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I see you've had FM for a long time & feel like your Dr. can't help you.... Maybe try keeping a notebook or journal to record your symptoms, pain and fatigue? This way your Dr. will hear you loud & clear. It worked for me. I realized that telling my Dr. "I hurt all over" wasn't very detailed. LOL
Hope your having a better day *hugs*View Thread


Definitely keep track of all your symptoms, it helps with a diagnosis. (worked for me.... finally)
I hear you about family, some of my family members are wonderful and supportive. Some don't seem to "get it". Or don't WANT to get it. Ya know? Glad your posting here, I've found lots of support and advice, it means a lot!
Hopefully your appt. in November will get you some answers.
*hugs*View Thread

What helped me finally get a diagnosis was keeping track of all my pain, symptoms and fatigue. By doing this, you can be absolutely clear with your Dr. Good luck, and hope you feel better soon!View Thread

xperky: That's interesting about blood tests, I thought something would come up for sure if you had arthritis. Shows how little I know. =P Some days, I think my fingers look swollen, some not. I don't wear rings, so I wouldn't notice on a daily basis. One thing I have noticed, my finger joints are big. Kind of hard to describe, but it's the joint in the middle of your finger. Not sure if this is "normal" or not.
We definitely need a celeb spokesperson! Some celebrity out there HAS to have this! They're probably keeping it mum though.View Thread

So true about fighting for a diagnosis! I was happy to know what "it" was, followed by anger and sadness at it all. I was down for a few days, then started to learn more about FM. I have talked to my close family members (all VERY supportive) about this and am feeling better. I know I'm lucky to have support and understanding.

I did laugh at the "groundhog day" reference, it's so true! And coffee, gotta have my coffee! LOL Again, thank you for your advice and support, it means a lot!View Thread

CLKWC1964: Thank you for your support
I also have a hypothryroid and allergies. Plus, psoriasis and Cervical Spinal Stenosis. I wasn't terribly surprised to learn I have FM too. *sigh* LOL Thanks again everybody!View Thread

*HUGS*View Thread
Glad to know I'm not alone on this, thank you

P.S. LOL @ road eating machine, good analogy!View Thread


Have you had or asked for an MRI on your neck/upper back? I know there can be lots of different issues with the back, but it sounds like it would be worth it to have it checked. Hope you have a better day!View Thread
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