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Reducing T3 - please help me understand
Hi all, I am baffled with my situation. I would be so grateful for any ideas. First, after being extremely sick for over 5 years I was finally diagnosed with mold exposure early in 2023 and now being treated by a top specialist at Cleveland Clinic in the US. Making progress. This doc warned me
Hi all, I am baffled with my situation. I would be so grateful for any ideas. First, after being extremely sick for over 5 years I was finally diagnosed with mold exposure early in 2023 and now being treated by a top specialist at Cleveland Clinic in the US. Making progress. This doc warned me
jstein1979
in
Thyroid UK
5 months ago
blood results
Hi, I have had my blood results back from blue horizon. The only one they said was low was the TSH at 0.06. I was expecting this as I’ve been self sourcing T3 . Little worried about what my endo will say when he reruns bloods next month, as he’s not keen to raise my levo above 50. Results are below,
Hi, I have had my blood results back from blue horizon. The only one they said was low was the TSH at 0.06. I was expecting this as I’ve been self sourcing T3 . Little worried about what my endo will say when he reruns bloods next month, as he’s not keen to raise my levo above 50. Results are below,
Clauds123
in
Thyroid UK
5 months ago
Help with results
Auto immune hypothyroid taking 100mcg Levo. Take iron tablets as ferritin usually 50-60 without. Suspected IBS and lots of gut issues. Feeling tired, aching weak feeling and some symptoms of low B12/folate but all results are in range and considered normal. Serum TSH level: 0.7 mIU/L (range 0.4
Auto immune hypothyroid taking 100mcg Levo. Take iron tablets as ferritin usually 50-60 without. Suspected IBS and lots of gut issues. Feeling tired, aching weak feeling and some symptoms of low B12/folate but all results are in range and considered normal. Serum TSH level: 0.7 mIU/L (range 0.4
pinklady756
in
Thyroid UK
5 months ago
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INR control
Hi don't know if this is of any interest to anyone ,but my INR has always been impossible to stabilize My heamatologist suggested taking a small dose of vitamin K and increasing the warfarin dose I didn't do this as don't want to be taking any more supplements, So I decided to massively increase my intake
Hi don't know if this is of any interest to anyone ,but my INR has always been impossible to stabilize My heamatologist suggested taking a small dose of vitamin K and increasing the warfarin dose I didn't do this as don't want to be taking any more supplements, So I decided to massively increase my intake
mully
in
Hughes Syndrome APS Forum
5 months ago
Scartgabe13
My wife wss diagnosed with PA 3 years ago, after our daughter suggested she should have a blood test to find out if her b12 was low,it was36 ,our daughter who has had PA for 10 years, was right .my wife had loading doses then started to have one every3 months but recently noted she has,nt had one since
My wife wss diagnosed with PA 3 years ago, after our daughter suggested she should have a blood test to find out if her b12 was low,it was36 ,our daughter who has had PA for 10 years, was right .my wife had loading doses then started to have one every3 months but recently noted she has,nt had one since
scartgabe12
in
Pernicious Anaemia Society
5 months ago
Latest blood test results
Happy New Year!A bit of a long post so please accept my apologies. Firstly thanks for the previous advice on taking vitamins to help with my Hashi diagnosis, which l got last September. I received my blood results from Medichecks this afternoon. Bloods were done 24 hrs after my last levo at 9.30 am
Happy New Year!A bit of a long post so please accept my apologies. Firstly thanks for the previous advice on taking vitamins to help with my Hashi diagnosis, which l got last September. I received my blood results from Medichecks this afternoon. Bloods were done 24 hrs after my last levo at 9.30 am
DitzyGrandma
in
Thyroid UK
5 months ago
Desperate for direction
I am diagnosed hypothyroid. I take 75mg levothyroxine a day. i have had my latest thyroid results from Monitor My Health. I think they use NHS ranges. 15/01/2024 3.7 pmol/L FT3 levels normal (normal range 3.1 - 6.8 pmol/L) thyroxine 15/01/2024 16.4 pmol/L FT4 levels normal (normal range 12 -
I am diagnosed hypothyroid. I take 75mg levothyroxine a day. i have had my latest thyroid results from Monitor My Health. I think they use NHS ranges. 15/01/2024 3.7 pmol/L FT3 levels normal (normal range 3.1 - 6.8 pmol/L) thyroxine 15/01/2024 16.4 pmol/L FT4 levels normal (normal range 12 -
Bluekipper
in
Thyroid UK
5 months ago
Folate Levels ?
I am still trying to feel well ? With symptoms including severe fatigue and weakness, disorientation, and joint and body pains. Can you please let meknow if I might need to increase my Folate level - as although within range - at 13 - I think I had read here that it is best if it is at least 50% through
I am still trying to feel well ? With symptoms including severe fatigue and weakness, disorientation, and joint and body pains. Can you please let meknow if I might need to increase my Folate level - as although within range - at 13 - I think I had read here that it is best if it is at least 50% through
Lemondrizz
in
Thyroid UK
5 months ago
Confused about latest blood tests - why are FT4 and FT3 rising, but I still feel awful and I'm undiagnosed and not on any meds?
Sorry for the super long post.... I would very much appreciate the help of you wonderful people on this forum. I am a bit confused with my latest blood test results that I just received yesterday, and am hoping that you will be able to help me understand what's going on. I'll try to keep it brief, while
Sorry for the super long post.... I would very much appreciate the help of you wonderful people on this forum. I am a bit confused with my latest blood test results that I just received yesterday, and am hoping that you will be able to help me understand what's going on. I'll try to keep it brief, while
Overlooked
in
Thyroid UK
5 months ago
DEXA results and nerves
Hello folks, I’m a 34 year old female with a complex medical history dating back pretty much my whole life. I recently had a DEXA scan due to current very low body weight on the advice of my GP. Ive been told that the fact I have Kyphoscoliosis & scoliosis (76 degrees fixed to 26 degrees - operated
Hello folks, I’m a 34 year old female with a complex medical history dating back pretty much my whole life. I recently had a DEXA scan due to current very low body weight on the advice of my GP. Ive been told that the fact I have Kyphoscoliosis & scoliosis (76 degrees fixed to 26 degrees - operated
Chaucer89
in
Bone Health and Osteoporosis UK
5 months ago
pulmonary fibrosis
hi everyone I have been prescribed ninintab haven't taken yet but the nurse said can't take NAC and quercetin and lots of other vitamins and alchhol and other rules, does anyone know anything about this seems like a change of lifestyle to me im supposed to use ambulatory oxegen as welwell !
hi everyone I have been prescribed ninintab haven't taken yet but the nurse said can't take NAC and quercetin and lots of other vitamins and alchhol and other rules, does anyone know anything about this seems like a change of lifestyle to me im supposed to use ambulatory oxegen as welwell !
Currygirl
in
Living with Interstitial Lung Disease (ILD)
6 months ago
high b12 high mch and mcv
Hi, b12 797 (145 - 637) folate 35.1 (7 - 39) mch 37.6 (27.4 - 33.9) mcv 110 (83 - 97) iron 12 (8 - 30) ferritin 69.30 (13 - 150) haemoglobin 124 (119 - 157) What does this mean? I am not taking b12 supplements or injections. My GP said that I had a b12 deficiency (she didn't measure my b12),
Hi, b12 797 (145 - 637) folate 35.1 (7 - 39) mch 37.6 (27.4 - 33.9) mcv 110 (83 - 97) iron 12 (8 - 30) ferritin 69.30 (13 - 150) haemoglobin 124 (119 - 157) What does this mean? I am not taking b12 supplements or injections. My GP said that I had a b12 deficiency (she didn't measure my b12),
nyx19
in
Pernicious Anaemia Society
2 months ago
vitamin D and magnesium deficiency from B12 loading doses
good day, I'm on my sixth month of loading methy B12 and learning so much on with every ones posts, I am trying to balance out my cofactors now that I've started to feel better along this journey. So with other factors I'm finding out I'm deficient in from all my gastritis from B12 deficiency for several
good day, I'm on my sixth month of loading methy B12 and learning so much on with every ones posts, I am trying to balance out my cofactors now that I've started to feel better along this journey. So with other factors I'm finding out I'm deficient in from all my gastritis from B12 deficiency for several
JesusMercy60
in
Pernicious Anaemia Society
2 months ago
vitamin d advice please
I’m sub clinic apparently. I plan to start V D but my first look at what’s available is confusing. Is there more than one V D as I see some are called D3? Is the RDA amount available or do you just take lots to make it up. I’m 61 female with AI rheumatoid conditions and veggie.
I’m sub clinic apparently. I plan to start V D but my first look at what’s available is confusing. Is there more than one V D as I see some are called D3? Is the RDA amount available or do you just take lots to make it up. I’m 61 female with AI rheumatoid conditions and veggie.
Stills
in
Thyroid UK
5 months ago
recovery
Hello, does how quickly you feel better after initial b12 injection(s) and iron infusion depend on your deficiencies severity?
Hello, does how quickly you feel better after initial b12 injection(s) and iron infusion depend on your deficiencies severity?
TheLabSquad
in
Pernicious Anaemia Society
5 months ago
recurrent fungal infections & reaction to probiotics
I have been on the same dose of Levothyroxine for about 13 months (212.5mcg) and seem to be doing ok thyroid wise. However, I have had a fungal infection in my nails and excessive gas for as long as I can remember, and I get recurring fungal infections on my face, scalp, back, chest and feet. Last year
I have been on the same dose of Levothyroxine for about 13 months (212.5mcg) and seem to be doing ok thyroid wise. However, I have had a fungal infection in my nails and excessive gas for as long as I can remember, and I get recurring fungal infections on my face, scalp, back, chest and feet. Last year
BreifneKing
in
Thyroid UK
5 months ago
Vit B12 deficient again after being taken off injections two years ago.
Hello Everyone, I haven’t been here for years and I need some advice please. My hubby started having strange symptoms over ten years ago and it was discovered that he had low vitamin b12, despite eating meat. His GP said he likely had Pernicious Anaemia and gave him a loading dose of injections and
Hello Everyone, I haven’t been here for years and I need some advice please. My hubby started having strange symptoms over ten years ago and it was discovered that he had low vitamin b12, despite eating meat. His GP said he likely had Pernicious Anaemia and gave him a loading dose of injections and
CarolineAnne
in
Pernicious Anaemia Society
5 months ago
Interesting B1 observation
Five days ago, my husband stopped taking sublingual B1. His head has been foggy and his balance had been getting progressively worse for many months, falling to the side weekly of late and of course we put it down to his PD getting worse. We have been trying to get the ‘right dose’ of thiamine for 4
Five days ago, my husband stopped taking sublingual B1. His head has been foggy and his balance had been getting progressively worse for many months, falling to the side weekly of late and of course we put it down to his PD getting worse. We have been trying to get the ‘right dose’ of thiamine for 4
Jennyjenny2
in
Cure Parkinson's
1 year ago
Why did my infusions get stopped?
I’ve had several Rituximab infusions, usually every 9 months to a year apart; the last one was in 2021. In 2022 I was informed that Rituximab would be replaced by Rituxithon ( I hope that’s right) as its cheaper. I haven’t got a problem with this. In March 2020, the week before lockdown, I went
I’ve had several Rituximab infusions, usually every 9 months to a year apart; the last one was in 2021. In 2022 I was informed that Rituximab would be replaced by Rituxithon ( I hope that’s right) as its cheaper. I haven’t got a problem with this. In March 2020, the week before lockdown, I went
SwimmerBTC
in
NRAS
5 months ago
I found this helpful
I evaluated the information on injecting available regarding injecting insulin with regards to risk of self preloading syringes and multi use vials. I also evaluated information available for clinical environment injections. I found this information and my evaluation more credible and helpful than
I evaluated the information on injecting available regarding injecting insulin with regards to risk of self preloading syringes and multi use vials. I also evaluated information available for clinical environment injections. I found this information and my evaluation more credible and helpful than
WIZARD6787
in
Pernicious Anaemia Society
5 months ago
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