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Too much Methylcobalamine?
I took methylcobalamine 5000 mcg sublingual for about 10 months. Just had my blood tested and found the B-12 level was > 1999 and the normal range is 211-946. Doc said to stop taking methylcobalamine immediately. Stopped 3 weeks ago . I have tingling on both feet. Should I gradually withdraw rather
I took methylcobalamine 5000 mcg sublingual for about 10 months. Just had my blood tested and found the B-12 level was > 1999 and the normal range is 211-946. Doc said to stop taking methylcobalamine immediately. Stopped 3 weeks ago . I have tingling on both feet. Should I gradually withdraw rather
Donhturner
in
Pernicious Anaemia Society
7 years ago
Hi I'm new to this group low vitamin B9 folate
Hi I'm new to this group I have slightly low vitamin B9 folate I'm told I was looking it up and this group came up. Can anyone tell me what this means as I have long term health problems too many to mention, I suffer with lots of muscle joint pain and fatigue recently suffered a bout of moderate gastritis
Hi I'm new to this group I have slightly low vitamin B9 folate I'm told I was looking it up and this group came up. Can anyone tell me what this means as I have long term health problems too many to mention, I suffer with lots of muscle joint pain and fatigue recently suffered a bout of moderate gastritis
GillyGangGong
in
Pernicious Anaemia Society
7 years ago
Donor identified
It's been a while since my last update but I'm pleased to say that I have a donor lined up for a stem cell transplant. A young man from Germany. I am to stay on Ibruitinin for 6 more months and then good to go.
It's been a while since my last update but I'm pleased to say that I have a donor lined up for a stem cell transplant. A young man from Germany. I am to stay on Ibruitinin for 6 more months and then good to go.
KAS8
in
CLL Support
7 years ago
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Really feel confused
I'm new on this forum I just don't know what to ask now !! This sickle cell trait I've got I have been suffering for quite a long time now some days I get my crisis the pains in my stomach legs feel weird but my GP don't listen she thinks I'm mad or on drink or even drugs !!!!!! So where do I get some
I'm new on this forum I just don't know what to ask now !! This sickle cell trait I've got I have been suffering for quite a long time now some days I get my crisis the pains in my stomach legs feel weird but my GP don't listen she thinks I'm mad or on drink or even drugs !!!!!! So where do I get some
Healthbud
in
Sickle Cell Society
7 years ago
Phenomenal News
Some of you may have seen my recent post inquiring about full remission. The reason is that I have been in full remission since June 2nd without any of my prior symptoms. I have not had one moment of cog fog, muscle spasm, fatigue, numbness, or loss of balance. I have not: changed my diet, changed my
Some of you may have seen my recent post inquiring about full remission. The reason is that I have been in full remission since June 2nd without any of my prior symptoms. I have not had one moment of cog fog, muscle spasm, fatigue, numbness, or loss of balance. I have not: changed my diet, changed my
Karen-x
in
My MSAA Community
7 years ago
It's a Nice Day for a White Wedding
Hi Folks , , just a social post to prove that despite my current issues battling my inner GVHD 'friend', there is life after undergoing a Stem cell transplant. My beautiful wife and I attended a Nieces wedding this weekend. It was a casual event as weddings go and very enjoyable. I was keeping everything
Hi Folks , , just a social post to prove that despite my current issues battling my inner GVHD 'friend', there is life after undergoing a Stem cell transplant. My beautiful wife and I attended a Nieces wedding this weekend. It was a casual event as weddings go and very enjoyable. I was keeping everything
JediReject
in
MPN Voice
7 years ago
Friends and Fans from around the World
I Thank all those for the messages of support at times they can make a huge difference. I am back home now just been watching the highlights of the Final day of the Tour I was there but you can't see everything hey. I had a great time and meet some lovely people, our group had no punctures like all the
I Thank all those for the messages of support at times they can make a huge difference. I am back home now just been watching the highlights of the Final day of the Tour I was there but you can't see everything hey. I had a great time and meet some lovely people, our group had no punctures like all the
TheFlyer
in
CLL Support
7 years ago
GP didn't order intrinsic factor test!
Hello, I went to my GP practice and got print-outs of all my blood test results, but discovered I never even had the IF test! Instead she did the gastric parietal cell antibody test (negative) as well as a number of others (all negative): Anti Mitochondrial Antibody Anti Smooth Muscle Antibody Liver
Hello, I went to my GP practice and got print-outs of all my blood test results, but discovered I never even had the IF test! Instead she did the gastric parietal cell antibody test (negative) as well as a number of others (all negative): Anti Mitochondrial Antibody Anti Smooth Muscle Antibody Liver
Curlygal
in
Pernicious Anaemia Society
7 years ago
GCA and Tocilizumab
I have just heard that I have funding and approval from the NHS to take Tocilizumab and will be having my first infusion this week or the week after. Then I have weekly injections after. I wondered if anyone knew if there are any immediate effects. Also do you go on taking other medications. I am on
I have just heard that I have funding and approval from the NHS to take Tocilizumab and will be having my first infusion this week or the week after. Then I have weekly injections after. I wondered if anyone knew if there are any immediate effects. Also do you go on taking other medications. I am on
christine2715
in
PMRGCAuk
7 years ago
IF Antibody test back - so what next
Following up on my previous posts (low B12, started on B12 loading shots - had second today so too early to tell results on symptoms) Finally got my IF antibody test back today Results: 2.9 U/mL (Normal: < 6 U/mL) I'm aware of the inherent reliability of the test (40-60%) so realise that it doesn't
Following up on my previous posts (low B12, started on B12 loading shots - had second today so too early to tell results on symptoms) Finally got my IF antibody test back today Results: 2.9 U/mL (Normal: < 6 U/mL) I'm aware of the inherent reliability of the test (40-60%) so realise that it doesn't
GavinUK
in
Pernicious Anaemia Society
7 years ago
MPN Voice Patients’ Forum – Birmingham. Friday 6th October 2017, 12.30 – 4 pm, registration and buffet lunch 12 – 12.30 pm
Suite 7, Fazeley Studios, 191 Fazeley Street, Digbeth, Birmingham, B5 5SE
Programme
The programme is yet to be finalized, but will include talks from haematologists, a haematology specialist nurse, and patients, plus breakout groups for each MPN where patients can meet in smaller groups
Suite 7, Fazeley Studios, 191 Fazeley Street, Digbeth, Birmingham, B5 5SE
Programme
The programme is yet to be finalized, but will include talks from haematologists, a haematology specialist nurse, and patients, plus breakout groups for each MPN where patients can meet in smaller groups
Mazcd
MPNVoice
in
MPN Voice
7 years ago
MPN Voice Patients’ Forum – Inverness. Friday 8th September, 10 am - 2 pm, registration 9.30 – 10 am
Eden Court Theatre, Bishops Road, Inverness, IV3 5SA
The forum will be held in The MacLean Room
Programme
The programme is yet to be finalized, but will include talks from haematologists, the haematology nurse specialist from Guy’s Hospital and patients, plus breakout groups for each
Eden Court Theatre, Bishops Road, Inverness, IV3 5SA
The forum will be held in The MacLean Room
Programme
The programme is yet to be finalized, but will include talks from haematologists, the haematology nurse specialist from Guy’s Hospital and patients, plus breakout groups for each
Mazcd
MPNVoice
in
MPN Voice
7 years ago
Stem Cell Transplant Research
Trying to find a way to eliminate the need for bone marrow donors ... http://tinyurl.com/y8rm9p6u
Trying to find a way to eliminate the need for bone marrow donors ... http://tinyurl.com/y8rm9p6u
Shar0n
Volunteer
in
Non Hodgkin's Lymphoma Friends
7 years ago
JUST THE FACTS: SCT/Sickle Cell Trait ==> "People with Diabetes and Sickle Cell Trait Should Have Reliable A1C Test"
Source: NIH (National Institutes of Health) Web site https://www.nih.gov/news-events/news-releases/people-diabetes-sickle-cell-trait-should-have-reliable-a1c-test) Wednesday, November 28, 2007 ARTICLE TITLE: "People with Diabetes and Sickle Cell Trait Should Have Reliable A1C Test" QUOTE #1: ""In the
Source: NIH (National Institutes of Health) Web site https://www.nih.gov/news-events/news-releases/people-diabetes-sickle-cell-trait-should-have-reliable-a1c-test) Wednesday, November 28, 2007 ARTICLE TITLE: "People with Diabetes and Sickle Cell Trait Should Have Reliable A1C Test" QUOTE #1: ""In the
RadiantSue
in
Sickle Cell Society
7 years ago
Question on Complete Stem Cell Transplant
Has anyone out there ever had a complete stem cell transplant? I will be going with my sister in law this coming week to Emory Hospital in Atlanta to find out the details. Would like to hear the good and the bad if you or if you know anyone who has had this done. She has CLL but has the P17 deletion
Has anyone out there ever had a complete stem cell transplant? I will be going with my sister in law this coming week to Emory Hospital in Atlanta to find out the details. Would like to hear the good and the bad if you or if you know anyone who has had this done. She has CLL but has the P17 deletion
evetom
in
CLL Support
7 years ago
Is this the right test?
I've been diagnosed with B12 (113) and folate (3.1) deficiency. I'm getting the loading injections at the moment. The doctor has given me a blood test form to get a "gastic parietal cell antibody" test. Is this the right test? I thought I should be getting the Anti intrinsic factor antibody test as that
I've been diagnosed with B12 (113) and folate (3.1) deficiency. I'm getting the loading injections at the moment. The doctor has given me a blood test form to get a "gastic parietal cell antibody" test. Is this the right test? I thought I should be getting the Anti intrinsic factor antibody test as that
Orpheusss
in
Pernicious Anaemia Society
7 years ago
Giant Cell Arteritis and Tocilizumab Patient Experience Needed
If you have been treated with Tocilizumab for Giant Cell Arteritis VUK would like to hear of your experiences both good and bad. Please contact John Mills email John.mills@vasculitis.org.uk as soon as possible
If you have been treated with Tocilizumab for Giant Cell Arteritis VUK would like to hear of your experiences both good and bad. Please contact John Mills email John.mills@vasculitis.org.uk as soon as possible
Suzym2u
Vasculitis UK
in
Vasculitis UK
7 years ago
Sickle Cell Trait
Hi Im 21 years old and have been diagnosed with Sickle Cell Trait when i was seven, I have been experiencing some dizziness a couple days now which is very uncomfortable. It feels as if i am very intoxicated, moving my head and neck in certain directions is extremely discomforting as it feels like if
Hi Im 21 years old and have been diagnosed with Sickle Cell Trait when i was seven, I have been experiencing some dizziness a couple days now which is very uncomfortable. It feels as if i am very intoxicated, moving my head and neck in certain directions is extremely discomforting as it feels like if
Miguelf
in
Sickle Cell Society
7 years ago
Just the facts / In Summer Heat Stay Hydrated - Please
FACT about sickle cell trait "The defect in urine concentrating ability in persons with sickle cell trait is thought to result from intracellular polymerization of Hb S in erythrocytes, leading to microvascular occlusion, in the vasa recta of the renal medulla. Reasoning that the severity of the concentration
FACT about sickle cell trait "The defect in urine concentrating ability in persons with sickle cell trait is thought to result from intracellular polymerization of Hb S in erythrocytes, leading to microvascular occlusion, in the vasa recta of the renal medulla. Reasoning that the severity of the concentration
RadiantSue
in
Sickle Cell Society
7 years ago
For those diagnosed with Giant Cell Arteritis - this was tweeted just a few minutes ago
A breakthrough in the treatment of GCA @RheumatologyUK @PMRGCAuk @vascuk Please follow this link https://www.ncbi.nlm.nih.gov/pubmed/28745999
A breakthrough in the treatment of GCA @RheumatologyUK @PMRGCAuk @vascuk Please follow this link https://www.ncbi.nlm.nih.gov/pubmed/28745999
Suzym2u
Vasculitis UK
in
Vasculitis UK
7 years ago
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