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iron and b12 test results
How am I doing with iron and b12? i posted before about my thyroid results and have reduced my Levo a tiny amount pending testing again in a few weeks time I now have the rest of my results (minus ferritin and folate ) from MMH. I can see that my iron and b12 are not dire but neither are they optimal
How am I doing with iron and b12? i posted before about my thyroid results and have reduced my Levo a tiny amount pending testing again in a few weeks time I now have the rest of my results (minus ferritin and folate ) from MMH. I can see that my iron and b12 are not dire but neither are they optimal
Bearo
in
Thyroid UK
3 months ago
Still having symptoms of hypothyroidism despite medication - any advice?
I wondered if anyone could please share their thoughts on my situation. I was diagnosed with subclinical hypothyroidism around 8 years ago, but didn’t have any symptoms (apart from some fatigue). Then, after contracting COVID in 2020, I began to have symptoms like 30-35lb weight gain (unexplained),
I wondered if anyone could please share their thoughts on my situation. I was diagnosed with subclinical hypothyroidism around 8 years ago, but didn’t have any symptoms (apart from some fatigue). Then, after contracting COVID in 2020, I began to have symptoms like 30-35lb weight gain (unexplained),
melissa-b
in
Thyroid UK
3 months ago
why i have so much anxiety in my stomach thats causing me nausea and missing heart pulse
i been to cardiologist today i have skiped heart beats 5 days now also tightness on chest brain fog am angry and depresed cant even talk to any doctor how i feel all say is not from levothyroxine tat is all in my head is no side effects... but all this heart missing beats started
i been to cardiologist today i have skiped heart beats 5 days now also tightness on chest brain fog am angry and depresed cant even talk to any doctor how i feel all say is not from levothyroxine tat is all in my head is no side effects... but all this heart missing beats started
morcan54
in
Thyroid UK
3 months ago
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Supplements Autism
Hi, Anyone tried supplements for high functioning autism symptoms? What was your experience? Omega-3 fatty acids Vitamin D Methyl-B12. Probiotics Etc.
Hi, Anyone tried supplements for high functioning autism symptoms? What was your experience? Omega-3 fatty acids Vitamin D Methyl-B12. Probiotics Etc.
anymusic
in
Autism Support
3 months ago
Gluten free diet
Hi all, hope you’re not suffering too much today. Just wanted to bring to your attention an article I was reading today about gluten, which you can find on google. https://en.m.wikipedia.org/wiki/Non-celiac_gluten_sensitivity I’ve recently been trialing a gluten free diet, which has helped me considerably
Hi all, hope you’re not suffering too much today. Just wanted to bring to your attention an article I was reading today about gluten, which you can find on google. https://en.m.wikipedia.org/wiki/Non-celiac_gluten_sensitivity I’ve recently been trialing a gluten free diet, which has helped me considerably
Kryptonite59
in
Fibromyalgia Action UK
3 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
dose increase?
Good morning I’m looking for a bit of advice about whether I should increase my Levothyroxine dose now, or wait a little while. I currently take 125/137.5 alternate days. I took a test after 6 weeks and have attached a picture of the results. I also had an iron panel done at the same time and, as per
Good morning I’m looking for a bit of advice about whether I should increase my Levothyroxine dose now, or wait a little while. I currently take 125/137.5 alternate days. I took a test after 6 weeks and have attached a picture of the results. I also had an iron panel done at the same time and, as per
BethBeezle
in
Thyroid UK
4 months ago
Taking Vitamin C
This might seem a daft question but I need to increase my iron & read I should take it with 100mg of VitC. How do I take 100mg of VitC? All the tablets are 1000mg. The average tangerine is 50mg & not what I’d choose to eat at night. Do I buy a VitC powder?
This might seem a daft question but I need to increase my iron & read I should take it with 100mg of VitC. How do I take 100mg of VitC? All the tablets are 1000mg. The average tangerine is 50mg & not what I’d choose to eat at night. Do I buy a VitC powder?
BoojaBooja
in
Restless Legs Syndrome
3 months ago
I've been thinking a lot about people's misdiagnoses........
We talk a lot about the vast number of people who have been misdiagnosed, who went on to self treat, and subsequently improved their health, and their quality of life. But what about those who have received a diagnosis, and accepted it?? My GP at the time of my B12 crash wanted to diagnose me with Fibromyalgia
We talk a lot about the vast number of people who have been misdiagnosed, who went on to self treat, and subsequently improved their health, and their quality of life. But what about those who have received a diagnosis, and accepted it?? My GP at the time of my B12 crash wanted to diagnose me with Fibromyalgia
BeachArt
in
Pernicious Anaemia Society
3 months ago
B supplement
Please could you advise me if it is OK to take Homocystix Plus as a B supplement? I have been taking Thorne Basic Plus and Nature's Best Vit B 12. However Vit B12 now over 500. I started flushing more and think I'm developing Rosacea . Looked online and found Niacin can be a factor in flushing. Also
Please could you advise me if it is OK to take Homocystix Plus as a B supplement? I have been taking Thorne Basic Plus and Nature's Best Vit B 12. However Vit B12 now over 500. I started flushing more and think I'm developing Rosacea . Looked online and found Niacin can be a factor in flushing. Also
Shellian
in
Thyroid UK
3 months ago
Thyroid scan advice and recommendations please
Good Afternoon everyone 😊 Thyroid UK recommends London Private Ultrasound Clinic. Please could anyone who has used them private message me with your experiences, good or bad, or anything I should be aware of beforehand? I'm thinking of having a scan with them as I will be in London for another reason
Good Afternoon everyone 😊 Thyroid UK recommends London Private Ultrasound Clinic. Please could anyone who has used them private message me with your experiences, good or bad, or anything I should be aware of beforehand? I'm thinking of having a scan with them as I will be in London for another reason
Bertiepuss
in
Thyroid UK
5 months ago
Multi vitamins
I take bisoprolol, apixaban for AF and a statin.Can I take a multivitamin daily tablet as well or are there any contransdictions? Thanks
I take bisoprolol, apixaban for AF and a statin.Can I take a multivitamin daily tablet as well or are there any contransdictions? Thanks
gateman
in
AF Association
5 months ago
Just diagnosed. Does this explain my life? Especially my recent experiences?
For as long as I can remember, I have been suffering with various levels of depression and anxiety, lack of energy, poor sleep habits and headaches.Yet both times I have come out of hospital with B12 shots, I have felt like a new man with a new brain, like nothing previous worried me as much anymore.
For as long as I can remember, I have been suffering with various levels of depression and anxiety, lack of energy, poor sleep habits and headaches.Yet both times I have come out of hospital with B12 shots, I have felt like a new man with a new brain, like nothing previous worried me as much anymore.
Valid94
in
Pernicious Anaemia Society
3 months ago
B12 supplements recommendations please.
Hi All! My B12 last year was : 641 - ranges: 197-771 ng/l I have recently been retested at it is now 579 - ranges: 197-771 ng/l - so has gone down a bit. Can anyone please recommend a good source of B12 supplements please? Thank you in advance.
Hi All! My B12 last year was : 641 - ranges: 197-771 ng/l I have recently been retested at it is now 579 - ranges: 197-771 ng/l - so has gone down a bit. Can anyone please recommend a good source of B12 supplements please? Thank you in advance.
Lavender-Blue
in
Thyroid UK
3 months ago
GGT level
Hi, I was told that in 2015 I had a fatty liver from having a scan for suspected gall stones. I wasn't told much more and no advice or follow up given. Last year I started getting pain and a kind of tight feeling on my right side just under my lowest rib. Gp did some blood tests and said nothing came
Hi, I was told that in 2015 I had a fatty liver from having a scan for suspected gall stones. I wasn't told much more and no advice or follow up given. Last year I started getting pain and a kind of tight feeling on my right side just under my lowest rib. Gp did some blood tests and said nothing came
Vavoomm
in
British Liver Trust
3 months ago
Better Understanding
I knew and expressed here that I was fearful of crashing this winter as I have since 1995 to varying degrees. I had set a marker of April 01 as a measure. I was successful although I will wait until April 01 to see it in my rear view mirror, and have a celebration although I am already celebrating. Some
I knew and expressed here that I was fearful of crashing this winter as I have since 1995 to varying degrees. I had set a marker of April 01 as a measure. I was successful although I will wait until April 01 to see it in my rear view mirror, and have a celebration although I am already celebrating. Some
WIZARD6787
in
Pernicious Anaemia Society
3 months ago
Tiny Levo increase but FT4 well over range
Just got results back from MMH. I’ll add historical results for comparison but they may be irrelevant as I am where I am! I take Levo only. Ranges were 3.1-6 for FT3 and 12-22 for all tests. 2021 on 100mcg TSH 0.01 FT4 24.9=129% (12-22) FT3 6.5=91.89% (3.1-6.8) Note: insomnia much improved
Just got results back from MMH. I’ll add historical results for comparison but they may be irrelevant as I am where I am! I take Levo only. Ranges were 3.1-6 for FT3 and 12-22 for all tests. 2021 on 100mcg TSH 0.01 FT4 24.9=129% (12-22) FT3 6.5=91.89% (3.1-6.8) Note: insomnia much improved
Bearo
in
Thyroid UK
4 months ago
advice, thoughts please, feeling rather desperate?!
hi I only got one response to my recent post which was so kind but no feedback so am trying again as I’m a bit stumped. I’d hoped going on NDT would relieve fibro symptoms and generally help me feel better, and give me more energy, but despite latest test results I don’t feel that much different. Certainly
hi I only got one response to my recent post which was so kind but no feedback so am trying again as I’m a bit stumped. I’d hoped going on NDT would relieve fibro symptoms and generally help me feel better, and give me more energy, but despite latest test results I don’t feel that much different. Certainly
Starseed56
in
Thyroid UK
3 months ago
B12 result after 6 months…
Hi, So initially in October I was diagnosed with what they suspect to be pernicious anaemia, I had a negative IF test but due to me having diabetes and no other factors which could indicate why I was so low in B12 they put it down to me having pernicious anaemia. I had 6 loading doses after which my
Hi, So initially in October I was diagnosed with what they suspect to be pernicious anaemia, I had a negative IF test but due to me having diabetes and no other factors which could indicate why I was so low in B12 they put it down to me having pernicious anaemia. I had 6 loading doses after which my
Nikkim236
in
Pernicious Anaemia Society
3 months ago
B12 injections
Hi,I've been diagnosed with PA since 2021. I was on loading doses, then 3 monthly. This didn't agree with me and I was exhausted so I was moved from 3 months to 6 weeks. I was still finding myself wiped after 4 weeks ish so was moved to 3 weeks. During my 3 weekly treatment I began getting facial tingling
Hi,I've been diagnosed with PA since 2021. I was on loading doses, then 3 monthly. This didn't agree with me and I was exhausted so I was moved from 3 months to 6 weeks. I was still finding myself wiped after 4 weeks ish so was moved to 3 weeks. During my 3 weekly treatment I began getting facial tingling
GranolaLover60
in
Pernicious Anaemia Society
3 months ago
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