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Fibromyalgia Online Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia, together.
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03/30/2008 14:31
jomama
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I am glad to join you, have no support at my house, or family, seems they think this is a joke. Not me, wish some of them understood. Have had fibromyalgia now for 11 years, my medical doctor is the only I see, seems to understand the pain, and depression parts well. Hope to hear any suggestions.
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03/30/2008 14:50
Red2
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jomama,

Welcome! I think a lot of us are in the same boat. It's really hard to get others to understand what's going on with us. I have had others who also make me feel as though they think I am just making things up. Well, all of us know this is REAL and NO joke!! So, you will find a lot of support here.

Red

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03/30/2008 14:56
ladycrowe
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Welcome! You are at the right place for support! These men and women are the most incredible people I have ever "met"! I hope you find it comfy and supportive here!
We are all soldiers in this battle to reclaim our lives from the beast within!
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03/30/2008 15:01
jgamble409
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Welcome Jo mama,

Here we all understand the hurt, the pains, the lack of understanding that the "normal" people don't have. We are all helping and yes, even laughing together so we can better each others lives. Jean

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03/30/2008 15:21
JLCarter
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I understand all too well about having no support at home.I felt that I was reading about myself when I read your post.Its very difficult for anyone to understand what we Fibro sufferers go thru,unless thay have it too!thats why we are here.Anytime you need someone,or your having an emotional moment(with me its an hour or so)someone is here for you!This support group is a blessing.Welcome!~gentle huggs~
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03/30/2008 15:50
AngelBooze
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Welcome Jomama,

I just joined just a couple of weeks ago but I was diagnosed about 17 years ago with Fibro. And I will tell you that this is best thing that ever came around. I have made more friends and had so much comfort from fellow members that even when my bad days are extreme there is someone here that understands what I am going through. I also have not laughed so much in a very long time. And they say that laughter is the best medicine. I hope that you find all the comfort, friends and laughter that I have found here.

very gentle hugs

Rita

AngelBooze
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03/30/2008 17:28
amyj298
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Hi Jomama,

Welcome to the best support group you will ever find! I too have very little family support. My kids are great by my mom is tired of hearing about Fibro this or Fibro that. I was recently diagnosed and I am doing a lot of research. It is not that I am complaining ... except for now.

Anway, you are in the right place because when you are having a bad day, one of us who is having an okay day, will be here to lift you up. If one of us is having a bad day, it might be you that makes all the difference.

We laugh here and we cry here. Sometimes member don’t sign on for weeks but when they come back, it is as if they never left.

I hope you find what you need here. We all are living our lives with FM so never be afraid to vent or ask ANY question you may have.

HUGS!

Amy

We made up FM car magnet ribbons as a group. They are really nice. I have some extra at cost. They are $1.50 if you want one, just PM me. Thanks!

LIFE IS A ROUND-A-BOUT WITH NO STREET SIGNS

***I HAVE FM CAR MAGNETS AT COST PM IF YOU WANT ONE!***
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03/30/2008 17:31
mamanordy
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Welcome to this amazing board! You will get lots of support here!
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03/30/2008 18:32
jomama
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I certainly understand that, my husband is the same way. He too is disabled with crippling back problems, but thinks his pain is far more worse than mine. But smile and enjoy the time when you do and hope it can be more often than not. I thank god for when we can have time and enjoy it while I can.
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03/30/2008 18:34
mamanordy
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I think that is a lot with mine too, he has horrible back pain and diabetic neuropathy but he seems to be able to do more so he thinks I should
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