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Hi from AZ
Hi, m name is Michelle and I live in the VERY hot state of Arizona. I was recently (and finally) diagnosed with fibromyalgia. There are no support groups where i live, and I am exhausting my husband with all my questions, rants etc. So I thought I would exhaust all of you LOL! http://neurotalk.psychcentral.com/im...es/biggrin.gif Seriously I am having a hard time coping with this, and I am hoping that by talking to people who have similar issues , I can be enlightened. I used to be very active...working out, riding horses and harleys, singing in a band, and hanging with my kids. I am getting back to the gym, but it is SO frustrating not being able to do ANYTHING i was more than capable of doing before. Anyone else have that problem? I also go to school PT and still sing. I am "retiring" from my PT job because of the hours (5am-10 am), and trying to find a way to get back on my cycle. My horse has arthritis so we both just stare at each other now!
Thanks in advance! I hop that you all can help me get over the "whiney baby" stage and get me on the road to acceptance! |
Hi, Michelle! :Wave-Hello: Welcome to NeuroTalk!
Here's a link to the FM forum: http://neurotalk.psychcentral.com/forumdisplay.php?f=12 You seem like you have a good grip on things and that is probably your best defense. Do visit with the others in the FM forum, you'll find a good group of supportive, friendly new friends.:) |
Welcome to NeuroTalk Michelle. I see that After has taken good care of you. :D
Ahhhhh, that long elusive road to acceptance...take my hand and maybe we can find it together! :rolleyes: |
Michelle,
Hello and welcome to NeuroTalk. Nice to see you have come to be with us. You will find a great number of caring members here willing to help others as they are able. Again welcome, looking forward to seeing you around. Darlene:hug: |
Hi Michelle and Welcome! :welcome_sign:
I understand 100% what you are feeling. I have FM and it's very painful and unpredictable. I know it's with me every day. I have a Neuro, but since he's a royal pain, (and I don't need more pain) I see a Rheumatologist, who is wonderful. He understands and treats FM. Maybe that would be a start. Hang in there and I am glad you found us. Like Cindy said, the FM forum here is very helpful. |
HI Michelle,
Welcome! Arizona is a great place but it is sure hot there. We love to visit your state. Like DM I have Fibro and my rheumy has helped a lot with the pain and muscles spasms I get. THere are also some great books out there that I have read on fibro. I'll go looking under my bed to find some of the titles. None was a cure all but some had tips that worked for me. :hug: |
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