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Customs duty on methylcobalamin
Hi. Can anyone tell me if there is now a duty to pay on b12/methyl etc.,? I've just received an order from Germany. I was expecting the 20% vat but not a large duty fee at Customs. Not really sure exactly what I'm looking for but I had a look on the Customs website and found a code for vitamin
Hi. Can anyone tell me if there is now a duty to pay on b12/methyl etc.,? I've just received an order from Germany. I was expecting the 20% vat but not a large duty fee at Customs. Not really sure exactly what I'm looking for but I had a look on the Customs website and found a code for vitamin
Missd66
in
Pernicious Anaemia Society
4 months ago
Slippery Elm & Lansoprazol
I'm asking advice for my son. It's about timings etc re slippery elm, supplements and slippery elm. He's 40 and on Lazoprasole for almost 12 years for slight hiatus hernia. Each time he's not taken it, due to prescription mix up, he gets bad acid symptoms. At the moment he's having an acid flare up.
I'm asking advice for my son. It's about timings etc re slippery elm, supplements and slippery elm. He's 40 and on Lazoprasole for almost 12 years for slight hiatus hernia. Each time he's not taken it, due to prescription mix up, he gets bad acid symptoms. At the moment he's having an acid flare up.
Cal_
in
Acid Reflux Support
4 months ago
Fighting for corrections is so hard.
I am coming up on the one year of my wife's passing. On this day last year, she was sitting in her hospital bed eating frozen fruit. She was at 99% Sat with 1l of O2, and the plan was to turn it off in the morning. LFT's bang on Normal. Indirect Billi is still high, direct normal. Albumin low Plat low
I am coming up on the one year of my wife's passing. On this day last year, she was sitting in her hospital bed eating frozen fruit. She was at 99% Sat with 1l of O2, and the plan was to turn it off in the morning. LFT's bang on Normal. Indirect Billi is still high, direct normal. Albumin low Plat low
ceward204
in
British Liver Trust
4 months ago
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Daughter’s results causing confusion - Hashimoto’s AND Graves??
Hi everyone, This post comes with a caveat. I’m sat looking through my daughter’s blood test results from the second part of last year. I’m doing this because she’s off college again with some sort of virus, this follows a week of Covid. I’m ashamed to say that I’m only looking at these results
Hi everyone, This post comes with a caveat. I’m sat looking through my daughter’s blood test results from the second part of last year. I’m doing this because she’s off college again with some sort of virus, this follows a week of Covid. I’m ashamed to say that I’m only looking at these results
J972
in
Thyroid UK
4 months ago
symptoms of B12 deficency
I continue to suffer from tingling feet and feeling tired also sweating for no good reason. Has anyone got suggestions of how to cope with this. I get injection for condition every 12 weeks.
I continue to suffer from tingling feet and feeling tired also sweating for no good reason. Has anyone got suggestions of how to cope with this. I get injection for condition every 12 weeks.
Infob12quest
in
PMRGCAuk
4 months ago
Cure for Parkinson's - neverending story
There are thousands of substances with some beneficial effects on Parkinson's, from vitamins, herbs,spices ,minerals,off label medications, types of exercise, or whatever or however you name it.. sometimes i feel lost, exhausted from trying and experimenting, physically mentally and.... financially bankrupted
There are thousands of substances with some beneficial effects on Parkinson's, from vitamins, herbs,spices ,minerals,off label medications, types of exercise, or whatever or however you name it.. sometimes i feel lost, exhausted from trying and experimenting, physically mentally and.... financially bankrupted
realk
in
Cure Parkinson's
6 months ago
Anxiety relief
Other than getting the right amount of B12, has anyone found something that helps with the anxiety aspects of deficiency and PA? Medication or therapy. On numerous occasions my GP and neurologists have suggested antidepressants but I’m very loathe to do down that route. Even the medication being suggested
Other than getting the right amount of B12, has anyone found something that helps with the anxiety aspects of deficiency and PA? Medication or therapy. On numerous occasions my GP and neurologists have suggested antidepressants but I’m very loathe to do down that route. Even the medication being suggested
Pa234aw
in
Pernicious Anaemia Society
4 months ago
new to group
I developed strange heavy lower leg sensation in 10/23; always been very healthy active 54 year old female. This issue coincided with a lower back flare up after playing pickle ball. MRI revealed a small disc bulge at L4-5 but no one was sure if these symptoms were related. I also got brain MRI
I developed strange heavy lower leg sensation in 10/23; always been very healthy active 54 year old female. This issue coincided with a lower back flare up after playing pickle ball. MRI revealed a small disc bulge at L4-5 but no one was sure if these symptoms were related. I also got brain MRI
Corolla1
in
Restless Legs Syndrome
4 months ago
B1 HDT Protocol with Sinemet
Does anyone happen to know should the thiamine be taken before, after, or at the same time as sinemet?Or does it even matter?
Does anyone happen to know should the thiamine be taken before, after, or at the same time as sinemet?Or does it even matter?
lionessroar
in
Cure Parkinson's
4 months ago
Peripheral neuropathy
Just researching vitamin K2 and found this..... Peripheral neuropathy (PN) Diabetic peripheral neuropathy is a frequent and severe complication of diabetes. A recent study aimed to evaluate factors associated with sensitive diabetic neuropathy in Type 2 Diabetes, and, in particular, dephospho-uncarboxylated
Just researching vitamin K2 and found this..... Peripheral neuropathy (PN) Diabetic peripheral neuropathy is a frequent and severe complication of diabetes. A recent study aimed to evaluate factors associated with sensitive diabetic neuropathy in Type 2 Diabetes, and, in particular, dephospho-uncarboxylated
tomdickharry
in
Pernicious Anaemia Society
4 months ago
New response on BMJ B12 article
Hi All, There was a new response on recent BMJ article B12 Deficiency by B. Wolffenbuttel by a haematologist. Just wondered what people thought. Link to article https://www.bmj.com/content/383/bmj-2022-071725 Link to responses https://www.bmj.com/content/383/bmj-2022-071725/rapid-responses
Hi All, There was a new response on recent BMJ article B12 Deficiency by B. Wolffenbuttel by a haematologist. Just wondered what people thought. Link to article https://www.bmj.com/content/383/bmj-2022-071725 Link to responses https://www.bmj.com/content/383/bmj-2022-071725/rapid-responses
Sleepybunny
in
Pernicious Anaemia Society
4 months ago
supplements
Does anyone on here know if there are any otc vitamins or supplements that increase levels of RLS/Myoclonus.
Does anyone on here know if there are any otc vitamins or supplements that increase levels of RLS/Myoclonus.
soupersuzy
in
Restless Legs Syndrome
6 months ago
serum methylmalonic acid testing
just had my medicheck results with dr recommendations including and they have suggested that I should get a serum methylmalonic acid test. My B12 is normal but in lower range. Question is whether this is worth testing or to just go ahead and supplement (I would do this in support of my dr I just don’
just had my medicheck results with dr recommendations including and they have suggested that I should get a serum methylmalonic acid test. My B12 is normal but in lower range. Question is whether this is worth testing or to just go ahead and supplement (I would do this in support of my dr I just don’
Gosierunn
in
Thyroid UK
4 months ago
Trapped nerve/ shoulder pain
last July I was diagnosed with low b12, I started on a series of 6 injections before starting on a three monthly top up regime. In that time I also received my annual flu vaccination and most recent covid jab. in December 2023 I started having numbness in three fingers, index, middle and ring and
last July I was diagnosed with low b12, I started on a series of 6 injections before starting on a three monthly top up regime. In that time I also received my annual flu vaccination and most recent covid jab. in December 2023 I started having numbness in three fingers, index, middle and ring and
J200george
in
Pernicious Anaemia Society
4 months ago
T4 low TSH normal
Evening, I've had more blood tests done and I'm fed up of feeling so badly every day. I've done medichecks TSH tests and cortisol. Only test low is my T4 which tbh never changed since 2016 TSH fluctuates. I had telephone appointment before my test results came back. Due to my chronic fatigue. Weight
Evening, I've had more blood tests done and I'm fed up of feeling so badly every day. I've done medichecks TSH tests and cortisol. Only test low is my T4 which tbh never changed since 2016 TSH fluctuates. I had telephone appointment before my test results came back. Due to my chronic fatigue. Weight
Lillygirl66
in
Thyroid UK
4 months ago
Anyone else have severe daily heartburn?
Diagnosis of autoimmune atrophic gastritis with intestinal metaplasia and also PA. Currently SI B12 (cyanobalamin ) EOD. Does anyone else with this get severe heartburn? I’ve cut out acidic and spicy. It seems to happen mostly on an empty stomach right before lunch. Sometimes Pepsid Complete works and
Diagnosis of autoimmune atrophic gastritis with intestinal metaplasia and also PA. Currently SI B12 (cyanobalamin ) EOD. Does anyone else with this get severe heartburn? I’ve cut out acidic and spicy. It seems to happen mostly on an empty stomach right before lunch. Sometimes Pepsid Complete works and
ReallyWondering
in
Pernicious Anaemia Society
4 months ago
Can anyone recommend a good haematologist or Neurologist for pernicious anaemia
Hi can anyone recommend a haematologist or neurologist who has a good understanding of pernicious anaemia anywhere in England? (Needs to be NHS as GP said they won't act on any recommendation from a private doctor). Many of my neurological symptoms, although much improved, never went away completely
Hi can anyone recommend a haematologist or neurologist who has a good understanding of pernicious anaemia anywhere in England? (Needs to be NHS as GP said they won't act on any recommendation from a private doctor). Many of my neurological symptoms, although much improved, never went away completely
Rett713
in
Pernicious Anaemia Society
4 months ago
Tingling and pricking
Hi friends Two weeks ago I started with tingling and pricking in my feet, legs, arms and hands. When I lie down at night it is also in most of my torso and a bit in my face. Occasionally I get little stabs in my feet. It comes and goes every few days and lasts a couple of days. Massage helps. It does
Hi friends Two weeks ago I started with tingling and pricking in my feet, legs, arms and hands. When I lie down at night it is also in most of my torso and a bit in my face. Occasionally I get little stabs in my feet. It comes and goes every few days and lasts a couple of days. Massage helps. It does
Viveka
in
PMRGCAuk
4 months ago
can you tell me what the best brand to take for low folate
I had full thyroid check with medicheck just over a year ago. the result for my vitamins were Folate. 2.38ugl ( 3.89 - 19.45) Vitamin b12 69.5 pmol/L ( 37.5 - 150) Vitamin D 67 ( 50-200) I did get my folate check with my doctors, after I told them of my private blood test but they
I had full thyroid check with medicheck just over a year ago. the result for my vitamins were Folate. 2.38ugl ( 3.89 - 19.45) Vitamin b12 69.5 pmol/L ( 37.5 - 150) Vitamin D 67 ( 50-200) I did get my folate check with my doctors, after I told them of my private blood test but they
Bookworm90
in
Thyroid UK
4 months ago
Help with results - what would you do?
Hello I finally got a private endo to agree to up my meds from 75mcg levothyroxine to 100 or112.5 if I felt it necessary in July 2023 allowing my TSH to fall below range, and that I understood and was willing to take the risks. My 3 pm slump was dangerous as I was fighting to stay awake on the way
Hello I finally got a private endo to agree to up my meds from 75mcg levothyroxine to 100 or112.5 if I felt it necessary in July 2023 allowing my TSH to fall below range, and that I understood and was willing to take the risks. My 3 pm slump was dangerous as I was fighting to stay awake on the way
66olives
in
Thyroid UK
4 months ago
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