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I have not tried the actipatch but I like the the #lidoderm patches.
Has anyone tried Fibrorelief supplements?i want to try them to see if they help but they are kind of expensive. I just want to make sure i am not falling for a scam. Are there any scams out there that i should be aware of that target people with chronic illness such FM?
I tried Fibrorelief. The pills are kind of large and it says 4 per day. I could only manage to take 1 or 2 per day because I have some swallowing issues. Since it's a capsule, I couldn't cut them in… read more
I'm late to the answers here, been MIA. I also experience this, and while I seem to be prone to frequent mild UTIs, in my case this pain is usually due to my pelvic organ prolapse (which sounds… read more
Anyone with spinal stenosis is this what makes your legs pain and feel like they will colapse or you can only walk a little then have to sit and would exercise help legs or not?
I have a friend who has COPD she gets out of breath all the time .she cannot walk at all without getting out of breath .she has a rescue inhaler. And she also has other inhaler treatments.
So when i get my flares i get pain in my legs, chest, arms, neck and head. Everytime ive had a flare lately though in addition to my usual symptoms and pain ive been getting pain under my left rib. Sometimes in my shoulder, sometimes my side , and sometimes under my breast. Its gotten more intense with each flare. Im hoping its just fibro related and not something more nefarious. The last two flares sent me to the er and they did a ct among all the other work ups and it was clear. Ive had (prior… read more
Sorry bluebird21!!! I didnt realize i missed you!!! Its just constant lately . Pressure infer my left ribcage! Used to always be at the end of a flare and now it seems steady! My legs are a little… read more
I itch a lot as either I am too warm, or my clothing is not soft enough. I have to feel everything before I buy it as my skin is super sensitive.
Does anyone feel like they may have been misdiagnosed? I've been speaking with a friend a lot recently who has fibro and she feel she has and the more I speak to her the more I feel I may have been. Just given fibro diagnosis as there was nothing else they could think of. Another friend has mentioned MS which has never been mentioned by a doctor before but reading up on it I have a lot of the symptoms. Obviously I will be discussing this with a doctor ASAP as I would explain a lot. Be intrested… read more
My MRI was clear too so they wanted to do a spinal tap. Hard no there.
Does anyone else here get sever migraines lasting over a week? I’ve been dealing with migraines for 15 years but over the last two I get some that last a couple of weeks. No medicine has ever helped them. I have had ct scans mris and specific eye tests that are all normal. The pain gets unbearable and I have yet to talk to someone that can relate.
I use Coenzyme Q10, 200-250mg once daily for migraine prevention. I used to get a migraine every 3-5 days, now once a month and it only lasts for one day. I found this useful.
There is nothing wrong dentally. The pain is accompanied by debilitating headaches on the left of my head. I’ve had MRIs and CT scans of my head and nothing is wrong. My sinuses are clear.
I am assuming that this is another symptom of the Fibro.
I forgot to say I have started taking 50 mg of CBD per day as well as increasing the gabapentin to 600 mg 3x per day and it’s helped some . Along with my pain meds I can cope better some days
Hi everyone ♥️ I have an mri scheduled for this Monday, December 4th for my shoulder with contrast dye. I’ve never had the dye before. Is there anyone who has that can tell me their story? Thank you
I lost count of how many MRIs I’ve had. If you are claustrophobic at all, let them know ahead of time. You can request something to help calm you down.