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will the demand for potassium always remain
hello all, I am my 4th week of daily 9 days now EOD of meth b12 injections and doing all my cofactors , trying them all. The potassium has helped with episodes of panic and anxiety and I am also trying the iron and folate as well at different times, I was wondering does this stay like this or about
hello all, I am my 4th week of daily 9 days now EOD of meth b12 injections and doing all my cofactors , trying them all. The potassium has helped with episodes of panic and anxiety and I am also trying the iron and folate as well at different times, I was wondering does this stay like this or about
JesusMercy60
in
Pernicious Anaemia Society
1 month ago
FBC interpretation
I live in France and so therefore cannot obtain private blood test results for Folate, B12, and Ferritin without catching a ferry and returning to the UK which I am too ill to do at present. I do however have a full blood count from a few months ago. My questions is can anybody on this site help me
I live in France and so therefore cannot obtain private blood test results for Folate, B12, and Ferritin without catching a ferry and returning to the UK which I am too ill to do at present. I do however have a full blood count from a few months ago. My questions is can anybody on this site help me
Brightness14
in
Thyroid UK
1 month ago
Can't use Panpharma 😫
Although I'm prescribed B12 ampoules via my gp, I can only use certain brands without agonising stinging and burning. My local pharmacy hasn't been able to source anything for over a month. It's the added sodium acrylate that I react to. Decided to order online and I thought I'd thoroughly researched
Although I'm prescribed B12 ampoules via my gp, I can only use certain brands without agonising stinging and burning. My local pharmacy hasn't been able to source anything for over a month. It's the added sodium acrylate that I react to. Decided to order online and I thought I'd thoroughly researched
Myoldcat
in
Pernicious Anaemia Society
1 month ago
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please help mi
hi my wife yanett was diagnosed with parkinson in 2002 and a nervous depression, and also has a hart time to sleep and has a strong jaw and left hand tremor, problems to swallow food and a daily nevous state. since the diagnose she has been taken aproximatly 75mg of lovadopa daily and diazepan 5mg
hi my wife yanett was diagnosed with parkinson in 2002 and a nervous depression, and also has a hart time to sleep and has a strong jaw and left hand tremor, problems to swallow food and a daily nevous state. since the diagnose she has been taken aproximatly 75mg of lovadopa daily and diazepan 5mg
ANDRESVALDES
in
Cure Parkinson's
1 month ago
Bit of a success with frequency of B12 injections
Hi, I just wanted to share a bit of a positive experience. I had about a year long history of feeling jittery, bit light headed, palpitations, classic anxiety symptoms. In desperation I asked the GP if she could check to make sure there was no physical reason for this. She kindly ran some basic checks
Hi, I just wanted to share a bit of a positive experience. I had about a year long history of feeling jittery, bit light headed, palpitations, classic anxiety symptoms. In desperation I asked the GP if she could check to make sure there was no physical reason for this. She kindly ran some basic checks
Charlie2024
in
Pernicious Anaemia Society
1 month ago
Latest Results for advice
Latest Results from BH for advice. Currently taking 1 grain 60mg Armour , 1/2 am, 1/2 pm, under supervision with private endo I had bloods drawn at 9am, day before bloods I split my doze 1/2 am and 1/2 grain at 10:30pm and I stopped Biotin/Bcomplex 1 week before. Usual symptoms, temple hairloss and
Latest Results from BH for advice. Currently taking 1 grain 60mg Armour , 1/2 am, 1/2 pm, under supervision with private endo I had bloods drawn at 9am, day before bloods I split my doze 1/2 am and 1/2 grain at 10:30pm and I stopped Biotin/Bcomplex 1 week before. Usual symptoms, temple hairloss and
Albaangel
in
Thyroid UK
1 month ago
Parkinsons
Hello My dad has parkinsons and I have read that most patients with a parkinsons diagnosis have low b12. My dad has been taking cyanocobalamin for years so he must have had a low reading at some point. It frustrates me that this hasn't been reviewed. When we arrange a test, will he be required to
Hello My dad has parkinsons and I have read that most patients with a parkinsons diagnosis have low b12. My dad has been taking cyanocobalamin for years so he must have had a low reading at some point. It frustrates me that this hasn't been reviewed. When we arrange a test, will he be required to
RedOne1
in
Pernicious Anaemia Society
1 month ago
High vitamin D results but have symptoms of low D. Is this possible?
I have osteoporosis, and spinal stenosis, waiting for surgery.My latest blood test for vit. D is - Serum total 25-hydroxy vitamin D levels. 174nmol/L. [. >51]at risk of toxicity, consider discontinuation of suppliments. I have discontinued but I remember reading somewhere that as I have coeliacs disease
I have osteoporosis, and spinal stenosis, waiting for surgery.My latest blood test for vit. D is - Serum total 25-hydroxy vitamin D levels. 174nmol/L. [. >51]at risk of toxicity, consider discontinuation of suppliments. I have discontinued but I remember reading somewhere that as I have coeliacs disease
Everdean
in
Thyroid UK
1 month ago
Feeling dismissed on results, am I clutching at straws??
Hello! New here and hoping for some advice from people with a bit more knowledge.Ended up having some private bloods done (was afternoon, have now seen first time in morning best) due to really struggling over the last 12 months. Under the care of a rheumatologist for inflammatory arthritis but have
Hello! New here and hoping for some advice from people with a bit more knowledge.Ended up having some private bloods done (was afternoon, have now seen first time in morning best) due to really struggling over the last 12 months. Under the care of a rheumatologist for inflammatory arthritis but have
weedee41
in
Thyroid UK
1 month ago
Please advise on iron panel blood test results
Please can anyone advise if I need to take iron tablets with these results. I feel so tired. Due to see the endo on Monday but I know he might say it is in range.The blood tests are as follows: I sent the TSH, T3and t4 in a previous email. Folic acid 9.6 range e >2.7 B12 695 ng/L range 160-800ng/L MCV
Please can anyone advise if I need to take iron tablets with these results. I feel so tired. Due to see the endo on Monday but I know he might say it is in range.The blood tests are as follows: I sent the TSH, T3and t4 in a previous email. Folic acid 9.6 range e >2.7 B12 695 ng/L range 160-800ng/L MCV
cbraffe
in
Thyroid UK
1 month ago
Recent blood test result, TPO is high
Hi everyone! I've read many threads and responds in this forum to try to educate myself more, understand and manage my symptoms. I've been experiencing symptoms for years and self-diagnosed myself with Hashimoto through private lab. Fatigue, low heart rate, dizzy spells, anxiety, stomach issues (mild
Hi everyone! I've read many threads and responds in this forum to try to educate myself more, understand and manage my symptoms. I've been experiencing symptoms for years and self-diagnosed myself with Hashimoto through private lab. Fatigue, low heart rate, dizzy spells, anxiety, stomach issues (mild
TheRightSide
in
Thyroid UK
1 month ago
New test results. Comments?
Hi everyone! Sharing my last test results!My levels all seem to be better, Antibodies are still high though, do you think is still worth keeping a GF and DF diet? I had the idea that removing gluten and dairy would magically reduce antibodies 😅 My symptoms have improved a bit, but I cannot say I'm
Hi everyone! Sharing my last test results!My levels all seem to be better, Antibodies are still high though, do you think is still worth keeping a GF and DF diet? I had the idea that removing gluten and dairy would magically reduce antibodies 😅 My symptoms have improved a bit, but I cannot say I'm
Marinot
in
Thyroid UK
1 month ago
at last
more than 12 months several trips to neurologist, scans and blood tests I’ve now been put back on B12 injections (on the advice of the neurologist to the GP surgery) every 8 weeks, my original GP said my levels were high enough to last for years and he thought it was masking something else so he stopped
more than 12 months several trips to neurologist, scans and blood tests I’ve now been put back on B12 injections (on the advice of the neurologist to the GP surgery) every 8 weeks, my original GP said my levels were high enough to last for years and he thought it was masking something else so he stopped
Imcn1960
in
Pernicious Anaemia Society
1 month ago
Does any1 know if immunoglobulin treatment inhosp for someone recently diagnosed peripheral neuropathy/lots infections linked tob12inanyway?
Hi, I'm not sure of all the facts but wonder if anyone can help advise please? it's a family member of a family member. He has been in and out of hosp this year, now in again with more breathing problems, tho has covid on top of it this time. He's recently been diagnosed with peripheral neuropathy last
Hi, I'm not sure of all the facts but wonder if anyone can help advise please? it's a family member of a family member. He has been in and out of hosp this year, now in again with more breathing problems, tho has covid on top of it this time. He's recently been diagnosed with peripheral neuropathy last
Jo5454
in
Pernicious Anaemia Society
1 month ago
Just a quick update, Endo appointment 👿
went to Royal Liverpool Endo dept , was hoping to see the consultant who is on TUK Uk list. Unfortunately this did not happen, the person I saw was less than helpful, see I can be tactful, sometimes. Introduced herself as diabetes consultant and she lived up to that name. The first thing she said
went to Royal Liverpool Endo dept , was hoping to see the consultant who is on TUK Uk list. Unfortunately this did not happen, the person I saw was less than helpful, see I can be tactful, sometimes. Introduced herself as diabetes consultant and she lived up to that name. The first thing she said
Polo22
in
Thyroid UK
1 month ago
I was starting to feel a little better, then........
Following the advice given in reply to my first email 3 months ago and using all the knowledge I have learnt from the questions and answers in the blog, I spoke to my GP and she agreed that I should increase my Levo from 75mcg to 100mcg. She also suggested that I should try Magnesium in the evening
Following the advice given in reply to my first email 3 months ago and using all the knowledge I have learnt from the questions and answers in the blog, I spoke to my GP and she agreed that I should increase my Levo from 75mcg to 100mcg. She also suggested that I should try Magnesium in the evening
man1412
in
Thyroid UK
1 month ago
Hot flushes
Hello I’m on week 4 of daily pred (20mg), 30mg lanzaprozole, 70mg alendronic acid (weekly not daily). I’ve suddenly started having horrendous hot flushes - mainly at night but yesterday evening had a horrible sweaty and ill feeling 30 mins. Very reminiscent of my early menopause days pre HRT. I have
Hello I’m on week 4 of daily pred (20mg), 30mg lanzaprozole, 70mg alendronic acid (weekly not daily). I’ve suddenly started having horrendous hot flushes - mainly at night but yesterday evening had a horrible sweaty and ill feeling 30 mins. Very reminiscent of my early menopause days pre HRT. I have
NewPMR53
in
PMRGCAuk
1 month ago
Monitoring
Hello everyone Its been a while since i've been on this forum so apologies if this is a common question or if it has been asked recently but I'll make it short and sweet. I am a pernicious anemia sufferer since diagnosis in 2012 and have been on injections ever since now I don't know if it's just me
Hello everyone Its been a while since i've been on this forum so apologies if this is a common question or if it has been asked recently but I'll make it short and sweet. I am a pernicious anemia sufferer since diagnosis in 2012 and have been on injections ever since now I don't know if it's just me
Davy28
in
Pernicious Anaemia Society
1 month ago
New results, scared doctor will dismiss me
Hi everyone, So, my levothyroxine was put up to 88mcg at the end of November. I tested in March and results were: TSH 1.270 µUI/mL 0.380 - 5.330 T4 (free) 1.16 ng/dL 0.54 - 1.24 (88% through range) T3 (free) 3.79 pg/mL 2.50 - 3.90 (92% through range) I always test before 9am, fasted, no
Hi everyone, So, my levothyroxine was put up to 88mcg at the end of November. I tested in March and results were: TSH 1.270 µUI/mL 0.380 - 5.330 T4 (free) 1.16 ng/dL 0.54 - 1.24 (88% through range) T3 (free) 3.79 pg/mL 2.50 - 3.90 (92% through range) I always test before 9am, fasted, no
catpotter44
in
Thyroid UK
1 month ago
Methinks it's time to add some T3 ......thoughts ?
these Vits were done 3 mths ago ~ nothing really awful, but have been working on improving them : Vit D 75 (aiming for 80-100) activeB12 90 (aiming for 100+) Folate 11 (aiming for 14) Ferritin 73 (aiming for 100+) ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
these Vits were done 3 mths ago ~ nothing really awful, but have been working on improving them : Vit D 75 (aiming for 80-100) activeB12 90 (aiming for 100+) Folate 11 (aiming for 14) Ferritin 73 (aiming for 100+) ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
tattybogle
in
Thyroid UK
1 month ago
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