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Best way to take B12 chewable tablets?
Hi, Do I take them with food? In the morning/evening? Thanks
Hi, Do I take them with food? In the morning/evening? Thanks
LifeintheMed
in
Pernicious Anaemia Society
17 days ago
strange horrendous pain
Hi, I’m wondering if any of you lovely lot have had a similar experience please? I got very ill in January , extreme tiredness, stumbling, having visions, breathlessness , poor memory and pain and parathesia down right side of body . Long story short I was diagnosed with pernicious anaemia in February
Hi, I’m wondering if any of you lovely lot have had a similar experience please? I got very ill in January , extreme tiredness, stumbling, having visions, breathlessness , poor memory and pain and parathesia down right side of body . Long story short I was diagnosed with pernicious anaemia in February
Karenedawson
in
British Heart Foundation
17 days ago
B12 ampoules
Could someone take a look at this link for me before I order as I don't want to make a mistake... I'd be grateful of all advice.Thanks in advance Allywales https://www.arzneiprivat.de/product/vitamin-b12-depot-hevert-ampullen.245042.html
Could someone take a look at this link for me before I order as I don't want to make a mistake... I'd be grateful of all advice.Thanks in advance Allywales https://www.arzneiprivat.de/product/vitamin-b12-depot-hevert-ampullen.245042.html
Allywales8663
in
Pernicious Anaemia Society
18 days ago
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Help with test results
Hi,I'm hoping to get insights into my latest test results and symptoms I continue to have. I had my thyroid out in 2012 (Graves), I'm located in Australia and currently taking 100mcg of Eltroxin and 16mcg of slow release (compounded) t3 daily. Around 2yrs ago I got quite sick, I had extremely heavy fatigue
Hi,I'm hoping to get insights into my latest test results and symptoms I continue to have. I had my thyroid out in 2012 (Graves), I'm located in Australia and currently taking 100mcg of Eltroxin and 16mcg of slow release (compounded) t3 daily. Around 2yrs ago I got quite sick, I had extremely heavy fatigue
Miso_soup
in
Thyroid UK
18 days ago
Feeling desperate
I'm feeling very low at the moment, and quite isolated. I'm hoping to get some advice here. I'm a 45 year old male, and have had Hashimoto's since my early 20s. After a terrible few years on thyroxin I found NDT and on the whole have been relatively well on it. However, since around 2019 I've had bouts
I'm feeling very low at the moment, and quite isolated. I'm hoping to get some advice here. I'm a 45 year old male, and have had Hashimoto's since my early 20s. After a terrible few years on thyroxin I found NDT and on the whole have been relatively well on it. However, since around 2019 I've had bouts
ci00aaj
in
Thyroid UK
3 months ago
Colonoscopy/gastroscopy
Hello, me again! Or should I say “g’day”? I’ve just had my first ever hospital procedure with sedation - A colonoscopy and gastroscopy (top and tail) to check why I might not be absorbing B12 and iron. I’ve been terrified about it for so long and it was a complete non-event. The hospital staff were
Hello, me again! Or should I say “g’day”? I’ve just had my first ever hospital procedure with sedation - A colonoscopy and gastroscopy (top and tail) to check why I might not be absorbing B12 and iron. I’ve been terrified about it for so long and it was a complete non-event. The hospital staff were
PlatypusProfit8077
in
Pernicious Anaemia Society
18 days ago
blood test results help please
hi everyone I hope you don’t mind me asking for help again. I had a blood test request from my endocrinologist last January and was very disappointed he hadn’t requested T4 let alone T3. He’s only interested in TSH and my cholesterol. He also tells me to Jake my Levothyroxine just before a blood test
hi everyone I hope you don’t mind me asking for help again. I had a blood test request from my endocrinologist last January and was very disappointed he hadn’t requested T4 let alone T3. He’s only interested in TSH and my cholesterol. He also tells me to Jake my Levothyroxine just before a blood test
Boohooby
in
Thyroid UK
18 days ago
Sally Pacholok tonight 7pm UK time (Daylight Savings Time) in 90 minutes. Monday 9 Sept
I know it's been mentioned before but we have a very important speaker tonight. Meeting URL: https://us02web.zoom.us/j/84471004296?pwd=ZDlLV0JZdEZsNllCcjlMUnRVK1RtZz09 Meeting ID: 844 7100 4296 Passcode: 656898 Sally Pacholok doesn’t need an introduction – she’s one of the most courageous and longstanding
I know it's been mentioned before but we have a very important speaker tonight. Meeting URL: https://us02web.zoom.us/j/84471004296?pwd=ZDlLV0JZdEZsNllCcjlMUnRVK1RtZz09 Meeting ID: 844 7100 4296 Passcode: 656898 Sally Pacholok doesn’t need an introduction – she’s one of the most courageous and longstanding
HugoMinney
in
Pernicious Anaemia Society
18 days ago
Latest blood test - advice please
I would welcome thoughts from the community on my latest blood tests please? I had these taken in August results via Medichecks. I have Hashimotos and the bloods were taken first thing in the morning. Interestingly, my Thyroglobulin antibodies are slightly down from 362 in 2022 to 287 in 2024. Not sure
I would welcome thoughts from the community on my latest blood tests please? I had these taken in August results via Medichecks. I have Hashimotos and the bloods were taken first thing in the morning. Interestingly, my Thyroglobulin antibodies are slightly down from 362 in 2022 to 287 in 2024. Not sure
Mantras131
in
Thyroid UK
18 days ago
RLS and iron
HOW TO HAVE YOUR IRON STATUS CHECKED IRON INFORMATION FOR RLS PATIENTS As we know, low iron in the brain is one of the two major causes of Restless Leg Syndrome. (The other is a dopamine imbalance in the brain. In any event, RLS occurs in the brain - it is manifested in the limbs.) With regard
HOW TO HAVE YOUR IRON STATUS CHECKED IRON INFORMATION FOR RLS PATIENTS As we know, low iron in the brain is one of the two major causes of Restless Leg Syndrome. (The other is a dopamine imbalance in the brain. In any event, RLS occurs in the brain - it is manifested in the limbs.) With regard
fritzb43
in
Restless Legs Syndrome
18 days ago
Neurology appointment today!
I have a follow up appointment with the NHS neurologist today. Saw her over 18 months ago when I had some tingling nerve pain in my abdomen/hip/groin. (Follow up was supposed to be 12 months, but not surprised it’s longer). At the time she didn’t know what was causing it so referred me to Birmingham
I have a follow up appointment with the NHS neurologist today. Saw her over 18 months ago when I had some tingling nerve pain in my abdomen/hip/groin. (Follow up was supposed to be 12 months, but not surprised it’s longer). At the time she didn’t know what was causing it so referred me to Birmingham
Chickens44
in
Pernicious Anaemia Society
18 days ago
Update on neurology appointment
Has said he will get GP to up the tablets to 3 times
a
day (as I had had before) and add in
vitamin
C and then recheck bloods. It wasn’t appropriate to bring up Buprenorphine at this time but I will next time if things haven’t improved.
Has said he will get GP to up the tablets to 3 times
a
day (as I had had before) and add in
vitamin
C and then recheck bloods. It wasn’t appropriate to bring up Buprenorphine at this time but I will next time if things haven’t improved.
Islay9
in
Restless Legs Syndrome
18 days ago
Insights on 4 years of results?
Hello to everyone on here. Does anyone have any insights to share on my results, please? I'm due another blood test with my GP next week and I have asked for a full thyroid panel, but so far they haven't agreed to that. I asked last year too, but they were only willing to measure TSH. I have read on
Hello to everyone on here. Does anyone have any insights to share on my results, please? I'm due another blood test with my GP next week and I have asked for a full thyroid panel, but so far they haven't agreed to that. I asked last year too, but they were only willing to measure TSH. I have read on
FrancesD
in
Thyroid UK
19 days ago
Hypo crash after going too fast with T3, saliva cortisol readings
Hi, community. So I’ve been on a bit of a wild run over the past 2.5 months trying to get my thyroid therapy back in good shape. To give you a bit of the context, I am a 25 yo female, have been diagnosed with Hashimoto and subclinical hypothyroidism since 2018, started combo therapy (T4+T3) around
Hi, community. So I’ve been on a bit of a wild run over the past 2.5 months trying to get my thyroid therapy back in good shape. To give you a bit of the context, I am a 25 yo female, have been diagnosed with Hashimoto and subclinical hypothyroidism since 2018, started combo therapy (T4+T3) around
anakondratenko
in
Thyroid UK
19 days ago
Anaemia anyone?
I am wondering if anyone with PMR and/or GCA (both of which I've got/had) has also been diagnosed with anaemia. I notice that Pernicious Anaemia is another autoimmune condition. My GP called me in as my monthly blood tests had suggested I might have anaemia. He's running more tests but of course I'm
I am wondering if anyone with PMR and/or GCA (both of which I've got/had) has also been diagnosed with anaemia. I notice that Pernicious Anaemia is another autoimmune condition. My GP called me in as my monthly blood tests had suggested I might have anaemia. He's running more tests but of course I'm
DogAgilityObsessed
in
PMRGCAuk
19 days ago
Sore, swollen lips; lethargy and weakness
Hello all.... over the last year or so I have had worsening health. I have been managing ok for a good few years my hypothyrodism / hashimoto's / menopause via Thyroid-S x 2 grains / strictly gluten free for over 5 years / Oestrogel x4 pumps/day. Had reasonable energy levels, body composition, mood
Hello all.... over the last year or so I have had worsening health. I have been managing ok for a good few years my hypothyrodism / hashimoto's / menopause via Thyroid-S x 2 grains / strictly gluten free for over 5 years / Oestrogel x4 pumps/day. Had reasonable energy levels, body composition, mood
richar03
in
Thyroid UK
19 days ago
Problem absorbing T4/T3
Just wondering if anyone knows how you can tell if you are not absorbing thyroxine and liothyronine due to gut/stomach problems. Will your TSH and T4/T3 blood levels show you have enough hormone - i.e. will it still get into your blood but not other parts of your system. I currently have a diverticulosis
Just wondering if anyone knows how you can tell if you are not absorbing thyroxine and liothyronine due to gut/stomach problems. Will your TSH and T4/T3 blood levels show you have enough hormone - i.e. will it still get into your blood but not other parts of your system. I currently have a diverticulosis
JRosemaryW
in
Thyroid UK
19 days ago
Can Hashimotos change into hypothyroidism
I've been back on Amour thyroid and started to feel like the real me again, in early January this year. At the last check I had in March 2024, my T3 and free T3 were both on the higher end of normal; my T4 was good, but my TSH, as always, stayed around zero. My vitamins are good levels, too, and I'm
I've been back on Amour thyroid and started to feel like the real me again, in early January this year. At the last check I had in March 2024, my T3 and free T3 were both on the higher end of normal; my T4 was good, but my TSH, as always, stayed around zero. My vitamins are good levels, too, and I'm
Me1157
in
Thyroid UK
4 months ago
IBSA USA debuts three new dietary supplements - FilmTec B12.
Having produced Tirosint and Tirosint SOL levothyroxine (under their various names - brands and re-branded), IBSA appear to see supplements as a money-spinner. I'm just putting this here for information - hopefully at some point we will find out more. Like whether there is some basis for their absorption
Having produced Tirosint and Tirosint SOL levothyroxine (under their various names - brands and re-branded), IBSA appear to see supplements as a money-spinner. I'm just putting this here for information - hopefully at some point we will find out more. Like whether there is some basis for their absorption
helvella
in
Pernicious Anaemia Society
20 days ago
Supplement absorption
I posted the other day about being newly diagnosed and I received loads of brilliant support and advice from people on here about supplements and lifestyle changes that can help with PD progression. I haven’t yet managed to do all the recommended reading but I’m working on it. I’m still looking into
I posted the other day about being newly diagnosed and I received loads of brilliant support and advice from people on here about supplements and lifestyle changes that can help with PD progression. I haven’t yet managed to do all the recommended reading but I’m working on it. I’m still looking into
SallyBeeBobs
in
Cure Parkinson's
20 days ago
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