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Dry mouth

I was wondering if anybody else up for some dry mouth from your medications and what you use for if that works

posted about 1 hour ago by A MyFibroTeam User

I recently had to switch my Rheumatologist because Dr. Janet Kromes is no longer practicing in my area.

How can I update this information on the Provider Directory? I don't have her new location I just know she's not in Langhorne, PA any longer.

tags: Update to Provider Directory

posted about 2 hours ago by A MyFibroTeam User

I've had fibro for 20 years. I also have chronic dizziness. It's like a motion sickness dealing. Does anyone else have This?

posted about 3 hours ago by A MyFibroTeam User

Yes have it now it drives me mad can't go anywhere or do anything feel like I'm going to faint some time s I take serc 16tablets but they not doing much… read more

posted about 2 hours ago

Vitamin deficiencies??

Not a scientist or detective but ive spent a lot of time trying to understand my body (sadly through internet searches) and why I have autoimmune disorders and if things are linked together. Im just curious how many of you had some type of vitamin deficiencies before or leading up to diagnosis of fibro?

tags: #vitamindeficiencies #

posted about 8 hours ago by A MyFibroTeam User
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Yes I had almost no vitamin d before they said I had fibro

posted about 4 hours ago

Has anyone been prescribed trazadone for fibromyalgia?

After much discussion, my doctor and I chose not to go the route of Cymbalta or Lyrica, but instead try trazadone (to combat fibro symptoms of weight gain, insomnia, constant headaches, and overall chronicpain.) The results have been amazing! Has anyone else tried this?

posted about 9 hours ago by A MyFibroTeam User
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I have taken trazodone for sleep for many years. It is very helpful and has few side effects. Gabapentin has massive side effects when discontinued and… read more

posted about 8 hours ago

Sleep Study Report

I spent the night at one of the top sleep study clinics in the USA. The bottom line is that I am not reaching deep sleep and wake up often. I am not on any medications.

They told me absolutely no sleep medications as they ( and many fibro drugs) alter deep sleep and prevent human growth hormone formation that is critical for fibro recovery and stopping the pain.

They gave me a sheet of sleep hygiene recommendations and suggested stretching for 30 minutes before bed, meditation 2 to 3 times a… read more

posted about 9 hours ago by A MyFibroTeam User
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Tried it. I use it for my kids in gummie form when they have problems with sleep. It is helpful but for me I found after taking it for a week at a time… read more

posted about 4 hours ago

Has anyone taken Dosulepin a prescription med for fibro pain? If you have, did it help the fibro pain?

I was on Nortriptyline and when my Dr increased the dose I got really bad migraines. He has now put me on Dosulepin, I have been on it for a week and have had no improvement with pain. The only thing it has changed is made me have a really really low mood. Not sure whether to stop it or keep on it for another week. I'm a bit nervous to stay on it as the side effects and low mood has me very worried. My partner has… read more

posted about 13 hours ago by A MyFibroTeam User

Have you tried cymbolta and neuronin?

posted about 12 hours ago

Dogs & cats other animals ❤

In the short time I've been on this lovely site ..I have noticed a very common theme between us fibro people ..and that is how much we LOVE our animals ..
I thought it might be fun to kind of pay homage to our pets !
I have already posted pics of my two German shepherds khali and Acer ,so I thought I would also pay homage to my beautiful cat Albie the half Maine coon!
My animals mean everything to me ..they are always there for me ..they don't question me ,they dont have,any… read more

posted about 13 hours ago by A MyFibroTeam User
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Wow Nicola a full on menagerie !I love horses but I wouldn't be able to fit one on my sofa !xx

posted about 5 hours ago

My pain is getting worse

My pain is getting worse. It's to the point, where I'm up for days with no sleep. My rheumatologist has tried different medication, and nothing is helping me. I bought a wii fit plus, cause my rheumatologist told me to do yoga. And it hasn't helped me. I've tried my tens unit, it don't help. I've tried a hot bath, no relief. Anyone have any suggestions for me, to help manage my pain? My rheumatologist only wants me to work, every other Friday and Saturday nights only. I don't know how… read more

posted about 15 hours ago by A MyFibroTeam User
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One other thing I have noticed. If I stay hydrated I do a lot better with pain. When I get dehydrated I hurt all over. I also d take vitamin D and… read more

posted about 8 hours ago
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