Search
Search
About
Log in
Join
Experiences with
Sickle-cell anaemia
Posts
Communities
8,357 public posts
Filter results
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
You are what you breath - but what you breath varies...
[i]MY reason for writing this is one or two people liked my answers about the strange world of breathing. I am not a clinician, nor a scientist so beware taking me literally. However some things are self-evident dear Watson. [/i] We breath in a mixture of oxygen (20%) , nitrogen (79%) and a tiny amount
[i]MY reason for writing this is one or two people liked my answers about the strange world of breathing. I am not a clinician, nor a scientist so beware taking me literally. However some things are self-evident dear Watson. [/i] We breath in a mixture of oxygen (20%) , nitrogen (79%) and a tiny amount
Timberman
in
Lung Conditions Community Forum
1 year ago
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
1 year ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
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
Could ET mask a diagnosis of Vitamin B12 deficiency/Pernicious anaemia?
I have an ET JAK2 mutation diagnosis (on aspirin) and have some neurological type symptoms that are similar to those associated with a Vit B12 deficiency. Athough I'm now taking a B12 supplement, I was wanting to see if I could get a B12 injection in case my issue related to an inability to absorb B12
I have an ET JAK2 mutation diagnosis (on aspirin) and have some neurological type symptoms that are similar to those associated with a Vit B12 deficiency. Athough I'm now taking a B12 supplement, I was wanting to see if I could get a B12 injection in case my issue related to an inability to absorb B12
Cb1001
in
MPN Voice
2 years ago
Miraculous Story of a person who underwent stem cell transplant in 1999
I have taken this portion of the the report from the article elaborating the results of double blind trial in 1999. "Patient 133 (video segments 17–19) developed parkinsonism at age 42 in 1986. His major problems were wearing-off episodes as well as levodopa-induced dyskinesias, particularly of the
I have taken this portion of the the report from the article elaborating the results of double blind trial in 1999. "Patient 133 (video segments 17–19) developed parkinsonism at age 42 in 1986. His major problems were wearing-off episodes as well as levodopa-induced dyskinesias, particularly of the
Farooqji
in
Cure Parkinson's
1 year 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
parietal cell antibody lab results
I’m having trouble interpreting my lab results. My Parietal Cell Antibody IgG value is 33.2 units and it said the standard range is 0.0-24.9 units. So it’s above the standard range but not by much. Apparently above 25 units is positive so that means I’m positive? I just want to confirm.
I’m having trouble interpreting my lab results. My Parietal Cell Antibody IgG value is 33.2 units and it said the standard range is 0.0-24.9 units. So it’s above the standard range but not by much. Apparently above 25 units is positive so that means I’m positive? I just want to confirm.
Purplegirl2
in
Pernicious Anaemia Society
1 year ago
Mexican sarsaparilla ( Smilax aristolochiifolia) for anaemia, CLL
Has anyone heard about this herb for anemia or blood cancer
Has anyone heard about this herb for anemia or blood cancer
Family2017
in
CLL Support
2 years ago
High Neutrophils
I was diagnosed with PA 3 years ago. It runs in my family. I took loading does of methylcobalamin then went to once a month. No doctor ever told me to take folate or adenosyl. I recently learned that folate is a vital co-factor. Started 5 mg folate daily, loading doses of cyanocobalamin daily
I was diagnosed with PA 3 years ago. It runs in my family. I took loading does of methylcobalamin then went to once a month. No doctor ever told me to take folate or adenosyl. I recently learned that folate is a vital co-factor. Started 5 mg folate daily, loading doses of cyanocobalamin daily
Auburn9144
in
Pernicious Anaemia Society
2 years ago
Do natural supplements work to reduce high cholesterol?
While strictly not a PMR issue I know there are a few whose cholesterol has risen markedly since being diagnosed. I am one of them. I have always had high-ish cholesterol but my last fasting blood test showed everything else perfectly normal but my cholesterol was up. I haven't seen the results
While strictly not a PMR issue I know there are a few whose cholesterol has risen markedly since being diagnosed. I am one of them. I have always had high-ish cholesterol but my last fasting blood test showed everything else perfectly normal but my cholesterol was up. I haven't seen the results
Pr0jection
in
PMRGCAuk
1 year ago
Feeling worse after B12 Injections
Hi all, I am a 21 y/o male who eats meat and was diagnosed with a B12 deficiency (not PA) about 2 months ago. I went into the walk-in about 3 months ago with heart palpitations, fatigue, severe anxiety, inability to focus, and some vision issues. I was diagnosed with generalized anxiety disorder and
Hi all, I am a 21 y/o male who eats meat and was diagnosed with a B12 deficiency (not PA) about 2 months ago. I went into the walk-in about 3 months ago with heart palpitations, fatigue, severe anxiety, inability to focus, and some vision issues. I was diagnosed with generalized anxiety disorder and
juanpablo111
in
Pernicious Anaemia Society
2 years ago
A giant cell arteritis suffer
A giant cell arteritis suffer on methotrexate and prednisolone. Has anyone been on this combination as well? How long did it take you to get off the steroids as i'm still on 4mg as struggling to get off them as symptoms keep returning once I reduce down any further.
A giant cell arteritis suffer on methotrexate and prednisolone. Has anyone been on this combination as well? How long did it take you to get off the steroids as i'm still on 4mg as struggling to get off them as symptoms keep returning once I reduce down any further.
BM16
in
PMRGCAuk
1 year ago
Am Iwell?
I have my bi-monthly consultant review next week, which always starts with the question, well how are you? My usual reaction, is that perhaps you should tell me! I have just got the results (After 1 hour) of my latest blood test but I'm not sure which questions to ask. I started treatment with 6xRituximab
I have my bi-monthly consultant review next week, which always starts with the question, well how are you? My usual reaction, is that perhaps you should tell me! I have just got the results (After 1 hour) of my latest blood test but I'm not sure which questions to ask. I started treatment with 6xRituximab
Dawson21
in
CLL Support
2 years ago
help please, migraine meds
does anyone know if migraleve is contra-indicated with T3? I know I'm OK with T4 but: paracetamol, codeine phosphate & buclizine hydrochloride, anyone? @helvella ? sorry to tag just can't find info
does anyone know if migraleve is contra-indicated with T3? I know I'm OK with T4 but: paracetamol, codeine phosphate & buclizine hydrochloride, anyone? @helvella ? sorry to tag just can't find info
turquoisea7
in
Thyroid UK
1 year ago
Levo doses and side effects
Hi everyone, I've had hypothyroidism (Hashimotos) for several years now and never felt 'well' that whole time, but at times have been able to cope and others (like now) absolutely can't. It seems to be constant and I wanted some advice/thoughts from what seems to be a very knowledgeable group who can
Hi everyone, I've had hypothyroidism (Hashimotos) for several years now and never felt 'well' that whole time, but at times have been able to cope and others (like now) absolutely can't. It seems to be constant and I wanted some advice/thoughts from what seems to be a very knowledgeable group who can
Stevensnj87
in
Thyroid UK
1 year ago
Allogenic Stem Cell Transplant
I [i]received a Stem cell transplant six months ago. My decision was based on the availability of a suitable donor and being able to get to remission through aggressive chemotherapy. Other treatments had no effect on my rapidly growing leukemia. As of today I’m still in remission, showing 97% chimerism
I [i]received a Stem cell transplant six months ago. My decision was based on the availability of a suitable donor and being able to get to remission through aggressive chemotherapy. Other treatments had no effect on my rapidly growing leukemia. As of today I’m still in remission, showing 97% chimerism
GarciaB
in
MPN Voice
1 year ago
Bone marrow transplant
Hi, I am being offered a bone marrow transplant and wonder if anyone can offer me positive advice. Obviously the process is quite scary, but would like to think I'm doing the right thing. Thank you George
Hi, I am being offered a bone marrow transplant and wonder if anyone can offer me positive advice. Obviously the process is quite scary, but would like to think I'm doing the right thing. Thank you George
Georgehb
in
MPN Voice
1 year ago
Questions & Advice for a newbie please!
Hi all, I've been investigating possible causes of long-term fatigue. My symptoms & PA risk factors are listed below. I'm currently waiting on results for the Intrinsic factor antibodies test (bloods taken over 2 weeks ago through GP). On advice of a nutritionist I've been taking an oral B complex,
Hi all, I've been investigating possible causes of long-term fatigue. My symptoms & PA risk factors are listed below. I'm currently waiting on results for the Intrinsic factor antibodies test (bloods taken over 2 weeks ago through GP). On advice of a nutritionist I've been taking an oral B complex,
Spiralizer
in
Pernicious Anaemia Society
2 years ago
Folate deficiency
Please can you give me some advice as to what supplement should be take for a folate deficiency. Is it folic acid tablets or folate tablets? I am somewhat confused. Also what is the optimal folate level for a person with Hashimotos? Thanks in advance
Please can you give me some advice as to what supplement should be take for a folate deficiency. Is it folic acid tablets or folate tablets? I am somewhat confused. Also what is the optimal folate level for a person with Hashimotos? Thanks in advance
Pinkisland
in
Thyroid UK
2 years ago
1
...
61
62
63
...
100
Next page
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Pernicious Anaemia Society
3540 results
Thyroid UK
2438 results
MPN Voice
363 results
View top 10 communities
Sort by
Most Relevant
Newest