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Improvement Timeline after starting B12 deficiency treatment.
I wish there was a specific thread here where we could read about improvements/ changes after starting treatment. Lab test showed my B12 was 99 pg/ml. So far I have taken 7 alternate day shots of hydroxycobalamine. I haven't observed any improvement yet. Still have unsteady gait/dizziness, tinitus, numbness
I wish there was a specific thread here where we could read about improvements/ changes after starting treatment. Lab test showed my B12 was 99 pg/ml. So far I have taken 7 alternate day shots of hydroxycobalamine. I haven't observed any improvement yet. Still have unsteady gait/dizziness, tinitus, numbness
nkindia
in
Pernicious Anaemia Society
5 years ago
Living with peripheral neuropathy
Hi all neuropathy people I know your Pain and despair with this crazy ailment I have lived the angst with you all but could not focus to contribute to the forum After trying nearly everything I am now doing a mindfulness course I have chronic peripheral neuropathy in my feet and legs legs up to waist
Hi all neuropathy people I know your Pain and despair with this crazy ailment I have lived the angst with you all but could not focus to contribute to the forum After trying nearly everything I am now doing a mindfulness course I have chronic peripheral neuropathy in my feet and legs legs up to waist
Jim7bo
in
Neuropathy Support
5 years ago
Garlik and Parkinson d
Hi! I found on this forum a recipe of Ayurveda with garlic, from 1 to 21 cloves of garlic, every day increasing by 1 clove. Everything was fine, my gait even improved, but on day 16 my stomach ached and I stopped. Someone tried it too? How to protect the stomach from garlic? I would like to repeat this
Hi! I found on this forum a recipe of Ayurveda with garlic, from 1 to 21 cloves of garlic, every day increasing by 1 clove. Everything was fine, my gait even improved, but on day 16 my stomach ached and I stopped. Someone tried it too? How to protect the stomach from garlic? I would like to repeat this
Difg
in
Cure Parkinson's
5 years ago
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Dr Winkleman Dr Buchfuhrer
Hi Restless Team Just wondering what the difference in care is between the 2 specialist Dr Winkleman and Dr Buchfuhrer. We are on route to NYC and hoping to get appointment with Dr Winkelman in Boston . I have sent all my paper work but still awaiting contact from liaison officer . If he cannot
Hi Restless Team Just wondering what the difference in care is between the 2 specialist Dr Winkleman and Dr Buchfuhrer. We are on route to NYC and hoping to get appointment with Dr Winkelman in Boston . I have sent all my paper work but still awaiting contact from liaison officer . If he cannot
Shumbah
in
Restless Legs Syndrome
5 years ago
In focus: managing the effects of chemotherapy - neuropathy
Hello For October, we're looking at some of the effects of chemotherapy and how they can be managed. We're continuing today with a post about neuropathy. In this post about the possible side effects of chemotherapy, we’ll be looking at peripheral neuropathy, what it is and how it can be managed by your
Hello For October, we're looking at some of the effects of chemotherapy and how they can be managed. We're continuing today with a post about neuropathy. In this post about the possible side effects of chemotherapy, we’ll be looking at peripheral neuropathy, what it is and how it can be managed by your
OvacomeSupport
Administrator
in
My Ovacome
5 years ago
Need advice about urilogical symptoms....
Anyone else have burning after urination and bladder irritarion? What does your doctor say about this? Could this be IC? Could this just be a result of hypertonic pelvic floor dysfunction? My pelvic floor therapist thinks it is a result of the spasms in my pelvic floor. I am getting a second opinion
Anyone else have burning after urination and bladder irritarion? What does your doctor say about this? Could this be IC? Could this just be a result of hypertonic pelvic floor dysfunction? My pelvic floor therapist thinks it is a result of the spasms in my pelvic floor. I am getting a second opinion
aften16
in
Pelvic Pain Support Network
5 years ago
Pins and needles in hand/arm
I have a pacemaker for trifacicular block but I also have an areterial flutter. I was having pins and needles on diagnosis but gp/cardiologist said it was not related and would go away. It did but returned with a vengeance....burning in hand and tingling up arm (left only) .... everything I read says
I have a pacemaker for trifacicular block but I also have an areterial flutter. I was having pins and needles on diagnosis but gp/cardiologist said it was not related and would go away. It did but returned with a vengeance....burning in hand and tingling up arm (left only) .... everything I read says
Beffohol
in
AF Association
5 years ago
Plasmapheresis for itching
I AM NERVOUS HAVING PLASMAPHERESIS THIS FRODAY AT NOON 😬 HAS ANYONE ELSE HAD THIS PROCEDURE DONE. I AM BEING REFERRED BY MY UNIVERSITY OF MICHIGAN HEPATOLGIST DUE TO MY SEVERE ITCHING FROM PBC AS THEYVE TRIED PRESCRIBING SEVERAL MEDICATIONS, CREAMS ETC.. NOTHING WORK SO CROSSINGS MY FINGERS AS I HAVE
I AM NERVOUS HAVING PLASMAPHERESIS THIS FRODAY AT NOON 😬 HAS ANYONE ELSE HAD THIS PROCEDURE DONE. I AM BEING REFERRED BY MY UNIVERSITY OF MICHIGAN HEPATOLGIST DUE TO MY SEVERE ITCHING FROM PBC AS THEYVE TRIED PRESCRIBING SEVERAL MEDICATIONS, CREAMS ETC.. NOTHING WORK SO CROSSINGS MY FINGERS AS I HAVE
genj65
in
PBC Foundation
5 years ago
Pain
Ok here goes I had this put in last Thursday 10/10/19 and I've felt nothing but pain in my back from this date. I was told by the rep it should be better by second day mmmmm WRONG. I have this trial to see if it helps with my foot pain well yeah it helps because my pain in my back now is the focus of
Ok here goes I had this put in last Thursday 10/10/19 and I've felt nothing but pain in my back from this date. I was told by the rep it should be better by second day mmmmm WRONG. I have this trial to see if it helps with my foot pain well yeah it helps because my pain in my back now is the focus of
Noles43
in
Pain Concern
5 years ago
How do I know if I have RLS
Hi everyone, Can you help - I don’t know if the following symptoms will help determine whether I have RLS or not and would appreciate any advice? Pain, ache in ankles and calves predominantly. Most severe at night, can’t sleep and whilst I don’t get electric shock like effect, I can’t settle and feel
Hi everyone, Can you help - I don’t know if the following symptoms will help determine whether I have RLS or not and would appreciate any advice? Pain, ache in ankles and calves predominantly. Most severe at night, can’t sleep and whilst I don’t get electric shock like effect, I can’t settle and feel
RoisinW
in
Restless Legs Syndrome
5 years ago
Skin biopsy to detect peripheral neuropathy
I came across an interesting article called The Fire Within from John Hopkins about peripheral neuropathy. It only mentions b12 briefly but what I found interesting was a description of an objective method to detect and evaluate peripheral neuropathy using skin biopsies. I imagine it would be easier
I came across an interesting article called The Fire Within from John Hopkins about peripheral neuropathy. It only mentions b12 briefly but what I found interesting was a description of an objective method to detect and evaluate peripheral neuropathy using skin biopsies. I imagine it would be easier
palmier
in
Pernicious Anaemia Society
5 years ago
Neuropathy and magnesium
Just wondered if anyone can advise the best magnesium supplement for idiopathic neuropathy. I have tried citrate but that doesn't do anything. It is so confusing because there appear to be quite a few different types of magnesium.
Just wondered if anyone can advise the best magnesium supplement for idiopathic neuropathy. I have tried citrate but that doesn't do anything. It is so confusing because there appear to be quite a few different types of magnesium.
Twitchen
in
Foggy's "Invisible Illness" Support
5 years ago
Neuropathy
Hi does anyone have any advice regarding spinal compression neuropathy. Recently been diagnosed as I’ve been suffering constantly with tingling in arms,hands,legs and feet and feeling lightheaded. Have been prescribed pregablin 25mg twice a day but feel a little apprehensive about taking them due to
Hi does anyone have any advice regarding spinal compression neuropathy. Recently been diagnosed as I’ve been suffering constantly with tingling in arms,hands,legs and feet and feeling lightheaded. Have been prescribed pregablin 25mg twice a day but feel a little apprehensive about taking them due to
Timothy3
in
Restless Legs Syndrome
5 years ago
Questions about OIC
Hi everyone. I have had excellent luck for the past seven months with being on 150mg of Tramadol and 600mg of horizant. This combination seems to work very well for me. I have had absolutely no RLS for the past 7 months. Been able to sleep well every night. And sometimes even take a nap. My problem
Hi everyone. I have had excellent luck for the past seven months with being on 150mg of Tramadol and 600mg of horizant. This combination seems to work very well for me. I have had absolutely no RLS for the past 7 months. Been able to sleep well every night. And sometimes even take a nap. My problem
Tennwalker1
in
Restless Legs Syndrome
5 years ago
Pain
Good morning, I'm trying to find out if any one with lupus has ever had Renal colic?
Good morning, I'm trying to find out if any one with lupus has ever had Renal colic?
djsema
in
LUPUS UK
5 years ago
Update to my Intro
Hello, again ! I would like to add that i have full blown neuropathy extending even to my face and mouth started from a little tingling in my feet and lips about thirty years ago . With the strongest pain in my feet, it has progressed up my legs and into my arms and hands somewhat as well. I have taken
Hello, again ! I would like to add that i have full blown neuropathy extending even to my face and mouth started from a little tingling in my feet and lips about thirty years ago . With the strongest pain in my feet, it has progressed up my legs and into my arms and hands somewhat as well. I have taken
Hopinggh
in
Pain Concern
5 years ago
Symptom Free
Everyone is different, and what works for one may not for another. I suffered with RLS for so long, I can’t even remember how long. However in the past 5 years it had become unbearable. I wouldn’t sleep for days on end. I was depressed, tired, and thoughts of suicide starting dancing around in my pea
Everyone is different, and what works for one may not for another. I suffered with RLS for so long, I can’t even remember how long. However in the past 5 years it had become unbearable. I wouldn’t sleep for days on end. I was depressed, tired, and thoughts of suicide starting dancing around in my pea
Restlesssufferer
in
Restless Legs Syndrome
5 years ago
Neuropathy pain
I have neuropathy of the motor and sensory neves,I have had all the usual medicines for this condition which didn't work,the latest being butran patches which I have now stopped as they made me feel worse,can anyone tell me if they take tramadol.I'm also on citalopram so I don't know if they would interact
I have neuropathy of the motor and sensory neves,I have had all the usual medicines for this condition which didn't work,the latest being butran patches which I have now stopped as they made me feel worse,can anyone tell me if they take tramadol.I'm also on citalopram so I don't know if they would interact
Shihtz6
in
Fibromyalgia Action UK
5 years ago
AF, Sotalol & Me
I have constant AF which started after bypass surgery and found out after cardio-version I am allergic to Sotalol. Extremely allergic to Sotalol - Never, ever according to the manufacturer and other medical websites take Sotalol unless under hospital observation. It literally killed me!
I have constant AF which started after bypass surgery and found out after cardio-version I am allergic to Sotalol. Extremely allergic to Sotalol - Never, ever according to the manufacturer and other medical websites take Sotalol unless under hospital observation. It literally killed me!
Mimibest
in
AF Association
5 years ago
Rytary and Bydureon updates
I have posted about this in the past six months and wanted to give an update. I started Rytary about 6 months ago and struggled to find a way to control my symptoms. It is a slow acting form of Carbidopa and Levodopa that is a controlled release capsule. I said “slow acting” because it takes a while
I have posted about this in the past six months and wanted to give an update. I started Rytary about 6 months ago and struggled to find a way to control my symptoms. It is a slow acting form of Carbidopa and Levodopa that is a controlled release capsule. I said “slow acting” because it takes a while
Hidden
in
Cure Parkinson's
5 years ago
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