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150 total results
Comments (132)
I've been on Gabapentin for years. Started at 100mg per day now I take 3200 mg...
https://connect.mayoclinic.org/comment/246924/
headaches and twice as much pain from the neuropathy ... patients, epileptic, people with ME and ALS ... Pray that they find a good drug for neuropathy
Discussion: Gaba Lyrica Addiction
Support Group: Neuropathy
Posted: Feb 13, 2019
I was tested for ALS, MS, MG, etc. 8 years ago not because of my fasciculations,...
https://connect.mayoclinic.org/comment/854469/
I was tested for ALS, MS, MG, etc. 8 ... I was afraid I had ALS. ... was all part of my HNPP (Hereditary Neuropathy ... I was relieved it wasn't ALS!
Discussion: Benign fasciculation syndrome (BFS)
Support Group: Brain & Nervous System
Posted: May 4, 2023
I am no expert but it sounds similar to peripheral neuropathy……. Als twitches usually do not...
https://connect.mayoclinic.org/comment/860232/
but it sounds similar to peripheral neuropathy ... Als twitches usually do not start randomly ... spasticity then twitch for it to be Als
Discussion: Need some insight. Cannot see neurologist for 7 months.
Support Group: Brain & Nervous System
Posted: May 15, 2023
@faithwalker007 I'm not in your league when it comes to surgeries, but I've had my share,...
https://connect.mayoclinic.org/comment/99200/
almost certainly related to autonomic neuropathy ... But because neuropathy isn't curable ... control and therapy for depression et al
Discussion: Chronic Pain members - Welcome, please introduce yourself
Support Group: Chronic Pain
Posted: Oct 5, 2020
Good morning! I don't know for sure, but now that I have PN and am learning...
https://connect.mayoclinic.org/comment/887203/
than to say in an offhand way it was neuropathy ... ), my parents, grandparents, et al.,
Discussion: Peripheral Neuropathy? Family history? Don't wait!
Support Group: Neuropathy
Posted: Jun 29, 2023
Chronic use of PPIs ( prilosec et al) or H2RAs (Pepcid et al) or metformin all...
https://connect.mayoclinic.org/comment/1049594/
Chronic use of PPIs ( prilosec et al ... ) or H2RAs (Pepcid et al) or metformin ... development or worsening of peripheral neuropathy
Discussion: Neuropathy + Proton-pump Inhibitor use?? Anyone had this experience?
Support Group: Neuropathy
Posted: Apr 12 12:36pm
Hi there, I have the exact same symptoms as you and I am scheduled for a...
https://connect.mayoclinic.org/comment/980344/
on the 29th to confirm or rule out AL ... in an area where you have the most neuropathy
Discussion: Amyloidosis and Polyneuropathy?
Support Group: Autoimmune Diseases
Posted: Dec 14, 2023
Haha, I too must be old, or an old soul, at least, in terms of expecting...
https://connect.mayoclinic.org/comment/1085032/
typical suggestions for chronic pain/neuropathy ... /fibromyalgia/chronic fatigue, et al
Discussion: Paxlovid as treatment/trial fails
Support Group: Post-COVID Recovery & COVID-19
Posted: Jun 11 2:25pm
Neuro issues are frustrating and scary but it could be so many things including something non-life...
https://connect.mayoclinic.org/comment/1093909/
out to be HNPP, a rare hereditary neuropathy ... answers and it’s nothing as serious as ALS ... years ago I was tested for suspected ALS
Discussion: Having ALS-like symptoms and can't get a neurologist referral
Support Group: Brain & Nervous System
Posted: Jun 25 11:08am