Fibromyalgia Medication and treatment

Posted by Sundance(RB) @sundance6, Jun 1, 2019

I have been on the Mayo Connect for over six months. My symptoms point to the umbrella of things, Lyme disease, West Nile, Fibromyalgia, Lupus, and Chronice Fatigue. I have seen every doctor in my hospital system. Had every test and scans done. JUST MADE MORE $$ FOR THE HOSPITAL SYSTEM!

Yesterday I finally went to a Rheumatologist for a consultation on a blood test. When I expalined what I had been going through the last ten months he finally gave me a diagnoses. (First one after 10 months and 10 doctors.)There is a small chance I may have Lyme Disease, but to late to tell. He said he was sure it is Fibromyalgia. He said I should have been directed to him when it first started. (Again as many of you agree they put you through unecessay test and perscribe pills to make $$ for the industry.

So now that I finally have some direction to move, I need some advice, information, what helps, what causes it and such. He said he feels mine is in the area of sleep. Does this make sense to anyone? He is sending me to a sleep clinic for evaluation.

I know I have seen many postings about Fibromyalgia, but I guess it is the "Fibro Fog" that dosen't remember all.

I had been on Gabretentian but the side effects were worse than my pain! We are tryng Cymbalta. Can anyone let me know how it has worked for them. Anything to watch for?
As always this site is the Best! People are so honest and open about helping.
Thanks,
Sundance 🙂

Interested in more discussions like this? Go to the Fibromyalgia Support Group.

@freedom05

I was looking for this site because I am starting to think I am just lazy. I am 69 yrs old, been diagnosed for 13 years, have a great GP Dr who is very observant and takes good care of me. I am just so tired I cannot get anything done most days then all of a sudden I am a speed demon going thru the house. I do hurt in every inch of my body, and I have other things I cannot spell. I take Gabapentin, Effexor, Hydrocodine for my Fibro all of which I tolerate very well. This is after 13 years of trying all sorts of meds. this is what we settled on. The lazy thing is so foreign to me. I raised 3 boys, worked full time, had 2 elderly parents and you could eat off my floors. It was just my beautiful life back then. Now I am by myself and no one sees the dishes, floor. Just too high of bar I have set for myself.

Jump to this post

Hi Freedom,
How are you doing today?

REPLY

@freedom05 - You are not alone!
Fibromyalgia seems to run in families at times. I have it as does my sister and our mother had it. In addition, my 2 daughters and son have it.
It appears to wax and wane through life.
One important factor I learned when my 2 youngest were evaluated is SLEEP. Fibro is also a sleep disorder. You may sleep for hours, but wake up unrefreshed. With poor sleep, the pain and other symptoms get worse.
The Rheumatologists prescribed a certain medication to help with sleep.
Physical activity is recommended- swimming is good. It doesn’t put so much stress on your joints.
You may look online for in-person support groups. Sometimes local hospitals have educational meetings.

REPLY

Hello @freedom05 and @sundance. Forgive me for the dual response. I'm struck by each of you, and your struggles with chronic symptoms, such as pain and sleep disturbances, due to fibromyalgia.

Sundance, I read in your bio that "you never give up". I love that because neither do I.

Freedom05, you most definitely are not lazy, because anyone who consciously has concern for such, is typically not a lazy person.

A little about me...in my search for proper diagnosis of my chronic situations, I was Dr. hopping and swore fibro must be next on my list. The rheumatologist said that I had mirroring symptoms, but not actually fibro. A couple of years later, by process of elimination, and the failure of multiple treatments, meds, and tests, Central Sensitization Syndrome (CSS) became the answer.

Last October, I graduated Mayo Clinic's Pain Rehabilitation Center (PRC). It was life changing. What brought me there was that I refused to give up, like the both of you. I was fed up with opiates which increased my pain and symptoms, fed up with my body deconditioning, fed up with lack of sleep and my reclining chair being my bed for over 3 years, fed up with dependence on doctors to treat my chronic pain verses myself, and just plain fed up with not being present.

Did you know Mayo PRC treats a multitude of chronic pain issues, including fibromyalgia? I'm wondering if either of you folks might consider looking into this amazing program as an option?

Here is a link to learn more. You will find patient testimonials as well.
https://www.mayoclinic.org/departments-centers/pain-rehabilitation-center/sections/overview/ovc-20481691
I will be curious to know what you think. Do you mind getting back to me with any questions, comments, or concerns you may have?

REPLY

In reply to @rwinney…..I have multiple chronic pain issues including fibro and was accepted into the PRC 3 week program two years ago but broke my foot and could not attend. My foot is finally to the point that I could probably resubmit a request. However, as part of my fibro diagnosis (done at Mayo) it was directed to follow up with a sleep specialist; which I did and was prescribed medication that I believe is heaven sent. The PRC program has already stated they would want me to discontinue at least, this medication. I’m not into lying and will not do this, so I don’t know if this program would be the right choice for me. Everything else about the program, as laid out to me, sounded very helpful and hopeful in assisting me in managing my chronic pain.

REPLY

My wife suffers from fibrimialgia for the last 10 years. She was first having cimbalta and lyrica . But since 2018 she stopped the medications and takes cannabis oil C10T10 -a few drops 3 time a day. The result is unbelivable -much lesser pain and full night sleep. No side effects.

REPLY
@rwinney

Hello @freedom05 and @sundance. Forgive me for the dual response. I'm struck by each of you, and your struggles with chronic symptoms, such as pain and sleep disturbances, due to fibromyalgia.

Sundance, I read in your bio that "you never give up". I love that because neither do I.

Freedom05, you most definitely are not lazy, because anyone who consciously has concern for such, is typically not a lazy person.

A little about me...in my search for proper diagnosis of my chronic situations, I was Dr. hopping and swore fibro must be next on my list. The rheumatologist said that I had mirroring symptoms, but not actually fibro. A couple of years later, by process of elimination, and the failure of multiple treatments, meds, and tests, Central Sensitization Syndrome (CSS) became the answer.

Last October, I graduated Mayo Clinic's Pain Rehabilitation Center (PRC). It was life changing. What brought me there was that I refused to give up, like the both of you. I was fed up with opiates which increased my pain and symptoms, fed up with my body deconditioning, fed up with lack of sleep and my reclining chair being my bed for over 3 years, fed up with dependence on doctors to treat my chronic pain verses myself, and just plain fed up with not being present.

Did you know Mayo PRC treats a multitude of chronic pain issues, including fibromyalgia? I'm wondering if either of you folks might consider looking into this amazing program as an option?

Here is a link to learn more. You will find patient testimonials as well.
https://www.mayoclinic.org/departments-centers/pain-rehabilitation-center/sections/overview/ovc-20481691
I will be curious to know what you think. Do you mind getting back to me with any questions, comments, or concerns you may have?

Jump to this post

Wow. I had no idea. I cannot get any opiates period. The strongest sis Ultram which helps some. I don’t think my rheumatologist is much on treating fibro tbh.
I have 3 other autoimmune disorders with one being a new diagnosis this past Tuesday.
So it’s multiple specialists etc and going through the figuring out what’s happening.
I’ll check out the link above.

REPLY
@nanajoy

Wow. I had no idea. I cannot get any opiates period. The strongest sis Ultram which helps some. I don’t think my rheumatologist is much on treating fibro tbh.
I have 3 other autoimmune disorders with one being a new diagnosis this past Tuesday.
So it’s multiple specialists etc and going through the figuring out what’s happening.
I’ll check out the link above.

Jump to this post

Great! I'll be curious to know your thoughts after checking it out.

REPLY
@migizii

In reply to @rwinney…..I have multiple chronic pain issues including fibro and was accepted into the PRC 3 week program two years ago but broke my foot and could not attend. My foot is finally to the point that I could probably resubmit a request. However, as part of my fibro diagnosis (done at Mayo) it was directed to follow up with a sleep specialist; which I did and was prescribed medication that I believe is heaven sent. The PRC program has already stated they would want me to discontinue at least, this medication. I’m not into lying and will not do this, so I don’t know if this program would be the right choice for me. Everything else about the program, as laid out to me, sounded very helpful and hopeful in assisting me in managing my chronic pain.

Jump to this post

Thank you for your reply. Well, dang! Of all the luck with a broken foot to deter you from getting to Mayo PRC.

I 100% encourage you to move forward with trying to go again. Please do not let your sleep medicine deter you from attending this program. PRC is voluntary, and is open to anyone who is willing, and has desire to make changes in order to progress in a healthy positive direction and take back control. What you take away from PRC is life changing and well worth the investment, but you've got to want it.

Here is a members post that I found helpful:
https://connect.mayoclinic.org/discussion/pain-rehabilitation-21da8b/
Are you willing to contact the front desk of PRC again? You are already in their system from your prior attempt to go, so you're that much closer.

REPLY
@rwinney

Thank you for your reply. Well, dang! Of all the luck with a broken foot to deter you from getting to Mayo PRC.

I 100% encourage you to move forward with trying to go again. Please do not let your sleep medicine deter you from attending this program. PRC is voluntary, and is open to anyone who is willing, and has desire to make changes in order to progress in a healthy positive direction and take back control. What you take away from PRC is life changing and well worth the investment, but you've got to want it.

Here is a members post that I found helpful:
https://connect.mayoclinic.org/discussion/pain-rehabilitation-21da8b/
Are you willing to contact the front desk of PRC again? You are already in their system from your prior attempt to go, so you're that much closer.

Jump to this post

Thanks for your input…I will give it some consideration but I do not want to discontinue my sleep medication; regardless of the other valuable insights I may gain from the program. If they are willing to accept me with this limitation, I would definitely be open to trying again. A call to discuss would be an idea.

REPLY
@migizii

Thanks for your input…I will give it some consideration but I do not want to discontinue my sleep medication; regardless of the other valuable insights I may gain from the program. If they are willing to accept me with this limitation, I would definitely be open to trying again. A call to discuss would be an idea.

Jump to this post

You're welcome. I understand where you're coming from. lt never hurts to call, and PRC does a great job with communication. Good luck!

REPLY
Please sign in or register to post a reply.