Search
Search
About
Log in
Join
Experiences with
Vitamin B12 / Folic acid
Posts
Communities
51,480 public posts
Filter results
Mucousy
Some one on this forum used the term mucousy. I had never read that term and looked it up. Expecting it to be a UK situation. "We should take a wee walk and go behind that wee bush and take a wee. 🙂 I have been wracking my brain trying to find a way to evaluate not only my supplementation regime but
Some one on this forum used the term mucousy. I had never read that term and looked it up. Expecting it to be a UK situation. "We should take a wee walk and go behind that wee bush and take a wee. 🙂 I have been wracking my brain trying to find a way to evaluate not only my supplementation regime but
WIZARD6787
in
Pernicious Anaemia Society
10 months ago
Update
I have written here often that I suffer more with less B12 and less with more B12. I heal more effectively with my latest trial of supplementation. (See Profile) It is not knowable what which of the supplements are effective and it well may be they work together. It is working out that I inject 4
I have written here often that I suffer more with less B12 and less with more B12. I heal more effectively with my latest trial of supplementation. (See Profile) It is not knowable what which of the supplements are effective and it well may be they work together. It is working out that I inject 4
WIZARD6787
in
Pernicious Anaemia Society
10 months ago
Blue Horizon Active B12 ref range
A quick question - can anyone tell me what the BH range is for Active B12? It would be a separate/different test to the Thyroid Gold Premium which has the Serum B12. I looked but couldn't see it on the BH site. Cheers.
A quick question - can anyone tell me what the BH range is for Active B12? It would be a separate/different test to the Thyroid Gold Premium which has the Serum B12. I looked but couldn't see it on the BH site. Cheers.
Sneedle
in
Thyroid UK
10 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Test Results and heart flutters
Hello everyone, I'm new on here. So glad to have found this site! I've posted before for a friend but now I'm looking for some help with my own thyroid medication. I've had hashimotos for 34 years (since I was 20yrs old) and been on levothyroxine for most of that time. Mostly I've been ok-ish. Just
Hello everyone, I'm new on here. So glad to have found this site! I've posted before for a friend but now I'm looking for some help with my own thyroid medication. I've had hashimotos for 34 years (since I was 20yrs old) and been on levothyroxine for most of that time. Mostly I've been ok-ish. Just
LoveAndPeas
in
Thyroid UK
3 months ago
B1 therapy side effects
Hi, I am 55 years old male diagnosed with PD about 5 years ago. Started B1 therapy couple of days ago in consultation with my Neurologist. He suggested 100 mg Thiamine oral tablets 3 times a day for 10 days and taper down after 10 days. However severe side effects like feverish, body aches, headache
Hi, I am 55 years old male diagnosed with PD about 5 years ago. Started B1 therapy couple of days ago in consultation with my Neurologist. He suggested 100 mg Thiamine oral tablets 3 times a day for 10 days and taper down after 10 days. However severe side effects like feverish, body aches, headache
ashok200
in
Cure Parkinson's
6 months ago
TTFD promotes voluntary activity through dopaminergic activation
Thiamine tetrahydrofurfuryl disulfide promotes voluntary activity through dopaminergic activation in the medial prefrontal cortex
https://www.nature.com/articles/s41598-018-28462-2
Thiamine tetrahydrofurfuryl disulfide promotes voluntary activity through dopaminergic activation in the medial prefrontal cortex
https://www.nature.com/articles/s41598-018-28462-2
Gcf51
in
Cure Parkinson's
6 months ago
Daridexorant / quvuviq and RLS
Just wondering if anyone else has experience of this sleep aid and RLS? I have bought (not available in my region on NHS yet) a month’s supply of 50mg tablets and ….. I am sleeping normally!!!! It is a new drug to the UK but tried and tested in USA I believe? Apparently minimal side effects. I have
Just wondering if anyone else has experience of this sleep aid and RLS? I have bought (not available in my region on NHS yet) a month’s supply of 50mg tablets and ….. I am sleeping normally!!!! It is a new drug to the UK but tried and tested in USA I believe? Apparently minimal side effects. I have
Lacey_
in
Restless Legs Syndrome
1 month ago
Dr Sarah Myhill B12 injections
Hi allI know alot people on the forum get their B12 injections from Germany but I'm just wondering if anyone has bought from Dr Myhills website?
Hi allI know alot people on the forum get their B12 injections from Germany but I'm just wondering if anyone has bought from Dr Myhills website?
Hollybushroad
in
Pernicious Anaemia Society
10 months ago
Daughter- overactive?
Morning all, My daughter has had 2 blood tests 6 months apart which suggest over active thyroid. High T3 and T4, low TSH They have started her on Carbimazole 15mg Her folate is 9 B12 - High normal 712 We have requested a VIT D test and ferritin. Her lymphocytes are 1.3 slightly out of range.
Morning all, My daughter has had 2 blood tests 6 months apart which suggest over active thyroid. High T3 and T4, low TSH They have started her on Carbimazole 15mg Her folate is 9 B12 - High normal 712 We have requested a VIT D test and ferritin. Her lymphocytes are 1.3 slightly out of range.
Rockerfella
in
Thyroid UK
6 months ago
Next step in solving the mystery of my burning feet, but need a little bit of advice
Hi all I’m in need of some more advice. As suggested, I’ve tried raising my vitamin levels since Nov 2023 and although not perfect, they’ve gone up. I’m still having burning in my feet so decided to go to a consultant. Below are my most recent bloods. 7th Feb 2024 Medichecks Blood tests
Hi all I’m in need of some more advice. As suggested, I’ve tried raising my vitamin levels since Nov 2023 and although not perfect, they’ve gone up. I’m still having burning in my feet so decided to go to a consultant. Below are my most recent bloods. 7th Feb 2024 Medichecks Blood tests
FW23
in
Thyroid UK
3 months ago
Riboflavin (b2) supplementation is a no-brainer for Parkinsons
Riboflavin (b2) is a complete no-brainer. 0 side effects and dirt cheap. Especially if your second and third toes any toenails are full of fungus/athletes foot. The Chinese believe that your second and third toe is a place where toxins leave the body. The Chinese believe PD is “stuck” in fight or
Riboflavin (b2) is a complete no-brainer. 0 side effects and dirt cheap. Especially if your second and third toes any toenails are full of fungus/athletes foot. The Chinese believe that your second and third toe is a place where toxins leave the body. The Chinese believe PD is “stuck” in fight or
38yroldmale
in
Cure Parkinson's
4 months ago
B12 Vitamin
hi Could someone be so kind as to interpret the vitamin B12, do I need to supplement this and if so what is recommended and best supplement. Thank you in advance
hi Could someone be so kind as to interpret the vitamin B12, do I need to supplement this and if so what is recommended and best supplement. Thank you in advance
Thesun
in
Thyroid UK
4 months ago
B12 injections
My needles arrived today and I can’t believe I did my first subcutaneous injection, it wasn’t perfect but I did it! Thank you to everyone who helped me, I couldn’t have done it on my own.
My needles arrived today and I can’t believe I did my first subcutaneous injection, it wasn’t perfect but I did it! Thank you to everyone who helped me, I couldn’t have done it on my own.
Inishfree
in
Pernicious Anaemia Society
10 months ago
optimal bloods?
Looking at my bloods I think they are near enough spot on? (Any input would be great). However I still feel terrible with severe fatigue & body aches. I am taking vit D, multi vit, iron (heme) and going to restart cortex adrenal. As my cortisol is coming back low. currently on 1 1/4 grain armour
Looking at my bloods I think they are near enough spot on? (Any input would be great). However I still feel terrible with severe fatigue & body aches. I am taking vit D, multi vit, iron (heme) and going to restart cortex adrenal. As my cortisol is coming back low. currently on 1 1/4 grain armour
Ajva
in
Thyroid UK
6 months ago
Blood results interpretation required
Hi there, I need help interpreting my results. My symptoms are brain fog, joint aches, lack of energy and anxiety. These have been with me all my life. They got better in 2022 when I started combination therapy. However, I do not think I have reached my optimum (whatever that is) because these symptoms
Hi there, I need help interpreting my results. My symptoms are brain fog, joint aches, lack of energy and anxiety. These have been with me all my life. They got better in 2022 when I started combination therapy. However, I do not think I have reached my optimum (whatever that is) because these symptoms
Carlax
in
Thyroid UK
3 months ago
Benfotiamine In The Mix For PD Again?
The following new animal study (December 2023) suggests that the fat soluble form of vitamin B1, Benfotiamine, may also be suitable for PD : https://www.sciencedirect.com/science/article/abs/pii/S0014299923007483?via%3Dihub Here is a relevant study quote :
' The results demonstrated that treatment
The following new animal study (December 2023) suggests that the fat soluble form of vitamin B1, Benfotiamine, may also be suitable for PD : https://www.sciencedirect.com/science/article/abs/pii/S0014299923007483?via%3Dihub Here is a relevant study quote :
' The results demonstrated that treatment
chartist
in
Cure Parkinson's
6 months ago
Heart Arrhythmia
Hello All. I've posted in the past and remember that some have said that I could increase my dose of T3 to perhaps alleviate the arrhythmia I have been experiencing for many years. I take 75 MCG LEVO (for 35+ years with varying dosages) and 5 MCG Lio each morning. Any comments at this time would be greatly
Hello All. I've posted in the past and remember that some have said that I could increase my dose of T3 to perhaps alleviate the arrhythmia I have been experiencing for many years. I take 75 MCG LEVO (for 35+ years with varying dosages) and 5 MCG Lio each morning. Any comments at this time would be greatly
saritadelmar
in
Thyroid UK
3 months ago
Ferritin Levels/Hair Loss/Thyroid
Good morning I have started to loose my hair and the doctor is insistent its not a change in my thyroid levels, although my TSH has changed over the last couple of readings. So I was told to have a ferritin test and take vitamin D, I also take B12. Thinking that it would be low hence the hair loss
Good morning I have started to loose my hair and the doctor is insistent its not a change in my thyroid levels, although my TSH has changed over the last couple of readings. So I was told to have a ferritin test and take vitamin D, I also take B12. Thinking that it would be low hence the hair loss
MurphysMama
in
Thyroid UK
6 months ago
Some Blood Tests - Not lots of..
Just wanted to set out my lastest blood tests. I am getting a new set of Thyroid function, FBC, B12 and U&E tests later this month. mid 2022 - TSH = 1.16 uUmL Mid 2023 TSH = 0.90uUmL / FT4 = 17.1 pmol / FT3 3.7 pmol - updated for latest ft4 I have been borderline anaemic for three
Just wanted to set out my lastest blood tests. I am getting a new set of Thyroid function, FBC, B12 and U&E tests later this month. mid 2022 - TSH = 1.16 uUmL Mid 2023 TSH = 0.90uUmL / FT4 = 17.1 pmol / FT3 3.7 pmol - updated for latest ft4 I have been borderline anaemic for three
Treesong2023
in
Thyroid UK
6 months ago
Preparing for GP appt
Hello I have a GP appointment in a few weeks to discuss blood tests results and symptoms (tiredness, weight gain, low mood, pins and needles). Based on what I've read on this forum, it sounds like these symptoms and results could be indicative of hypothyroid, but because TSH is within range I'm unlikely
Hello I have a GP appointment in a few weeks to discuss blood tests results and symptoms (tiredness, weight gain, low mood, pins and needles). Based on what I've read on this forum, it sounds like these symptoms and results could be indicative of hypothyroid, but because TSH is within range I'm unlikely
Fb104
in
Thyroid UK
3 months ago
1
...
77
78
79
...
100
Next page
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
21448 results
Pernicious Anaemia Society
13044 results
Cure Parkinson's
1534 results
View top 10 communities
Sort by
Most Relevant
Newest