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Scientists say mystery of how red wine headaches occur may be solved
Thought this could be relevant on at least two grounds: First, so many members say they have issues tolerating alcoholic drinks, especially red wine. And it is specifically in this respect that I am posting. Not ordinary excessive drinking. Second, there are numerous posts here which advocate taking
Thought this could be relevant on at least two grounds: First, so many members say they have issues tolerating alcoholic drinks, especially red wine. And it is specifically in this respect that I am posting. Not ordinary excessive drinking. Second, there are numerous posts here which advocate taking
helvella
Thyroid UK
in
Thyroid UK
9 months ago
Vagus nerve stimulation'
I've posted here a few times to discuss gut health for those of you suffering from PA who also have gut issues. In my quest to find some relief from visceral hypersensitivity and massive intolerances (leading to malabsorption) I began acupuncture treatment this year. I am very lucky to have an anethesist
I've posted here a few times to discuss gut health for those of you suffering from PA who also have gut issues. In my quest to find some relief from visceral hypersensitivity and massive intolerances (leading to malabsorption) I began acupuncture treatment this year. I am very lucky to have an anethesist
expatkerry
in
Pernicious Anaemia Society
9 months ago
small fibre neuropathy
How long does small fibre neuropathy due to prolonged B12 deficiency for many years take to be reversed, if possible ? After 14 months of self injecting daily and pathology results finally returning to normal (holotranscobalamin and serum B12 normal) and taking Lyrica for my neuropathy the past six
How long does small fibre neuropathy due to prolonged B12 deficiency for many years take to be reversed, if possible ? After 14 months of self injecting daily and pathology results finally returning to normal (holotranscobalamin and serum B12 normal) and taking Lyrica for my neuropathy the past six
GoneWithTheWind1972
in
Pernicious Anaemia Society
9 months ago
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Living with Disc Issues
Hi all. So i herniated my L4-L5 lumbar disc (and minor abnormalities from L2 to L4) from doing too much weight on an inclined leg press and bad form. I also somehow caused bulging discs in my neck (cervical vertebrae, can't remember which ones) from either years of scrunching my neck during workouts
Hi all. So i herniated my L4-L5 lumbar disc (and minor abnormalities from L2 to L4) from doing too much weight on an inclined leg press and bad form. I also somehow caused bulging discs in my neck (cervical vertebrae, can't remember which ones) from either years of scrunching my neck during workouts
GoToHealth
in
Pain Concern
9 months ago
Taxotere causing horrible neuropathy on just the 3rd day.
I had my first infusion last Thursday and starting yesterday I've had a severe worsening of my existing neuropathy. I can barely walk. I'm experiencing a wide variety of nerve pains from my waist downward. From nearly total numbness in my toes and feet to rippling pain coursing down from my hips. Sometimes
I had my first infusion last Thursday and starting yesterday I've had a severe worsening of my existing neuropathy. I can barely walk. I'm experiencing a wide variety of nerve pains from my waist downward. From nearly total numbness in my toes and feet to rippling pain coursing down from my hips. Sometimes
V10fanatic
in
Advanced Prostate Cancer
9 months ago
buzzing in foot
Hi all, I’m new to the this post, but I have not been diagnosed by a doctor yet. I have my vitamin B 12 check six months ago and it was fine a few weeks ago I started to have the buzzing in my foot, it felt like I had a cell phone buzzing in the bottom of my foot, and it would start at night when I was
Hi all, I’m new to the this post, but I have not been diagnosed by a doctor yet. I have my vitamin B 12 check six months ago and it was fine a few weeks ago I started to have the buzzing in my foot, it felt like I had a cell phone buzzing in the bottom of my foot, and it would start at night when I was
Sandalsforever
in
Pernicious Anaemia Society
9 months ago
For People With Parkinson's Taking Levodopa Medication: The Danger of B6 Deficiency Is Dire and Vastly Outweighs the Danger of B6 Excess
Vitamin B6 is an essential cofactor for over 100 enzymatic reactions. We need abundant B6 to keep what is left of our dopaminergic neurons as healthy as possible, especially since they are already compromised by Parkinson's. Levodopa medication depletes vitamin B6. B6 is only present in foods in low
Vitamin B6 is an essential cofactor for over 100 enzymatic reactions. We need abundant B6 to keep what is left of our dopaminergic neurons as healthy as possible, especially since they are already compromised by Parkinson's. Levodopa medication depletes vitamin B6. B6 is only present in foods in low
park_bear
in
Cure Parkinson's
10 months ago
B6 - advice
I’m confused about B6. is the advice with Co-Careldopa not to take, at all. Or to take after Co-Careldopa has been absorbed. my recent blood tests showed me deficient in B6. thanks
I’m confused about B6. is the advice with Co-Careldopa not to take, at all. Or to take after Co-Careldopa has been absorbed. my recent blood tests showed me deficient in B6. thanks
Nb11
in
Cure Parkinson's
10 months ago
Some good news
Just to keep you all up to date. I have been on 50mg daily of Agomelatine, for depression, foe the padt month. I feel the best I have felt in years!. Severe restless legs are 75% better. Some nights I have no rls at all. Always good to have a good news story - especially for me after the last 6 months
Just to keep you all up to date. I have been on 50mg daily of Agomelatine, for depression, foe the padt month. I feel the best I have felt in years!. Severe restless legs are 75% better. Some nights I have no rls at all. Always good to have a good news story - especially for me after the last 6 months
Trish8433
in
Restless Legs Syndrome
10 months ago
Hip pain
I started V/O treatment in April of this year. Finished O in September, will take 4 V daily to end February. Oncologist says I’m in remission and bloodwork agrees. Side effects are getting worse every day and include pain in both hips and lower back. Bad in morning, better during the day, bad again in
I started V/O treatment in April of this year. Finished O in September, will take 4 V daily to end February. Oncologist says I’m in remission and bloodwork agrees. Side effects are getting worse every day and include pain in both hips and lower back. Bad in morning, better during the day, bad again in
Cottager1989
in
CLL Support
10 months ago
Sotalol
Hi there. I saw my specialist last week and he took me off Sotalol 80mg morning and night. My pulse has been low ever since CHF. My heart pulse is generally between41 &46, Today when I took my blood pressure & pulse my pulse is upto 98. I waited awhile and took it again, 91. I will wait and
Hi there. I saw my specialist last week and he took me off Sotalol 80mg morning and night. My pulse has been low ever since CHF. My heart pulse is generally between41 &46, Today when I took my blood pressure & pulse my pulse is upto 98. I waited awhile and took it again, 91. I will wait and
Gulmarrad
in
AF Association
10 months ago
Krebs Cycle
Has anyone’s heard of the Krebs Cycle, also known as the Citric Acid Cycle? It’s a series of biochemical reactions that happen in the mitochondria and is critical for the formation of energy. Krebs has a book called “The Principles and Applications of Ozone Therapy”. The cycle converts NADH to NAD
Has anyone’s heard of the Krebs Cycle, also known as the Citric Acid Cycle? It’s a series of biochemical reactions that happen in the mitochondria and is critical for the formation of energy. Krebs has a book called “The Principles and Applications of Ozone Therapy”. The cycle converts NADH to NAD
LagLag37
in
Cure Parkinson's
10 months ago
Switching from Gabapentin to Horizant?
I'm currently taking 2400mg of Gabapentin, for my PLMs, and gradually reducing..my plan is to switch to Horizant/Gabapentin enacarbil. Does anyone know how much Gabapentin I need to be taking, in order to switch to 600mg of Horizant? I'm looking for a website that will give me this specific info
I'm currently taking 2400mg of Gabapentin, for my PLMs, and gradually reducing..my plan is to switch to Horizant/Gabapentin enacarbil. Does anyone know how much Gabapentin I need to be taking, in order to switch to 600mg of Horizant? I'm looking for a website that will give me this specific info
pianoplayerPLMD
in
Restless Legs Syndrome
10 months ago
Not impressed
Decided to go through my medical notes such as they are, and blood tests again now I'm more sensible again. All hospital consultations are missed off and consequently diagnoses. Oh, and there is a gp consultation noted that never took place. Basically my notes appear to be a mess. What really
Decided to go through my medical notes such as they are, and blood tests again now I'm more sensible again. All hospital consultations are missed off and consequently diagnoses. Oh, and there is a gp consultation noted that never took place. Basically my notes appear to be a mess. What really
Wheat
in
Pernicious Anaemia Society
10 months ago
Nifedipine mr
Hi I'm taking nifedipine for reynauds/ scleroderma again after not being successful with it in the past ... also just been given siledipine 25mg 3 times daily .I'm not really getting any side affects yet as it's only been a few days on both together .. last time I tried nifedipine MR I found it made
Hi I'm taking nifedipine for reynauds/ scleroderma again after not being successful with it in the past ... also just been given siledipine 25mg 3 times daily .I'm not really getting any side affects yet as it's only been a few days on both together .. last time I tried nifedipine MR I found it made
Tmontana
in
Scleroderma & Raynaud's UK (SRUK)
10 months ago
Creatine For Advanced Prostate Cancer Patients
A new study at Huntsman Cancer Institute is going to look at potential benefits of creatine for maintaining muscle mass in APC patients. Here's the link: https://www.onclive.com/view/new-clinical-trials-test-innovative-ways-to-preserve-muscle-mass-during-metastatic-prostate-cancer?utm_medium=email&
A new study at Huntsman Cancer Institute is going to look at potential benefits of creatine for maintaining muscle mass in APC patients. Here's the link: https://www.onclive.com/view/new-clinical-trials-test-innovative-ways-to-preserve-muscle-mass-during-metastatic-prostate-cancer?utm_medium=email&
CocoTheAlphaCat
in
Advanced Prostate Cancer
10 months ago
Targinact
I have had RLS for over 20 years and have tried most medications, the latest being Pregabalin, which was good but is now not working so well. I therefore asked my GP if I could try Targinact as I read this is now licensed for RLS. He has agreed and I just need to taper Pregabalin. Can anyone
I have had RLS for over 20 years and have tried most medications, the latest being Pregabalin, which was good but is now not working so well. I therefore asked my GP if I could try Targinact as I read this is now licensed for RLS. He has agreed and I just need to taper Pregabalin. Can anyone
Quiltingmum
in
Restless Legs Syndrome
10 months ago
Peripheral neuropathy without diabetes
I have peripheral neuropathy of the feet. Doctors cannot find a reason. I do not have diabetes nor autoimmune issues. Nothing is helping me. I am desperately trying to find out the cause and to find something to help minimize or eliminate the pain and numbness. I got this 2 weeks after getting my
I have peripheral neuropathy of the feet. Doctors cannot find a reason. I do not have diabetes nor autoimmune issues. Nothing is helping me. I am desperately trying to find out the cause and to find something to help minimize or eliminate the pain and numbness. I got this 2 weeks after getting my
laurelb
in
AF Association
10 months ago
RLS and neuropathy?
hey all, hope you’re doing well. Although I’ve been on Oxycodone consistently enough to keep the RLS at bay, I have noticed new symptoms of what seems to be peripheral neuropathy. in addition to the feelings of electrocution, which is what my RLS feels like, I have burning in my extremities. My
hey all, hope you’re doing well. Although I’ve been on Oxycodone consistently enough to keep the RLS at bay, I have noticed new symptoms of what seems to be peripheral neuropathy. in addition to the feelings of electrocution, which is what my RLS feels like, I have burning in my extremities. My
Marlayna67
in
Restless Legs Syndrome
10 months ago
update on prolotherapy
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
Hidden
in
Neuropathy Support
10 months ago
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