Search
Search
About
Log in
Join
Experiences with
Ageing well
Posts
Communities
943 public posts
Filter results
Positive parietal cell antibody
After eventually seeing a neurologist with regard to my tingling limbs, I have today received a copy of a letter he sent to my GP. He says that the MRI scan was normal, so pleased about that. However, he then says, quote: "I note she as a positive parietal cell antibody and that some provisional blood
After eventually seeing a neurologist with regard to my tingling limbs, I have today received a copy of a letter he sent to my GP. He says that the MRI scan was normal, so pleased about that. However, he then says, quote: "I note she as a positive parietal cell antibody and that some provisional blood
Twitchen
in
Thyroid UK
10 years ago
Narrowed esophagus
My Rheumy has asked me if I have difficulty swallowing. So I wonder if this is a symptom of GCA. I recently had a colonoscopy and endoscopy with a stretching of the esophagus. The gastro doctor informed me that my esophagus was very narrowed and wondered if it had been bothering me. He wondered if it
My Rheumy has asked me if I have difficulty swallowing. So I wonder if this is a symptom of GCA. I recently had a colonoscopy and endoscopy with a stretching of the esophagus. The gastro doctor informed me that my esophagus was very narrowed and wondered if it had been bothering me. He wondered if it
Asbeck
in
PMRGCAuk
10 years ago
Progress
I joined the PAS and this forum at the beginning of Sept this year having been diagnosed with PA in May 2013. I hadn't received any loading doses and was put immediately onto 3 monthly injections. My readings on each subsequent visit to the Doc were around the 200 mark. Thanks to the forum I realised
I joined the PAS and this forum at the beginning of Sept this year having been diagnosed with PA in May 2013. I hadn't received any loading doses and was put immediately onto 3 monthly injections. My readings on each subsequent visit to the Doc were around the 200 mark. Thanks to the forum I realised
Weewull
in
Pernicious Anaemia Society
10 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
MPDlife - the newsletter for people with MPNs
November 2014 issue now available, the newsletter is packed full of interesting articles: •Rapid changes in MPN research and treatment options – Professor Claire Harrison reports on the European School of Haematology MPN meeting held in Estoril, Portugal in October 2014, and tells us about the new scientific
November 2014 issue now available, the newsletter is packed full of interesting articles: •Rapid changes in MPN research and treatment options – Professor Claire Harrison reports on the European School of Haematology MPN meeting held in Estoril, Portugal in October 2014, and tells us about the new scientific
Mazcd
MPNVoice
in
MPN Voice
10 years ago
Is there a better test for F1 antibodies?
Hi, I've been (blood) tested for F1 antibodies and the results were negative, but I've heard the test is notoriously unreliable - does anyone know of a better test that I could request or is the standard blood test the only one out there? I'm going to ask for a parietal cell antibody test, and possibly
Hi, I've been (blood) tested for F1 antibodies and the results were negative, but I've heard the test is notoriously unreliable - does anyone know of a better test that I could request or is the standard blood test the only one out there? I'm going to ask for a parietal cell antibody test, and possibly
Chancery
in
Pernicious Anaemia Society
10 years ago
MPN Voice Patients’ Forums 2015
We are pleased to announce that we have 2 patients’ forums confirmed for 2015, Colchester and Cardiff. Colchester – Wednesday 4th February 2015, 4 pm – 6 pm, (registration from 3.45 pm) in Room 2, Post Graduate Medical Centre, Villa 8, Colchester General Hospital, Turner Road, Colchester, Essex, CO4
We are pleased to announce that we have 2 patients’ forums confirmed for 2015, Colchester and Cardiff. Colchester – Wednesday 4th February 2015, 4 pm – 6 pm, (registration from 3.45 pm) in Room 2, Post Graduate Medical Centre, Villa 8, Colchester General Hospital, Turner Road, Colchester, Essex, CO4
Mazcd
MPNVoice
in
MPN Voice
10 years ago
Zoom Zoom, CAR-T Cells to Treat Myeloma
An exciting approach to refractory myeloma is the development of CAR-T cells to recognize and kill the malignant plasma cells which mutate and are responsible for recurrence. Chimeric Antigen Receptor - T cell therapy has now been used in hundreds of patients with recurrent leukemia (89% success) and
An exciting approach to refractory myeloma is the development of CAR-T cells to recognize and kill the malignant plasma cells which mutate and are responsible for recurrence. Chimeric Antigen Receptor - T cell therapy has now been used in hundreds of patients with recurrent leukemia (89% success) and
Janstafl
in
Myeloma America Support
10 years ago
Help with test results please
Hi I have finally got my test results from my GP. I was wondering if anyone could look at them and let me know what they think please. Sorry but have added everything as not sure what I could miss out. I cannot find my original B12 result as not sure what I am reading but know at the time I was
Hi I have finally got my test results from my GP. I was wondering if anyone could look at them and let me know what they think please. Sorry but have added everything as not sure what I could miss out. I cannot find my original B12 result as not sure what I am reading but know at the time I was
lal2502
in
Pernicious Anaemia Society
10 years ago
OH NOES! Have I ruined my chances for parietal cell antibody testing?
For reasons that are too embarrassing to explain, I suspect I might have something wrong with my parietal cells. I've had the full blood tests, plus B12 serum, folate, and IF antibody tests - all 'normal' (i.e. B12 in the 'grey zone'), but I wasn't tested for Parietal Cell Antibody. Would anything have
For reasons that are too embarrassing to explain, I suspect I might have something wrong with my parietal cells. I've had the full blood tests, plus B12 serum, folate, and IF antibody tests - all 'normal' (i.e. B12 in the 'grey zone'), but I wasn't tested for Parietal Cell Antibody. Would anything have
Chancery
in
Pernicious Anaemia Society
10 years ago
Question
My dad has non Hodgkin and hodgkin cancer and is has just had stem cell transplant. I believe that it's not a gene related diesease but I've had enlarged lymphones under my arms previously and just worried incase, do I need to speak to anyone. Thanks
My dad has non Hodgkin and hodgkin cancer and is has just had stem cell transplant. I believe that it's not a gene related diesease but I've had enlarged lymphones under my arms previously and just worried incase, do I need to speak to anyone. Thanks
dora21
in
Lymphoma Canada
10 years ago
You've hit a milestone! 300 of you now have joined the Sickle Cell Society HU community
Congratulations for building a true Sickle Cell Disorders health movement in HealthUnlocked! Whenever you write a post, ask a question or reply to someone, you are touching the lives of other people with Sickle Cell Disorders by spreading the benefit of shared, personal health experiences. And beyond
Congratulations for building a true Sickle Cell Disorders health movement in HealthUnlocked! Whenever you write a post, ask a question or reply to someone, you are touching the lives of other people with Sickle Cell Disorders by spreading the benefit of shared, personal health experiences. And beyond
HealthUnlocked
HealthUnlocked
in
Sickle Cell Society
10 years ago
Stem cell transplantation
Are there any myelofibrosis sufferers out there who are considering stem cell transplantation? If so, please get in touch. Thank you.
Are there any myelofibrosis sufferers out there who are considering stem cell transplantation? If so, please get in touch. Thank you.
daisystar
in
MPN Voice
10 years ago
Stem Cell Transplant
I'm celebrating three years of partial remission after two years of treatment with little or no change. I feel like I've been given the gift of three additional years of life. If the opportunity is given...take it and run. Still feeling well and back to being my very busy involved self.
I'm celebrating three years of partial remission after two years of treatment with little or no change. I feel like I've been given the gift of three additional years of life. If the opportunity is given...take it and run. Still feeling well and back to being my very busy involved self.
jc--rb--2--0
in
Myeloma America Support
10 years ago
Blood Stem Cell Transplant
Hi I m a 46 year old woman diagnosed with Cll in April 2014 with 17p deletion. I have been in watchful Waiting but now doctors have suggested I take Imbrivica and prepare to have a stem cell blood transplant because I am young and not showing symptoms. Has anyone had a stem cell blood transplant? What
Hi I m a 46 year old woman diagnosed with Cll in April 2014 with 17p deletion. I have been in watchful Waiting but now doctors have suggested I take Imbrivica and prepare to have a stem cell blood transplant because I am young and not showing symptoms. Has anyone had a stem cell blood transplant? What
Jameelah
in
CLL Support
10 years ago
Introducing Myself
Hi, My name is Kim Marrelli. I was diagnosed with Myeloma 4 years ago. I am considered high risk with t(4:14) (MMSET/FGFR/IGH). To be honest, I only partially understand what all that means. In the past, I have been teated with Revlimid, Velcade, Kyprolis, Pomalyst and the ever popular, Dexamethasone
Hi, My name is Kim Marrelli. I was diagnosed with Myeloma 4 years ago. I am considered high risk with t(4:14) (MMSET/FGFR/IGH). To be honest, I only partially understand what all that means. In the past, I have been teated with Revlimid, Velcade, Kyprolis, Pomalyst and the ever popular, Dexamethasone
KimMarr
in
Myeloma America Support
10 years ago
Benefits
My husband had a letter from the DWP today to say that his DLA is being stopped as he currently doesn't score a high enough mark on their points system for PIP. Along with losing DLA, he also has to send back his Blue Badge. FYI: My husband was diagnosed with Multiple Myeloma (blood cancer) in August
My husband had a letter from the DWP today to say that his DLA is being stopped as he currently doesn't score a high enough mark on their points system for PIP. Along with losing DLA, he also has to send back his Blue Badge. FYI: My husband was diagnosed with Multiple Myeloma (blood cancer) in August
Amanda1234
in
PMRGCAuk
10 years ago
What does this test involve?
Hi there, Has anyone had their 'anterior pituitary function' tested? I've got to spend a full morning in hospital on Friday having the test done and it sounds pretty comprehensive! Endo says he will be checking my GnRH, TRH, Short Synacthen. Does anyone know what kind of diagnoses or indications these
Hi there, Has anyone had their 'anterior pituitary function' tested? I've got to spend a full morning in hospital on Friday having the test done and it sounds pretty comprehensive! Endo says he will be checking my GnRH, TRH, Short Synacthen. Does anyone know what kind of diagnoses or indications these
Amalie105
in
Thyroid UK
10 years ago
What to do next
My teenage relative was given six loading doses of B12 after their level tested at 136. Iron levels were low normal folate normal blood count etc normal. Three months after loading doses b12 levels were 288. Intrinsic factor anti body was not tested for as Gastric Parietal Cell antibody was negative
My teenage relative was given six loading doses of B12 after their level tested at 136. Iron levels were low normal folate normal blood count etc normal. Three months after loading doses b12 levels were 288. Intrinsic factor anti body was not tested for as Gastric Parietal Cell antibody was negative
Hensa
in
Pernicious Anaemia Society
10 years ago
You've hit a milestone! 1000 of you now have joined the PMRGCAuk HU community
Congratulations for building a true PMRGCAuk health movement in HealthUnlocked! You've built the biggest Polymyalgia Rheumatica and Giant Cell Arteritis community in the world. Whenever you write a post, ask a question or reply to someone, you are touching the lives of other people with Polymyalgia
Congratulations for building a true PMRGCAuk health movement in HealthUnlocked! You've built the biggest Polymyalgia Rheumatica and Giant Cell Arteritis community in the world. Whenever you write a post, ask a question or reply to someone, you are touching the lives of other people with Polymyalgia
HealthUnlocked
HealthUnlocked
in
PMRGCAuk
10 years ago
Dealing with sickle cell anaemia.
ever since I knew I had sickle cell, I've been taking much of folic acid. How does the folic acid help sustain me?
ever since I knew I had sickle cell, I've been taking much of folic acid. How does the folic acid help sustain me?
Indahi-keith
in
MPN Voice
10 years ago
1
...
42
43
44
...
48
Next page
10
20
30
40
Filter results
Clear filters
Posted in
All communities
PMRGCAuk
202 results
MPN Voice
130 results
CLL Support
118 results
View top 10 communities
Sort by
Most Relevant
Newest