Search
Search
About
Log in
Join
Experiences with
Naturopathy
Posts
Communities
2,488 public posts
Filter results
Gait changes
The last time I saw my neurologist, she did EMG and nerve tests and said I had only about 50% of the muscle strength needed to be able to lift my feet up. She said it was due to peripheral neuropathy. This is a Parkinson’s symptom, right? Does/can PD cause peripheral neuropathy? I have so many questions
The last time I saw my neurologist, she did EMG and nerve tests and said I had only about 50% of the muscle strength needed to be able to lift my feet up. She said it was due to peripheral neuropathy. This is a Parkinson’s symptom, right? Does/can PD cause peripheral neuropathy? I have so many questions
Alwezonmymind
in
Cure Parkinson's
6 years ago
Help needed with work
Hi, I also suffer from epidural fibrosis following spinal surgery, i have constant pain in my lower back as well as nerve damage in both legs, my feet are numb and tingly all of the time, I am taking strong medication constantly, everyday, I am unable to try physio and hydro as I did before the pain
Hi, I also suffer from epidural fibrosis following spinal surgery, i have constant pain in my lower back as well as nerve damage in both legs, my feet are numb and tingly all of the time, I am taking strong medication constantly, everyday, I am unable to try physio and hydro as I did before the pain
Kellee75
in
Pain Concern
6 years ago
Amitriptyline for carpal tunnel syndrome?
Hello, my GP has just diagnosed carpal tunnel syndrome and prescribed amitriptyline 10mg. I did some research but didn’t find anything about this drug being used for CTS. I’ve only just started taking it, and I just feel so wiped out. Is that normal? Has anyone else heard of amitriptyline to treat
Hello, my GP has just diagnosed carpal tunnel syndrome and prescribed amitriptyline 10mg. I did some research but didn’t find anything about this drug being used for CTS. I’ve only just started taking it, and I just feel so wiped out. Is that normal? Has anyone else heard of amitriptyline to treat
JasonP
in
Pain Concern
6 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Preliminary
I'm new to HealthUnlocked.I am 82 years today and still with it despite health problems ( obviously) Had mastectomy at 44 years,lymphoedema shortly after and in70's developed nerve damage issues .anyone got brachial neuropathy ?
I'm new to HealthUnlocked.I am 82 years today and still with it despite health problems ( obviously) Had mastectomy at 44 years,lymphoedema shortly after and in70's developed nerve damage issues .anyone got brachial neuropathy ?
Belvidere
in
LSN
6 years ago
Spinal cord stimulator experiences
Hi folks, I am 37 years old and slipped on ice last year, twisted back and my injury was made far worse following physio intervention in which I was asked to lift 5kg weight repetively as quick as I could in a minute. I had an instant flare up resulting in numbness lower back, groin, lower legs ext
Hi folks, I am 37 years old and slipped on ice last year, twisted back and my injury was made far worse following physio intervention in which I was asked to lift 5kg weight repetively as quick as I could in a minute. I had an instant flare up resulting in numbness lower back, groin, lower legs ext
Kerrycop
in
Pain Concern
6 years ago
Breath/Lung/Breathing shortness
Parkinson's disease (PD) patients apart from motor dysfunctions exhibit respiratory disturbances. Their mechanism is still unknown and requires investigation. Our research was designed to examine the activity of phrenic (PHR) and hypoglossal (HG) nerves activity during a hypoxic respiratory response
Parkinson's disease (PD) patients apart from motor dysfunctions exhibit respiratory disturbances. Their mechanism is still unknown and requires investigation. Our research was designed to examine the activity of phrenic (PHR) and hypoglossal (HG) nerves activity during a hypoxic respiratory response
Hidden
in
Cure Parkinson's
6 years ago
Ataxia or not?
My wife has had lifelong epilepsy since birth. She has had 2 brain operations to remove a Hypothalamic Hamartoma and has suffered the effects of many anti convulsant drugs. I overheard on consultant mutter "Ataxia like gait." He said nothing more. Then another asked if she had problems swallowing (she
My wife has had lifelong epilepsy since birth. She has had 2 brain operations to remove a Hypothalamic Hamartoma and has suffered the effects of many anti convulsant drugs. I overheard on consultant mutter "Ataxia like gait." He said nothing more. Then another asked if she had problems swallowing (she
Zombi
in
Ataxia UK
6 years ago
Update on Oxycodone
Hello all my restless friends. I said I would let you know how I fared with starting oxycodone. I have now been taking 5 mg. Longtec (oxycodone) for two weeks. This tablet is slow release over 12 hours. For the first few days I played about with the time of taking and have now settled on 8.00 p.m
Hello all my restless friends. I said I would let you know how I fared with starting oxycodone. I have now been taking 5 mg. Longtec (oxycodone) for two weeks. This tablet is slow release over 12 hours. For the first few days I played about with the time of taking and have now settled on 8.00 p.m
Jelbea
in
Restless Legs Syndrome
6 years ago
Neuropathy?
My problem is not knowing whether I am overworking or under working my body. Either way I get exhausted. Everyone seems to have so much pain, which I do not. Luckily. So, is it neuropathy or not? Sure wished I knew! Sooo frustrating!
My problem is not knowing whether I am overworking or under working my body. Either way I get exhausted. Everyone seems to have so much pain, which I do not. Luckily. So, is it neuropathy or not? Sure wished I knew! Sooo frustrating!
Largo
in
Neuropathy Support
6 years ago
Neuropathy
Morning all, When I was having chemo, although I was asked if I had pains in my hands and feet and answered yes and explained those feelings, I was never told about peripheral neuropathy. Perhaps I should have asked why they were asking but if I did that for every question I'd have been there a week
Morning all, When I was having chemo, although I was asked if I had pains in my hands and feet and answered yes and explained those feelings, I was never told about peripheral neuropathy. Perhaps I should have asked why they were asking but if I did that for every question I'd have been there a week
ZenaJ
in
My Ovacome
6 years ago
Use of Essential Oils to help feel better
Hello all... Again :) Has anyone on here currently use or have tried essential oils to remedy things like sluggishniss, fatigue, sleepless/restless nights, headaches and just feeling terrible and dont no how to pinpoint what your feeling?? especially after having surgery (like an ablation and so forth
Hello all... Again :) Has anyone on here currently use or have tried essential oils to remedy things like sluggishniss, fatigue, sleepless/restless nights, headaches and just feeling terrible and dont no how to pinpoint what your feeling?? especially after having surgery (like an ablation and so forth
Flo2pen
in
AF Association
6 years ago
Hail Mary approach to neuropathy
The neuropathy started last autumn. Turned out I had low b12, low vitamin d, MGUS and low IgA. Despite intensive b12 by injections, folic acid and vitamin d treatment all of which I'm still receiving, the parasthesia is still spreading. It extends up both legs and both arms now and is accompanied by
The neuropathy started last autumn. Turned out I had low b12, low vitamin d, MGUS and low IgA. Despite intensive b12 by injections, folic acid and vitamin d treatment all of which I'm still receiving, the parasthesia is still spreading. It extends up both legs and both arms now and is accompanied by
ABC852031
in
Gluten Free Guerrillas
6 years ago
Docetaxel and leg/groin pain?
First post on this site but read everyday to absorb as much information on fighting this awful disease. My husband has had second round of Docetaxel 5 days ago. He has multiple bone mets in lower back, right hip and right femer. Yesterday he started with severe groin and hip/leg pain on the left side
First post on this site but read everyday to absorb as much information on fighting this awful disease. My husband has had second round of Docetaxel 5 days ago. He has multiple bone mets in lower back, right hip and right femer. Yesterday he started with severe groin and hip/leg pain on the left side
roseanduwe
in
Advanced Prostate Cancer
6 years ago
Low magnesium
Does anyone else have persistently low magnesium, not just when you are on chemo? My oncs are concerned about mine. I'm currently having 3 magnaspartate sachets a day. And they say that if they don't bring it up to near normal levels, they want to refer me to another department for investigations.
Does anyone else have persistently low magnesium, not just when you are on chemo? My oncs are concerned about mine. I'm currently having 3 magnaspartate sachets a day. And they say that if they don't bring it up to near normal levels, they want to refer me to another department for investigations.
Di16
in
My Ovacome
6 years ago
Foot pain could it be referred pain?
I was wondering if anyone else suffers with painful feet? I have had them X-rayed and scanned and both showed very little. I visited the orthodontist last week and they confirmed there is nothing wrong mecanically wrong with my feet. It has been suggested that my foot pain is a referred pain from my
I was wondering if anyone else suffers with painful feet? I have had them X-rayed and scanned and both showed very little. I visited the orthodontist last week and they confirmed there is nothing wrong mecanically wrong with my feet. It has been suggested that my foot pain is a referred pain from my
Foxy07
in
Pain Concern
6 years ago
Blood results
This may not be related to thyroid but due to the advise given from my last post (fainting or feeling faint) my bloods were taken for analysis. One of the results is LDH which Which I haven't a clue about. The range is 120 - 250 my result was 587. Is this anything to worry about?
This may not be related to thyroid but due to the advise given from my last post (fainting or feeling faint) my bloods were taken for analysis. One of the results is LDH which Which I haven't a clue about. The range is 120 - 250 my result was 587. Is this anything to worry about?
Bessiedog
in
Thyroid UK
6 years ago
Finally sleeping without too much pain!
Hi everyone❣️I'm Xindi and I'm self diagnosed PN. I've been suffering with it on and off with it moving around my body, for 3 years...but the past 4 months...it has gotten incredibly worse...pain 24/7. Tried chiropractors, Chinese medicine...no pain relief. Had lots of test (CT, MRI, Gastric and Colon
Hi everyone❣️I'm Xindi and I'm self diagnosed PN. I've been suffering with it on and off with it moving around my body, for 3 years...but the past 4 months...it has gotten incredibly worse...pain 24/7. Tried chiropractors, Chinese medicine...no pain relief. Had lots of test (CT, MRI, Gastric and Colon
Xindirock11
in
Foggy's "Invisible Illness" Support
6 years ago
Lymphovascular lesion
Hello all, I’m wondering if anyone has had any experience of lymphovascular lesions and how it presented and was diagnosed. My young daughter (11 years) has primary lymphoedmea of her lower body including her pubic mound. Last year she was also diagnosed with lymphorrea. A great MCT diet has controlled
Hello all, I’m wondering if anyone has had any experience of lymphovascular lesions and how it presented and was diagnosed. My young daughter (11 years) has primary lymphoedmea of her lower body including her pubic mound. Last year she was also diagnosed with lymphorrea. A great MCT diet has controlled
ssc123
in
LSN
6 years ago
I’m new here. Have neuropathy. Decreasing my intake of gabapentine. Anyone taking this medication?
Hello I had spinal cord surgery 4 months ago and ever since i have neuropathy. Worst on my hands, feet, stomach (like the feeling of a very painful belt), lower back. I started on Lyrica which gave me swollen hands and feet so i was stopped on that. I am now on the Gabapentine which is not helping much
Hello I had spinal cord surgery 4 months ago and ever since i have neuropathy. Worst on my hands, feet, stomach (like the feeling of a very painful belt), lower back. I started on Lyrica which gave me swollen hands and feet so i was stopped on that. I am now on the Gabapentine which is not helping much
ellenhamid
in
Foggy's "Invisible Illness" Support
6 years ago
Marijuana (Medical Grade) & Neouropathic Pain
I was diagnosed with Neouropathy over 85% of of my body. The numbness was bad enough but the neuropathic pain was unbelievable. The pain had now interupted my life. No driving, hard to walk. I felt like I was on a slippery slope and didn't know when it was going to STOP!!!!!!!!!!, It was suggested to
I was diagnosed with Neouropathy over 85% of of my body. The numbness was bad enough but the neuropathic pain was unbelievable. The pain had now interupted my life. No driving, hard to walk. I felt like I was on a slippery slope and didn't know when it was going to STOP!!!!!!!!!!, It was suggested to
Hidden
in
Foggy's "Invisible Illness" Support
6 years ago
1
...
59
60
61
...
100
Next page
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Fibromyalgia Action UK
276 results
Pernicious Anaemia Society
251 results
Pain Concern
245 results
View top 10 communities
Sort by
Most Relevant
Newest