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Vintage Pammy has non diabetic Peripheral Neuropathy :(
Hi my name is Pammy and I have PN Peripheral Neuropathy. I am new to being connected to any support group but at the risk of totally going round the bend, I thought I might ought to do something productive and join in a support group. If nothing else by some of the posts I have read and responded to
Hi my name is Pammy and I have PN Peripheral Neuropathy. I am new to being connected to any support group but at the risk of totally going round the bend, I thought I might ought to do something productive and join in a support group. If nothing else by some of the posts I have read and responded to
VintagePammy
in
Foggy's "Invisible Illness" Support
8 years ago
Lyrica for Neuropathy
Hi! Hope you all are having a good day! Another question about Neuropathy. Anyone been put on Lyrica because of Neuropathy. Did it help? My doctor called in a prescription cream but it hasn't helped at all. My hands hurt continously & I just want relief. Thanks in advance for insight!!!
Hi! Hope you all are having a good day! Another question about Neuropathy. Anyone been put on Lyrica because of Neuropathy. Did it help? My doctor called in a prescription cream but it hasn't helped at all. My hands hurt continously & I just want relief. Thanks in advance for insight!!!
alnovca
in
My Ovacome
8 years ago
Stomach problems
Hi guys it's been a while since I've been on here and last time I said I had problems with my stomach by weight gaining and bad pains and I thought it was my meds so I changed them but it wasn't anything to do with my meds I'm 99% certain it's a stomach ulcer so my doctor put me on a course of ranitadine
Hi guys it's been a while since I've been on here and last time I said I had problems with my stomach by weight gaining and bad pains and I thought it was my meds so I changed them but it wasn't anything to do with my meds I'm 99% certain it's a stomach ulcer so my doctor put me on a course of ranitadine
Mal69
in
HIV Partners
8 years ago
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Happy story - three months later
Hello Warriors, my wife Gauri had her bloods and scan done today. Last chemo was end May and now three months later her CA125 and scan are in normal range. With His Grace and all your Blessings may she remain this way forever. Her hair is also coming back, softer than it was earlier. Fatigue, weight
Hello Warriors, my wife Gauri had her bloods and scan done today. Last chemo was end May and now three months later her CA125 and scan are in normal range. With His Grace and all your Blessings may she remain this way forever. Her hair is also coming back, softer than it was earlier. Fatigue, weight
Naimish
in
My Ovacome
8 years ago
Help please! NHS definition of each number on pain scale
Hi I'm new to the group, had Fibro since I can remember (Rheumatologist thinks since I was 11 now 33) and first was a battle to be believed and get a diagnosis, which only came in 2011/2 (can't remember fog!) now a battle to sort med's given new research I've found on here. I want my old GP back he
Hi I'm new to the group, had Fibro since I can remember (Rheumatologist thinks since I was 11 now 33) and first was a battle to be believed and get a diagnosis, which only came in 2011/2 (can't remember fog!) now a battle to sort med's given new research I've found on here. I want my old GP back he
Hidden
in
Fibromyalgia Action UK
8 years ago
Newbie
Hi everyone just joined the site and I'm so glad I did. My story is very similar to some of yours diagnosed December 2014 stage 3c OC. From then on I felt I had a blue flashing light on my head operated on Xmas eve and spent all Xmas in hospital. Don't get me wrong I'm so grateful they acted so quickly
Hi everyone just joined the site and I'm so glad I did. My story is very similar to some of yours diagnosed December 2014 stage 3c OC. From then on I felt I had a blue flashing light on my head operated on Xmas eve and spent all Xmas in hospital. Don't get me wrong I'm so grateful they acted so quickly
SuSue
in
My Ovacome
8 years ago
Pain in legs
Diagnosed with peripheral neuropathy and having every other day injections plus taking b12 boost and Berocca. My legs are now painful rather than just weak and feeble - is this a good or bad sign?
Diagnosed with peripheral neuropathy and having every other day injections plus taking b12 boost and Berocca. My legs are now painful rather than just weak and feeble - is this a good or bad sign?
Carolyn1964
in
Pernicious Anaemia Society
8 years ago
Needing extra b12
Hi. Can someone please recommend a good supplement to take daily? I am currently on injections every other day for foreseeable future due to peripheral neuropathy and also have a berrocca and b12 boost spray but am worse now than before!!, really need some help, advice and more b12 - any suggestions
Hi. Can someone please recommend a good supplement to take daily? I am currently on injections every other day for foreseeable future due to peripheral neuropathy and also have a berrocca and b12 boost spray but am worse now than before!!, really need some help, advice and more b12 - any suggestions
Carolyn1964
in
Pernicious Anaemia Society
8 years ago
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
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
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