I think that I posted this question in the wrong forum so here I go again.

I am seeing a FMS Specialist next Thursday and I was wondering what type of questions I should be asking? I have just been diagnosed with this and I am still trying to wrap my head around it. I am at a loss....if anyone can lead me in the right direction, I would truly appreciate it very much.

Thanks

Puddles

good luck and let us know how you make out. and don't be afraid to ask us these people can help as well, because i always walk out with more questions then i went in with. i also take my husband with me because he doesn't suffer from fibro fog or anxiety so he will catch what i miss.

teri

I have had fibro for 17yrs now (result of work injury). I think the most important thing I have learned is to take good care of myself, which includes finding the right balance of everything...pacing yourself, eating right, exercising some, resting enough, etc...basically not giving so much of yourself to others that you forget to save something for yourself. (This is my tendency. ) It's difficult to ask for help sometimes, but we all need it whether we like it or not. If you have an understanding doc (which I hope you do) they will be patient with you and recognize that you need them to be a partner with you in taking the best care of you as possible rather than them telling you what you have to do & that's it. I hope I am making some sense.

If you have further ?'s, you can always PM me as well. I will do my best to help you any way that I can.

Sending loving gentle hugs your way....{{{{{HUGS}}}}}

Sending you more hugs.....Let us know how your appt goes!

Coolmamma brought up a good point about the medications.

Another thought, some of the meds can be costly & you also don't know how they will effect you. So, try asking your doctor for samples before you fill the prescription if the doctor gives you a prescription. See if the doc will give you like a 2 week supply or more.

Good luck with your appointment.

Just recently got back from seeing the Fibro Specialist. Wow, was he wonderful!! He spent a total of an HOUR AND A HALF with me!! Can you believe it!! I wish you all had access to him as I do. He even told me that I could call and see him ANYTIME I needed to. He did give me a sample for 14 days until I could get to my doctor for a prescription. The specialist wants to make certain that my body can deal with it.

Has anyone heard of or uses: Ralivia

He is giving me 200 mg to start. Once a day every day. Would like to hear your take on this drug.

Interesting enough: The specialist told me to "check out" the Fibromyalgia Support Group on line. The one he suggested, was THIS ONE!!! I feel so happy right now! Having anyone, believe that this does exist and the chronic pain is indeed real........is a great day to celebrate!

Soft hugs to all!

Puddles

So glad your appointment went well!!! Finding a doctor you like is REALLY wonderful!! Sounds like you had a productive visit. I have not heard of Ralivia...but I bet some others may have. I hope it works for you! You will have to let us know if it helps.

How funny he recommended THIS support group!!! I knew we were a wonderful group of people I'm so happy that YOU are so happy!! Thank you for sharing the good news!

Hugs to you too!

Red