Experiences with

Naturopathy

What kind of doctor do I see to address RLS or whatever this is? I'm diagnosed by my PCP who thinks that, given the leg/arm pain and leg spasms, it might be something else. She's not well-versed and has just been Googling stuff.

I spoke our hospital’s new rheumatologist In May about the recurring burning sensation I have in my feet and hands, particularly at night, and he prescribed Amitriptyline. I asked my fellow Lupies here for advice and experiences of this drug and the response was brilliant thank you. However, by the

Hi, When my husband massages whatever area on my legs are playing up with RLS the area is really painful when he massages it , Anyone know why this is ? as the same area is not painful if it is not affected by the RLS ,

PD symptoms first appeared about five years ago. Officially diagnosed last fall. Not taking any allopathic meds or mucuna so far. My sleep is terrible, typically 3-5 hours per night. The problem is not physical stiffness or pain. Just difficulty falling asleep and staying asleep. I am not particularly

Hello all! I have such a lot of health problems and here I am again. Besides my long list of pains I have Peripheral Neuropathy. I have a few questions to people here who also suffer from it. I am not a diabetic but I had cancer and my PN was caused by chemotherapy. I always say chemo destroyed me.

Hello everyone. My father is dealing with peripheral neuropathy after having several rounds of docetaxel and jevtana. Hence, I would like to ask what can he take that would significantly improve this adverse effects from the chemotherapy agents? He is only taking 100 mg of gabapentin a day because

Hi. Do you think sore, painful feet with burning and tingling sensation is associated with Low thyroid? I used to have painful burning feet before I was diagnosed with hypothyroidism. A few months after taking Levothyroxine, it went away and I didn’t think much about it. Now, 5 years later, the painful

Not really a question but I've discovered AZO pain killer really works for urinary pain etc. within 20mminutes feel so much better. Not a cure of course but what a relief ! Doctor has me on 25mg nitrofurantoin for a month. The colour of my urine when taking AZO is bright red/orange. Doesnt interfere

Hello everyone, One day ,about 4 months ago ,when i woke up I had a strange feeling of of ants crawling/electricity going through my calves.It wasn't painful just very annoying.I didn't really notice it during the day ,because i was focusing on work but it was there.When the night came it kept me from

Ridiculously tired and headaches, thought it was heatstroke but now my knees are throbbing and my hand joints hurt I’m thinking it’s a flare?! Anyone else get similar, only diagnosed in January..

Part 2 in free mini series: Holistic Nutrition How we feel about ourselves, will be reflected by how we nourish ourselves. Read that over. Feel it. And now, dear one, consider your current eating habits. Self enquiry. No judgement. Just curiosity. Habits are easy to form....not so easy

Hi everyone - I’ve finally been told I have palindromic rheumatism and fibromyalgia, prescribed Amitriptyline to take at bedtime. How have you found this as a treatment? ss

Two years later after near death experience due to PA. Neuropathy still alive, but changing very SLOWLY and still making progression. I found out a website that sells ampules 5MG (5000ug A.K.A. micro grams) methylcobalamin the good stuff. http://balans-arnhem.ccvshop.nl/Webwinkel-Product-143400297

Hi Donna First time posting in this forum . Have read your post and I have experienced similar sensations since March . Neurologist did basic tests and referred me for nerve conduction tests . However these have not happened because of lockdown . She did order a bank of blood tests which I had last

I was on ropinarole for 10 years and progressed from 1mg to 3mg and it still worked for my restless leg and the only reason I came off it was because I couldn't sleep and had heard of augument in relation to these tablets. Since I have come off them nothing else seems to work for me ie Gabapentin Pregabalin

Hi everyone I was just wondering if anyone else suffered with numbness or pins and needles as i get it bad jn my hands it also occurs in my feet and legs sometimes my hips how do youll cope with it sometimes my hand so bad cant hold anything

Searching mode continues for: 1. Naturopathic Med professionals 2. Integrative Med professionals Within a 100-150 mile radius of my home front. Ft. Wayne,IN.... Nalakrats and Tall_Allen have helped. Still looking and will keep on looking

Getting ready to start six cycles of docetaxel in a few weeks. Have been reading about the use of ice mittens, booties and ice skull cap to ward off peripheral neuropathy and hair lose. Does this acutely work? Also, my OM at Moffitt Center in Tampa has been delaying the beginning of chemotherapy while

Dear all We have a virtual meeting of the Medical Advisory Panel of Ataxia UK in a couple of weeks. One of the topics we will be discussing is how neurology appointments have been affected by the coronavirus climate that we unfortunately find ourselves in. I would be so grateful if you could let me

I received a bonus container of “Pure Creatine” with a mail order, a couple months ago. I decided to go to the internet to see what it was used for and was surprised to see claims that some people feel it has been helpful for PwP. I use an electrolyte drink mix recommended by my primary care doctor.