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1,282 total results
Comments (1,172)
During my research of what to take for my polyneuropathy I learned from Dr Emily Splichal’s...
https://connect.mayoclinic.org/comment/1232751/
my research of what to take for my polyneuropathy
Hello and thank you for bringing up hand controls for driving. I am considering going for...
https://connect.mayoclinic.org/comment/1149537/
I have had axonal polyneuropathy for
Hi @nukhan, There does seem to be a connection between high levels of uric acid and...
https://connect.mayoclinic.org/comment/760890/
severity of diabetic sensorimotor polyneuropathy
Thanks for response and info on pinched nerve. I have had biopsies in both feet and...
https://connect.mayoclinic.org/comment/618402/
Last EMG and NCT was 3 years ago and polyneuropathy
@offthegrid Do you know if Medicare covers ldn? I read in research studies that it shouldn't...
https://connect.mayoclinic.org/comment/288743/
primary pain is small fiber peripheral polyneuropathy
Have you seen a neuromuscular neurologist? Have EMG/nerve conduction test. Small fiber biopsy. ( the reason...
https://connect.mayoclinic.org/comment/1116083/
Severe axonal sensorimotor peripheral polyneuropathy
It’s very frustrating when doctors don’t believe you. I have been very fortunate that the doctors...
https://connect.mayoclinic.org/comment/923909/
it has been G.I., respiratory, and polyneuropathy
Hi Tab, welcome to Connect. I'd like to introduce you to a few other members who...
https://connect.mayoclinic.org/comment/155479/
(chronic inflammatory demylenating polyneuropathy
I had a moderate TBI 30 years ago, including damage to my left temporal and frontal...
https://connect.mayoclinic.org/comment/1024164/
contributing factors (in my case, polyneuropathy
I have had MGUS and polyneuropathy for around 8 years, mostly minor loss of feeling and...
https://connect.mayoclinic.org/comment/1116869/
I have had MGUS and polyneuropathy for
I was diagnosed with IgA kappa light chain MGUS 8 years ago (69 yo woman) and...
https://connect.mayoclinic.org/comment/1008159/
I have mild polyneuropathy but my oncologist
Hello @txamo, Welcome to Mayo Clinic Connect. You will notice that we have moved your post...
https://connect.mayoclinic.org/comment/238696/
(chronic inflammatory demylinating polyneuropathy
@nanashelly Good Afternoon, Myelopathy is just a general term that there is a problem with the...
https://connect.mayoclinic.org/comment/261864/
have Neuropathy, I have Peripheral Polyneuropathy
Hello, web28 (@web28) That is indeed scary! It would be foolish for anyone to have experienced...
https://connect.mayoclinic.org/comment/1172363/
My life with, first, peripheral polyneuropathy
I also have what they're calling idiopathic polyneuropathy which came on quickly after my admission to...
https://connect.mayoclinic.org/comment/888152/
what they're calling idiopathic polyneuropathy
My calve muscles were extremely tight as an early symptom of the sensory and motor polyneuropathy...
https://connect.mayoclinic.org/comment/878245/
early symptom of the sensory and motor polyneuropathy
I have just been diagnosed with peripheral polyneuropathy. For a couple of years on and off...
https://connect.mayoclinic.org/comment/820472/
just been diagnosed with peripheral polyneuropathy
Hello @26sabrina and @danawyn, I would like to welcome you both to Connect. One of the...
https://connect.mayoclinic.org/comment/782523/
Chronic Inflammatory Demyelinating Polyneuropathy
@dckuke @maryflorida Hi. I have Small Fiber Polyneuropathy, via skin punch biopsy, with a b12 deficiency...
https://connect.mayoclinic.org/comment/299231/
I have Small Fiber Polyneuropathy, via
I was diagnosed with peripheral sensorimotor polyneuropathy last year with symptoms mostly in my feet and...
https://connect.mayoclinic.org/comment/896792/
diagnosed with peripheral sensorimotor polyneuropathy
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