Search
Search
About
Log in
Join
Experiences with
Stem cell mobilization
Posts
Communities
926 public posts
Filter results
multiple sclerosis and sickle cell trait
Very hard to get doctors to discuss sickle cell trait causing health problems. Have always had blood show up in my urine when examined even when I don't have an infection. I believe this is because of SCT.
Very hard to get doctors to discuss sickle cell trait causing health problems. Have always had blood show up in my urine when examined even when I don't have an infection. I believe this is because of SCT.
shestlouis
in
Sickle Cell Society
7 years ago
1st week on venetoclax - WOW, not what we expected...
After reviewing jtaeross's post from 3 months ago I wanted to share our experience on venetoclax. My husband just stared venetoclax 20mg we are on day 6 after failing on Ibrutinib after 18months and he is 17p, 52 years old - diagnosed at 45 It has been a hell of a week with threats of TML - he had to
After reviewing jtaeross's post from 3 months ago I wanted to share our experience on venetoclax. My husband just stared venetoclax 20mg we are on day 6 after failing on Ibrutinib after 18months and he is 17p, 52 years old - diagnosed at 45 It has been a hell of a week with threats of TML - he had to
NMMP
in
CLL Support
7 years ago
Autologous stem cell transplantation
Going to do autologous stem cell transplant.for relapsed follicular lymphoma. And new dbcl. After 2 weeks. Any body has been through that? Let me know please. Thanks. And God bless you all.
Going to do autologous stem cell transplant.for relapsed follicular lymphoma. And new dbcl. After 2 weeks. Any body has been through that? Let me know please. Thanks. And God bless you all.
Bhlool
in
LSN
7 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Autologous Stem Cell Transplantation for MS
Autologous Stem Cell Transplantation for MS: Progression-Free Survival Seen in Nearly Half of Patients By Amy Orciari Herman Edited by David G. Fairchild, MD, MPH, and Jaye Elizabeth Hefner, MD Autologous stem cell transplantation for multiple sclerosis might help slow neurologic progression in nearly
Autologous Stem Cell Transplantation for MS: Progression-Free Survival Seen in Nearly Half of Patients By Amy Orciari Herman Edited by David G. Fairchild, MD, MPH, and Jaye Elizabeth Hefner, MD Autologous stem cell transplantation for multiple sclerosis might help slow neurologic progression in nearly
erash
in
My MSAA Community
7 years ago
actemra
Basel, 24 January 2017 FDA grants priority review for Roche’s Actemra/RoActemra (tocilizumab) supplemental biologics license application for giant cell arteritis, a form of vasculitis Roche recently announced positive results from a Phase III clinical trial in giant cell arteritis (GCA) There have
Basel, 24 January 2017 FDA grants priority review for Roche’s Actemra/RoActemra (tocilizumab) supplemental biologics license application for giant cell arteritis, a form of vasculitis Roche recently announced positive results from a Phase III clinical trial in giant cell arteritis (GCA) There have
mamacline
in
PMRGCAuk
7 years ago
My recent experience of Giant Cell Arteritis
Hello, for the information of others, I am posting my recent experience of GCA as follows:- I have been suffering from pains in my neck, shoulders and cheeks. My head got so sensitive I could not even comb my hair and my jaws were so painful I could hardly eat any solids. After several visits to my
Hello, for the information of others, I am posting my recent experience of GCA as follows:- I have been suffering from pains in my neck, shoulders and cheeks. My head got so sensitive I could not even comb my hair and my jaws were so painful I could hardly eat any solids. After several visits to my
marpil
in
PMRGCAuk
7 years ago
Post transplant feedback
Hello again. I am three months post stem cell transplant for NHL that crossed the blood brain barrier into my CNS. There are many restrictions for me and I wondered who else was in the same boat? Thank you.
Hello again. I am three months post stem cell transplant for NHL that crossed the blood brain barrier into my CNS. There are many restrictions for me and I wondered who else was in the same boat? Thank you.
Jennchap1
in
Non Hodgkin's Lymphoma Friends
7 years ago
Yellow eyes and Red lips
Ever since I was young I had yellow eyes,now at 22 I still do,and the most irritating question I get even from strangers is "why are your eyes yellow",this really brings my spirit down,Because I cant ever explain to everybody I meet why my eyes are so,although I havent tried any medication that would
Ever since I was young I had yellow eyes,now at 22 I still do,and the most irritating question I get even from strangers is "why are your eyes yellow",this really brings my spirit down,Because I cant ever explain to everybody I meet why my eyes are so,although I havent tried any medication that would
macogola
in
Sickle Cell Society
7 years ago
New here...
Diagnosed in July 2014- RCHOP treated in Pittsburgh at the Mario Lemieux Center for Blood Cancers. Relapsed in November of 2015, received RICE then BEAM before April 2016 auto stem cell transplant.
Diagnosed in July 2014- RCHOP treated in Pittsburgh at the Mario Lemieux Center for Blood Cancers. Relapsed in November of 2015, received RICE then BEAM before April 2016 auto stem cell transplant.
Mrjackwagon
in
Non Hodgkin's Lymphoma Friends
7 years ago
Gastroenterologist says a positive IFA & Parietal Cell antibody result does not mean I have P.A. ?! HELP & advice please
Just returned from Hospital Appointment to see Gastro, at request of my G.P`s, one who does not think I have a B12 issue, and another who will not agree to alternate day jabs without ok from Hospital because afraid of overdosing issues ( he quoted side affects from his BNF book ). The Gastro said that
Just returned from Hospital Appointment to see Gastro, at request of my G.P`s, one who does not think I have a B12 issue, and another who will not agree to alternate day jabs without ok from Hospital because afraid of overdosing issues ( he quoted side affects from his BNF book ). The Gastro said that
Barry1955
in
Pernicious Anaemia Society
7 years ago
Trying Something New
http://nattokinasehearthealth.com/20/what-is-nattokinase-and-health-benefits/ http://nattokinasehearthealth.com/60/what-is-lumbrokinase/ http://nattokinasehearthealth.com/142/serrapeptase-benefits/ This is the third time I am trying to write this post. I keep clicking on the wrong thing and losing my
http://nattokinasehearthealth.com/20/what-is-nattokinase-and-health-benefits/ http://nattokinasehearthealth.com/60/what-is-lumbrokinase/ http://nattokinasehearthealth.com/142/serrapeptase-benefits/ This is the third time I am trying to write this post. I keep clicking on the wrong thing and losing my
Cynt-ann53
in
Sickle Cell Society
7 years ago
I'm new to this, please be gentle
So starting at the beginning I was diagnosed with Leukemia in 2014 at 23, then I had a stem cell transplant which is where it all went wrong; Being on all sorts of medication including steroids made me gain weight, then loose it, then gain it again; this wasn't helped by the fact I wasn't able to do
So starting at the beginning I was diagnosed with Leukemia in 2014 at 23, then I had a stem cell transplant which is where it all went wrong; Being on all sorts of medication including steroids made me gain weight, then loose it, then gain it again; this wasn't helped by the fact I wasn't able to do
lynn_dee_lou
in
Weight Loss Support
7 years ago
HCST
Has anyone looked into doing stem cell transplant? My neurologist told me that they wouldn't accept me because of my age 48 and because I have had MS for 9 years, think I want to try, this disease is so frustrating.
Has anyone looked into doing stem cell transplant? My neurologist told me that they wouldn't accept me because of my age 48 and because I have had MS for 9 years, think I want to try, this disease is so frustrating.
cnichols
in
My MSAA Community
7 years ago
Key questions to ask your consultant
Hi everyone, sorry if you thought from the title of this message that I am providing the answers - instead, I would like your views. If you want the main point of this post skip to end, but it might help give better answers if you read through] [
aside:
For anyone with the stamina, here is my
Hi everyone, sorry if you thought from the title of this message that I am providing the answers - instead, I would like your views. If you want the main point of this post skip to end, but it might help give better answers if you read through] [
aside:
For anyone with the stamina, here is my
Davdow
in
CLL Support
7 years ago
sickle cell traits problems
I have sickle traits and I'm anemia and I get sick sometimes and always have low vitamin d I get tired a lot because my low blood (anemia) I think a new research needs to be done. I been getting sick since I was young. I got the traits from my dad mother.
I have sickle traits and I'm anemia and I get sick sometimes and always have low vitamin d I get tired a lot because my low blood (anemia) I think a new research needs to be done. I been getting sick since I was young. I got the traits from my dad mother.
lavette40
in
Sickle Cell Society
7 years ago
Help to come off of Sertraline and change to 5-HTP!!
I am brand new here to the forum. I am looking for some guidance on how to come off Sertraline which I have been on for as long as I can remember. 20 years plus. I am on 150 mg a day and I tried to come off them before by reducing to 100 mg but side effects of feeling really low, confused and irritable
I am brand new here to the forum. I am looking for some guidance on how to come off Sertraline which I have been on for as long as I can remember. 20 years plus. I am on 150 mg a day and I tried to come off them before by reducing to 100 mg but side effects of feeling really low, confused and irritable
debgou
in
Thyroid UK
7 years ago
Daughter update
I lost my daughter on the 11th Jan. Th funeral is Friday , i believe its the first of the day, 9-00 . I am suffering with a bit of stress. Though at this time I'm trying to be positive and look to the future. I have another daughter who is fighting fit, two sons of whom are both in good health. Tracey
I lost my daughter on the 11th Jan. Th funeral is Friday , i believe its the first of the day, 9-00 . I am suffering with a bit of stress. Though at this time I'm trying to be positive and look to the future. I have another daughter who is fighting fit, two sons of whom are both in good health. Tracey
fastball
in
Lung Conditions Community Forum
8 years ago
GP does not do loading dose as per BNF guidelines due to pressure on appointment availability !1
Hi all, Finally had a reply from my letter to GP questioning why my loading dose of 6 jabs was over 6 weeks, not 2 weeks as per guidelines. ( I enclosed copies of EVERY treatment protocol ) and reminded him I had tested positive for IFA antibodies and Parietal Antibodies, and had neuro symptoms even
Hi all, Finally had a reply from my letter to GP questioning why my loading dose of 6 jabs was over 6 weeks, not 2 weeks as per guidelines. ( I enclosed copies of EVERY treatment protocol ) and reminded him I had tested positive for IFA antibodies and Parietal Antibodies, and had neuro symptoms even
Barry1955
in
Pernicious Anaemia Society
7 years ago
Relapsed Mantle Cell Lymphoma--I'm new here!
My name is Gail and I am 66 years old. I was diagnosed with MCL in February, 2008 when I was 58 years old and living in Cleveland, Ohio. The only side effect I had were weight loss and swollen lymph nodes under my arms. I had HYPER C-VAD chemo with Rituxin and then had a stem cell transplant in October
My name is Gail and I am 66 years old. I was diagnosed with MCL in February, 2008 when I was 58 years old and living in Cleveland, Ohio. The only side effect I had were weight loss and swollen lymph nodes under my arms. I had HYPER C-VAD chemo with Rituxin and then had a stem cell transplant in October
Gail2050
in
Non Hodgkin's Lymphoma Friends
8 years ago
CD8 T Cell Lymphoma in skin tissue and muscle
Diagnosed Nov 15 with above without suffering from any of the normal symptons, had 6 courses of CHOP treatment, finished Mar 16. Scan revealed I was in complete remission. Had to undergo stem cell transplant in May/Jun 16. Didn't suffer some of the side effects but wouldn't wish on my worst enemy. Further
Diagnosed Nov 15 with above without suffering from any of the normal symptons, had 6 courses of CHOP treatment, finished Mar 16. Scan revealed I was in complete remission. Had to undergo stem cell transplant in May/Jun 16. Didn't suffer some of the side effects but wouldn't wish on my worst enemy. Further
squashman
in
Non Hodgkin's Lymphoma Friends
8 years ago
1
...
33
34
35
...
47
Next page
10
20
30
40
Filter results
Clear filters
Posted in
All communities
PMRGCAuk
200 results
MPN Voice
130 results
CLL Support
118 results
View top 10 communities
Sort by
Most Relevant
Newest