Experiences with

Naturopathy

I have neuropathy in my legs and arms and my feet some due to pinched nerves and herniated discs I am having trouble taking gabapentin three times a day because I'm on a lot of other meds it just seems not to work two times a day any suggestions would be appreciated thank you Evan

I am also taking ginger root and ginkgo bilboa (these for tinnitus) so maybe that has helped along with the gaba. Anyway the restless legs is about gone after years so I will keep on taking those 3 things!

I meet with my doctor next week and will bring up increased neuropathy, pain, balance issues and new areas of numbness. I suspect she may tell me this is to be expected as I get older with PA. Is it? Or is it an indication that I am not SI frequently enough? For 20 years I have been sticking

I experience extreme flare ups of my Raynaud's in the form of foot pain, numbness and leg shakes. I eat very healthy, exercise daily and stay warm wearing thermal insoles, compression or thermal socks but these do not ease the flare ups or prevent them. Also experience the flares at certain times of

I have Raynaud’s. I’m on nifedipine and Sildenafil for circulation. Sometimes I experience throbbing pain in my fingers. Does anyone else go through this and if so what do you do for immediate pain relief?

My daughter has had a-fib since she was 19. 1 ablation that failed after she got pregnant. Multiple meds and a cardioversion and she is in and out all the time. They started her on Sotalol 80mg 2x a day two days ago at home. I'm a retired nurse and have never heard of starting Sotalol at home. Today

I have a numbing/tingling sensation in thumb and fingers of both hands at times. Usually several times over a two or three day period, then a break for several days. When I experience the problem, my thumb may be numb and inflexible for several minutes. I slower try to close my fist and eventually

Cluneal nerve entrapment. Already have pudendal neuralgia. Thank you!

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Hi All, I finished 6 cycles of chemotherapy (Docetaxel) in October 2019 and have had Peripheral Neuropathy ever since. For about the first 7-9 months I suffered the usual sharp pains in my feet (like they were being stabbed) and electric shock type pains as well. The other effect of PN has been numbness

Looking for some advice. Received oral sex only as a male. 3 months later freaked out and got tested for hiv, syphilis twice. I also got bacterial test for all bacterial sti gonnoreah, chlamydia, mycoplasma, herpes etc and negative. Didn’t quite believe tests as I am anxious person and obsessed for

A friend of mine who had some anxiety issues, among other things went to a psychotherapist who did Neuro feedback sessions. He did not want to take any psychotropic drugs to treat his problems. It consisted of mapping the brain's activity then correcting the imbalances with very tiny impulses of electricity

I’m on Sotalol, have been for a lot of years now. It was originally prescribed for SVT, but I’ve developed PAF since 2014, after a nasty coughing virus and the Drs are keeping me on it. I’ve been fine on it, but what worries me, is the huge amount of drugs that Sotalol reacts with and are red flag reactions

Hello, I've been doing some research and it seems like my symptoms tend to be a more rare result of B12 deficiency and was wondering if anyone else has experienced these. I have had the common symptoms of pins and needles and burning in my hands and feet, however, these occur less frequently. My face

Hello all .. Hope you are all keeping well X I wonder if anyone with fibromyalgia has tried Alpha Lipoic Acid for pain relief ? My mum is newly diagnosed with Fibro and she's in terrible pain, depressed , sleepless nights ( the usual with this diagnosis ) ..but she quite a complicated case as she also

My mother is 82yrs old and has had Parkinson's for 10 years. She finds it very difficult to sit still and concentrate. It makes it difficult for Dad who is her carer as she is always up and down. Has anyone else experienced this and is there anything we can do.. Mum suffered from Restless Legs until

A restriction or prohibition that has survived almost 50 years (1975-2020) without any scientific reason since levodopa was linked to carbidopa or benserazide. by Jesus Marquez Rivera Project "Parkinsons Here and Now" (2012-2021) "What is Science? Learn from Science that you must doubt of the experts

Hi guys I’m writing this as the last few months I’ve been in excruciating pain . I have sero negative inflammatory arthritis. I’m on weekly benpali injection and arcoxia for day time pain along with tramadol and amitriptaylin on a night . The pain is getting worse my meds don’t seem to be working apart

Hi everyone. Recently I underwent a n EMG (electromyograph) and Nerve Conduction Study to verify the nerve damage since I’m having symptoms of peripheral neuropathy. Both studies were normal. Have any of you underwent such study to confirm peripheral neuropathy (nerve pain, muscle weakness) due to Pernicious

Has anyone tried therapy lights or mood or depression that constantly accompanies Parkinson’s?