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Vitamin B12 / Folic acid
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Help interpreting results
Hi, apologies for long post. I’m a 34yo female. I’ve had symptoms that line up with hypothyroid symptoms for years. Had a few tests when my eczema flared up really badly around 12 years ago, which coincides with the time that a lot of the symptoms began. Have had fatigue basically since catching Epstein-Barr
Hi, apologies for long post. I’m a 34yo female. I’ve had symptoms that line up with hypothyroid symptoms for years. Had a few tests when my eczema flared up really badly around 12 years ago, which coincides with the time that a lot of the symptoms began. Have had fatigue basically since catching Epstein-Barr
KTEO
in
Thyroid UK
5 months ago
High T4 - Test Results
CRP -HS 2-690 mg/L Range under 3 Ferritin 185.00 ug/L ( 30-650) Folate - sample error Vit B12 Active 83.2 pmol/L (37.5 - 188) Vit D
CRP -HS 2-690 mg/L Range under 3 Ferritin 185.00 ug/L ( 30-650) Folate - sample error Vit B12 Active 83.2 pmol/L (37.5 - 188) Vit D
Fortie
in
Thyroid UK
5 months ago
results
lets try again Result. Range Vit D 109 50-200 Optimal 75-200 Magnesium. 0.93. 0.66-0.99 CRP.
lets try again Result. Range Vit D 109 50-200 Optimal 75-200 Magnesium. 0.93. 0.66-0.99 CRP.
Honeybee66
in
Thyroid UK
5 months ago
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MORE ADVICE ON RESULTS PLEASE !
Hi again kind people, Further to my last posts-I reduced Levo from 125ug to -100ug from 12/01/24 on Endo’s advice ( previous results as below ,he said ,still showed overmedication) 08/01/24: TSH 0.02 (0.27-4.3) FT4 4.2 ( 3.1- 6.8) FT4 21.9 (12.00-22.00) My latest blood results taken on 22/02/
Hi again kind people, Further to my last posts-I reduced Levo from 125ug to -100ug from 12/01/24 on Endo’s advice ( previous results as below ,he said ,still showed overmedication) 08/01/24: TSH 0.02 (0.27-4.3) FT4 4.2 ( 3.1- 6.8) FT4 21.9 (12.00-22.00) My latest blood results taken on 22/02/
Koababy20
in
Thyroid UK
5 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
3 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
3 months ago
IV Zoledronic acid.
unfortunately time to move to Zoledronic acic fractures happening. Tried calcium and Vit D weight bearing exercises. Has anybody got any advice before I travel down the road of no return!!! thank you in advance.
unfortunately time to move to Zoledronic acic fractures happening. Tried calcium and Vit D weight bearing exercises. Has anybody got any advice before I travel down the road of no return!!! thank you in advance.
Lion321
in
Advanced Prostate Cancer
6 months ago
DELIRIUM
Dear All, Just so you know, in medicine, we use the acronym PINCH ME for this symptom.
P - Pain
We can experience severe pain due to P.A./B12 deficiency needed to make the outer covering of nerves.
Dear All, Just so you know, in medicine, we use the acronym PINCH ME for this symptom.
P - Pain
We can experience severe pain due to P.A./B12 deficiency needed to make the outer covering of nerves.
Narwhal10
in
Pernicious Anaemia Society
11 months ago
Can I get some advice on my latest results, please?
Hello All I recently had my blood test through my GP for my Vitamin D and other tests. (Currently on 100mcg T4 and 10mcg T3 due to see my endo around July 2024) Date: 02/05/2024 (Early morning fasting after taking my Levo and T3). Serum Vitamin B12 239 ng/L [200 - 900] Serum Vitamin D 101 nmol
Hello All I recently had my blood test through my GP for my Vitamin D and other tests. (Currently on 100mcg T4 and 10mcg T3 due to see my endo around July 2024) Date: 02/05/2024 (Early morning fasting after taking my Levo and T3). Serum Vitamin B12 239 ng/L [200 - 900] Serum Vitamin D 101 nmol
BookLover2020
in
Thyroid UK
2 months ago
Results
Hello everyone. Firstly I want to say a big thanks to everyone that helped me understand my mum's results and situation. I also got my wires crossed and gave some wrong info. My mum did have a test before they prescribed 25mg, TSH 8.58. They said as she was 'borderline' they would try levo before considering
Hello everyone. Firstly I want to say a big thanks to everyone that helped me understand my mum's results and situation. I also got my wires crossed and gave some wrong info. My mum did have a test before they prescribed 25mg, TSH 8.58. They said as she was 'borderline' they would try levo before considering
RedOne1
in
Thyroid UK
5 months ago
Further to my post of 9 months ago
Hi Until December last I was taking 40 mg iron bisglycinate with orange juice every two days. Since this had little impact on my RLS I increased the iron dose to 40mg every day from December until now. As yet I have noticed little change to my RLS symptoms. A blood test this month showed my ferritin
Hi Until December last I was taking 40 mg iron bisglycinate with orange juice every two days. Since this had little impact on my RLS I increased the iron dose to 40mg every day from December until now. As yet I have noticed little change to my RLS symptoms. A blood test this month showed my ferritin
Rameau
in
Restless Legs Syndrome
4 months ago
Could it be MS?
For the last 11 months, I have been experiencing numbness and tingling in both feet. I have noticed when its cold I feel worse. I also have numbness, tingling and weakness on my left side in my hand and lower arm. I had a MRI in April 2023 with no contrast; both came back normal. My symptoms have
For the last 11 months, I have been experiencing numbness and tingling in both feet. I have noticed when its cold I feel worse. I also have numbness, tingling and weakness on my left side in my hand and lower arm. I had a MRI in April 2023 with no contrast; both came back normal. My symptoms have
brwnbaby
in
My MSAA Community
7 months ago
NHS Endocrinology appointment with results of NHS T3 tests. Are latest bloods in my favour or will they work against me?
Hi All, I am hoping to have T3 prescribed on the NHS (aren’t we all?!) or at least to have an understanding Endocrinologist. I am also hoping to increase T3 (See * below) My new NHS Endocrinologist I saw last month asked for me to take my morning NHS T4 and self-prescribed T3 as usual, then 2-4hrs
Hi All, I am hoping to have T3 prescribed on the NHS (aren’t we all?!) or at least to have an understanding Endocrinologist. I am also hoping to increase T3 (See * below) My new NHS Endocrinologist I saw last month asked for me to take my morning NHS T4 and self-prescribed T3 as usual, then 2-4hrs
Abi-Abster
in
Thyroid UK
7 months ago
Any suggestions for how to improve my poos
Hello all. My apologies for the title of this post, but I didn’t know how to phrase it. I was diagnosed with GCA in January 2023 and have been on Prednisone ever since, along with other meds that are given to mitigate the side effects of the Pred. I also started Methotrexate this January. My first attempt
Hello all. My apologies for the title of this post, but I didn’t know how to phrase it. I was diagnosed with GCA in January 2023 and have been on Prednisone ever since, along with other meds that are given to mitigate the side effects of the Pred. I also started Methotrexate this January. My first attempt
Handloomweaver
in
PMRGCAuk
4 months ago
B12 and remyelization
This article was interesting to me due to frequent mention of the importance of B12 to nerve remyelization: https://journals.sagepub.com/doi/full/10.1177/2192568218758633 I inject B12 daily because of the possibility that it helps to insure presence of B12 whenever and wherever remyelization might
This article was interesting to me due to frequent mention of the importance of B12 to nerve remyelization: https://journals.sagepub.com/doi/full/10.1177/2192568218758633 I inject B12 daily because of the possibility that it helps to insure presence of B12 whenever and wherever remyelization might
WiscGuy
in
Pernicious Anaemia Society
11 months ago
Got GP appointment but what to say to get him to test anything more than TSH
Hi 3 months ago I wrote a post about my daughters results since 2018 & her vitamin levels which are dire. It has taken her this long to manage to get a telephone appointment with a GP next Wednesday. My question is what does she say to convince them to test more than just her TSH. I went through
Hi 3 months ago I wrote a post about my daughters results since 2018 & her vitamin levels which are dire. It has taken her this long to manage to get a telephone appointment with a GP next Wednesday. My question is what does she say to convince them to test more than just her TSH. I went through
Otto11
in
Thyroid UK
3 months ago
Exhaustion
Hi All Finally have a full set of results: FT3. 4.1 (range 3.1 - 6.8) FT4 22.2 (range 12 - 22) TSH 0.08 (range 0.27 - 4.2) Vit D. 113 nmol/L reduced supplements from 10000iU/wk to 6000/wk Anaemia HB 152 g/L Normal Ferritin 324 if/L Normal TSAT 40% Normal Active B12 51 pmol/L Normal Folate
Hi All Finally have a full set of results: FT3. 4.1 (range 3.1 - 6.8) FT4 22.2 (range 12 - 22) TSH 0.08 (range 0.27 - 4.2) Vit D. 113 nmol/L reduced supplements from 10000iU/wk to 6000/wk Anaemia HB 152 g/L Normal Ferritin 324 if/L Normal TSAT 40% Normal Active B12 51 pmol/L Normal Folate
DylanA
in
Thyroid UK
5 months ago
Have taken the plunge full Thyroid test!
Hi After reading many posts on here regarding Thyroid testing I have just received a full Thyroid Function test from Blue Horizon. My Thyroid has not been medicated correctly since I started taking 100mg Levothyroxine 4 yrs ago. Everytime I have a test the parameters seem to change from one test to
Hi After reading many posts on here regarding Thyroid testing I have just received a full Thyroid Function test from Blue Horizon. My Thyroid has not been medicated correctly since I started taking 100mg Levothyroxine 4 yrs ago. Everytime I have a test the parameters seem to change from one test to
Ontherun81
in
Thyroid UK
3 months ago
DX 5 years on Dec 26th. What I’ve learned about my PD. Please Read! It might be helpful.
PD is very common in my family. My dad and his dad had it. I have almost no hope they will ever cure it because it’s so complex. Here is what caused my Parkinson’s. (IMO) 1.Genetics. This is something you cannot change. I know my genes have issues with clearing out toxins? PD is a man made disease
PD is very common in my family. My dad and his dad had it. I have almost no hope they will ever cure it because it’s so complex. Here is what caused my Parkinson’s. (IMO) 1.Genetics. This is something you cannot change. I know my genes have issues with clearing out toxins? PD is a man made disease
38yroldmale
in
Cure Parkinson's
7 months ago
park_bear made a very compelling argument for taking P5P (active B6)
park_bear made a very compelling argument for taking P5P (active B6)(a). My comments are: 1) When I tried taking (his recommended) 2 hours after C/L, I started walking side to side and the problem didn’t clear until I took my C/L again. 2) I am afraid to take P5P before bed because I did not sleep
park_bear made a very compelling argument for taking P5P (active B6)(a). My comments are: 1) When I tried taking (his recommended) 2 hours after C/L, I started walking side to side and the problem didn’t clear until I took my C/L again. 2) I am afraid to take P5P before bed because I did not sleep
Gcf51
in
Cure Parkinson's
7 months ago
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