Why wear a ribbon?

"I wear this ribbon because Alzheimer's in in our family, I have fibromyalgia, I'..." (igimom)

MDJunction to me

"All I can say is that this has been the best place ever. It has been six to seven months since I joined, and I have learned so much. I now believe in myself and accept myself on a completely different level. The people on MDJunction has been so supportive and accepting that I have been able to adopt it into my personal life. That has reduced a lot of stress in my life. Thanks to all." (bunnyfly)
We comply with the HONcode standard for trustworthy health information:
verify here.
Fibromyalgia Online Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia, together.
Join This Group
Group Home   Forums   Articles   Members (1758)   Diaries   Leaders   Guidelines
FMS Community FMS Support Forums Introductions & Personal Stories I am new to the group-would luv to hear from u all
Related discussions:
11/25/2008 13:33
Virva
Posts: 4
New Member

Send a PM
Give a Hug
Hi everyone....I have FMS-diagnosed in 1995--so i have a lot of experiences and traumas that i have gone thru, including doctors & family (you name it) telling me it's all in my head, etc......I mostly denied that i had this diagnosis for years due to the reason I was only 22 yrs old at the time...well...if anyone has been recently diagnosed, I would not suggest doing what I did...everyday is a struggle...the reports say that FMS doesn't get worse----WRONG!!! they forget to tell you that the normal stresses in life can make it worse, or bad relationships, etc....I am not sure what to say, but i do know I need a support group...I don't know anyone else with FMS, except for my mother....

I guess i will say what treatments i have tried...

the anti-depressant SSRI's -- made me very ill..i would vomit for no reason, literally tried to attempt suicide...and the doctors still kept me on the anti-depressant - Effexor - the side effects of quitinq was pure hell--I did it on my own...did my research 1st---tappered off them slowly-- I refuse to go back on SSRI's for that reason and Effexor didn't help with the pain----i found out that with FMS, the person has to be pro-active in their treatment and reasearch everything....because one persons meds may not work for you...and the doctors half the time really don't care...luckily, my rheumatoligist (sp) has 2 nurse's with master's degree's that see me for follow -up appointments..and they have been the compassionate ones--- one grace from God...I would like to know if anyone in this group has experienced the dread of living....anyone....and how does one cope with dating or marriage....what do you say to them about FMS??? How do they cope?


Popular posts by Virva
    HUSBANDS OR BOYFIRENDS!!!!!
Reply  


11/25/2008 14:09
livn4jc4evr
Purple Ribbon
Posts: 163
Member

Send a PM
Give a Hug
Welcome to the group! There are many days I too have dreaded life. Last week I asked someone how you are and they replayed "I am great because I woke up on the right side of the dirt today!" I thought about it and I said hmmm... did I wake up on the right side of the dirt because I am still here suffering and I just wish it would stop.

I remember meeting my husband 3 years ago and someone introducing us. I have been sick since I was 15 so I never had time to do the whole dating thing due to having to do school at home and all the hospital stays etc. When we went out on our second date I remember being so scared because I was so sick we had 1st gone to the movie and now we where out to eat and then he says do you want to go out to a club and go dancing? I did not want him to think I did not want to go out with him or something. I had to tell him no. The following week we went out and watched another movie followed by food and boy do I tell you I was so embraced because after we ate I felt something dripping and I was having more nose bleeds which was a side effect of one of the medications I was taking at that time. I staid in the bathroom for 10minutes and it still did not stop. So I came back out and said that we needed to go. After that he asked if there was anything he could do and guess what he has never left my side since.

The point to this is if you are looking for a man, if he really loves you he will be understanding and love you for who you are and what’s going on with you. I spent the longest time worried about what he would think and then something happened and I had to tell him and he was so happy I told him and after that he was so supportive. If you are married or looking for away to explain to a boyfriend or anyone else what is going on with you, you might consider sharing this letter. Star another member here once shared with me. It is the greatest thing I have ever read. I showed it to my husband of only 6 months and for the 1st time he really understood.

It is a letter that I think was originally called A Letter to Normal’s, but when it reached my hands, it was called A Letter to the One I Love:

Fibromyalgia isn't all in my head, and it isn't contagious. It doesn't turn into anything serious and nobody ever died from fibro though they might have wished they could on really awful days. I can't control how often I feel good or how often I feel terrible. If you want to read articles about fibro I can show you some that I think are good. If you just want to learn as we go along, that's fine too. This is definitely going to be a process. The first step is for you to believe that there is an illness called fibro and that I have it. This may sound simple, but when you hear about some of the symptoms I don't want you to think I am making this up.

Fibro is a high maintenance condition with lots and lots of different kinds of symptoms. There's no way to just take a pill to make it go away, even for a little while. Sometimes a certain medication can make some of my symptoms more bearable. That's about the best I can hope for. Sometimes I can take a lot of medication and still not feel any better. That's just the way it goes.

There's no cure for fibro, it won't go away. If I am functioning normally, I am having a good day. This doesn't mean I'm getting better, because I suffer from chronic pain and fatigue for which there is no cure. I can have good days, weeks, or even months. But a good morning can suddenly turn into a terrible afternoon. I get a feeling like someone has pulled out a plug and all my energy has just run out of my body. I may get more irritable before these flares, and suddenly get more sensitive to noise, or just collapse from deadening fatigue. Other times there may be no warning, I may just suddenly feel awful. I can't warn you when this is likely to happen, because there isn't any way for me to know. Sometimes this is a real spoiler and I'm sorry.

Fibromayalgics have a different kind of pain that is hard to treat. It is not caused by inflammation like an injury. It is not a constant ache in one place like a broken bone. It moves around my body daily and hourly and changes in severity and type. Sometimes it is dull and sometimes it is cramping or prickly. Sometimes it is jabbing and excruciating. If Eskimos have a hundred words for snow, fibromyalgics should have them for pain. Sometimes it just hurts all over.

Besides pain we have muscle stiffness, which is worse in the mornings. Sometimes when I get up out of a chair I feel like I am ninety years old. I may ask you to pull me up. I'm creaky and I'm clutzy. I trip over things no one can see, and I bump into the person I'm walking with and I drop things and spill things because my finders are stiff or my coordination is off. I just don't seem to connect the way I shoud. Hand-eye coordiation; it's all off. I walk slowly up and down stairs because I'm stiff and I'm afraid I might fall.

Because I feel badly most of the time I am always pushing myself and sometimes I push myself too hard. When I do this, I pay the price. Sometimes I can summon the strength to do something special, but I will usually have to rest for a few days afterwards because my body can only make so much energy. I pay a big price for overdoing it, but sometimes I have to. I know it's hard for you to understand why I can do one thing and not another. It's important for you to believe me, and trust me about this. My limitations, like my pain and my other symptoms, are invisible but they are there.

Another symptom I have is problems with memory and concentration, which is called fibrofog. Short-term memory is the worst! I am constantly looking for things I have no idea where I put, I walk into rooms and have no idea why. Casualties are my keys, which are always lost, my list of errands, which I write up and leave on the counter when I go out. Even if I put notes around to remind myself of important things I'm still liable to forget them. Don't worry, this is normal for fibros - most of us are fightened that we are getting Alzheimer's.

I mentioned my sensitivities earlier and I need to talk about them again. It's more like an intolerance to everything. To noise, especially certain sounds like the television, or shrill noises. Too bright lights, to fluorescent lights. To smells like fish or some chemicals, or fragrance or perfume. I also have a problem with heat and with cold. It sounds like I'm never happy but that isn't it. These things make me physically ill. They strees me out and make my pain worse, and I get exhausted. Sometimes I just need to get away from something, I just don't know how to say it. I know that sometimes this means I will have to go outside, or out to the car, or home to sit alone, and that's really all right. Sometimes when I feel lousy I just want to be by myself. When I'm like this there's nothing you can do to make me feel better, so it's just best to let me be.

I have problems sleeping. Sometimes I get really restless and wake up and can't get back to sleep. Other times I fall into bed and sleep for fourteen hours. I'm sure that's confusing to be around, and I know there are times when my tossing and turning and getting up and down to go to the bathroom disturbs you. We can talk about solutions to this.

All these symptoms and the chemicals in my brain can make me depressed, as you'd imagine. I get angry and frustrated and I have mood swings. Sometimes I know I'm being unreasonable but I can't admit it. Sometimes I just want to pull the covers over my head and stay in bed. These emotions are all very strong and powerful. I know this is a very hard thing about being with me. Every time you put up with me when I'm in one of my moods, secretly I'm so grateful. I can't always admit it at the time, but I'm admitting it now.

I have other symptoms like irritable bowel and pelvic pain that will take their toll on our physical intimacies. Some of these symptoms are embarrassing and hard to talk about but I promise to try. I hope that you will have the patience to see me through these things. It is very hard for me too because I love you and I want to be with you, and it makes everything worse when you are upset and tired of dealing with all my problems. I have made a promise to myself and now I am making it to you. I will set aside time for us to be close. During that time we will not talk about my illness. We both need time to get away from its demands. Though I may not show it always, I love you a million times more for standing by me. Having to slow down physically and having to get rid of unnecessary stresses will make our relationship stronger.

Sorry for the rambling hope this somewhat helps. Have a great day! And remember if the people around you love you they will always be supportive or all of your problems.

Post edited by: livn4jc4evr, at: 11/25/2008 14:10

Spread love everywhere you go. Let no one ever come to you without leaving happier. "Mother Teresa"

"Judge your success by what you had to give up to get it."
Reply  


11/25/2008 14:23
Kestral
Purple Ribbon
Posts: 64
Member

Send a PM
Give a Hug
I sent a copy of that letter, slightly modified, to my parents. My husband and my sister understand, but, though they try, my parents have problems understanding exactly what I'm going through. When I told them I was on nine medications now, my Dad nearly blew a gasket. He's so frustrated for me because of all the crap the military has put me through, both while on active duty and since I've been "retired." *sigh*

Post edited by: Kestral, at: 11/25/2008 14:24

"What is a friend? A single soul dwelling in two bodies." ~Aristotle
Reply  


11/25/2008 14:36
Cori
Purple Ribbon
Posts: 1249
Senior Member

Send a PM
Give a Hug
Wow very well said.

The point to this is if you are looking for a man, if he really loves you he will be understanding and love you for who you are and what’s going on with you.



Sometimes it's hard to walk, talk, or even know what tomorrow brings. But as long as I have a smile on my face I can give a little bit of sunshine!
Reply  


11/25/2008 15:43
Starr
Purple Ribbon
Posts: 2432
Senior Member

Send a PM
Give a Hug
Yes, Livn, I have a copy of that letter saved on my computer. It was very well written, and I have shared it with many others who benefitted from it. I don't give it to IH because it's over for me. I just don't care. But that's my life and I don't need to burden anyone here with it any more than I already have. Thank you for thinking of me though.

That's a beautiful love story you told about you and your DH. How fortunate you are. I'm really happy for you.

Virva, please try not to reach the point where you're dreading life. Try to find ways to live within the limitations set by this disease. Find acceptance. Only then can yo be happy again. Life is good...live it!

Reply  



Start a New Discussion

Disclaimer: The information provided in MDJunction is not a replacement for medical diagnosis, treatment, or professional medical advice. Read more.
Contact Us | Bookmark Us | Add a Doctor | For Doctors | FAQ | Awareness Ribbons
About Us | Terms & Conditions | Privacy | Spread the Word | Advertise
Copyright (c) 2008 MDJunction.com All Rights Reserved