This condition is being written by our editorial team, so please check back soon! In the meantime connect with others through Posts and People!
Recent posts about Neuropathy
hey fam. I got some difficult news this week😞. Turns out I have EDS, Mast Cell Activation Syndrome, Fibromyalgia and now I am seeing another Dr about possibly POTS and Small Fiber Neuropathy. I already knew about the fibro and painful joints but these new diagnostic realities have me a bit shaken. I could really use some love and assurance from you guys! Tips and treatment suggestions welcomed 🥰
Anyone have burning feet? It started for me after I contracted Bartonella a few years ago and it gets a little better every year, but it’s still bad. An EMG showed I technically don’t have neuropathy, but no dr can figure out what’s causing the burning. It’s mostly when I have shoes on and especially when I’m walking or exercising
Hey, I’m new! Have any of you heard of the new transdermal CBD patch that’s been approved for use with fibromyalgia patients? I’ve heard it’s a game changer when it comes to body pain and specifically peripheral neuropathy!
Just started Cymbalta for depression, neuropathy, & chronic pain management. Does anyone have experiences with this medication? I’ve been on Zoloft for 6 years and weened off of it for the purpose of trying something new.
I’ve been diagnosed with Idiopathic Small Fiber Neuropathy (SFN) with a side of POTS and possible other heart related issues. I’ve been learning to live with pain and pins/needles tingling daily. Even with the meds I’m still a mess and having trouble accepting that this is my new reality....and being okay with that. Just need some friends...