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Haemolytic anaemia
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Above range MCV and MCH
Hi I always get results saying my MCV and MCH are both above range. I’ve read it can be due to hypothyroid Anyone know if ft3 plays a part in this ?
Hi I always get results saying my MCV and MCH are both above range. I’ve read it can be due to hypothyroid Anyone know if ft3 plays a part in this ?
130396
in
Thyroid UK
3 years ago
Diagnosis of results?
Hi, could someone in the know translate for me. I haven't seen Haematologist for some time, like most and have had letter today with blood results from tele consultation end July. Haemoglobin of 155 g/L with a satisfactory PCV of 0.448. White count of 5.61 x 10 power of 9 /L with a normal differential
Hi, could someone in the know translate for me. I haven't seen Haematologist for some time, like most and have had letter today with blood results from tele consultation end July. Haemoglobin of 155 g/L with a satisfactory PCV of 0.448. White count of 5.61 x 10 power of 9 /L with a normal differential
Jennytheb
in
MPN Voice
3 years ago
COVID /copd
Hey guys hope Everyone is ok , my 20 year old sons tested positive for COVID yesterday on a lft so just waiting for the pcr results now , so I’m confused and to say I’m scared aswell , his fit and healthy luckily has his own room and toilet so he hasn’t left his room but me with my lung issues I’m scared
Hey guys hope Everyone is ok , my 20 year old sons tested positive for COVID yesterday on a lft so just waiting for the pcr results now , so I’m confused and to say I’m scared aswell , his fit and healthy luckily has his own room and toilet so he hasn’t left his room but me with my lung issues I’m scared
Hometeam2016
in
Lung Conditions Community Forum
3 years ago
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NICE CKS - suspected B12 and folate deficiency -investigations
NICE CKS link about investigations doctors should order for those with suspected B12 or Folate deficiency https://cks.nice.org.uk/topics/anaemia-b12-folate-deficiency/diagnosis/investigations/ NICE CKS link about how to interpret investigation results https://cks.nice.org.uk/topics/anaemia-b12-folate-deficiency
NICE CKS link about investigations doctors should order for those with suspected B12 or Folate deficiency https://cks.nice.org.uk/topics/anaemia-b12-folate-deficiency/diagnosis/investigations/ NICE CKS link about how to interpret investigation results https://cks.nice.org.uk/topics/anaemia-b12-folate-deficiency
Sleepybunny
in
Pernicious Anaemia Society
3 years ago
Pernicious anaemia
Good morning from the UK. After being without my B12 injections for 5 years due to a young doctor saying they weren’t need any longer and feeling so poorly thankfully I found this post and I was so grateful to so many of you rallying to help me. I’m asking for advice again please, I have now had 2 injections
Good morning from the UK. After being without my B12 injections for 5 years due to a young doctor saying they weren’t need any longer and feeling so poorly thankfully I found this post and I was so grateful to so many of you rallying to help me. I’m asking for advice again please, I have now had 2 injections
Hedgehogs15
in
Pernicious Anaemia Society
3 years ago
Iron Infusions - the type of iron used may matter.
Here is a rather long and confusing article. Read it if you need to be lulled to sleep. https://journals.physiology.org/doi/full/10.1152/japplphysiol.91076.2008 In it I found a ridiculously interesting paragraph as follows: "Deficits in regional brain iron and changes in uptake and efflux of brain
Here is a rather long and confusing article. Read it if you need to be lulled to sleep. https://journals.physiology.org/doi/full/10.1152/japplphysiol.91076.2008 In it I found a ridiculously interesting paragraph as follows: "Deficits in regional brain iron and changes in uptake and efflux of brain
Hidden
in
Restless Legs Syndrome
3 years ago
Intrinsic factor and parietal cell antibody positive but MMA normal is it PA?
I have intrinsic factor abs and anti parietal cells but methylmalonic acid level is normal. B12,folate, hb are all in range.I have Hashis and a range of B12 deficiency systems Could anyone please advise if there is ever a situation when a GP would not prescribe B12 given the ap and IFabs? I am beginning
I have intrinsic factor abs and anti parietal cells but methylmalonic acid level is normal. B12,folate, hb are all in range.I have Hashis and a range of B12 deficiency systems Could anyone please advise if there is ever a situation when a GP would not prescribe B12 given the ap and IFabs? I am beginning
Aumshantii
in
Pernicious Anaemia Society
3 years ago
Advice please
Hi, I was advised by someone over on the thyroid community to post my Vitamin b12 blood test results here for advice. I had a rest with Thriva while testing my thyroid and based on those results my GP tested me again on the NHS. He now tells me my levels are normal, but the input from the thyroid community
Hi, I was advised by someone over on the thyroid community to post my Vitamin b12 blood test results here for advice. I had a rest with Thriva while testing my thyroid and based on those results my GP tested me again on the NHS. He now tells me my levels are normal, but the input from the thyroid community
Allyfin1
in
Pernicious Anaemia Society
3 years ago
I am improving I hope
Hi, I don't have P.A. but neurological symptoms. It started as itching in upper feet alone for almost an year. I mistook it as dey skin. Then a slight tingling ( once or twice) around may end of 2021. Immediately I checked my B12 . Yes it was 166. Luckily I am not anaemic. But slight lower end, at the
Hi, I don't have P.A. but neurological symptoms. It started as itching in upper feet alone for almost an year. I mistook it as dey skin. Then a slight tingling ( once or twice) around may end of 2021. Immediately I checked my B12 . Yes it was 166. Luckily I am not anaemic. But slight lower end, at the
Gettingbette
in
Pernicious Anaemia Society
3 years ago
Methylcobalamin injections?
Hi, I am a B12 deficienct newbie and was reading that the methylcobalamin has some advantages over cyanocobalamin. Do you know if this can be purchased in injectable form anywhere please. I have not been able to find anywhere as yet. My GP has just diagnosed chronic fatigue syndrome after an initial
Hi, I am a B12 deficienct newbie and was reading that the methylcobalamin has some advantages over cyanocobalamin. Do you know if this can be purchased in injectable form anywhere please. I have not been able to find anywhere as yet. My GP has just diagnosed chronic fatigue syndrome after an initial
AngelaWoo
in
Pernicious Anaemia Society
3 years ago
Shall I try injections?
After the advice I received 11 months ago on this forum I decided to try supplements (igennus super b) rather than MMA test which is expensive. After a few months I started to feel a bit better and could do more physically. Up to a couple of weeks ago I felt quite normal although still couldn’t do
After the advice I received 11 months ago on this forum I decided to try supplements (igennus super b) rather than MMA test which is expensive. After a few months I started to feel a bit better and could do more physically. Up to a couple of weeks ago I felt quite normal although still couldn’t do
Sa-ja-ca
in
Pernicious Anaemia Society
3 years ago
Test for intrinsic factor antibodies - when to do?
Quick questions, I hope! My doctor has agreed to this test but said we should wait until after 4 weeks after a third monthly injection of b12. I don't really see the point in waiting, because if it confirms a Pernicious Anemia diagnosis, that would hopefully mean I could start on more frequent loading
Quick questions, I hope! My doctor has agreed to this test but said we should wait until after 4 weeks after a third monthly injection of b12. I don't really see the point in waiting, because if it confirms a Pernicious Anemia diagnosis, that would hopefully mean I could start on more frequent loading
fireflymairi
in
Pernicious Anaemia Society
3 years ago
Nerves are just raw
MRI came back good. Guess it's the Pernicious Anaemia. I am experiencing some numbness in my face again along with extreme sensitivity in my legs to the point I can't even stand anything to touch them. I have not slept well in a couple weeks because I wake up with mild panic. I do notice when I'm
MRI came back good. Guess it's the Pernicious Anaemia. I am experiencing some numbness in my face again along with extreme sensitivity in my legs to the point I can't even stand anything to touch them. I have not slept well in a couple weeks because I wake up with mild panic. I do notice when I'm
Hidden
in
Pernicious Anaemia Society
3 years ago
B12 levels are high but.......
Hi - I’m new to this, but will try to write my query. Got diagnosed with PA by a gastroenterologist about 6 years ago ( I don’t have the intrinsic factor) B12 injections every 3 months until about 3 years ago, then down to every 2 months. But at 6 weeks, I go downhill fast. This past year, it’s been
Hi - I’m new to this, but will try to write my query. Got diagnosed with PA by a gastroenterologist about 6 years ago ( I don’t have the intrinsic factor) B12 injections every 3 months until about 3 years ago, then down to every 2 months. But at 6 weeks, I go downhill fast. This past year, it’s been
Space69
in
Pernicious Anaemia Society
3 years ago
First post - help please 😊
Hi everyone, I was diagnosed in May this year with Pernicious Anaemia (I had actually contacted the doctor as I had deteriorating memory- I’m 45years old) I had 2 weeks of loading b12 doses then yesterday I had my first 3 month b12 shot. I asked the doctor if I could go to 2 monthly but they aren’t keen
Hi everyone, I was diagnosed in May this year with Pernicious Anaemia (I had actually contacted the doctor as I had deteriorating memory- I’m 45years old) I had 2 weeks of loading b12 doses then yesterday I had my first 3 month b12 shot. I asked the doctor if I could go to 2 monthly but they aren’t keen
Sassybob
in
Pernicious Anaemia Society
3 years ago
Ghost: for those who feel invisible
This is an eggshell mosaic on slate called Ghost. It depicts the weird trickling sensation just under your skin with the delightful name of formication: to me, this felt like a physical depletion of self, trickling down to my fingertips and soles of my feet- always started when exhausted (a supermarket
This is an eggshell mosaic on slate called Ghost. It depicts the weird trickling sensation just under your skin with the delightful name of formication: to me, this felt like a physical depletion of self, trickling down to my fingertips and soles of my feet- always started when exhausted (a supermarket
Cherylclaire
Forum Support
in
Pernicious Anaemia Society
3 years ago
How high fat diet and exercise can affect myelin sheaths production by oligodendrocytes while the person is on high dose of B12 vitamin l
I'm wondering how to get our damaged nerves get repaired faster by oligodendrocytes which are responsible in most vertebrates for production of damaged myelin sheaths. Based on Mayo clinic research high fat diet and exercise catalyzes this repair process but saturated fat and sugar damage this process
I'm wondering how to get our damaged nerves get repaired faster by oligodendrocytes which are responsible in most vertebrates for production of damaged myelin sheaths. Based on Mayo clinic research high fat diet and exercise catalyzes this repair process but saturated fat and sugar damage this process
Hamayeshguy
in
Pernicious Anaemia Society
3 years ago
Can anyone tell me what these blood results mean
I have pernicious anaemia and have been suffering really badly with head shaking, arm shaking and weakness also im really tired. Could this be B12 related? Here are my results Full blood count - FBC Haemoglobin estimation131 g/L115 - 160 g/L Total white cell count4.15 10*9/L4.00 - 11.00 10*9/L Platelet
I have pernicious anaemia and have been suffering really badly with head shaking, arm shaking and weakness also im really tired. Could this be B12 related? Here are my results Full blood count - FBC Haemoglobin estimation131 g/L115 - 160 g/L Total white cell count4.15 10*9/L4.00 - 11.00 10*9/L Platelet
Cultivate
in
Pernicious Anaemia Society
3 years ago
Not sure if having a flare
Hi all - need advice: Diagnosed with PMR Feb 2017. I have Mast Cell Activation Syndrome on top of the PMR. Seems that I probably have had it for a long time - but getting viral pneumonia in Dec 2018 along with the meds for that - just made it truly haywire! Do I have been happily reducing over a long
Hi all - need advice: Diagnosed with PMR Feb 2017. I have Mast Cell Activation Syndrome on top of the PMR. Seems that I probably have had it for a long time - but getting viral pneumonia in Dec 2018 along with the meds for that - just made it truly haywire! Do I have been happily reducing over a long
Slosh
in
PMRGCAuk
3 years ago
Dream job
Hello British liver trust,am hepatitis carrier on Tenofovir, my question is i want to study nursing, is that possible or there is restrictions on hepatitis b carrier
Hello British liver trust,am hepatitis carrier on Tenofovir, my question is i want to study nursing, is that possible or there is restrictions on hepatitis b carrier
adexbola86
in
British Liver Trust
3 years ago
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