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Bloods Results
These where printed out for me as requested, any advice most welcome 🌸 Was taking teva levo 75mcg, thybon henning t3 10mcg, prior to these results. Now taking 5mcg three times a day. Supplement vit D with k2, mk7 and magnesium glycinate
These where printed out for me as requested, any advice most welcome 🌸 Was taking teva levo 75mcg, thybon henning t3 10mcg, prior to these results. Now taking 5mcg three times a day. Supplement vit D with k2, mk7 and magnesium glycinate
Geegee777
in
Thyroid UK
2 years ago
B-12 is Low (398), Folate is High, HCY is 55.6, uMMA is 1.7 , vitamin D and C and Magnesium are Low, all B vitamins are low.
Why is the GP not taking my labs seriously, I've been taking methylcobalamin tablets for a year and just began 5-MTHF because of Folate Deficiency found in my DNA, GP declined to do a MMA Blood serum test, I have been allergic to milk and beef since birth, peanuts followed with life threatening allergies
Why is the GP not taking my labs seriously, I've been taking methylcobalamin tablets for a year and just began 5-MTHF because of Folate Deficiency found in my DNA, GP declined to do a MMA Blood serum test, I have been allergic to milk and beef since birth, peanuts followed with life threatening allergies
Hoyle
in
Pernicious Anaemia Society
2 years ago
Neuropathy and the Cold weather
If only there was a cure to reverse the damage caused by B12 deficiency which I'm sure was caused by Metformin tablets given to me for type 2 diabetes 🤔 I have looked into the side effects of this drug and on the Drug makers website it clearly states that this drug can cause Pernicious
Anaemia
If only there was a cure to reverse the damage caused by B12 deficiency which I'm sure was caused by Metformin tablets given to me for type 2 diabetes 🤔 I have looked into the side effects of this drug and on the Drug makers website it clearly states that this drug can cause Pernicious
Anaemia
dl56uk
in
Pernicious Anaemia Society
2 years ago
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nerve conduction test
We had a good open discussion on pernicious
anaemia
patients vs nerve results, and he said that my case is unusual as pernicious
anaemia
patients tend to have depressed nerve speed on symmetrical sides of the body.. mine shows one side.
We had a good open discussion on pernicious
anaemia
patients vs nerve results, and he said that my case is unusual as pernicious
anaemia
patients tend to have depressed nerve speed on symmetrical sides of the body.. mine shows one side.
PAapr22
in
Pernicious Anaemia Society
2 years ago
co-trimoxazole and anaemia/folate deficiency
I was wondering if anyone in the community has had any experience of taking Co-trimoxazole long term and
anaemia
/folate deficiency ?
I was wondering if anyone in the community has had any experience of taking Co-trimoxazole long term and
anaemia
/folate deficiency ?
fapumpkin
in
CLL Support
2 years ago
Advice on current symptoms
I have been taking 50mg and 75mg levothyroxin on alternate days and would say I haven’t felt particularly well for a long time - suffering hair loss,
anaemia
, fatigue and muscle stiffness as well as memory impairment. In the past couple of years digestive issues have become a significant issue.
I have been taking 50mg and 75mg levothyroxin on alternate days and would say I haven’t felt particularly well for a long time - suffering hair loss,
anaemia
, fatigue and muscle stiffness as well as memory impairment. In the past couple of years digestive issues have become a significant issue.
DaisyTed
in
Thyroid UK
2 years ago
Urine Calcium Test tips?
As my GP has me down as a hypochondriac malingerer I need some evidence to force testing of calcium properly. I can’t afford a £150 6 hour round trip London clinic test so some internet research led me to a £25 set of 10 dipsticks. I’m ready for the ‘waste of time’ responses and see an endo responses
As my GP has me down as a hypochondriac malingerer I need some evidence to force testing of calcium properly. I can’t afford a £150 6 hour round trip London clinic test so some internet research led me to a £25 set of 10 dipsticks. I’m ready for the ‘waste of time’ responses and see an endo responses
Regenallotment
in
Thyroid UK
2 years ago
Diagnosed with b12 deficiency not pernicious anemia so far.
Wondering if anyone suspects covid vaccine and b12 deficiency. I have tinnitus b12. speech impairment headaches last about 2 minutes also transulent zig zags over my eyes again lasts 2 minutes. Taking b12 injections monthly. Is this enough given my symptoms. Would like to hear if others have my symptoms
Wondering if anyone suspects covid vaccine and b12 deficiency. I have tinnitus b12. speech impairment headaches last about 2 minutes also transulent zig zags over my eyes again lasts 2 minutes. Taking b12 injections monthly. Is this enough given my symptoms. Would like to hear if others have my symptoms
Janeames
in
Pernicious Anaemia Society
2 years ago
B12 test
Hi I fear I've been deficient for many years, digestion issues for 20 years, always exhausted hair loss, teeth enamel worn away. stuttering dizziness memory loss confusing words and palpitations (got worse)started about 3 years ago. October 2022 my health took a nose dive, dementia like symptoms, extreme
Hi I fear I've been deficient for many years, digestion issues for 20 years, always exhausted hair loss, teeth enamel worn away. stuttering dizziness memory loss confusing words and palpitations (got worse)started about 3 years ago. October 2022 my health took a nose dive, dementia like symptoms, extreme
Hidden
in
Pernicious Anaemia Society
2 years ago
Latest appointment update…..ET investigation
I must admit I always thought you had to be actually Anaemic to affect your platelets but apparently in some cases Iron deficiency without
anaemia
alone can do this….
I must admit I always thought you had to be actually Anaemic to affect your platelets but apparently in some cases Iron deficiency without
anaemia
alone can do this….
Purdy13
in
MPN Voice
1 year ago
Which iron supplement is the best and what dose?
Hi there, having found this forum two weeks ago, am fascinated by everything I am finding out about this damn RLS! But had a blood test this morning and my ferritin levels are 48ug/L, serum iron is 14.1 and serum TIBC 53.7 and the transferring sat index 26% When I talked to my doctor last week, having
Hi there, having found this forum two weeks ago, am fascinated by everything I am finding out about this damn RLS! But had a blood test this morning and my ferritin levels are 48ug/L, serum iron is 14.1 and serum TIBC 53.7 and the transferring sat index 26% When I talked to my doctor last week, having
Jukebox55
in
Restless Legs Syndrome
2 years ago
anaemia
My consultant today told me I’m very anaemic and was surprised my gp hasn’t put me on medicine for it. I have methotrexate tablets during the week and because of that I have to take folic acid- iron tablets. So I don’t know really know what exactly the consultant it’s going to do writing to my gp. I
My consultant today told me I’m very anaemic and was surprised my gp hasn’t put me on medicine for it. I have methotrexate tablets during the week and because of that I have to take folic acid- iron tablets. So I don’t know really know what exactly the consultant it’s going to do writing to my gp. I
Junny123
in
Pain Concern
2 years ago
Deep Brain Stimulation
Study from China on Parkinson's patients with RLS showed Deep Brain Stimulation reduced RLS & helped sleep.I certainly wouldn't consider it. Seems too extreme but if the Parkinson's patients are having the treatment to help tremor, it would be sensible to see if stimulation in another area relieves RLS
Study from China on Parkinson's patients with RLS showed Deep Brain Stimulation reduced RLS & helped sleep.I certainly wouldn't consider it. Seems too extreme but if the Parkinson's patients are having the treatment to help tremor, it would be sensible to see if stimulation in another area relieves RLS
Joolsg
in
Restless Legs Syndrome
2 years ago
Hyperparathyroidism
Hi there! I have been diagnosed as having possible primary hyperparathyroidism. I am a shocked that there is not a group for this disease. Can anyone help with this? So many people think I have something wrong with my thyroid when I say I have it, when in fact it is to do with the parathyroid glands
Hi there! I have been diagnosed as having possible primary hyperparathyroidism. I am a shocked that there is not a group for this disease. Can anyone help with this? So many people think I have something wrong with my thyroid when I say I have it, when in fact it is to do with the parathyroid glands
love25032607
in
Thyroid UK
2 years ago
This might be of interest for anyone who struggles to raise their iron levels or is frequently anaemic or nearly anaemic
Further research is needed to understand the roles of individual and combined vitamin deficiencies on
anaemia
to design appropriate micronutrient interventions to prevent
anaemia
.[/i]
Further research is needed to understand the roles of individual and combined vitamin deficiencies on
anaemia
to design appropriate micronutrient interventions to prevent
anaemia
.[/i]
humanbean
in
Thyroid UK
2 years ago
can you have normal iron cells and not megablastic and still have pernicious anemia ?
I am curious to know if megablastic anemia whereby the bloodcells are larger in shape has to be present in PA patient. And my second question would be, wouldn’t one know at birth of the shape of their bloodcells were bigger than usual of different enough to suspect PA? Excuse my ignorance but I’m trying
I am curious to know if megablastic anemia whereby the bloodcells are larger in shape has to be present in PA patient. And my second question would be, wouldn’t one know at birth of the shape of their bloodcells were bigger than usual of different enough to suspect PA? Excuse my ignorance but I’m trying
Reembow
in
Pernicious Anaemia Society
2 years ago
Hello and thank you for having me!
Other things I think may be relevant: - I was diagnosed with mild asthma a few years ago - I was diagnosed with iron-deficiency
anaemia
(low ferritin) late in 2021 and now take daily iron to keep it to an acceptable level (I am veggie and was donating blood, have stopped that now, but do eat a very
Other things I think may be relevant: - I was diagnosed with mild asthma a few years ago - I was diagnosed with iron-deficiency
anaemia
(low ferritin) late in 2021 and now take daily iron to keep it to an acceptable level (I am veggie and was donating blood, have stopped that now, but do eat a very
Hollyinthewild
in
LUPUS UK
1 year ago
Slow progress getting ferritin up... any advice?
Previously: https://healthunlocked.com/rlsuk/posts/148663707/rls-differential-diagnosis Have taken iron for the last three months - 75mg iron (as bisglycinate) every evening with 500mg Vitamin C. Ferritin levels have gone from 25 to 57 to 81µg/L, so they're definitely getting there slowly. I believe
Previously: https://healthunlocked.com/rlsuk/posts/148663707/rls-differential-diagnosis Have taken iron for the last three months - 75mg iron (as bisglycinate) every evening with 500mg Vitamin C. Ferritin levels have gone from 25 to 57 to 81µg/L, so they're definitely getting there slowly. I believe
howbeit-abroad
in
Restless Legs Syndrome
2 years ago
shingles
on Saturday night I felt dreadful like I did when the doctor refused to give me my B12 for my pernicious
anaemia
but the strange think was my blood pressure kept going up to over 200/90. I was really scared and rang 111 and of course I got someone who hadn’t a clue about B12 deficiency.
on Saturday night I felt dreadful like I did when the doctor refused to give me my B12 for my pernicious
anaemia
but the strange think was my blood pressure kept going up to over 200/90. I was really scared and rang 111 and of course I got someone who hadn’t a clue about B12 deficiency.
Hedgehogs15
in
Pernicious Anaemia Society
2 years ago
Possible Uveitis
My main problems are fatigue and brain fog, joint pain, generalised aches and pains, raynauds, mouth ulcers, and recurring
anaemia
. I have always had dry eyes. About a week ago I suddenly noticed a large floater in one of my eyes. I also noticed flashing.
My main problems are fatigue and brain fog, joint pain, generalised aches and pains, raynauds, mouth ulcers, and recurring
anaemia
. I have always had dry eyes. About a week ago I suddenly noticed a large floater in one of my eyes. I also noticed flashing.
Ophelia1
in
LUPUS UK
2 years ago
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