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Neuropathy
So my doctor finally told me some of my pain in my arm is neuropathy. I've heard about this before because its a complication of my mum and brothers condition, so it's not new to me. But it does reinforce the idea that my nerve was damaged in my op =( He is doing his best to rush my referral which I'm
So my doctor finally told me some of my pain in my arm is neuropathy. I've heard about this before because its a complication of my mum and brothers condition, so it's not new to me. But it does reinforce the idea that my nerve was damaged in my op =( He is doing his best to rush my referral which I'm
vampress
in
Pain Concern
8 years ago
Essential Oils
I bought some before the diagnosis and was looking online to buy a diffuser when I came across information specifically about Essential Oils and Parkinsons. Have any of you used them? I bought mine from the company called Young Living which is supposed to sell the purest forms. I was just helping a
I bought some before the diagnosis and was looking online to buy a diffuser when I came across information specifically about Essential Oils and Parkinsons. Have any of you used them? I bought mine from the company called Young Living which is supposed to sell the purest forms. I was just helping a
Boyce3600
in
Cure Parkinson's
8 years ago
Henoch-schonlein Purpura.
Hi. My wife is being passed around GP's who admit no experience of this condition- Henoch-schonlein Purpura. Just had 1 blood test - still waiting results. No treatment. Both very worried about what we have read in terms of possible deveopments. Are there any experts in North Wales or North West UK
Hi. My wife is being passed around GP's who admit no experience of this condition- Henoch-schonlein Purpura. Just had 1 blood test - still waiting results. No treatment. Both very worried about what we have read in terms of possible deveopments. Are there any experts in North Wales or North West UK
Yeprat
in
Vasculitis UK
8 years ago
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tablets for pain
Before I was dx with PBC the doctor prescribed Metamizol Aristo 575 mg capsules EFG for pain/discomfort, can I still take these, I worry now what I can take.
Before I was dx with PBC the doctor prescribed Metamizol Aristo 575 mg capsules EFG for pain/discomfort, can I still take these, I worry now what I can take.
Sandie1
in
PBC Foundation
8 years ago
Student Research Request: Opportunity to win a £25 Amazon voucher
Good afternoon, my name is Ella and I’m a student studying Geography at Cambridge University. Having lived with severe chronic pain myself, I chose to investigate the effects of the UK’s 2012 Welfare Reform on the experiences of those in chronic pain. I hope that it will give people in chronic pain a
Good afternoon, my name is Ella and I’m a student studying Geography at Cambridge University. Having lived with severe chronic pain myself, I chose to investigate the effects of the UK’s 2012 Welfare Reform on the experiences of those in chronic pain. I hope that it will give people in chronic pain a
ellasivan
in
Pain Concern
8 years ago
Pins and needles
Hi, I have been having pins and needles in hands and feet since my loading injections 2 months ago. I have read on here many times that this could be part of recovery process however it has started to travel up to elbows and knees. Is this normal or should I go back to GP? Not due another b12 jab until
Hi, I have been having pins and needles in hands and feet since my loading injections 2 months ago. I have read on here many times that this could be part of recovery process however it has started to travel up to elbows and knees. Is this normal or should I go back to GP? Not due another b12 jab until
HeidiO
in
Pernicious Anaemia Society
8 years ago
Ideas for Restless Legs
Hi I am a newbie to the site ! Have had RLS for about 30 odd years had various treatments, patches and tablets am now on Oprymea (pramipexole) 3.15mg prolonged release tablets and now they do not work very well, the Doctor has said as I am now on the strongest dose they can not up it and there is nothing
Hi I am a newbie to the site ! Have had RLS for about 30 odd years had various treatments, patches and tablets am now on Oprymea (pramipexole) 3.15mg prolonged release tablets and now they do not work very well, the Doctor has said as I am now on the strongest dose they can not up it and there is nothing
desperate_41
in
Restless Legs Syndrome
8 years ago
ITCH😤
Hi Everyone🙅 Has anyone had Jaundise relating to gallbadder problems. Just needing some help with this, as I did develop Jaundise and taken into hospital had stone removed this is about a month ago now two of the medications I was put on was for this awful itch I got through having Jaundise, Chlorphenamine
Hi Everyone🙅 Has anyone had Jaundise relating to gallbadder problems. Just needing some help with this, as I did develop Jaundise and taken into hospital had stone removed this is about a month ago now two of the medications I was put on was for this awful itch I got through having Jaundise, Chlorphenamine
Jeaniep
in
Thyroid UK
8 years ago
Help with neuropathy in feet
Hi everyone especially those who also have problems with neuropathy. Just wanted to pass on a tip which might help you as it has me. A physio recommended rolling a tennis ball under each foot to stimulate circulation and to reduce painful spasms in bed. I tried it and it has been successful so maybe
Hi everyone especially those who also have problems with neuropathy. Just wanted to pass on a tip which might help you as it has me. A physio recommended rolling a tennis ball under each foot to stimulate circulation and to reduce painful spasms in bed. I tried it and it has been successful so maybe
Barlow1951
in
My Ovacome
8 years ago
OT: feeling a phantom drop of water on leg, arm
I've had a recurring feeling of a drop of cold water on my bare right shin, exactly like if you were wearing shorts and dripped a single drop of cold water on your shin. Often it will happen somewhere (on the street or in the kitchen) where I might have trod in a puddle or dripped water on myself, so
I've had a recurring feeling of a drop of cold water on my bare right shin, exactly like if you were wearing shorts and dripped a single drop of cold water on your shin. Often it will happen somewhere (on the street or in the kitchen) where I might have trod in a puddle or dripped water on myself, so
puncturedbicycle
in
Thyroid UK
8 years ago
:/ periphial neuropathy
Along with my PD. I have periphial neuropathy causing numbness in both lower legs,, this affects my walking any distance considerably, my neurologist has suggested this is not necessarily related to my PD, l would welcome any comments from fellow sufferers. I live in the UK.
Along with my PD. I have periphial neuropathy causing numbness in both lower legs,, this affects my walking any distance considerably, my neurologist has suggested this is not necessarily related to my PD, l would welcome any comments from fellow sufferers. I live in the UK.
ramondo4
in
Cure Parkinson's
8 years ago
Peripheral neuropathy??? burning?
Hi, out of nowhere today my fingers are really burning and tingling on and off (its not painful but just hot and burns)... they say dont google your symptoms but I did, and most results say 'peripheral neuropathy' which can be caused by diabetes (which as far as I know I dont have).... so I am very confused
Hi, out of nowhere today my fingers are really burning and tingling on and off (its not painful but just hot and burns)... they say dont google your symptoms but I did, and most results say 'peripheral neuropathy' which can be caused by diabetes (which as far as I know I dont have).... so I am very confused
Sarahskittles
in
Foggy's "Invisible Illness" Support
8 years ago
Neuropathy........Ouch
Hi all! I haven't written in a while & so I hope you all are doing well. I've tried to read and keep up with posts. I've had 3 of 6 treatments of carbo/taxol so far & last night, neuropathy was awful in my hands and fingers. It hurt so bad & couldn't seem to get relief. Is there anything you can do
Hi all! I haven't written in a while & so I hope you all are doing well. I've tried to read and keep up with posts. I've had 3 of 6 treatments of carbo/taxol so far & last night, neuropathy was awful in my hands and fingers. It hurt so bad & couldn't seem to get relief. Is there anything you can do
alnovca
in
My Ovacome
8 years ago
CBD Rich topicals against pain
read this review first : I use this for restless leg syndrome (RLS), INSTANT relief!! The tingling sensations are gone within in seconds and the need to kick or move my leg is gone within a few minutes. I gave some to my mom to use for her arthritis in her hand, she had movement in her fingers (normally
read this review first : I use this for restless leg syndrome (RLS), INSTANT relief!! The tingling sensations are gone within in seconds and the need to kick or move my leg is gone within a few minutes. I gave some to my mom to use for her arthritis in her hand, she had movement in her fingers (normally
Hidden
in
Restless Legs Syndrome
8 years ago
Peripheral neuropathy
Any tips? My feet have been especially bad, although I have some numbness and tingling in fingertips as well. They had to hold chemotherapy this latest time because of the neuropathy.
Any tips? My feet have been especially bad, although I have some numbness and tingling in fingertips as well. They had to hold chemotherapy this latest time because of the neuropathy.
westseraph
in
Prostate Cancer And Gay Men
8 years ago
I'm new to this . .
I have "pseudohypoparathyroidism" (yes it's a real mouthful!). I'm 57 and I've had this since I was born although it didn't come to light until I was 21. As a result of this above I've also got diabetes (type 2). I have suffered terribly with excessive sweating all my life and it gets worse if I'm at
I have "pseudohypoparathyroidism" (yes it's a real mouthful!). I'm 57 and I've had this since I was born although it didn't come to light until I was 21. As a result of this above I've also got diabetes (type 2). I have suffered terribly with excessive sweating all my life and it gets worse if I'm at
Mazzer59
in
Thyroid UK
8 years ago
Foot pain: can you solve my problem?
I suffer of PD from 8 years. My predominant symptoms are rigidity and bradikesia on right side, but my main problem now is a twisting of my right foot outwards and a strong pain below my foot. Walking has become difficult. Orthopedists say it is a neurologic problem, but none neurologist solves my pain
I suffer of PD from 8 years. My predominant symptoms are rigidity and bradikesia on right side, but my main problem now is a twisting of my right foot outwards and a strong pain below my foot. Walking has become difficult. Orthopedists say it is a neurologic problem, but none neurologist solves my pain
emmemi
in
Cure Parkinson's
8 years ago
Newbie
Hello all new to this group , I have small fiber nuropathy , had it for past 2 years in such pain with it , went to see gp yesterday asked for morphine patches as I have had bad wk , seem to be helping at the min . Nice to get some sleep last night for a change . Is there anybody on here from the northwest
Hello all new to this group , I have small fiber nuropathy , had it for past 2 years in such pain with it , went to see gp yesterday asked for morphine patches as I have had bad wk , seem to be helping at the min . Nice to get some sleep last night for a change . Is there anybody on here from the northwest
Soulgirl123
in
Foggy's "Invisible Illness" Support
8 years ago
Diabetic neuropathy - a little unusual
Hello all. Let me tell you about myself, for all who may be interested. When I noticed a balance problem a couple of years or so ago, I was diagnosed with diabetic peripheral neuropathy. I've been type 1 diabetic for over 30 years. However, I seem to be different from the run of the mill peripheral neuropathy
Hello all. Let me tell you about myself, for all who may be interested. When I noticed a balance problem a couple of years or so ago, I was diagnosed with diabetic peripheral neuropathy. I've been type 1 diabetic for over 30 years. However, I seem to be different from the run of the mill peripheral neuropathy
DozeyJohn
in
Foggy's "Invisible Illness" Support
8 years ago
Parkinsons and Periodontal Disease
Hi I am new to this I was diagnosed with PD in March and have been following conversations pretty well since I first got over the shock! I am wondering if there has been any research linking PD with Periodontal disease. I have been reading lots of material about Gut bacteria and it's connection with
Hi I am new to this I was diagnosed with PD in March and have been following conversations pretty well since I first got over the shock! I am wondering if there has been any research linking PD with Periodontal disease. I have been reading lots of material about Gut bacteria and it's connection with
Coling
in
Cure Parkinson's
8 years ago
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