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parietal cell antibody test.
My test was positive but an if test not was not done... what does this tell me please??
My test was positive but an if test not was not done... what does this tell me please??
xJJx
in
Pernicious Anaemia Society
9 years ago
Bloood exchange's
I have sickle cell anemia, Am 37, I've had 2 strokes, and i now have blood exchanges every 5 weeks because of the strokes. Does anyone else have blood exchanges? and how are you coping with them?
I have sickle cell anemia, Am 37, I've had 2 strokes, and i now have blood exchanges every 5 weeks because of the strokes. Does anyone else have blood exchanges? and how are you coping with them?
mzdonz
in
Sickle Cell Society
9 years ago
Pain
After stem cell transplant is the pain less, and does it simply go away for several years?
After stem cell transplant is the pain less, and does it simply go away for several years?
Price918
in
Myeloma America Support
9 years ago
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Dear ENDOTEXT and THYROIDMANAGER READERS
For your interest and information, I just received one of the emails I am subscribed to. For any of you who do not know of these resources, I commend them. Even though we often end up criticising doctors and "big pharma", there is no doubt that what is available here demonstrates that thyroid is an enormously
For your interest and information, I just received one of the emails I am subscribed to. For any of you who do not know of these resources, I commend them. Even though we often end up criticising doctors and "big pharma", there is no doubt that what is available here demonstrates that thyroid is an enormously
helvella
Thyroid UK
in
Thyroid UK
9 years ago
Scientists Studying Sickle Cell Trait
Studying Sickle Cell Trait Condition has killed 9 collegiate football players since 2000, researchers say WebMD News from HealthDay By Robert Preidt HealthDay Reporter THURSDAY, Sept. 18, 2014 (HealthDay News) -- Researchers are trying to learn more about a condition called sickle cell trait, which
Studying Sickle Cell Trait Condition has killed 9 collegiate football players since 2000, researchers say WebMD News from HealthDay By Robert Preidt HealthDay Reporter THURSDAY, Sept. 18, 2014 (HealthDay News) -- Researchers are trying to learn more about a condition called sickle cell trait, which
Wanda61
in
Sickle Cell Society
9 years ago
Week 5, Run 3 - Tick!
The
ageing
body seemed to say 'oh
well
, despite all of the aches and pains i've given him, he's obviously not going to give up, so i may as well jump in and give him a hand' And there it is, 20 minutes later and i'm still going and feeling fine. Maybe this plan does work after all ........ :)
The
ageing
body seemed to say 'oh
well
, despite all of the aches and pains i've given him, he's obviously not going to give up, so i may as well jump in and give him a hand' And there it is, 20 minutes later and i'm still going and feeling fine. Maybe this plan does work after all ........ :)
Linkin
in
Couch to 5K
9 years ago
Panorama
Hi Watching panorama where they are treating ms by giving patients chemo then a bone Marrow transplant and rebooting their immune system to before their MS. wouldn't it be wonderful if that could help RA X
Hi Watching panorama where they are treating ms by giving patients chemo then a bone Marrow transplant and rebooting their immune system to before their MS. wouldn't it be wonderful if that could help RA X
allanah
in
NRAS
9 years ago
Hastings Meet up
After a great start in November and December the Hastings group is looking forward to a successful 2016. If you would like to join us at a meeting please let us know. If you know of others in East Sussex or if you are visiting Hastings and would like to meet with others who have polymyalgia rheumatica
After a great start in November and December the Hastings group is looking forward to a successful 2016. If you would like to join us at a meeting please let us know. If you know of others in East Sussex or if you are visiting Hastings and would like to meet with others who have polymyalgia rheumatica
pennyw
Administrator
in
PMRGCAuk
9 years ago
I had a few questions
My nan had sickle cell anaemia, she pasted away from it in 2003 aged 59, however now I am 17 turning 18 soon i wanted to look in to it abit more. As far as I know I understand that it's on my dads side. My dad has never been tested for it and only found out my nan had sickle cell anaemia shortly after
My nan had sickle cell anaemia, she pasted away from it in 2003 aged 59, however now I am 17 turning 18 soon i wanted to look in to it abit more. As far as I know I understand that it's on my dads side. My dad has never been tested for it and only found out my nan had sickle cell anaemia shortly after
Jasonfaram17
in
Sickle Cell Society
9 years ago
Some Statistics regarding Large Vessel Vasculitis
Some statstics came through to us this morning so thought I would share them, but please do not shoot the messenger, I am just passing them on. There is estimated to be 1 new case of TAK (Takayasu Arteritis ) per million here in Europe per year. Average age of onset is 23 years. 50% of those diagnosed
Some statstics came through to us this morning so thought I would share them, but please do not shoot the messenger, I am just passing them on. There is estimated to be 1 new case of TAK (Takayasu Arteritis ) per million here in Europe per year. Average age of onset is 23 years. 50% of those diagnosed
Suzym2u
Vasculitis UK
in
Vasculitis UK
9 years ago
Daughter update
Well i have good news to tell you and that is she is HOME. The Drs. couldnt believe how quickly she has recovered from Stem Cell transplant. She has got to take it easy and rest not do anything. I have to take her for blood tests on Monday so fingers crossed nothing goes wrong. That all i have to tell
Well i have good news to tell you and that is she is HOME. The Drs. couldnt believe how quickly she has recovered from Stem Cell transplant. She has got to take it easy and rest not do anything. I have to take her for blood tests on Monday so fingers crossed nothing goes wrong. That all i have to tell
fastball
in
NRAS
9 years ago
husbands blood results suggestive of PA?
My husband suffers from psoriasis, has had Hodgekins lymphoma in past with stem cell transplant and chemo, has underactive thyroid, sarcoidosis of the lungs, heart attack and by pass surgery. Now he is fatigued, depressed, forgetful and his blood results show B12 at 253 (180-1000) Folate at 4.7 (>4)
My husband suffers from psoriasis, has had Hodgekins lymphoma in past with stem cell transplant and chemo, has underactive thyroid, sarcoidosis of the lungs, heart attack and by pass surgery. Now he is fatigued, depressed, forgetful and his blood results show B12 at 253 (180-1000) Folate at 4.7 (>4)
gillsie
in
Pernicious Anaemia Society
9 years ago
any advice on prednisolone for kids...
My 9 year old has ITP since he was one. So far no medication ,now at count of 7 heamatologist satrted giving predisolone, Im not sure if its helpful. I want to know what side effect it can cause. I've been told that bone marrow transplant is the only solution to this condition. I,m an Asian working
My 9 year old has ITP since he was one. So far no medication ,now at count of 7 heamatologist satrted giving predisolone, Im not sure if its helpful. I want to know what side effect it can cause. I've been told that bone marrow transplant is the only solution to this condition. I,m an Asian working
S38abcd
in
ITP Support Association
9 years ago
Stem cell transplant
Hi all I am at the moment awaiting a stem cell transplant for my systemic scleroderma as advised by professor Denton at royal free and was wondering wether anybody out there has had it and what was the result x
Hi all I am at the moment awaiting a stem cell transplant for my systemic scleroderma as advised by professor Denton at royal free and was wondering wether anybody out there has had it and what was the result x
Typicalmommy
in
Scleroderma & Raynaud's UK (SRUK)
9 years ago
update on daughter
Well daughter has been in hospital for a week, they found a nasty virus that they didnt want it to mature. It would do a lot of damage. The good news is there could be action on the bone marrow transplant in the middle of Dec. We all have our fingers crossed. I said to her there is a small light at the
Well daughter has been in hospital for a week, they found a nasty virus that they didnt want it to mature. It would do a lot of damage. The good news is there could be action on the bone marrow transplant in the middle of Dec. We all have our fingers crossed. I said to her there is a small light at the
fastball
in
NRAS
9 years ago
MDS World Awareness Day today 25th October 2015
Thought you may be interested. MDS is a rare bone marrow disease which is only curable by a cell stem or bone marrow transplant. I can't find any information or indeed references on this web site but anyone affected, see more here www.mdspatientsupport.org.uk. Best regards Glyn
Thought you may be interested. MDS is a rare bone marrow disease which is only curable by a cell stem or bone marrow transplant. I can't find any information or indeed references on this web site but anyone affected, see more here www.mdspatientsupport.org.uk. Best regards Glyn
Gforce1
in
CLL Support
9 years ago
Sickle Cell Society please advise me of what you mean when you say the following!!
Could you please explain to me why on you website it adamtly states, and I quote "People who ONLY (are you for real?) Have Sickle Cell Trait do not suffer any of the symptoms of Sickle Cell Anemia. Sickle Cell Trait is NOT an illness and people with trait are completely healthy" I feel that this is
Could you please explain to me why on you website it adamtly states, and I quote "People who ONLY (are you for real?) Have Sickle Cell Trait do not suffer any of the symptoms of Sickle Cell Anemia. Sickle Cell Trait is NOT an illness and people with trait are completely healthy" I feel that this is
benhudson444
in
Sickle Cell Society
9 years ago
Dr. Shpall on Therapeutic Agents for the Treatment of CLL
Elizabeth J. Shpall, MD, professor, deputy department chair, Department of Stem Cell Transplantation, Division of Cancer Medicine, medical director, Cell Therapy Laboratory, director, Cord Blood Bank, the University of Texas MD Anderson Cancer Center, discusses idelalisib and ibrutinib for the treatment
Elizabeth J. Shpall, MD, professor, deputy department chair, Department of Stem Cell Transplantation, Division of Cancer Medicine, medical director, Cell Therapy Laboratory, director, Cord Blood Bank, the University of Texas MD Anderson Cancer Center, discusses idelalisib and ibrutinib for the treatment
Justasheet1
in
CLL Support
9 years ago
New PMRGCAuk Café Meet-ups in Orpington, Maidstone, Sevenoaks and Hastings
PMRGCA café meet-ups are a great new way to meet others with polymyalgia rheumatica and giant cell arteritis who live in your area. Four new café meet-ups - Orpington, Maidstone, Sevenoaks and Hastings - are now open for you. All the details are on the PMRGCAuk website - links below: Orpington - http
PMRGCA café meet-ups are a great new way to meet others with polymyalgia rheumatica and giant cell arteritis who live in your area. Four new café meet-ups - Orpington, Maidstone, Sevenoaks and Hastings - are now open for you. All the details are on the PMRGCAuk website - links below: Orpington - http
pennyw
Administrator
in
PMRGCAuk
9 years ago
Hypothyroidism
Recently diagnosed, no overt symptoms,
well
maybe some but how to distinguish from
ageing
process - I'm 80? In second week of treatment so only 25 mg of levothyroxine. No reaction so far, just signed up so I can learn more first hand about the condition.
Recently diagnosed, no overt symptoms,
well
maybe some but how to distinguish from
ageing
process - I'm 80? In second week of treatment so only 25 mg of levothyroxine. No reaction so far, just signed up so I can learn more first hand about the condition.
GillH-february
in
Thyroid UK
9 years ago
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