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How quickly would B12 Levels drop post injection?
Hello, I had 6 loading doses of B12 in September following a B12 level of <145 (test doesn’t specify below that cut off) I had some symptoms including muscle aches particularly my legs above my knees, anxiety, panic attacks, fatigue, dizziness and pins and needles on my left hand. No evidence of anaemia
Hello, I had 6 loading doses of B12 in September following a B12 level of <145 (test doesn’t specify below that cut off) I had some symptoms including muscle aches particularly my legs above my knees, anxiety, panic attacks, fatigue, dizziness and pins and needles on my left hand. No evidence of anaemia
Sparkleros
in
Pernicious Anaemia Society
4 months ago
Hello everyone 😊
Hello, I hope no one minds me expressing my fears. What it is I struggle like many to get the same brand of liothyronine or just get any thats available on the nhs at times and wait time at times has been months. Its stressful just going to the chemist and I'm made to feel that I'm difficult
Hello, I hope no one minds me expressing my fears. What it is I struggle like many to get the same brand of liothyronine or just get any thats available on the nhs at times and wait time at times has been months. Its stressful just going to the chemist and I'm made to feel that I'm difficult
Elizajoe102
in
Thyroid UK
4 months ago
still confused about my iron results
I’ve now redone my iron panel with medichecks and have similar results to last time. I can’t work out why my ferritin continues to drop. And what I can do about it as I know I need higher ferritin levels for optimum thyroid hormone function. …………………………… Ferritin……….Iron……….. Trans. Sat………..TIBC……….
I’ve now redone my iron panel with medichecks and have similar results to last time. I can’t work out why my ferritin continues to drop. And what I can do about it as I know I need higher ferritin levels for optimum thyroid hormone function. …………………………… Ferritin……….Iron……….. Trans. Sat………..TIBC……….
Mazes
in
Thyroid UK
2 months ago
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Sunlight relief
For the last 4 days I have had no PMR pain or stiffness. Why? I am on St Kitts, where there is abundant sunshine. I'm probably making tons of vitamin D. Although since my PMR commenced in Dec 2022 I have taken a vitamin D pill daily, I can't trace any relief to that. As for "perfect" days, I've had
For the last 4 days I have had no PMR pain or stiffness. Why? I am on St Kitts, where there is abundant sunshine. I'm probably making tons of vitamin D. Although since my PMR commenced in Dec 2022 I have taken a vitamin D pill daily, I can't trace any relief to that. As for "perfect" days, I've had
papadapadoo
in
PMRGCAuk
4 months ago
Marie
My doctors have just done B12 and folic acid blood tests, I was diagnosed in 2002 with pernicious anaemia. I have just been told that both results are high and that a doctor may want to speak to me. There is rumours that the surgery are trying to cut back on prescription and I am worried they will stop
My doctors have just done B12 and folic acid blood tests, I was diagnosed in 2002 with pernicious anaemia. I have just been told that both results are high and that a doctor may want to speak to me. There is rumours that the surgery are trying to cut back on prescription and I am worried they will stop
Royalblue1
in
Pernicious Anaemia Society
4 months ago
advice on blood results please
Hi Thanks for reading my post I hope you can help me . I am 57 year old woman diagnosed with Hashimos November 2022. At the time I had hyper symptoms HR 120 at rest exhausted weak muscles aching and feeling hot . Doctor insisted it was the menopause , I had already been on HRT for 4 years and had been
Hi Thanks for reading my post I hope you can help me . I am 57 year old woman diagnosed with Hashimos November 2022. At the time I had hyper symptoms HR 120 at rest exhausted weak muscles aching and feeling hot . Doctor insisted it was the menopause , I had already been on HRT for 4 years and had been
Poppygriff691
in
Thyroid UK
4 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
4 months ago
New Year New Bloods! It's time to titrate! Please help!
I made it to 8 weeks. This feels like a long post - I have both Thyroid and Iron issues to work out... I tried to make it shorter, but did not succeed, so here is a 5 bullet summary first.
TL;DR: Got results I didn't quite expect:
- I only changed a wee bit... + 12.5 on the levo
Changed
I made it to 8 weeks. This feels like a long post - I have both Thyroid and Iron issues to work out... I tried to make it shorter, but did not succeed, so here is a 5 bullet summary first.
TL;DR: Got results I didn't quite expect:
- I only changed a wee bit... + 12.5 on the levo
Changed
FallingInReverse
in
Thyroid UK
4 months ago
Is 3 times enough? And inherit.
I've been si M,W & F for couple months now and beginning to think it's not enough. Not sure if this happens to anyone else, but I get very tired, and weak until I eat something. It's a night and day difference after I eat, then a few hours later that all repeats. Do you all think I may need to increase
I've been si M,W & F for couple months now and beginning to think it's not enough. Not sure if this happens to anyone else, but I get very tired, and weak until I eat something. It's a night and day difference after I eat, then a few hours later that all repeats. Do you all think I may need to increase
MrJustatip
in
Pernicious Anaemia Society
4 months ago
How to nurture bone health
Hello Community, Our bones are the structural architecture that connect us to the earth element. This mineralised matrix of collagen and calcium phosphate - magnesium an important bone nutrient too, helping to keep calcium in our bones. Osteocytes, osteoblasts and osteoclasts are bone cells. The activity
Hello Community, Our bones are the structural architecture that connect us to the earth element. This mineralised matrix of collagen and calcium phosphate - magnesium an important bone nutrient too, helping to keep calcium in our bones. Osteocytes, osteoblasts and osteoclasts are bone cells. The activity
WhollyAligned
Administrator
in
Nutrition and Yoga for Health
4 months ago
Test results - please advise
Hi everyone, Can I please ask your thoughts on my last test results? TSH: 2.77 mU/l (Range 0.35 - 5.5) 46.99% FT4: 9 pmol/l (Range 9 - 23) 0.00% FT3: 4.7 pmol/l (Range 3.5 - 6.5) 40.00% Vitamin D is still at 87 nmol/L (50nmol/L - sufficiency) , while on
Hi everyone, Can I please ask your thoughts on my last test results? TSH: 2.77 mU/l (Range 0.35 - 5.5) 46.99% FT4: 9 pmol/l (Range 9 - 23) 0.00% FT3: 4.7 pmol/l (Range 3.5 - 6.5) 40.00% Vitamin D is still at 87 nmol/L (50nmol/L - sufficiency) , while on
Dandelions
in
Thyroid UK
4 months ago
Help with b12 deficiency
I have neurofibromatosis 1 and now I have low b12 my nerves help just wondering if there is something can help
I have neurofibromatosis 1 and now I have low b12 my nerves help just wondering if there is something can help
Vegan10
in
Changing Faces
4 months ago
interpreting results
Hi everyone, I’ve recently ordered a blood test to check my TSH, T4 and T3 levels. I’m also having my antibodies, ferritin, vit D, B12 and folate checked aswell. I’m fine interpreting the results of the vitamins and minerals, and I also understand that the higher the TSH the more underactive you are
Hi everyone, I’ve recently ordered a blood test to check my TSH, T4 and T3 levels. I’m also having my antibodies, ferritin, vit D, B12 and folate checked aswell. I’m fine interpreting the results of the vitamins and minerals, and I also understand that the higher the TSH the more underactive you are
MarvelDC
in
Thyroid UK
4 months ago
Iron Levels
79yo male with classic tale of RLS. Started at 17yo. Progressing over the years. Augmentation last Christmas on Pramipexole and a hell of a time transitioning to gabapentin. Unfortunately though I could not stop the attacks even on high doses and taking it as advised by Sue Johnson. Helpful doc allowed
79yo male with classic tale of RLS. Started at 17yo. Progressing over the years. Augmentation last Christmas on Pramipexole and a hell of a time transitioning to gabapentin. Unfortunately though I could not stop the attacks even on high doses and taking it as advised by Sue Johnson. Helpful doc allowed
JOBAN1uk
in
Restless Legs Syndrome
4 months ago
thyroid?cortisol?
hello everyone , I’m writing from France, where information about thyroid/adrenals correlation are quite inexistants , as well as doctors aware of. One year ago I’ve been diagnostics of secondary hypothyroidism (TSH 0,6 FT4 7,9 range 9,2-17) FT3 2,5 range 2-4,4). At the ecography my gland is small
hello everyone , I’m writing from France, where information about thyroid/adrenals correlation are quite inexistants , as well as doctors aware of. One year ago I’ve been diagnostics of secondary hypothyroidism (TSH 0,6 FT4 7,9 range 9,2-17) FT3 2,5 range 2-4,4). At the ecography my gland is small
Ir18
in
Thyroid UK
4 months ago
Hello and happy new year everyone!! Aching legs when I walk more then 50 yards (in a nutshell)!!
Hello All, It's been ages since I wrote a post. I have been relatively OK for a while and then went down hill middle of December with my annual COPD freakout chest infection - heavy duty antibiotics sorted that out but of course, as I have discovered, "old age don't come alone". I am 70 now and although
Hello All, It's been ages since I wrote a post. I have been relatively OK for a while and then went down hill middle of December with my annual COPD freakout chest infection - heavy duty antibiotics sorted that out but of course, as I have discovered, "old age don't come alone". I am 70 now and although
sheenah
in
Thyroid UK
4 months ago
newly diagnosed anemia
Hi. I’m new to HealthUnlocked and to this group. I’m also in America, so I hope it’s OK that I post here. I’ll try to put in all the info I have and follow proper posting guidelines. It’s taken me a while to be able to get this post all typed up due to tiredness and brain fog. I just had 3 month follow-up
Hi. I’m new to HealthUnlocked and to this group. I’m also in America, so I hope it’s OK that I post here. I’ll try to put in all the info I have and follow proper posting guidelines. It’s taken me a while to be able to get this post all typed up due to tiredness and brain fog. I just had 3 month follow-up
SugarMint
in
Thyroid UK
8 days ago
CT scan instead of gastroscopy / colonoscopy with all PA tests normal
My Active B12 was just about into the sufficient range. My H Pylorii was negative, as was anti IFAB and coeliac. Homocysteine was fine too. My neurologist’s physical exam was normal ( though the sharp stimulus was a little less sharp on the feet. ) I have been taking sublingual B12 and the tingling
My Active B12 was just about into the sufficient range. My H Pylorii was negative, as was anti IFAB and coeliac. Homocysteine was fine too. My neurologist’s physical exam was normal ( though the sharp stimulus was a little less sharp on the feet. ) I have been taking sublingual B12 and the tingling
Applethorpe
in
Pernicious Anaemia Society
4 months ago
Tablets v Injections
Hi, After a few years of monitoring my B12 levels are now low enough for my GP to offer treatment. I was expecting injections but have been prescribed tablets. Is anyone else on these ? I assumed from what I had read that injections were the primary option. Thanks
Hi, After a few years of monitoring my B12 levels are now low enough for my GP to offer treatment. I was expecting injections but have been prescribed tablets. Is anyone else on these ? I assumed from what I had read that injections were the primary option. Thanks
Redmusic
in
Pernicious Anaemia Society
4 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
5 months ago
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