Tampilkan postingan dengan label Guest Posts. Tampilkan semua postingan
Tampilkan postingan dengan label Guest Posts. Tampilkan semua postingan

The Man in the Mirror, by The Rogue Blogger in Compression Pants

Posted by Unknown Kamis, 16 Januari 2014 0 komentar
We haven't had a guest post in a while, and it feels like it's time for one. This one came to me from a fellow blogger who initially was going to use his name. I suggested he go rogue, just on the off chance that people take offense to what he has to say. I said rogue, of course, then told him that it meant he would have to wear tights for me to protect his secret identity.

He came up with compression pants as a compromise. Seems fair.

Without further discussion, his observations on why we don't always like what is staring back at us in the mirror, and why we are quick to lash out at others instead of entertaining the idea that they just might be right.

~~~~~~~~~~~~~~~~~~~~~~~~~~~

My wife and I were celebrating our anniversary a while back. We found a babysitter. We had an evening to ourselves, a rare luxury for us. At the restaurant we went to, there was a lounge singer and he was playing some of my favorite songs. One in particular, which I haven’t heard in a long time. One, which once again, struck a new chord with me. It was “Man in the Mirror” by Michael Jackson. Great song, right? Great message, right?

It is a brutally honest song. It got me thinking about looking at myself in the mirror.

Scary thing to do. 

Scary thing to look for. 

Looking at those times where I was given or gave myself a brutally honest assessment. I thought, during the height of each assessment, that ‘this person’ or ‘that person’ was an asshole for pointing out something in me that I didn’t agree with. 

That’s thing about mirrors. 

We only like them when they show us something we agree with. 

I had a run in with a ‘mirror’ a couple months ago. This mirror was my father-in-law. We were visiting the in-laws for the weekend and I was in desperate need of a vacation. Not a vacation at my in-laws. They are great people, but I really wanted some “me” time with my wife and kids. 

The entire weekend, I tried to relax, remove myself from the stress from work and watch the opening weekend of the NFL and get my fantasy football teams off to a good start. The kids were just being kids...but I was telling them ‘no’ and ‘stop’ and ‘don’t do that’ far more than I should have. I never saw it. 

My father-in-law did. 

After we got back home, my wife got a text from her Dad expressing his concern about my actions. We both over-reacted because of wording, but the message itself was sound. 

I was pissed, beyond pissed. 

I thought he was calling me a bad Dad. I thought he was being dick. I knew what caused him to say what he said, and I knew I was in the wrong and I knew he was just looking out for our family. I just didn’t want to see that at first. I just thought he was being an asshole, when in truth, he was just being a great Dad, a great grandfather and an honest mirror. 


I was the one being the asshole. I was the one playing off like I was wronged. I was a hypocrite. I was just trying to stroke my own ego. As a response, just to prove him wrong, I overcompensated my fatherly duties. Like, full on going out of my way and making it really obvious that I was overcompensating. He’s wrong. I am right. I am the victim here. If there ever was an award for ‘most asshole thing to do’, I won it and by a landslide.

Whenever I get in a mood, I think about that whole situation. With kids, it happens a lot. But knowing is half the battle (GI JOE!!) and sometimes getting the truth, whether you like it or not, really helps. Admitting to yourself that you need to change your ways is such an awesome feeling. Honestly, since then, I have made my life less about me and more about my family. 

I made a rule for myself to follow: don’t be a dick. 

It’s super easy to enforce. I am a better man for it, but most of all, I am a better father to my children. 

Life is full of mirrors. We call them honest and accurate when we agree with them. We call them hypocrites and assholes when we don’t.

The thing we don't always realize is that they always tell the truth whether we like it or not. 

When was the last time you truly looked into the mirror? When was the last time you changed your ways?

Baca Selengkapnya ....

Hey, Guess What??? My Mom Has Cancer.

Posted by Unknown Kamis, 09 Januari 2014 0 komentar
January is Cervical Cancer Awareness Month.

Cervical cancer used to be the leading cause of cancer death in women. Thanks to better screening, detection and treatment, survival rates have increased dramatically. Each year in the US, about 12,000 women are diagnosed with cervical cancer, and approximately 4,000 die from it. Most cases of cervical cancer are caused by the HPV virus, a disease most frequently spread through sexual contact.

A while back now, my friend Emily confided something in me. She told me that she had cervical cancer and then waved her hand around dismissively about how she had to have surgery again but it was no big deal, right?

NBD. Uh huh.

I knew it was a big deal then, but I sensed that what she needed at that moment was a really inappropriate joke, so I said something naughty about her lady bits and we laughed. Turns out that I was right. It's been a long few years filled with a roller coaster of emotions for her. I asked if she would be willing to share her story here and she was kind enough to oblige.

I must warn you, though, she is my friend. So she's totally inappropriate. And candid. And honest. And real.

This is her story.

~~~~~~~~~~

While I was sitting in Starbucks waiting for her to come in, I realized that I hadn't written down a list of questions to ask her. I figured that it wouldn't much matter since the two of us rarely have a hard time finding things to talk about, and this time, we had a specific topic.

A serious one.

We usually tell each other fart jokes.

No, I'm not kidding.

She sat down and I could tell she was nervous. This isn't a story that she has told many people, not even really to me, not in much detail anyway. I told her that I was completely unprepared and didn't write any questions down. She winked and whispered, my vagina still works. Everyone always wants to know about that!

Tension broken.

Before we got to the story, she promised herself she wasn't going to cry, immediately teared up, then told me why she hadn't really told anyone. It's a reason I completely understand.

She didn't tell anyone because she was afraid that if she said the words out loud that it would be real. It was easier to pretend like it wasn't happening when other people were none the wiser. If other people knew, they would ask how she was. She didn't know how she was and she didn't even want to think about it. She didn't lose her hair. She didn't have to go through chemo and radiation. She just had to have surgery, so she felt like it wasn't even a real cancer anyway. It was all weird and she didn't want it to be weirder than it already was.

It was easier to tough it out alone than to face reality and say the words out loud.

Em has three children, all boys. Her middle son is one of Mini-me's best friends in the whole wide world. They are just like peas and carrots.

None of their deliveries were simple or easy. She went septic after the first and needed an emergency hysterectomy immediately after the last was born through Cesarean section.

She has never really even processed the loss of her future fertility and admitted as much. This whole experience is forcing her to do it now. The finality of it all sinking in. At the time of the hysterectomy, the gynecologist removed her uterus and about half of her cervix, needing to leave part of it because of swelling.

A year and a half later, she needed to have the remaining portion of her cervix cauterized for bleeding.

She was always on top of her annual checkups and Pap smears. She had never had a single abnormal Pap.

In the fall of 2012, she knew she had to go in to the doctor to have her check up before her insurance stopped. She was in the middle of divorcing her husband and wanted to make everything was taken care of while she was still covered. Had the Pap on a Friday, got a phone call on the next Tuesday. Never a good sign. There was some concern.

She needed a biopsy.

It was cancer.

Confused, she asked him how could this happen? I've been married forever.

The answer? HPV can lie dormant for years, decades even, then show up and cause trouble without warning.

In some ways, the impending divorce saved her life.

Her doctor sat her down and talked about options. It was early, it hadn't spread. Instead of doing an invasive surgery, he could try and remove what was left of her cervix in an in-office procedure. As long as the margins were good, this might be all that was necessary. She agreed, had the procedure, almost all of the cervix was taken.

Of course she sent me a text with a picture of the pieces of her cervix in a jar.

Of course.


Because that is the kind of relationship we have.

The margins were clear, everything looked good. She was relieved and ready to move on with this scary episode behind her.

Three months later, she had to go in for a check up. She was supposed to be declared cancer-free. She wasn't.

The cancer was back and she was out of options. She had to have the full surgery.

She's now had four surgeries in four years.

This time, both fallopian tubes, one ovary and what was left of her cervix were removed. The procedure was slightly complicated by the fact that her cervix had fused to her bladder. The healing was rougher this time around. A few weeks later, I sat by the pool with her and told her really bad jokes. But not the kind that make you laugh too much because that hurts.

Some of the jokes just presented themselves through no fault of my own. And that's totally an inside thing.

Just after the surgery, she used the C word for the first time with her boys. They'd known that Mom was sick before, that sometimes she didn't feel good, but this was the first time that they were told what was actually going on.

The first time that Mom and cancer were put in the same sentence.

Trying to explain why she was emotionally all over the place, she told them that when women have hormone changes, like when they have a baby, their bodies can't always manage the changes well. Since one of her ovaries was taken out and her body wasn't really sure what was going on with the sudden hormone drop, she was crying a lot for no reason.

Her middle son went to Sunday School at church the next day and said this:

"My Mom has cancer but her body thinks she just had a baby."

She hadn't told hardly anyone at church anything, and all of a sudden had a lot of explaining to do.

As word began to spread, months after she had actually been diagnosed, she realized in a hurry that having other people know wasn't all that helpful. She still didn't want to talk about it.

There was more though, this other part of it, the fact that this is the type of cancer that carries a stigma with it. People make assumptions about women with cervical cancer, none of which ever applied to her. She was married, monogamous and had been religious about checkups. This wasn't supposed to happen to her.

But it did.

We talked about this aspect of it for a while, because we both feel like all the education towards vaccination against certain strains of HPV has actually attached more of a stigma to cervical cancer than there ever was in the past.

It isn't just a cancer that women get from a virus that most people carry as adults anymore, it's a cancer that women who have sex get from partners who are infected. It's an STD gone bad now.

Cervical cancer has always been most commonly caused by HPV. People have always had HPV, men and women. It's just that now everyone talks about it. Which is good in some ways, certainly, but bad in others because it makes this cancer more than just a disease...it makes it something that, to some degree, is shamed.

Think about it.

It's impossible to have any conversation about the vaccines without it turning into some religious debate about condoning promiscuity and teen sex. Married, monogamous women can still get HPV, can still get cancer, can still die. Period.

Emily is proof of it.

When asked what she wants people to know, aside from that truth, she said that just because you are married or monogamous does not mean that you should feel comfortable waiting longer between Pap smears. She had never had an abnormal result, and had been dutiful about annual exams, before her diagnosis.

Next month, she goes back again. For another checkup.

She's been to the checkup where everything was supposed to be fine and it wasn't. She's scared.

That's the thing about cancer that you learn the hard way. Once you have been there, you live in fear of it coming back. It changes everything.

If you want moral support, Em, I'll go with ya. I can't imagine what the doc would do with both of us there though. That's got to be too much inappropriateness for such a tiny room.

Thank you for being brave enough to share your story.

Love you.

Baca Selengkapnya ....

A Desperate State of Affairs, a Guest Post from Anonymous

Posted by Unknown Jumat, 20 Desember 2013 0 komentar
In this strange and beautiful online world, I have had occasion to meet some truly amazing people. This writer today, one of them. She needed to let these words out of her head, and she needed a safe place to do it. She asked if I would be willing to share her story here. 

With my deepest love and respect, a tale of what it's like to live with and love someone with mental illness, with physical illness, and how hard it is to keep what affects them from defining who you are.

Thank you for sharing your story, my friend. I sincerely hope that you gain some peace by setting the words free.


~~~~~~~~~~~~~~~~~

A Desperate State of Affairs

I once made a friend the most incredibly stupid promise. Back when I was naïve, ignorant and pompous. I truly hadn’t the experience to make such a promise, and yet, with righteous indignation in my heart (and not one CLUE in my mind) I went ahead and made it: “I’ll never locate my self-esteem in my husband.”

What. A. Dickhead.

I had absolutely no business to be making such idiotic pronouncements – at the time, I wasn’t even married, for goodness sake! I was engaged; young, stupid, in love and yet still full of that sense of self which (semi)confident single-dom can bring.

We got married, and in my blinkered state, I managed to ignore that he was stressed beyond all reason. I was irritated at him, but chalked it down to the challenges of his job and the amount of organizing required by the mere act of getting married. We were both looking forward to married life. And its benefits – one above all (and yet untried by either of us).

Sex.

Through the historical strength of our individual convictions and our joint agreement to save ourselves until we had tied the knot, the limits of our temptations were tested and we waited.

The Wedding Night loomed. And in spite of all the stress and tiredness, it was good. I mean, it was nice. It was a very steep learning curve. But, ya know, the earth moved and we both had fits of the giggles and all was well. We congratulated ourselves on our first time being with each other, and reiterated how much we wanted to share the learning on this journey into a hitherto unexplored area of adulthood. We were happy.

I was dumb.

Because shortly after that, things began to go pear-shaped. Or at least, (if we’re using fruit analogies) not ‘nice, big, banana-shaped’. And gradually the realisation that having a spouse with relatively freshly diagnosed Type 1 Diabetes was a bit of a pain in the ass. It impacted HUGELY on his ability to function. Blood sugar too high? Say goodbye to sexy-fun-time. Blood sugar too low? Say hello to shaking and panic and urgent guttling of sugar while the furthest thing from anyone’s mind was their loins.

But there was more to it than even the diabetes. And as our (sadly already meager) sex life waned, illness and depression kicked in, and a long, awful slog towards an eventual diagnosis of autoimmune disorders gone mad and a broken endocrine system, leaving my poor husband with clinical depression, no energy, no spirit, and no spunk.

And because of the pressure (real? imagined?) of sex, he managed to develop a nasty little psycho sexual disorder into the bargain. When he (so, so rarely) was up for it, the chances of everything working as it should were so slim that the frustration of that expectation and the unhappiness of previous ‘failures’ would likely nix any chance of him achieving his happy place.

We began to argue more, and became distant from one another. I started to seek him less, taking matters into my own hands.

I nearly left him just before his diagnosis, and once we found out what was wrong with him, I thanked my lucky stars that I hadn’t gone off to seek a life of hedonism elsewhere, because in spite of my loneliness and wandering mind, deep down, I wanted him fixed – I wanted him back to the guy I fell for. I wanted us to grow old together.

Alas. The diagnosis held horror in store. His condition was treatable, but (because of the nature of the hormonal feedback loops, which are the mechanics of the endocrine system) the treatment would render him permanently infertile.

The doctors stayed the final medication to allow us to try for a child. I wavered, pondering the common sense of bringing a child into a world where his father was so unstable he’d already tried to kill himself twice (as I found out, one chilling day when I accompanied him to a doctor’s appointment to lend moral support). And yet…the idea of not having a child at all trumped everything, and we got busy (now cursing all former ideas of ‘having some time just to ourselves’ and anyone who’d ever told us ‘don’t start a family straight away’).

I found out that I was pregnant. And lost the baby mere weeks in. I was devastated. And he didn’t understand at all. To him it was a loss of potential. To me it was our dear child, whom we had longed for. I was so angry at him, and so hurt. And he so didn’t care, because the depression had taken root deep in his soul.

Eventually I got over my panic that sex might lead to another loss, and we tried again. With the same stumbling, awkward, pressurized, sometimes-ending-in-failure-and-tears methods we’d been used to. And four months later I was pregnant again. And then I wasn’t. Again.

We danced another dance of devastation and depression and wedges driven between us. And all the time, the deadline of that enforced infertility was moving ever-closer. When all of a sudden it hit us amidships, ahead of schedule, when a sperm count found one. solitary. sperm. No medication required. Just brokenness.

We both fell apart, but individually, and turned on each other instead of being able to offer comfort. I couldn’t tell him how upset I was because his guilt at making me upset would overwhelm him, and then my sorrow was transformed into a perceived attack on him and I lived in constant fear that he would try to kill himself again. He immersed himself in computer games, inappropriate amounts of sleep, and endless toy soldiers. No babies were getting tried for, and I could barely stand the sight of him.

The feeling was apparently almost mutual, because on the rare occasion I did feel that insistent yearning for some intimacy and the chance to ride the crest of our union into oblivious bliss, he was disinclined to participate. I vividly remember buying some new, vaguely sexy underwear and showing him, desperately hopeful that his interest would be piqued, but he murmured something vaguely placatory, then got all excited showing me his latest painted man-dolly; not caring – not able to care - that I was missing him or craving his
touch or falling rapidly out of love with him. The depression ruined all of it. We’d not been together for so long I wondered if my virginity was growing back.

And the rejection began to sink in, tapping into deep hurts from childhood, where my self-esteem and my physical appearance were consistently, wilfully, maliciously undermined by my father, who suffered the same brand of mental illness as had my husband in its grasp. The internal voices began rearing their vicious heads again “You’re so ugly. So fat. So disgusting. Even your husband doesn’t want you. No-one could ever desire you. No-one could possibly find you attractive – you’re repulsive, just give up. Don’t even try; there’s no point. Just LOOK at yourself in the mirror? Why would anyone ever fancy you? You’re vile.”

On and on and on they played, driving me near to the brink of succumbing to the depression myself! I admitted some responsibility and started trying to get healthier, slimmer, stronger (and hopefully, more attractive – at the same time feeling terrible about how vain and shallow I was being). Alas, even my shrinking figure was not enough to tempt him. It wasn’t about my size – it was about me. I was a terrible, unattractive, crap wife, and even when I made an effort, I couldn’t get him in the mood.

When you get married, you truly do hope that the one person who will always (or at least most of the time) find you desirable is the one who’s promised to love you forever. And when that person consistently would rather be dead, than alive and married to you, no matter what stupid-ass promises you made so flippantly all those years ago, your self-esteem will be BURIED. My sense of self-worth, already low, plummeted.

I gave up trying to get him in the mood. I focused on getting fitter for myself. So that I felt happy with the way I looked. Whenever one of my friends congratulated me on my success, or paid me a compliment, I brushed it off, but stored the words in my heart, beginning to think that perhaps I’d cracked it – maybe I was finally becoming the person I wanted to be – an attractive one. And slowly, the impetus of those friendly compliments increased, and my self-confidence began to grow.

But alas, the success was double-edged, and my slimmer, fitter self was still not enough to get him interested. It did get someone else interested though, which was in equal measures flattering and unsettling; because it was a friend who was very dear to me, and when she wrote me a letter simultaneously coming out to me and declaring that she had ‘far more than just a crush’ on me, my world got very confusing.

The guy I wanted had only indifference for me, and the girl I never sought, had anything but. And I was caught in the middle, pleased to have been found attractive (if by the wrong person) and wondering what on earth to do.

I shut them both out, unable to cope, and went seeking my validation in (marginally) less harmless ways, becoming an incorrigible flirt; enjoying the thrill of suggestion without promise and the return of the same. Meanwhile I was still awash with grief at my losses, the impending membership of the ‘Can’t Have Kids’ club, the lack of any kind of movement on the ‘Trying To Have Kids’ status and at the train wreck of my marriage, and I continued trying to get fitter (more beautiful? nah.), allowing myself to run in the dark, alone, deep in my tortured thoughts.

Because there was no way I could justify an affair. Even if I wanted one; craved one; was desperate to be desired and found womanly and attractive. And there was no way I could allow my desire for a baby, coupled with my need to be found desirable, to ruin the marriage I’d vowed to stay faithful to. But what if *something* happened to me, one night, in a dark corner of the city, which wasn’t my fault…which lifted all responsibility from me…which left me pregnant…what then?

Such shame. Such anger, that those kinds of thoughts were even entering my brain and at the same time, the idea of a completely guilt-free dalliance was alluring. I kept running alone, knowing all the while that the reality of that situation would be vastly removed from my sanitized fantasies. Fortunately, it never happened.
I went back to flirting with other people, instead. And things still weren’t fixed between my husband and I. But gradually, slowly, they began to improve. He finally got some much-needed help and the depression lifted ever-so slightly. I was 50lb lighter, far more pleasing to the eye (even to my own) and much fitter. But there was still the matter of sex, which is meant to bring such joy and unity in marriage, and which was so missing from ours. He was offered psycho sexual counselling to help overcome all the hooked-in negatives which accompanied the act for him. But he declined, unilaterally deciding that if he was beginning to be less depressed, he wouldn’t need it.

Except that I think he does.

And our baby deadline is February.

And I just don’t think it’s going to happen. And guess what, folks, there’s a whole vicious cycle right there – because if I’m stressed, I’m less likely to conceive. I’m also less likely to be ‘in the mood’. And as it frequently still takes a great deal of input on my part to get the mood going, guess what’s not happening…

We are truly (un)fucked.

And in spite of things (and one rather important one) being largely ‘on the up’, to quote a rather good movie – “It will all be alright in the end, and if it is not alright, then it is not yet the end.” - I know it’s not yet the end…because it’s really not all alright.

And I’m not sure I can see how it’s going to be.

But at least I look good.

Baca Selengkapnya ....

Type 2 Diabetes - Living With and Loving Those Who Have It ~ Stories of Family Members

Posted by Unknown Jumat, 15 November 2013 0 komentar
My deepest and most sincere gratitude to those who were willing to share their stories with me. Diabetes is a complex disease as it is, but the fact that so many people have an emotional relationship with food makes it worse. Add in the fact that food is a necessity to survive, and it becomes more so. We have to eat. Having diabetes just makes every meal difficult. Every choice becomes important. Every indulgence dangerous. The food you need to survive could be the very thing that kills you. 

Some people can't accept the lifestyle changes that are part of this disease. Some pretend they don't have it, minimize it's impact in their lives, convince themselves that they will escape the complications that happen to other people.  

With love and respect, their stories.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

My dad was diagnosed as diabetic at age 66. My mother had suspected for about 5 years that he was becoming diabetic. There were 2 problems in getting a proper diagnosis: He is extremely doctor-phobic, and he was getting close to retirement. Since mom prepares all of his meals due to his severe food allergies, she started trying to regulate his diet as much as possible. Also she made him cut down on sugary drinks and snacks. After he retired she finally got him to see a doctor.

She told the doctor all her observations and had to basically bully the doctor into doing a blood test because "I couldn't possibly know what I was talking about." Yeah Dad's blood sugar was in the 500s. Mom got a LOT more respect from the doctor at that point.

It took Dad about 3 years from diagnosis to be able to say "I'm diabetic." Mom did all the meter stuff, charted how well each different medication worked and consulted with the doctor until they found the right "mix". She still regulates his diet, hands him his meds on schedule, all that stuff.

Unfortunately, going that long undiagnosed had a very bad effect on Dad's eyesight, to the point that he can no longer drive and has trouble seeing large print. I'm sure there are other complications that they haven't shared with me.
- Joy

~~~~~~~~~~~~~~~~~~~~~~~~~~

I'm not totally sure where to start. My step dad, Bill Boye, came into my life when I was 15 yrs old. Since I had a strained relationship with my real father, Bill immediately became my hero. He had already been diagnosed with type 2 diabetes for about 15 yrs at that point. He and my mom got engaged, he moved into our house, that's when diabetes really became a part of my life. Blood glucose meters on counters, watching carbs and sugar grams on packages, seeing the different attitudes with the different sugar levels. Bill always said "I don't drink alcohol because I'm diabetic" .. Yet he was the 1st in line for chocolate cake. Regardless of his illness Bill was my rock, he supported me thru so MANY things, defended me when I made mistakes, lifted me up higher for my accomplishments. He encouraged me to apply for a dispatcher position w/ SDPD, I did and got the job, he was soooo proud. He was my DAD. 

As the years went on, Bill continued to not mind his diet, his weight was never under control. He ate junk food in secret, his car was full of wrappers and trash that he tried to hide from the family. My mom would get so frustrated, all of us would. We'd lecture, cook him meals, make him walk with us.. But just like leading a horse to water ... You can't force someone to take care of themselves. When I was 25 my real father died, February of 2003, hardest month of my life, so many unresolved issues and I felt like he didn't know I loved him. Bill hugged me, told me he loved me & he knew my dad was my angel. Then Bill got sick, ended up having quadruple bypass, heart valve replacement surgery. I went to see him after surgery & he didn't know me.. It was devastation all over again. He did recover though, thank god. He was forced to stop being a patrol officer, a job that defined who he was, he went to a desk job, retiring within 2 yrs. Even after his surgery he didn't eat right, didn't exercise. His legs were so sore and his circulation so bad that he got his 1st gangrenous sore, it was disgusting and painful. It healed slightly, but never fully. 

He and my mom decided to move from sunny SoCal to the wilds of Idaho, well Cour D'Alene, for their retirement. Very far from all their SoCal family, but something they wanted to experience. During the brief 3 yrs they lived there Bill became totally insulin dependent, but just didn't want to take it, he would take his oral meds, just not injections. He then went into total renal failure, got another gangrenous sore on his leg, this one led to an amputation just above his left knee. He rehab'd, sorta, he refused to try the prosthetic leg, stopped showering regularly, refused to shave his face. He became VERY depressed.

My mom and he moved back to San Diego, she needed her family to support & help her. 

My mom injured herself lifting his wheelchair in and out of her SUV, I had to go over there and help any time he needed to go somewhere. Of course, I did it, but it was hard.. I was a single mom who worked at least 50 hrs a week, I lived 30 mins from their house. I was the only one who he allowed to take him for haircuts, I shaved his face on a regular basis. I put diabetic lotion on his hands. My mom became very depressed. As mothers and daughters will do we fought. I got really mad at her and she got really mad at me. That was the weekend of July 4th, 2009. Bill was facing an amputation, from gangrene on his right hand. I had yelled at my mom to go see a counselor and get on depression meds. She left, Bill and I were alone, I convinced him to let me clean up his haircut and shave his beard. We chatted about a SWAT incident that I had worked and he had seen on tv. We laughed, I left for work. My mom left for a weekend at her moms, about 75 miles away in Hemet,CA. That Monday, she called me, I almost hit ignore for the call, but answered. All she said was "baby I need you, Billy is being transported to the hospital from dialysis. It doesn't sound good." I made it the 30 miles to her house in 15 minutes. We drove to the hospital and learned he had died from a massive heart attack. He was only 65 yrs old. 

I still think of him daily, I just got married this past Sunday and dedicated a "memorial" table with pictures of Bill, my father Dave and my grandpa, John. My husband reminds me SO MUCH of Bill. He's a police officer, he smiles just like Bill, he'd give you the shirt off his back just like Bill.. He however takes care of his type 2 diabetes with diet. Yup.. I married a man with type 2, even living thru that nightmare, I know that some can own the disease.. Eric is one of those. 

- Amber Miller

~~~~~~~~~~~~~~~~~~~~~~~~~~~~

My family has a history of diabetes. Two of my Aunts had it and had heart problems and strokes eventually. My older brother has recently been diagnosed with it and it's like he's given up. He won't walk anywhere, he rides a scooter. He's only 50. He won't come to family occasions anymore because he can't get the scooter up my 5 porch stairs. His legs are starting to swell probably due to inactivity and he's had a pacemaker put in. All in the past year. 

When they try to take him off his pain meds he throws a fit and won't take his other meds until he's back in the hospital again and gets more. He used to complain that no one would help him and then we finally got him some help and insurance and it seems like he's just gotten worse. He's getting to the point where he's getting does on his feet all the time and he could get nerve damage if the swelling continues. 

My younger sister also has diabetes and she has to use catheters to pee, she's only 40. She had to check her sugar at least twice a day and hers can go either way so she had to carry glucose tablets with her. 

Lately when I go to my Dr, she keeps checking my sugar, says it's fine, has ran blood tests that came back fine, but she still lectures me on diabetes. I find it very stressful and it's causing me to stress eat, lol. I actually want to avoid the Dr now cause I don't want the dumb diabetes lecture. I know about it. I see it everyday. I thought about switching Drs and decided that I was going to discuss it with her at my next appointment instead.
- Melissa

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My husband has been having medical issues lately. His last lab test showed sugar in his urine. Having a daughter with Type 1 Diabetes, we knew what that meant. The doctor was not diagnosing it yet and wanted to do an A1c test. 

The A1C showed slight elevation but the doctor still was not confirming what was inevitable. Meanwhile, our daughter's Diabetic Alert Dog started catching blood sugars over 200 in my husband. With the dog being able to find the high blood sugars and reporting it to the doctor, my husband was able to be diagnosed much sooner and we could start taking care of it right away.
- Anonymous

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Type 1 Diabetes - The Kids Were Old Enough to Know Something Was Wrong

Posted by Unknown Kamis, 07 November 2013 0 komentar
Today I am sharing the stories from two T1 Moms, about how their children were diagnosed with diabetes. I opted to run them together because there were so many similarities in the stories.

The lessons to take away here are these: know the symptoms and understand that most of them are totally non-specific, when in doubt always always always just go to the doctor just in case it is something to worry about and never underestimate the ability of a child to tell you that something is wrong.

I love both of these ladies, and they have both been tremendously supportive to me and my son in the past year. With love and respect, their stories.
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During the Christmas break of 2011, my son started to have issues with his stomach. Food started to not settle. Anything touching it, would come back up or hurt staying down. Should have been the first red flag. I didn't know. The month or so following that break, he spent either in his room sleeping or at school. He was 12, I thought he was either having a growth spurt or puberty was showing its ugly head. So, when he started losing weight because of the lack of desire for food and sleeping all the time, I blamed puberty. Second red flag. I didn't notice more thirst. I didn't notice more bathroom breaks.


February 6th, 2012. I got a phone call from the school nurse. She told me that she had a talk with my son. He had come to see her by way of the school psychologist. I found out he had gone to see the psychologist because he didn't feel well and he didn't think we (his parents) were listening to him. So he did something about it. And the psychologist took him to the nurse. Who in turn, called me at work. We talked about what was going on. I told her what I thought was going on. Puberty, and maybe a cold? I didn't know, so I agreed that he should be seen by his doctor. I got off the phone with the nurse from school and promptly called the doctor. That was a Monday. He got an appointment for Friday, February 10th.


I took him to the doctor. Told him all the things going on, and he ordered blood work and urinalysis. Now, my son is terrified of needles. Especially shots and draws from the arm. This was agonizing for him, damn near panic attack. We went back to the exam room. We waited. We joked. We laughed. Then the doctor came back in. He looked at my son. He looked at me. Then he said that my son was in something called Diabetic Ketoacidosis. And we needed to go directly to the Children's Hospital. Essentially his body was eating itself to keep going. My heart stopped. My brain exploded. My perfect baby. My 12 year old son HAS DIABETES.


He was in the hospital for a week. It took that long to bring his numbers down. And to educate him, as well as us. He learned what to do and when. He learned from endocrinologists. He learned from dietitians. He talked to pediatric psychologists. The Children's Hospital was AMAZING.


HE SAVED HIS OWN LIFE. HE did it. He talked to people until someone heard him. And for that I will forever be grateful.


Things don't always present with clear cut symptoms. Excessive drinking and peeing are classic indicators. But I didn't see them. I missed the other flags. I missed it all. I failed my son. My guilt over my part will never lessen. But my pride in my son? Never will diminish. He is amazing. He can calculate his ratios in his head, without a calculator. He still panics with a shot, or IV, or blood draw. BUT he does his testing on his fingers for his daily testing with no issue. Yes, he hits bottom from time to time. Yes, his numbers go all wonky when he's sick. BUT this is not the sum of him. He is NOT defined by his pancreas's inability to produce insulin.

- Anonymous


My daughter, Laura, turned 11 on February 11 2010. She played softball on 2 teams. The little league and a travel ball team. One Saturday in March she came to me carrying a laptop and crying. When I asked her what was wrong she showed me the web page on the laptop. It was web MD's symptoms of type 1 diabetes. 

She told me that she thought she had diabetes and she was scared. 

I read through the symptoms rationalizing each one for her. She drank a lot of water because she did softball practice/conditioning almost all year round. She went to the bathroom a lot because she drank so much water. Tiredness was also a result of softball. Her skin was breaking out because puberty. Don't worry, I told her. You are fine. 

The following Friday we were at softball practice and I had been noticing for a couple days that she looked taller or thinner. I asked a couple softball moms if they noticed the change in Laura. All the moms agreed she looked different. Laura was also white as a ghost. It was flu season, but I had gotten her the brand spanking new controversial swine flu vaccine a few months before because people were in a panic. Children were dying from that flu! So, I quickly ruled out the flu. 

While practicing it became obvious that there was something not right. She was slow and clumsy. She kept stopping to go to the water fountain in the gym. She was gasping for breath. The coach called a break and Laura came to get a bottle of water. She was shaking so bad that she spilled it down the front of her trying to drink it. The other moms and I looked at each other. One mom then told me Laura had been giving her food away at school. She hadn't eaten lunch all week. Immediately, I thought anorexia and I was scared. The coach's wife had a bag of peanut M&Ms and offered some to Laura. She ate a few, but said she didn't feel well. I decided we would leave practice early, and I told Laura that I wanted her to eat dinner. I would buy her whatever she wanted as long as she would eat. She chose peanut butter and banana sandwich with strawberries on the side. She ate half a sandwich and a few strawberries and went to bed. About 1 AM she woke me up because she had vomited. She was upset because she didn't make it to the bathroom in time. Of course I told her it was all right and got everything cleaned up. 

I knew for sure then that she had the flu, and had never been so thankful for my kid to have it. Saturday morning she woke up, ate a handful of dry cereal, and drank some ginger ale. She said her stomach felt better. I thought everything was A OK. About 20 minutes later she came to me shaking uncontrollably. She said "Mom, I'm shaking and I can't stop and I don't know why." I put her in the car and drove as fast as I could to the nearest hospital. 

By the time we got there, Laura's speech was slurred and she couldn't pick her feet up off the ground when she walked. The ER took her straight back, and instead of a nurse asking questions there was a doctor. I had to sign forms for spinal taps and blood work and god only knows what else. They hung an IV of fluids and drew tube after tube if blood. 20 minutes later, a nurse came in and said they had to stop the IV. I asked why and the nurse said that the doctor would be in shortly. 

When the doctor came in she told me my daughter's blood sugar was over 600. Her potassium was off, her blood pressure was high, her heart rate was too fast, she was in DKA. My daughter was dying right in front of my eyes. By this time she was in and out of consciousness. The hospital we went to did not have a peds endocrinologist so Laura had to be transported by ambulance to a children's hospital 2 hours away. 

We spent 5 days in pediatric ICU learning how to count carbs and give injections. It took those 5 days to clear the ketones out of my daughter's system and to get her potassium back to normal levels. It has been almost 4 years since her diagnosis. She is still deemed "uncontrolled" because her blood glucose levels swing from high to low to back again. 

A few years ago she would have been called a "brittle" diabetic. She has not let diabetes stop her. The day after she was released from PICU she went to softball practice. I will never get over the guilt of not believing her when she came to me with that laptop, but who would have believed a 11 year old could self diagnose Type 1 diabetes? Who wants to believe their child has an illness that can kill them without rhyme or reason? 

For the record, Laura had a physical in January for sports. She was given a clean bill of health. I recommend asking your pediatrician to do a simple finger stick if you suspect type 1. So many children die because they go undiagnosed. I would have lost my daughter if I had waited one more day. If you can't get your doctor to do a finger prick, go to Walmart and buy a blood glucose meter (Walmart has their own brand that is very inexpensive and the strips are as well) and do your own finger prick. Be proactive!! Be aware!! Don't let your child become a statistic like I almost did.

- Jerri Lynn

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I live with juvenile diabetes everyday, but....a guest post from Marlo from Nightdreams and Daymares

Posted by Unknown Senin, 04 November 2013 0 komentar
I live with juvenile diabetes everyday. But, I do not check my child’s sugars.

I live with juvenile diabetes everyday. But, I do not wake up to do 3 a.m. checks.

I live with juvenile diabetes everyday. But, I so not have to worry about keeping insulin cool.

I live with juvenile diabetes everyday. But, I do not have to worry about keeping pump supplies on hand.

I live with juvenile diabetes everyday. But, I sleep through the night without worrying if my child will be awake in the morning. Because she is already dead. You read that correctly. The last time I spoke to my daughter was September 15, 2011.


Sarah was diagnosed with diabetes January 6, 2005. She had just turned 8. It was the first week back to school after Christmas vacation. She had been getting up in the middle of the night and having accidents on just in front of the bathroom door. Early afternoon, I called her father and told him that I thought she might have a bladder infection or something of the nature. And, since it was Thursday and the doctor’s office closed at noon the next day, I wondered if we should go ahead and get her an appointment. We decided that if she did it again that night that we would take her in the morning.

That was until I received a phone call from Sarah’s teacher. She fell asleep standing up in the hall. Granted the kids had been tired most of the week, but this was Thursday. Something was off. I told her I was going to call the doctor and I would get back in touch with the school. I called the doctor’s office and explained what was going on.

“Get her here NOW.” It is incredibly frightening to hear a nurse be that adamant. I went to pick her up from school and take her to the office. They tried to draw her blood. It did not go well. Normally, she did not like needles. But, this wasn’t like her. Her father was about three minutes away. So, I called him and he came running. It took him laying over her 8 year old body talking her down, me holding down her feet and a nurse holding down her arm so that the second nurse could draw the blood.

After a short wait, the doctor came in and broke the news to us. We took it very calmly. Our closest endocrinologist was in Abilene, where I worked. It was twenty-five miles of so from home and the hospital. And, he would out of town until the following Monday. So, she was being admitted to our local hospital until we could get her sugar down to a more manageable number. She was in the mid-six hundreds at the time. By then, the other doctor would be back and we could transfer her to the children’s wing in Abilene. Up until this time, I was doing well.

It suddenly occurred to me that I needed to call my place of work and let them know what was going on. And, that I wasn’t sure when I would be back. I was blessed to have wonderful bosses that encouraged and expected you to put your family first. I did fine until I called them. The phones would go to voicemail at 5:30 and it was around 5:25. I dialed calmly. But, as soon as the girl answered the phone, I went into a tail spin. I was not making any sense. She put me on hold and transferred me to my boss. It gave me a moment to get myself together. “Sarah has diabetes.” I got the words out. My life was never the same.

Over the next seven years or so, we went through all sorts of trials and tribulations. There were the fights to get her to eat when she was sick. (When you are diabetic, you don’t have the option of letting your child be nauseated. It is life threatening.) There were the last minute realizations that you are down to your last syringe at 8:45. And, you are 20 minutes from the nearest pharmacy. So, you start digging in the cabinets while calling all of the grandparents to see if they have left at their house. The debating over whether to go trick or treating or not, since she can not just gorge on her candy like other kids. The not wanting to let her go to sleep overs for fear that her sugars would drop.

Not every diabetic reacts the same way to highs and lows. When he sugar would drop really fast, Sarah would have seizures. Her first one happened at 5 in the morning. I remember the morning very clearly. Her little brother had come into our room at 4:30 in the morning saying he couldn’t sleep. I sent him back to lie down. Half an hour later, I heard him walking back down the hall. I decided to go take him back to bed and maybe lay down with him or a bit. But, I realized that was not what I was hearing. I looked in Sarah’s room. She was having a full blown seizure. She had a day bed and her right arm was stiff and she was hitting her bed and wall with it. I do not think I have ever been so scared in my life. We rushed her to the ER. The guess is that her sugar went to somewhere in the mid-twenties. I rode in the ambulance to the hospital in Abilene, again. Her insulin was adjusted and we moved on. But, when her sugar would plummet, she would have a seizure. And, the oddest things would cause it to drop. Bad weather would even do it since she would get rather freaked out by it.

There is something upsetting about being calm when your child has a seizure. After the first couple, it becomes habit. Make sure they aren’t hurting themselves, check their sugar and get sugar in their system. It happened at the most inconvenient times, too. She had one in the computer lab at school. Not long after her father and I separated, he called from our local Walmart because she had one in the front of the store. The employees and fellow customers were awesome. But, yeah, we were “used” to seizures.

We will never know why she had her last one. All anyone can figure is that it may have been a result of having so many before. Her sugar did not drop. And, her heart had an arrhythmia. She never woke up. I received a call from her step mother that they had to call the ambulance and that they had to do CPR. Somehow, it just didn’t occur to me that she was dead. In hindsight, I should have known. But, it didn’t. Sarah’s father was driving in from out of state by himself. Luckily, he was a member of the local volunteer fire department for where he lives with the kids. So, there were people there to be with her step-mother and brothers until I could get there.

I walked into the ER waiting room and was told to sit down. “We tried everything we could.” I don’t remember much past that. There was crying and primal screaming. I terrified my son. He ran out of the room. I thought that someone had taken them out. But, he told me later that her left on his own. We had scared him.

They had to wait until I got there to actually say she was dead. 

They were as tactful and kind as they could be. Since she was a child, the Justice of the Peace had to talk to me and explain that they had to do an autopsy. I was calm for a good bit of the day. But, the rest of the time I was writhing in the floor crying.

That was two years ago. I still live with diabetes to this day. It took my child. If you think that your child might possibly have the most remote chance that your child, or if you are showing any signs that something is wrong. GET TO THE DOCTOR. Or, even go to the store to the glucometer and some strips. Checking a person’s sugar is simple. And, it barely hurts. There are small children that check their own every day. So, suck it up and do it.

If you have a child in your family that you think the parents are exaggerating and that it’s not a big deal to let
them have candy, STOP IT. There is not a parent on the planet that withholds sugar to be mean. They do it for their child’s health. Ask questions. As a diabetic parent, it’s the people that do not ask questions when they are going to keep our children that make us nervous.

This is serious business. A person’s life can be at stake. Don’t let the last picture of your child be one of their coffin.


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I came to know Marlo through a mutual friend a few months back when I was struggling with my youngest child's possible diagnosis of Type 1 Diabetes. 

She is a talented writer as you can already tell, and you can find her on her blog, Nightdreams and Daymares here and on her Facebook page here

I've come to know many people who deal with this condition daily, many of them the mothers of children living with it. Most of them tell me to be strong and be brave and that everything will be okay. 

She never did. 

She told me that this disease was something to be afraid of. That it is a big deal. That it will certainly change our lives, that it could end his. She told me to be strong and brave, yes...but she knows better than anyone that things may not always be okay.

I have had to deal with a great many people in the past year who don't understand T1. Who can't figure out why I carry a glucometer around, why I have Smarties in my purse and water in my car all the time. Who wonder why I take my son aside quietly at school and poke him with a needle before he can have a snack in a class party. Who can't understand why he isn't allowed just one piece of candy right now. Who tell me to just calm down and stay positive. Who act like this isn't a big deal.

It's a big deal. It's a very big deal. T1 is life changing. It can be life ending. 

It is what makes us poke our kids while they sleep at night, what makes us watch them breathe, what puts us on edge when someone seems a little more thirsty than usual. These kids don't just get colds, because any weakness in their immune system sets their blood sugars soaring and dropping. 

Marlo is one of the strongest, bravest women I know. She tells her stories, she shares her experiences, she opens up her life, she shows us the scary, ugly, real side of this disease.

She does it for Sarah and for all the other kids out there, for their families and friends. 

Thank you, Marlo, from the bottom of my heart. 

Your girl would be so proud of you for sharing her story. xoxo

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Mental Health Awareness ~ Welcome to My Crazy, by Dinner and a Nervous Breakdown

Posted by Unknown Rabu, 30 Oktober 2013 0 komentar
This post has been a few weeks in the making, and it all started when we were still in the middle of Mental Health Awareness Week. This very talented woman reached out to me and asked if she could share her story. Please check out her blog and Facebook page
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I thought I would share my story. Or rather, stories. Maybe it will help someone, or maybe I will just feel better after purging all the bullshit. Either way; welcome to my crazy

Before I had even hit middle school, I was diagnosed with the following. Although some of it kind of smooshes together, and some of it didn’t have such tidy, convenient names back then, here they are in all their glory along with MY definition of each. *IMPORTANT DISCLAIMER* I am NOT a doctor or an expert in any capacity, and each of these may be experienced differently by different people.

Social Anxiety Disorder – Social anxiety disorder is not about being shy, socially awkward, or uncomfortable at your new boyfriend’s cousin’s wedding. Everyone experiences social settings with varying degrees of discomfort. SAD goes beyond awkward and uncomfortable into excruciating and impossible. The thought of being placed into a social situation in which they are expected to be normal and carry on conversations and mingle, sets the SAD sufferer into a tailspin of dread, panic and thinking of any possible way that to get out of it.

Seasonal Depression – Apparently also called Seasonal Affective Disorder, Seasonal Depression strikes its sufferers, well, seasonally. As fall sets in and the weather gets colder, the days get shorter and the dark gets darker, the bleak also gets bleaker. Winter is approaching and it feels like the days of sunshine and summertime are never, ever going to come back and you’re doomed to wander this cold world, dark and alone, forever. And no, I’m not exaggerating.

Generalized Anxiety Disorder – GAD is an affliction that is the most counterproductive of all, in my opinion. It’s a cycle. Worry causes stress, stress causes fear, sleeplessness, soreness of body and mind. The constant and overwhelming worrying about something makes it impossible to productively focus on, let alone fix, whatever you began worrying about in the first place. Problems set off the GAD cycle, and, The GAD causes its symptoms, which cause more problems which give you more to worry about. It’s never ending and completely exhausting.

Claustrophobia – Everyone knows that this is the fear of closed, or small, spaces. While no one particularly likes being closed in small spaces, claustrophobics simply cannot handle it and will alter their life in whatever ways possible to avoid it. At all costs. They cannot handle the thought of being trapped in an airplane, so no trips. Elevators are absolutely not acceptable, so lots of stairs. Doctor’s offices - small rooms, closed doors, - cause panic so we usually just don’t go. Hospital? Surgery? Ha! Prescribing an MRI or a CAT scan is like prescribing death.

Agoraphobia – The actual definition of agoraphobia is “fear of open spaces.” It comes from the greek word agora, meaning market. And no, the irony is not lost on me. From a mental health standpoint, agoraphobia has basically come to mean the fear of any situation that may cause panic. Large crowds, tall buildings, unfamiliar surroundings for some. Being lost, not knowing where to find a bathroom or being somewhere by yourself for others. Agoraphobia is an all encompassing disorder and affects everyone differently. And it’s my least favorite.

Panic attacks – For me, and for many, any of the above situations can cause panic attacks, and are in turn worsened by panic attacks. I know that’s confusing, but I will get into it more later. A Panic attack never looks or feels the same for different people, or even for the same people in different situations. I’ll do my best to explain the way a panic attack most often feels to me:

I usually feel it coming and it usually starts with a heightened awareness of everything in the room. All of the noises and voices are suddenly closer, right in my ears and echoing in my head. The walls close in, while any chance of escape seems nearly impossible. I am sure everyone is looking at me, if not talking about me. And no, I don’t give a half a fuck what any of these people think about me, but why are they doing this? I’m sweaty and crampy, or nauseous. Extremely hot or extremely cold. I may be sick, or I may shit myself (seriously) and oh my god I am going to die. If I were being rational I would know that I am not actually, but panic replaces rationality. So no, not exactly literally, but I am still going to die. Or I am not going to die, instead I am going to feel this way forever and wish I would die. Why is this happening? Why can’t I just be normal dammit?! Fuck this, get me out of here. Now. No, I can’t leave, then the panic wins. I have to fight it. Why do I have to fight it? Why can’t I just stay home, where this won’t ever happen again and I don’t ever have to feel like this again and oh my god just please make it stop. It’s never going to stop. I am going to die. Where’s the door? Where’s the bathroom? When can I leave without it being awkward and making them all look at me and talk about me more than they already are….

That’s the best I can do and it doesn’t even come close.

Now, before I get into my personal experiences, I have to say something. I’m sure this is going to piss some people off, but I’ve been pissed off about it for a long time, so suck it up. If you feel like you have some kind of a disorder, please, please talk to somebody and get help. Please. But it you don’t – shut the fuck up. Allow me to explain; if you don’t like spiders, you do not have arachnophobia. You just don’t like spiders. Now if you refuse to go into some places, no matter how badly you need to, or alter your life in dramatic ways in order to avoid any situation in which you may possibly encounter an 8 legged asshole, then you may actually have arachnophobia. In the same sense; shy people do not have SAD, people who worry do not have GAD and people who prefer summer do not have seasonal depression. In order for any of these to be an actual condition, they have to be extreme, usually irrational and cause excruciating consequences. Not be simply uncomfortable. Uncomfortable is life. Everybody is uncomfortable. It seems like it has become trendy as of late to claim some sort of mental disorder or another. Everyone and their little sister has Generalized Anxiety Disorder now, or gets Panic Attacks. These are not things I would wish on my worst enemy, let alone want to have myself. Believe me, you DO NOT WANT this! Why pretend, or exaggerate, so that it looks like you have this? Seriously? Why? I think it is a result of drug companies and doctors. Someone has to be labeled in order to be medicated, and the more prescriptions they write the more money they make. But the whole thing makes me sick. The result is that those of us genuinely affected are not taken seriously. Try to tell someone that you suffer from a disorder that has exponentially hindered you in your life, and have them say, “Oh, me too.” Really? No.

Okay, rant over. You’re still here? Awesome. Lets continue.

Now, medication is usually viewed as the first and sometimes only treatment. Xanax, Valuim, Paxil, Effexor, Ativan and on and on and on. You’ve heard of them, I’m sure. You may take them. You may love them. I do not. I am on no medication. My opinion is that we are, as a society, completely over medicated and that these drugs do more to mask the problems, and zombify us, than to fix anything. While in some cases, medication may be a necessity, behavior modification, thought control and therapy are much more effective and may actually treat the issue instead of chemically covering it up. Though I do feel that medication has its purpose, that purpose is NOT in me. It’s not because I’m so strong, I don’t need drugs, I am going to fight this on my own. Nope. Most of the time I would so much rather pop a pill and have it go away. But I can’t. I literally cannot handle drugs. You know that little insert that comes with all the prescriptions? The one with the tiny print that lists all of the things that could possibly happen as a side effect? All of the things that could possibly go wrong? That list might as well be titled ALL OF THIS SHIT IS ABSOLUTELY GOING TO HAPPEN AS SOON AS YOU INGEST THIS PILL on anything prescribed to me.

I took Zoloft once. The doctor had been begging me to get on it for months,, and he finally convinced me by saying that it would likely lessen my panic attacks and my migraines. “I am going to get sick” I told him. “Just take it for 3 months and we will see” he responded. Okay. Here goes nothing. He gave me 25 milligrams, and I broke them in half. 12.5 milligrams a day. I was in bed for 2 weeks. I couldn’t eat, couldn’t really sleep, but couldn’t get up. I was nauseous and puking. It was like the worst flu AND hangover I had ever had, combined with not being able to grab onto any one thought for too long. I muscled through those miserable 2 weeks. By the third week I could get up, I could eat a little, but I was still all fuzzy, not really present. After a month I was almost normal, just felt a little disconnected. But if I forgot a pill, took one too early or too late, I was sick again. I sucked it up for 3 months, because I said I would. It did reduce my panic attacks and my migraines, but at the end of it all, I just couldn’t take it. My body does not like drugs.

So I’m pretty much on my own here.

All of these conditions that I have, essentially like to come out and play with each other and cause a clusterfuck for me. I’m going to try to keep it all straight, but sometimes you can’t. And by the end of this piece, you will see that they are all pretty much one big mess anyway.

I had my first panic attack in kindergarten. Of course, I didn’t know at the time that I was having a panic attack; I just thought that the entire world had flipped the fuck out and attacked me for a while. I told my mom about it and she brushed it off, said it was nothing and wouldn’t happen again. Mama didn’t respond this way to be heartless. You see, my 5 year old self had just explained to my mother her own worst nightmare. She had been suffering from her own panic disorders, to the point where she had been unable to leave the house for a period of years, and she thought that if she didn’t give it a name for me, didn’t give it any credibility, didn’t “feed the beast” I guess, then it wouldn’t happen to her baby as it had been happening to her. Mama was wrong.

I was too young to process it all really. The horrible thing had happened when I was in school. I loved school, but the horrible thing happened while I was in school, so I didn’t want to go ever again. But I had to. It wasn’t as simple as school being the problem though. For the first time ever I was being asked to socialize, and I was discovering that I just couldn’t. This talking and playing together thing that all the other kids were just effortlessly doing, was absolutely not working for me. I couldn’t. Welcome Social Anxiety Disorder. I was being asked to accomplish new things and follow new directions. I was a very smart kid, and certainly capable of all that they were asking me to do. But suddenly I was worried. What if I didn’t make my letters right? What if Suzy was better at coloring than me? What if I actually wasn’t smart, and I was doing it all completely wrong and everyone knew it? Welcome Generalized Anxiety Disorder. And as a result, welcome the Panic Attack. See how they all smoosh together?

As a kid I learned that I couldn’t go to sleepovers – I’d make it until about 2 am before I called mom to come get me. I couldn’t do the afterschool functions like parties or dances – I literally made myself sick with the nerves of trying. I couldn’t raise my hand in class, join any clubs or play any sports – I would be expected to talk. Out loud. While everyone looked at me. No. Oral presentations were an absolute nightmare. I skipped school, talked my way out of it with the teacher, or just took the E even though I was a straight A student. All the things caused the panic attacks, and the attacks caused me to avoid all the things. Simple. Fast forward a few years to when I was a young teenager and throw in hormones and seasonal depression. Then I had all the things plus an overwhelming desire to not get out of bed. Ever again. My poor mother had to physically pull me out of bed more than once. And every year I missed so much school that they threatened to fail me.

At some point my mother accepted the fact that I was suffering from many of the same things she had been suffering from. She took me to a doctor, they put some names on some of my crazy and discovered that pills hate me. My dear, well intentioned mother gave me some advice. Again, she was doing the best that she could with what she had. It went something like this;

“It’s a mental thing, honey. The panic attacks are going to happen all the time. Anytime there are too many people or too much noise, or sometimes for no reason at all. Try to fight through it. You’re not really going to die. It just feels like it. And sometimes makes you wish you could. But you can’t.”

Really, really bad advice. “It’s going to keep happening no matter what” and “just fight through it.’ Worst advice ever. But it was the best that she had, and it then became all that I had.

Now the funny – not at all funny – thing about all of these conditions is that they feed off of each other, cause each other to kick in and worsen one another. That’s confusing, I know, but here’s what I mean;

1. You go to Kroger, worried that you’ll have a panic attack

2. You have a panic attack and you either

a. Fight through it hoping to God it goes away once you’re out of the building

b. Get your ass kicked by it and abandon a full cart of groceries in isle 6 as you run for the door hoping that the screams that are inside your head don’t escape until your inside your car

3. But you survive it

4. You realize that you cannot go to that Kroger anymore because you will have another panic attack

5. Repeat steps 1-4 with every fucking place else.

That’s how my mama ended up staying not leaving the house for years. At my worst I made it 6 months before my then husband literally picked me up and deposited me (kicking and screaming unfortunately) in the middle of our front yard and held me there until I stopped. Actually, I pretended to be okay with it and ran back inside as soon as he let me go. But I didn’t want to end up like this, I didn’t want to be this, I didn’t want to do this. So I fought it.

I did avoid certain places and things that I knew would bring on an attack. Certain restaurants where I had experienced particularly nasty attacks, driving somewhere for the first time by myself (Before Siri could give me turn by turn, obviously), and small intimate gatherings were a no go. Everything else, I tried. Usually had an attack, sometimes fought through it, sometimes was beaten by it. I learned some tricks, though. My baby sister was born when I was 14. It didn’t take me long to discover that I didn’t panic when I had the baby with me. I don’t absolutely know why, but my guess is that my subconscious knew that I had a little person depending on me and wouldn’t allow me to lose my shit. So I brought the baby with me. Everywhere. Poor kid is 15 now and absolutely hates to be idle, she always wants to go, go, go. Oops. I learned that smokers had a very convenient, legitimate reason to periodically remove themselves from the situation. Looked like a great idea. And, it’s much easier to say “Be right back, gonna grab a smoke” than it is to say “If I don’t get the fuck out of here RIGHT NOW I am going to snap and this may be the one time that I don’t come back from the crazy.” I still smoke a pack a day and wish I had never started. I learned that if I was drunk, or even buzzed, I could almost handle a social situation. I still worried about it before, freaked during, and replayed it over and over in my head finding everything I did wrong after. But if I was not sober, I could participate some, it was a little less painful. I learned that if the attack didn’t go away when I left the situation, then I had to go home. Back to mom’s. Even after I moved out. Home was my safe place and mom was my safe person. I learned that relationships are even harder when you expect your boyfriend to put up with all of the things that you can’t do, all of the places that you can’t go, and all of the times that you have to go home (especially if you feel like you don’t deserve someone who will. But that’s a whole different post, isn’t it?). But I generally did better with a boyfriend around, so I pretty much always had one. And when I found one that would deal with all of my issues, I put up with whatever kind of treatment I got, because I’d likely never find anyone else willing to deal with the crazy anyway.

I went on like this for years. Missing out on so much, not enjoying the things that I couldn’t miss out on, and barely surviving things that other, normal people did every single day without even a thought. Constantly fighting panic and feeling extremely powerless and defeated anytime I let it win. Always tremendously, crushingly, unhappy and stressed out because I had to deal with all of this. Why the fuck couldn’t I just be normal? Everyone else could mingle at a party, even actually have fun, ride elevators, put gas in their cars for fucks sake, without issue! But not me. I was broken, and everything, all of the normal things, would always be hard.

I was doing it WRONG.

Once my fiancé and I started dating, I started dreading the obligatory I-have-issues-and-here-are-all-of-the-ways-that’s-going-to-suck-for-you conversation that was approaching. I never looked forward to this conversation. At best it was uncomfortable, at worst it put an end to whatever relationship was starting. But with this guy? I absolutely dreaded it. I didn’t know how he would respond, but I was pretty positive I wouldn’t like it. And I wasn’t wrong.

“…so that’s all of it,” I finished “I cant go some places, do some things, I have to leave in the middle of stuff a lot. And it sucks. What do you think?”

He then proceeded to say every single wrong thing possible.

“There’s no such thing as all that. Panic attacks? Its all in your head.”

Cue thunder and lightning, shocked face, middle finger, the entire array of nasty emotions available to a human being. Well, that’s pretty much done, I thought, so much for this guy. I still tried; I argued with him, tried to explain it, to make him see that it wasn’t all in my head, it was a very real thing, it wasn’t rational, I wasn’t rational once lost in it, I had no control over it . He didn’t buy it.

Until he saw a panic attack hit me, saw what it did to me. Then he believed it. And then he got pissed. He became angry that I had to deal with all of this, that I had been dealing with all of this for so long, frustrated that he couldn’t flip a switch and make it go away and kind of sad too I think, for all that I had missed. He understood, but he wasn’t willing to accept it. He was going to cure it. He was going to fix me. He told me this one day.

“Bahahahaha,” I laughed.”There is no fixing this babe, I’ve been dealing with it for more than 20 years! I do the best I can, but it’s not going to just go away.”

But the fiancé is stubborn. He’s also smart, has the patience to do extensive research, and has a passion for psychology and human behavior. Shortly after I laughed in his face, he approached me with a solution.

“Just decide you aren’t going to panic anymore.” He beamed. Like he had just solved fucking world peace and poverty all in one shot.

“Just decide, huh?” I asked. “Well, fuck! Why didn’t I think of that years ago?!?”

He tried to explain to me what he meant, how his solution would work. He talked about conditioning, behavior modification, conscious thinking. What in the actual fuck? Just what? He was psycho-babbling me, and really thought it would fix what had hindered my entire life. I quickly lost patience with it and insisted again that it wasn’t fixable, and that I as dealing with it the best that I could, and this was the best I was ever going to be.

He was patient when I lost my shit, stayed calm when I got frustrated (Totally opposite of the norm for us, by the way), and then he decided to take a different approach. “Just trust me.” He said. I knew that it would not work, but I went along with it. Mostly to shut him up.

That was almost 3 years ago. My panic attacks are down about 75% in frequency since then, and I am capable of doing 3 times as much shit as I could then. It’s not gone, fixed or cured, but it’s all so much better.

I’ll try to explain the process, try to minimize the psycho babble, and pray to God that I am able to get this across and that maybe someone else can benefit from it.

Before the fiancé decided to fix me, I started off every outing with “I am going to have a panic attack” running through my head like a mantra. I knew I was. I had been here before, and I had one then, so I would again (There’s that conditioning crap, y’all). Well, that was stupid. Human, but seriously stupid. Of course I am going to have one if I decide before I even leave the fucking house that I am going to have one. If you wake up in the morning and think “today is going to suck,” well then guess what? It probably will. I had to change that thought (There’s conscious thought). Well I immediately resisted that idea. I can’t control my fucking thoughts! What do you think I am? They just happen! But I tried. And it was ridiculously hard. It took a long time.

I started off thinking “I will probably have a panic attack.” Eventually it became “Maybe I will.” But about then, an amazing thing happened, and this is key; I went somewhere where I had always panicked, and I DIDN’T! I don’t know if it was a coincidence, or if it was that conscious thought shit working, but it was a huge fucking victory. And I grabbed it with both hands and ran with it. I started to be able to think “Maybe I won’t,” and sometimes even “I am not going to.” The whole conditioning thing, like the cycle I referred to earlier, had been working against me my whole life, and I was turning it around. I was making it work for me. I was making it my bitch!

What was previously:

All the things caused the panic attacks, and the attacks caused me to avoid all the things

Was becoming :

I can do stuff and not have an attack, so I can do stuff again and not have one again!

I know it all sounds kind of simple, but I promise you, it wasn’t. Its hard to change a thought pattern that is so ingrained. But every successful non-panicking thing fueled me. I gained confidence in myself. More importantly, I gained the desire to be not so damn afraid all the time, the desire to continue to accept this bullshit life with all these restrictions.

The fiancé helped me, tremendously. At first simply by distracting me while we were out, and it was sometimes enough to keep the panic away. And eventually, he saw the improvement, and the resulting confidence and so he challenged me.

“Drive out to this place tonight. I’ll meet you inside,” he said one night.

“Are you out of your mind?” I asked. “I can’t drive there by myself; I don’t know where it is. What if I get lost? And walk in by myself? To a place I’ve never been? What if I can’t find you? NO.”

“You can do it baby,” he assured me. “Remember last weekend? You made it through a whole afternoon at that crazy busy art fair!”

And he was right. I could. And I did! He played on my confidence, added to it and used it. More often than not I found out I could do it, and it was amazing. I was using that fucking god-awful cycle to my advantage. I was turning it around. Each new accomplishment allowed me the next one. It was like the best high of my life, every time I earned a victory.

They weren’t all victories, they still aren’t. I sometimes still slip into the old thinking. I just have to catch myself and pull out of it. And if I’m having a particularly crappy, weak day, and I have a panic attack, it still sometimes sets me back a bit. It’s still a battle. It’s still there. It always will be. But I have some of the control now. I just have to pay attention and keep it. It’s still a fight y’all, but now it’s a productive one, and one I can win.

And so can you. I’m not anybody special. I’m not super brave, or super strong. I was just super tired of it all, and I was handed a little piece of hope for change. And I took it. I built on it, I fought for it, and I refused to let it go. And now I’m handing it to you. If I can get better, even a little bit, you damn sure can.

And guys? Please try to keep in mind; no one ever knows what anyone else is going through. Be compassionate whenever you can. The world needs it.

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Mental Health Awareness - Anxiety and Depression, a guest post

Posted by Unknown Selasa, 29 Oktober 2013 0 komentar
This was shared with my by a very brave woman named Carla. She asked if she could tell her story so that others out there wouldn't feel alone. With love and respect, her words.
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It really starts with my parents divorce when I was 17. I began to feel anxious and depressed then, but was ashamed to say anything to anyone. It wasn't until I was about to get married, nearly three years later, that I was diagnosed with anxiety and depression. Since that time, I've been on and off medication. I was always very ashamed about having to take meds for it, therefore when I started "feeling better", I often stopped taking them.

Then the whole cycle would begin again. It was very hard to find something to fit all of my symptoms. So I began feeling like I could handle it myself. It wasn't until I had my second miscarriage that I finally got the courage to talk to my doctor about it again. By then I was 27. 

Since then, I've been on several different medications, but only two have really worked well. This summer I was on one, and it in particular gives a "black box warning" of signs to watch for. I took it for only two weeks, and I can tell you I never want to feel that way again in my life. 

I called people and had conversations with them that I don't remember having, and was inconsolable even by my own husband over something I had no control over. He can always redirect me, and calm me, but he couldn't then. It was two of the scariest days of my life, because it was like I couldn't stop myself, and had no control over my behavior. 

I can always tell when I'm getting more anxious, because I have a really hard time concentrating. My skin feels like it is crawling almost. Going out in public, to Walmart or the grocery store, is an ordeal. I have to make myself get up out of my recliner. It may take me a couple of hours to get to the point where I'm mentally ready to go. I'm an avid reader, but when I am dealing with increased anxiety it's hard for me to even focus on a book or tv show. 

If I am really honest, I don't even feel like talking to anyone besides a couple people while going through this. I've often thought I'm pretty good at "faking it". There's not more than a handful of people who can tell when anything is really wrong with me, I think. It's because I have gotten so good at putting on a mask.

I've currently taking different medication, and it works great. I can function, and even though I still have periods of ups and downs, it's no longer a living nightmare. Bottom line? Anxiety sucks, but I refuse to let it rule my life. 

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Mental Health Awareness ~ The Creative Beauty of the Bipolar Mind, by Anonymous

Posted by Unknown Rabu, 16 Oktober 2013 0 komentar
Today's post is being generously and courageously shared by someone I've come to know over the past few months through the wonders of Facebook. She is a tremendously creative spirit, and she reached out to me last week about possibly sharing a piece of her with you all. I was thrilled for many reasons, not the least of which is my own personal fascination with the artistic mind.

With much love and respect, her words and her art.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
I always thought it was just “mood swings”…. I didn’t think I needed a diagnosis, but… I got one in my mid-twenties. I wasn’t really surprised, in fact… I expected SOMEthing to be “wrong” with me. I knew that the rapid state at which my mind spun wasn’t very healthy, and I wanted someone to recognize that.

I have been in therapy for much of my life, it has been a life saver for me- in so many ways. I started SERIOUS therapy for my “issues” when I was….somewhere in my mid-twenties. I saw her for 3 years to cope with my behaviors, stress, kids, life, school, and anything else that came up. I knew SOMEthing needed to change with me, therapy was an option- so… I took it.

My therapist, Pam, was a nice woman. We clicked. I trusted her, and I opened up to her. She didn’t push meds, I liked that. I didn’t WANT meds, yet…anyway. During the time I was seeing her (sometimes twice a week) I was actively single. I had already been through a divorce at 22, and my fair share of relationships that weren’t working, this being one of the reasons I initially called her. I wasn’t emotionally healthy, and I wanted to be. I typed up a “cast list” for her, it was a compilation of people who were in my life, affect my life and otherwise need to be mentioned. Most of the people on that list I had slept with at one point. They were all my friends, so… why not? I wasn’t kidding when I said actively single, I dated (a lot). Don’t know what you like until you try it, right? (boy, does that open up a can of worms….)


I started classes at my local community college when I turned 25, I needed to wait until my boys were in school fulltime before I could quit my job and turn over a new leaf. I don’t remember the first time I heard the diagnosis bi-polar disorder in a psychology class I was taking….but- the more I read about it the more it resonated with me. I knew I had “issues”, but… I didn’t realize that “they” had a name.


After 3 years (at the ripe age of….29ish), I decided that it was too much for me. I was experiencing fits of rage, agitated depression, sleepless nights, a sexual appetite that made me think I was a sex addict, and a range of other crap. Pam was on board with me and my decision to try medication. It was never NOT an option, I just wanted to get my own shit together first before I actually walked down that road. So, now it’s time to look for a shrink…..ever tried looking for a shrink that listened to you? (for more than 10 minutes?). My first taste of meds (and a shrink) was a nightmare…. Wellbutrin, they had diagnosed me with…. (not bipolar)…. Something. They weren’t listening to me…. And, it annoyed me. Wellbutrin turned me into a totally different person, a zombie. I didn’t laugh anymore, life wasn’t FUN and EXCITING anymore…. I needed a change. So, I found a new shrink, one that came highly recommended, and… he listened.


Since 2001 I have been painting. That was the year after my brother passed in a very tragic car accident. That was the year I picked up a paintbrush, some oil pastels and a canvas. For 12 years I have been expressing myself though art and writing (however, I haven’t written much since being medicated), but the visual art…. That part I have never lost. Some days I have to fight for it, but… I always won. Or shall I say, the creative side of me always won.

Everyone loves the work I did in 2005. 2005 was one of many emotionally charged years…. Somewhere in the middle of the chaos. I loved the work that I was doing, but… it came at an emotional price. I wasn’t medicated then, my art was coming right out of my head… I lost myself in it every time. I can remember the manic nights- acrylic paint and pen & ink- back and forth, dancing with the media.


Soon after, I began medicating with pharmaceuticals. I was somewhere around 30/31 when I started taking the meds that made me “better”. Lamictal and Abilify. That was my cocktail. Seroquel when I got too manic or had too much anxiety (usually, hand in hand)…. And pot smoking always made me feel better. It also enhanced the creative side of me. Not only did I create art, I also modeled for photographers and fine art classes. I was always looking for a creative outlet, and I opened every door I could. I was just beginning to find ME.

For a few years, the meds did their job, I guess. I was still coping with some emotional issues in my life, luckily, I was still in therapy. I was looking for myself, I didn’t know WHO I was…. I just knew who I didn’t want to be. I had failed in 2 relationships after I stopped being “single”, and was looking for that “healthy” one.

I could tell stories of my role as a as a single mother, as a model, as an artist, as a survivor of domestic violence, or as a crazy as bat shit loon. But… I am here to talk about bipolar. Oh wait, those ARE all parts of me… my past has helped to define me. I have grown tremendously over the past 8 years of meds. However, it’s time. Time for me to remove that aspect of my life, and TRY to cope without them. I am tired, tired of a pill making me feel “better”, I am not sure how it will affect me. I have already (with the help of my shrink) taken myself off one. Now, it’s time for the other to go. However, I am both anxious and worried about how removing myself in the middle of grad school will affect my life.

I used to write incessantly, throwing up on the page, thoughts free flowing from my fingers. Sometimes I barely even stopped to see what I was writing. I didn’t edit, I just let it go.

2001

At the edge of the water- I sit- listen to the cracking of the waves....

the sky filled with grey- and the wind picking up speed. I can feel

dampness in the air- ready to explode down like a sheet of broken glass.

I can feel the moisture on my skin- it feels good- as the air is so

heavy- it needs to be cut. Patiently I wait for the rain to come, all

the while- I hold a stone in the palm of my hand. Projecting all of my

worries into it, feeling the energy of the dusk in my hands cascading

around the magick that I am creating.



At last- the rain falls... I raise my head to feel it fall on my face-

like warm tears... and then- a drop falls as if I was crying- and it

reminds me of my loss- and how I should heal. It felt as if my brother

were crying alongside of me - holding me- and keeping me strong.



With all of the energy I could muster- I lunge the stone into the

ocean, letting the current take all the worries away... and to deal with

them as it must.



I step away from the sea- looking into her- and all her glory....

feeling the rain in my clothes.... and smiling..... a small bit of sun

peeks through the clouds- and for a moment I could see beyond them- into

what I had been searching for....



I walked in the rain.... feeling a sense of clarity about what I must

do... and how I must achieve it- and knowing that I will always have my

brother at my side to guide me.



His death brought out my life... and the lives of so many others... and

as much as it hurts to say- had it not been for his spirit finding his

path - I would still be sitting on mine, instead of walking it with

pride.


2002

inside

wanting to scream

loud

and cry

and fight

and want

and have



Outside

laughing

smiling

loving

being



I see what I want

I see what I need

I can hold it in my mind

and it's screaming to me

I can see it

almost touch it

but stop


desperately looking

for that place

peace

of mind

of soul

looking

searching

yearning

hoping



missing

something

feeling it inside

outside

always



solitude

from the chaos

the suspect

the bullshit



in myself

in the room

in the mind

in my life



almost touching

what I need

for inner sanctity

the essence

of my being

yet afraid to embrace

what it really means



chaos

dysfunction

eruption

without it



days

weeks

months

each day a step to it

each hour a thought of it

each minute a way to get it



too many thoughts

close the mind

to the voices

to the funk

to the dreams



reality

sets in

and

reality

bites



2005
Life is full of would ofs and could ofs and should ofs, that is where people begin to regret, and really, think about what is going on in their lives, at least, one would hope. It’s full of things that distract us from the big picture, the larger things in life that really do matter. Instead of focusing on the tiny details that get lost in the mix. Unfortunately. it’s the tiny details , hundreds of them, thousands of them, times infinity that snowball, to make up what we call the big picture.

Hundreds of seconds of moments in time that we either run through aimlessly with no real direction, but just trying to move forward, as if somehow we will have another glorious moment- that *one* we are looking for…the pot at the end of the rainbow. And, in all reality, once that one moment is gone, there is no taking it back, there is no rewind button in this thing called life, and we can only hope that we have used most of our moments wisely, and with thought and sometimes deliberation, to form our paths, to lay the stones that will rest under our feet as we walk.

The art of free flow writing, to drop your pen onto a piece of stark white paper , allowing it so glide across, forming letters and words and sentences, and maybe it’s not even legible, but, if you stare at it long enough, you begin to see the dance that ensued. The dance between your mind and your hand, the pen and the paper. It’s hardly a dance I’d be willing to abandon, not even if my fingers do seem to guide themselves as they tap around the keyboard. Sometimes my words come fast, and furious, those are the times I wish for an old fashioned typewriter, so that the rhythmic tones of the keys penetrate the air…other times, I am stuck looking at a blank screen, with nothing to say. You can’t doodle with a keyboard, and sometimes starting the process is much like cranking up an old engine using the action of the pen, the turning of the gears, to get it started.

I miss writing. I miss poetry and prose and real life meanderings on the paper. I hope to regain that again, but… without the chaos in my mind.


I am 38 years old this year. I have lived a full life. One of hope, joy and happiness. I have also lived lives that only one can dream of- of fury and rage and hopelessness. I am a survivor of many things, and first being the demons in my mind. I am creating happy art these days, full of hope and faith and love.

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