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Vitamin B12 deficiency
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Pernicious Anaemia/
vitamin
B12
deficiency
can be the basis of psychiatric symptoms and diagnoses and developmental disabilities. I am terribly sorry that my knowledge of the latter is limited.
Pernicious Anaemia/
vitamin
B12
deficiency
can be the basis of psychiatric symptoms and diagnoses and developmental disabilities. I am terribly sorry that my knowledge of the latter is limited.
Narwhal10
in
Pernicious Anaemia Society
1 year ago
Cortisol tests
Hi, I just had my cortisol retested to see if there had been any improvement from February 2023. Since August 2023, I have been slowly titrating NDT Armour and taking vitamins, minerals and amino acids prescribed by a private thyroid Dr. My iron & B12 are good, working on increasing vit D. I'm still
Hi, I just had my cortisol retested to see if there had been any improvement from February 2023. Since August 2023, I have been slowly titrating NDT Armour and taking vitamins, minerals and amino acids prescribed by a private thyroid Dr. My iron & B12 are good, working on increasing vit D. I'm still
Insomania
in
Thyroid UK
5 months ago
low B12
hi can anyone help me? How do I link my old post to a new one today as I would like some advice many thanks (so people don’t get confused)
hi can anyone help me? How do I link my old post to a new one today as I would like some advice many thanks (so people don’t get confused)
Doris11
in
Thyroid UK
10 months ago
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Hypothyroid symptoms but Dr says normal
Hey! So my recent bloods show; Tsh 0.01 T4 11 (range 9- 19) T3 ( 4.5) (range 3 to 7) Dr says normal but I'm so fluid. My legs swell all the time and make indents in my leg. Confused. Legs are tingling due to water being so bad. I drink alot of water daily as I'm active but the retention is getting
Hey! So my recent bloods show; Tsh 0.01 T4 11 (range 9- 19) T3 ( 4.5) (range 3 to 7) Dr says normal but I'm so fluid. My legs swell all the time and make indents in my leg. Confused. Legs are tingling due to water being so bad. I drink alot of water daily as I'm active but the retention is getting
jparsss
in
Thyroid UK
5 months ago
Metatrexate
I am now back on 15 mil of Metx injection with 20m Pred. followed by folic acid 2 days later.and all seems to be going well and not affecting my blood sugar levels so badly. My B12 was very low so also had a course of injections it seems to be a fine balance between blood pressure, blood sugar levels
I am now back on 15 mil of Metx injection with 20m Pred. followed by folic acid 2 days later.and all seems to be going well and not affecting my blood sugar levels so badly. My B12 was very low so also had a course of injections it seems to be a fine balance between blood pressure, blood sugar levels
Doublef
in
PMRGCAuk
5 months ago
Update GP lied to our faces and some links for purchasing b12 please
So I updated you all last week on the visit to go last week where I believed she was gaslighting myself and my partner. Since then we have managed to access his medical records. One of the things I mentioned to her was his low result 5 years ago which was 222. She then went on to say he was tested 3
So I updated you all last week on the visit to go last week where I believed she was gaslighting myself and my partner. Since then we have managed to access his medical records. One of the things I mentioned to her was his low result 5 years ago which was 222. She then went on to say he was tested 3
Nic878
in
Pernicious Anaemia Society
10 months ago
Haematologist’s unsupportive B12 response
In a recent pathology test, my gastroenterologist was concerned with my low haemoglobin count and a high reticulocyte count. She mentioned that although I’m low in ferritin (40) I’m not yet needing an iron infusion just yet. My white cell count was seemingly low also and she suggested that I should get
In a recent pathology test, my gastroenterologist was concerned with my low haemoglobin count and a high reticulocyte count. She mentioned that although I’m low in ferritin (40) I’m not yet needing an iron infusion just yet. My white cell count was seemingly low also and she suggested that I should get
GoneWithTheWind1972
in
Pernicious Anaemia Society
3 months ago
levo increase!
Hi all about a month ago I increased my levo from 100mcgs to 112mcgs daily as per body weight thing! I am unfortunately 100kgs 😟 I am feeling a bit tired again sleeping a lot and not having much energy! I am doing something wrong? 😑 PS still have the ongoing saga with the deficient B12 and folate
Hi all about a month ago I increased my levo from 100mcgs to 112mcgs daily as per body weight thing! I am unfortunately 100kgs 😟 I am feeling a bit tired again sleeping a lot and not having much energy! I am doing something wrong? 😑 PS still have the ongoing saga with the deficient B12 and folate
Doris11
in
Thyroid UK
5 months ago
ferritin high
hello. I’m new to the group I’ve had under active thyroid for approx 2 years diagnosed during covid. I was just told over the phone you need thyroxine it’s sent to the chemist and that’s all the info I got. I’ve had another blood test as my shoulders and hips are in almost constant discomfort all that
hello. I’m new to the group I’ve had under active thyroid for approx 2 years diagnosed during covid. I was just told over the phone you need thyroxine it’s sent to the chemist and that’s all the info I got. I’ve had another blood test as my shoulders and hips are in almost constant discomfort all that
Puglady1981
in
Thyroid UK
5 months ago
on b12 treatment, when start folic acid?
Hi all, I was able to feel better over the last year with the help of this forum, a big thank you. My problem started with neurological symptoms without knowing what was happening! Then with the help of people here and researching I found out I was low in b12 when started treating with folic acid (5mg
Hi all, I was able to feel better over the last year with the help of this forum, a big thank you. My problem started with neurological symptoms without knowing what was happening! Then with the help of people here and researching I found out I was low in b12 when started treating with folic acid (5mg
Kat_88
in
Pernicious Anaemia Society
5 months ago
Inflammation and RLS
I have always believed that inflammation was part of my RLS. I believe this because my RLS responds well to ibuprofen. A recent blog was using this study http://www.smj.org.sg/sites/default/files/SMJ-57-514.pdf The study is from 2016. The study proposes to use the neutrophil-to-lymphocyte ratio
I have always believed that inflammation was part of my RLS. I believe this because my RLS responds well to ibuprofen. A recent blog was using this study http://www.smj.org.sg/sites/default/files/SMJ-57-514.pdf The study is from 2016. The study proposes to use the neutrophil-to-lymphocyte ratio
WideBody
in
Restless Legs Syndrome
5 months ago
Common Vitamin Deficiencies in PD?
I want to get a Vitamin deficiency blood test and I am wondering what vitamins to test for. The big ones I know I am going to look for are B1, B12 and D. Any other vitamins or non vitamins to look for?
I want to get a Vitamin deficiency blood test and I am wondering what vitamins to test for. The big ones I know I am going to look for are B1, B12 and D. Any other vitamins or non vitamins to look for?
RBDNoPDYet
in
Cure Parkinson's
6 months ago
Should I push for a test?
Update - I have realised that a few more results have come through. He ordered dsDNA but apparently the sample was lost or there wasn't enough? He ordered ENA Antibody test but the result says unknown? ANA Test - Anti-nuclear factor level POSITIVE - Titre > 1:640 ANA PATTERN SPECKLED In the presence
Update - I have realised that a few more results have come through. He ordered dsDNA but apparently the sample was lost or there wasn't enough? He ordered ENA Antibody test but the result says unknown? ANA Test - Anti-nuclear factor level POSITIVE - Titre > 1:640 ANA PATTERN SPECKLED In the presence
EllsBells591
in
Pernicious Anaemia Society
10 months ago
Postpartum depression
A recent release described a newly-developed drug for postpartum depression. Effects of the drug are said to last 45days. Cost is greater than $10,000 USD. No mention was made at all of nutrients. I seemed to recall a connection between postpartum depression and B12; a quick search on regular Google
A recent release described a newly-developed drug for postpartum depression. Effects of the drug are said to last 45days. Cost is greater than $10,000 USD. No mention was made at all of nutrients. I seemed to recall a connection between postpartum depression and B12; a quick search on regular Google
WiscGuy
in
Pernicious Anaemia Society
10 months ago
Blood test results
Repeated blood tests ordered by my GP trying to compare private ones I had a month ago with different ranges,I had both done at 9am and only glass of water can someone help please? 12th February 2024 repeat GP tests January 2024 Medichecks private test B12 344 range (187-883.00ng
Repeated blood tests ordered by my GP trying to compare private ones I had a month ago with different ranges,I had both done at 9am and only glass of water can someone help please? 12th February 2024 repeat GP tests January 2024 Medichecks private test B12 344 range (187-883.00ng
Bluenose69
in
Thyroid UK
5 months ago
Supplements to reduce glutamate
I was inspired by Widebody's comments on taurine and glycine to look into supplements that reduce glutamate. I found the following on an autism website that I cannot vouch for, but here is the list: (those of us taking gabapentin, pregabalin, horizont are taking medicine that is reducing brain glutamate
I was inspired by Widebody's comments on taurine and glycine to look into supplements that reduce glutamate. I found the following on an autism website that I cannot vouch for, but here is the list: (those of us taking gabapentin, pregabalin, horizont are taking medicine that is reducing brain glutamate
wantokporo
in
Restless Legs Syndrome
10 months ago
help… no longer tolerating meds
Hi all, I am having persistent issues after having Covid in May. Covid symptoms persisted for 2 weeks after which I felt ok until I didn’t at the beginning of June… very dehydrated, peeing a lot, adrenaline type feelings, indigestion and was getting neuropathic sensations in my skin. This so far
Hi all, I am having persistent issues after having Covid in May. Covid symptoms persisted for 2 weeks after which I felt ok until I didn’t at the beginning of June… very dehydrated, peeing a lot, adrenaline type feelings, indigestion and was getting neuropathic sensations in my skin. This so far
Littledancingtiger
in
Thyroid UK
3 days ago
Test results back - within range?
I posted last week that I suspected I was hypo (family history... that and coeliac) and you suggested I go away and get bloods tested. So results are as follows, all 'within range'... Slightly disappointed because I hoped that hypo might explain some of the symptoms I have that are otherwise unexplained
I posted last week that I suspected I was hypo (family history... that and coeliac) and you suggested I go away and get bloods tested. So results are as follows, all 'within range'... Slightly disappointed because I hoped that hypo might explain some of the symptoms I have that are otherwise unexplained
menochar
in
Thyroid UK
3 days ago
Graves Disease Private Endo recommendation (SW) London please PM 🙏
Hello, I’d appreciate a PM if anyone can recommend an Endo who specialises or is experienced in treating Graves’ disease in London or ideally SW London. I’ve been on NHS waitlist to see someone for three months and have only now started to get heart palpitations which are concerning so wanting to commence
Hello, I’d appreciate a PM if anyone can recommend an Endo who specialises or is experienced in treating Graves’ disease in London or ideally SW London. I’ve been on NHS waitlist to see someone for three months and have only now started to get heart palpitations which are concerning so wanting to commence
Gravie
in
Thyroid UK
4 days ago
latest bloods
I’m on a journey with t3 it’s taking a while. Latest bloods reflect 15mcg taken in one dose and 50mcg levothyroxine I think I need to increase levo but on 75 I was slightly over medicated I felt. A reply on here suggested 62.5mcg as middle road which makes sense to me but pills are tiny and crumbly
I’m on a journey with t3 it’s taking a while. Latest bloods reflect 15mcg taken in one dose and 50mcg levothyroxine I think I need to increase levo but on 75 I was slightly over medicated I felt. A reply on here suggested 62.5mcg as middle road which makes sense to me but pills are tiny and crumbly
Mag999
in
Thyroid UK
6 days ago
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