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Fitbit charge 2 - carpal tunnel syndrome and musculoskeletal disorders
My husband bought me a fitbit for Christmas. After reading the booklet, it would appear that I can not wear this due to having carpal tunnel syndrome and musculoskeletal disorder i.e. fibromyalgia. --- Is anyone wearing this Fitbit charge 2 with no side effects?
My husband bought me a fitbit for Christmas. After reading the booklet, it would appear that I can not wear this due to having carpal tunnel syndrome and musculoskeletal disorder i.e. fibromyalgia. --- Is anyone wearing this Fitbit charge 2 with no side effects?
FIBROWORK
in
Fibromyalgia Action UK
6 years ago
lavatory ani spasm
hi I have been suffering with lavatory muscle for 4 years . ive had injections and I'm on lyrica and palexia plus sleeoing tablets . any help much appreciatyed jeff
hi I have been suffering with lavatory muscle for 4 years . ive had injections and I'm on lyrica and palexia plus sleeoing tablets . any help much appreciatyed jeff
passat4932
in
Pelvic Pain Support Network
6 years ago
Amlodipine for Raynaud's?
I was diagnosed with Raynaud's (cold hands) about 5 years ago, and my doctor put me on Nifedipine ER which has helped significantly. I just got a notice from my drug insurance provider that for next year they will no longer covers the cost of Nifedipine, and suggest Amlodipine Besylate instead. The
I was diagnosed with Raynaud's (cold hands) about 5 years ago, and my doctor put me on Nifedipine ER which has helped significantly. I just got a notice from my drug insurance provider that for next year they will no longer covers the cost of Nifedipine, and suggest Amlodipine Besylate instead. The
shedridc
in
Scleroderma & Raynaud's UK (SRUK)
6 years ago
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PD & Mucuna
I was diagnosed with PD when I was 50 years old I'm now 55 but suspect it started three years prior. I held off taking medication not because the neurologist didn't want to drug me up I just felt I didn't need it at that time. This past December I reluctantly succumbed to the inevitable Carbidopa levodopa
I was diagnosed with PD when I was 50 years old I'm now 55 but suspect it started three years prior. I held off taking medication not because the neurologist didn't want to drug me up I just felt I didn't need it at that time. This past December I reluctantly succumbed to the inevitable Carbidopa levodopa
Stevenmast
in
Cure Parkinson's
6 years ago
Hypermagnesemia In Hypothyroidism
Hi everyone.. I found myself very sensitive to magnesium supplements and even foods rich in mag . Searching the internet I found hypothyroidism causes Hypermagnesemia. Anyone know more about this subject?
Hi everyone.. I found myself very sensitive to magnesium supplements and even foods rich in mag . Searching the internet I found hypothyroidism causes Hypermagnesemia. Anyone know more about this subject?
Ali1101
in
Thyroid UK
6 years ago
Re - do Ablation for 2018
Sort of knew this was coming ! I had Cryoablation in Feb this year ( for vagal AF) thought all was settling as the months were progressing until last 3 months when symptoms began reappearing more noticeably. Have had a brief trial of Sotalol in last couple of weeks which really didn't suit me making
Sort of knew this was coming ! I had Cryoablation in Feb this year ( for vagal AF) thought all was settling as the months were progressing until last 3 months when symptoms began reappearing more noticeably. Have had a brief trial of Sotalol in last couple of weeks which really didn't suit me making
Trilby8
in
AF Association
6 years ago
Rls
Hi I have had success with my rls and would like to help anyone out there who is suffering I know it can be hell . I searched the web some time ago and found a doctor who specialised in drug free treatment. He is based in Colchester difficult to get there but he is well qualified and worth the time and
Hi I have had success with my rls and would like to help anyone out there who is suffering I know it can be hell . I searched the web some time ago and found a doctor who specialised in drug free treatment. He is based in Colchester difficult to get there but he is well qualified and worth the time and
Hoochybaby
in
Restless Legs Syndrome
6 years ago
Axonal sensory peripheral neuropathy
Hi I have axonal sensory peripheral neuropathy had all blood test done they all come back negative vitamin's all ok they said it's hereditary my leg arms or always aching I'm on Gabapentin 3 times a day they don't seem to help much lately im starting to get blurred vision is this part of the Axonal sensory
Hi I have axonal sensory peripheral neuropathy had all blood test done they all come back negative vitamin's all ok they said it's hereditary my leg arms or always aching I'm on Gabapentin 3 times a day they don't seem to help much lately im starting to get blurred vision is this part of the Axonal sensory
tower-1
in
Foggy's "Invisible Illness" Support
6 years ago
Levodopa Medications and Vitamin B6
Introduction
Vitamin B6 is a cofactor in over 100 enzymatic reactions. In the process it is converted from the active form, principally P5P (pyridoxal-5-phosphate), to the inactive form, pyridoxine. An excess of pyridoxine is toxic because it occupies sites that require the active form. For this
Introduction
Vitamin B6 is a cofactor in over 100 enzymatic reactions. In the process it is converted from the active form, principally P5P (pyridoxal-5-phosphate), to the inactive form, pyridoxine. An excess of pyridoxine is toxic because it occupies sites that require the active form. For this
park_bear
in
Cure Parkinson's
6 years ago
Six months off all forms of b12
Hi I’ve been off all forms of b12 for six months now and got a serum b12 of 241pmol/l and an active b12 of 127 pmol/l on 21/11/17 (its 9/12/17 today). Does this mean I’m not b12d? I began self injecting back in April but had to stop due to developing awful anxiety after each one and then some very negative
Hi I’ve been off all forms of b12 for six months now and got a serum b12 of 241pmol/l and an active b12 of 127 pmol/l on 21/11/17 (its 9/12/17 today). Does this mean I’m not b12d? I began self injecting back in April but had to stop due to developing awful anxiety after each one and then some very negative
Steap
in
Pernicious Anaemia Society
6 years ago
Peripheral Neuropathy pain
I was diagnosed 1991 with CMT type 1(a) I am 67 now and had my knees replaced , my toes staightened etc etc. I get periferal neuropathy pains on just one toe. It last for 3_4 days and by using the T.E.N.S machine it allows me to get some sleep. Is there anything out there that would be helpful ? I walk
I was diagnosed 1991 with CMT type 1(a) I am 67 now and had my knees replaced , my toes staightened etc etc. I get periferal neuropathy pains on just one toe. It last for 3_4 days and by using the T.E.N.S machine it allows me to get some sleep. Is there anything out there that would be helpful ? I walk
Tandarts
in
Charcot-Marie-Tooth UK
6 years ago
Advice sought on peripheral neuropathy and doctors
I have suffered with uncomfortable feet with an unpleasant sensation crawling up my legs for well over a year. I had put it down to another auto immune disease that falls into the uncommon group so not a huge amount of information available other from those with the disease and their experiences. I
I have suffered with uncomfortable feet with an unpleasant sensation crawling up my legs for well over a year. I had put it down to another auto immune disease that falls into the uncommon group so not a huge amount of information available other from those with the disease and their experiences. I
butterflyEi
in
Pain Concern
6 years ago
selegiline and mortality
Comparison of therapeutic effects and mortality data of levodopa and levodopa combined with selegiline in patients with early, mild Parkinson's disease Levodopa in combination with selegiline seemed to confer no clinical benefit over levodopa alone in treating early, mild Parkinson's disease. Moreover
Comparison of therapeutic effects and mortality data of levodopa and levodopa combined with selegiline in patients with early, mild Parkinson's disease Levodopa in combination with selegiline seemed to confer no clinical benefit over levodopa alone in treating early, mild Parkinson's disease. Moreover
Hidden
in
Cure Parkinson's
6 years ago
Peripheral Neuropathy
Does anyone know if there is a link between peripheral neuropathy and hypothyroidism? I have seen my GP recently because of unexplained pain in two of my toes on my left foot. She said it could be due to neuropathy and has referred me for a scan of my foot. I know my B12 was low on my last blood test
Does anyone know if there is a link between peripheral neuropathy and hypothyroidism? I have seen my GP recently because of unexplained pain in two of my toes on my left foot. She said it could be due to neuropathy and has referred me for a scan of my foot. I know my B12 was low on my last blood test
Citta
in
Thyroid UK
6 years ago
Numbness and tingling problem
Hello dear all I m facing problem of numbness in legs alongwith tingling.my present hb1ac is 6.3.i also hv backache.i m taking b12.may be due to peripheral neuropathy..i m given calcium pantothenate.i m not on any med.
Hello dear all I m facing problem of numbness in legs alongwith tingling.my present hb1ac is 6.3.i also hv backache.i m taking b12.may be due to peripheral neuropathy..i m given calcium pantothenate.i m not on any med.
Manie
in
Diabetes India
6 years ago
Feet and ankles are screaming at me!
Sorry for being dramatic, but I'm so fed up with my feet and ankles. They are always a problem for me but at the moment they are awful, making walking anywhere a misery. I have sharp pain in ankles and constant burning on the top of my feet and toes. I can't find anything remotely comfortable to wear
Sorry for being dramatic, but I'm so fed up with my feet and ankles. They are always a problem for me but at the moment they are awful, making walking anywhere a misery. I have sharp pain in ankles and constant burning on the top of my feet and toes. I can't find anything remotely comfortable to wear
creaky
in
LUPUS UK
6 years ago
Csf protein
Did anybody have raised csf protein levels as part of their Vasculitis investigations
Did anybody have raised csf protein levels as part of their Vasculitis investigations
Perkles
in
Vasculitis UK
6 years ago
How To Stop and Prevent Sarcopenia (loss of muscle mass and strength)
"Sarcopenia, the loss of muscle mass and strength, becomes more common with age and can decrease lifespan and quality of life. "Eating enough calories and high-quality protein can slow down the rate of muscle loss. Omega-3 and creatine supplements may also help fight sarcopenia. "Nevertheless, exercising
"Sarcopenia, the loss of muscle mass and strength, becomes more common with age and can decrease lifespan and quality of life. "Eating enough calories and high-quality protein can slow down the rate of muscle loss. Omega-3 and creatine supplements may also help fight sarcopenia. "Nevertheless, exercising
PDConscience
in
Cure Parkinson's
6 years ago
RLS/Pain with BP and sugar
Hi every one, I am new in the group. My mother suffering from RLS in legs and in arms and pain in lega as well along with rest less legs since 10 years. She is currently using Ropinirol 1mg at night and 1mg after breakfast + Pregabalin 75mg, but she is not getting normal , i mean she feel relax sometimes
Hi every one, I am new in the group. My mother suffering from RLS in legs and in arms and pain in lega as well along with rest less legs since 10 years. She is currently using Ropinirol 1mg at night and 1mg after breakfast + Pregabalin 75mg, but she is not getting normal , i mean she feel relax sometimes
Wajidali25
in
Restless Legs Syndrome
6 years ago
Tingling/ numbness improved after SI but is now getting worse again!
Hi again x I was doing well SI every other day for 3 weeks and the tingling and numbness had completely gone. I then reduced SI down to twice a week and the tingling started to come back. I went back to alternate days and it improved for a week or so and now it's back almost all the time. I know I read
Hi again x I was doing well SI every other day for 3 weeks and the tingling and numbness had completely gone. I then reduced SI down to twice a week and the tingling started to come back. I went back to alternate days and it improved for a week or so and now it's back almost all the time. I know I read
Padders12
in
Pernicious Anaemia Society
6 years ago
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