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Feet and Leg Spasms
I have moderate peripheral neuropathy and started having feet/leg spasms this past year. Episodes getting worse until recently my right foot/calf was completely incapacitated for 4 hours. The spasms are worse in the right, but also present in the left. Worse during the night and when I get up in morning
I have moderate peripheral neuropathy and started having feet/leg spasms this past year. Episodes getting worse until recently my right foot/calf was completely incapacitated for 4 hours. The spasms are worse in the right, but also present in the left. Worse during the night and when I get up in morning
Hidden
in
Neuropathy Support
7 years ago
Ldn prescriber Dr. Cory Tichauer has 15 years experience and runs his naturopathic “Bear Creek Clinic” in Oregon.
He avoids opiates and antibiotics as much as possible, and does a great job of combining conventional western medicine with
Naturopathy
. Review by Ken Bruce https://vimeo.com/241816701
He avoids opiates and antibiotics as much as possible, and does a great job of combining conventional western medicine with
Naturopathy
. Review by Ken Bruce https://vimeo.com/241816701
liveurlife
Volunteer
in
LDN Research Trust
7 years ago
Burning sensation entire body-after knees surgery
My problem started about 1 month after surgery of both knees replacements same time over 1 1/2 yrs ago. First it started from the feet burning, slowly increasing to Knees and below, then from waist below and now , for the last 3-4 months entire body. My neurologist from Univ. of Michigan advised me
My problem started about 1 month after surgery of both knees replacements same time over 1 1/2 yrs ago. First it started from the feet burning, slowly increasing to Knees and below, then from waist below and now , for the last 3-4 months entire body. My neurologist from Univ. of Michigan advised me
alal42
in
Pernicious Anaemia Society
7 years ago
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Mild exercise or rest up
Having a session of uncomfortable AF, take Apixabam and Sotalol, but wondered what peeps do to help, a bit of exercise or just rest up. I get very breathless especially on standing, so not tried exercise as yet. My sessions last usually 3 days, this one probably triggered by Christmas which was when
Having a session of uncomfortable AF, take Apixabam and Sotalol, but wondered what peeps do to help, a bit of exercise or just rest up. I get very breathless especially on standing, so not tried exercise as yet. My sessions last usually 3 days, this one probably triggered by Christmas which was when
shorttail
in
AF Association
7 years ago
Brand change
The pharmacy switched me to a generic brand after my dosage was uped to .175. After two days of taking new meds. I’ve had extreme pins and needles and some foggy head feelings. Not quite vertigo or dizziness but right up there. Any thoughts on the medicine change? The pins numbness has almost all gone
The pharmacy switched me to a generic brand after my dosage was uped to .175. After two days of taking new meds. I’ve had extreme pins and needles and some foggy head feelings. Not quite vertigo or dizziness but right up there. Any thoughts on the medicine change? The pins numbness has almost all gone
Mattdwill
in
Thyroid UK
7 years ago
From oxy to cbd
Hello, i have severe fibro and a back injury and am currently taking 4 doses of 20mg oxycodone a day also 3 doses of 600mg gabbapentin a day. I wish to start using cbd oil and kick the oxy but am worried about first trying the cbd whilst taking the oxy ( you have to be weaned off oxycodone). My question
Hello, i have severe fibro and a back injury and am currently taking 4 doses of 20mg oxycodone a day also 3 doses of 600mg gabbapentin a day. I wish to start using cbd oil and kick the oxy but am worried about first trying the cbd whilst taking the oxy ( you have to be weaned off oxycodone). My question
maisiebess
in
Fibromyalgia Action UK
7 years ago
Is this telangiectasia ?
I noticed red dots on my stomach and on my chest but I also have quite a few purple/red lines above my knees that look like spiders. Are these both the red dots and the lines telangiectasias? I also noticed red dots below my nail. Thank you very much for your responses.
I noticed red dots on my stomach and on my chest but I also have quite a few purple/red lines above my knees that look like spiders. Are these both the red dots and the lines telangiectasias? I also noticed red dots below my nail. Thank you very much for your responses.
Rudiguer
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
peripheral neuropathy
Hello everyone, I hope you had a good Christmas As you can see from my post heading I suffer with Neuropathy and wondered if anyone else does. I have had this since 2014 and it has steadily been getting worse., my medication has been changed and now the Consultant wants it changed again, at the moment
Hello everyone, I hope you had a good Christmas As you can see from my post heading I suffer with Neuropathy and wondered if anyone else does. I have had this since 2014 and it has steadily been getting worse., my medication has been changed and now the Consultant wants it changed again, at the moment
OliveOyl
in
Pain Concern
7 years ago
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
7 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
7 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)
7 years ago
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
7 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
7 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
7 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
7 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
7 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
7 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
7 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
7 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
7 years ago
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