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Angel54
Last time I felt like this I had
Rituximab
infusion and had bad reaction. Any advice ?
Last time I felt like this I had
Rituximab
infusion and had bad reaction. Any advice ?
Angels54
in
NRAS
2 years ago
Immunosuppressed and Omicron
I am on
Rituximab
, does anyone know anyone who has had Omicron with
Rituximab
/ or any of the other biologicals? Mike
I am on
Rituximab
, does anyone know anyone who has had Omicron with
Rituximab
/ or any of the other biologicals? Mike
trenarren
in
NRAS
2 years ago
Access to Covid treatment and vaccines
JCVI Condition Group Those who were receiving or had received in the previous 3 months targeted therapy for autoimmune disease, such as JAK inhibitors or biologic immune modulators including B-cell targeted therapies (including
rituximab
but in this case the recipient would be considered immunosuppressed
JCVI Condition Group Those who were receiving or had received in the previous 3 months targeted therapy for autoimmune disease, such as JAK inhibitors or biologic immune modulators including B-cell targeted therapies (including
rituximab
but in this case the recipient would be considered immunosuppressed
Moomin8
in
NRAS
2 years ago
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COVID update: Who remains at higher risk? by LLS.org
These include: • Bruton tyrosine kinase (BTK) inhibitors, such as Imbruvica® (ibrutinib), Brukinsa® (zanubrutinib) and Calquence® (acalabrutinib) • Anti-CD20 antibody treatments, such as Rituxan® (
rituximab
) and Gazyva® (obinutuzumab) • CD-19 targeting CAR T-therapy (Breyanzi®, Kymriah®, Tecartus™
These include: • Bruton tyrosine kinase (BTK) inhibitors, such as Imbruvica® (ibrutinib), Brukinsa® (zanubrutinib) and Calquence® (acalabrutinib) • Anti-CD20 antibody treatments, such as Rituxan® (
rituximab
) and Gazyva® (obinutuzumab) • CD-19 targeting CAR T-therapy (Breyanzi®, Kymriah®, Tecartus™
lankisterguy
Volunteer
in
CLL Support
1 year ago
Neutropenia post Rituximab and Covid Jabs
My
Rituximab
Infusion was in June. I have been told to stop Methotrexate and isolate. Anyone had a similar experience? Thanks Anne
My
Rituximab
Infusion was in June. I have been told to stop Methotrexate and isolate. Anyone had a similar experience? Thanks Anne
annekelt
in
NRAS
2 years ago
Cashing in life insurance and pensions
Chemotherapy was not successful and now on 2 years of venetoclax and
Rituximab
in the UK. Has anyone been in a position, due to incurable cancer, to cash in life insurance and pensions? Due to also having MS and bot responding to chemotherapy - hope this treatment will work but unsure.
Chemotherapy was not successful and now on 2 years of venetoclax and
Rituximab
in the UK. Has anyone been in a position, due to incurable cancer, to cash in life insurance and pensions? Due to also having MS and bot responding to chemotherapy - hope this treatment will work but unsure.
bettyba
in
CLL Support
2 years ago
Rituximab
Thank you so much for your replies to my question. I had two infusions two weeks apart last summer. Reading your replies I’m optimistic that hopefully this next round will give me a greater improvement. Thanks very much x
Thank you so much for your replies to my question. I had two infusions two weeks apart last summer. Reading your replies I’m optimistic that hopefully this next round will give me a greater improvement. Thanks very much x
debjw
in
NRAS
2 years ago
Rituximab
Hi lovely people I’ve had one round of
rituximab
last summer. Can anyone tell me if the affects improve with each round please? Thank you x
Hi lovely people I’ve had one round of
rituximab
last summer. Can anyone tell me if the affects improve with each round please? Thank you x
debjw
in
NRAS
2 years ago
COVID: Staying Safe As The Virus Evolves - LLS Podcast / CLL Society’s COVID-19 Update December 5th, 2022 / Dec 15 2022 end Antibody Study
These include: • Bruton tyrosine kinase (BTK) inhibitors, such as Imbruvica® (ibrutinib), Brukinsa® (zanubrutinib) and Calquence® (acalabrutinib) • Anti-CD20 antibody treatments, such as Rituxan® (
rituximab
) and Gazyva® (obinutuzumab) • CD-19 targeting CAR T-therapy (Breyanzi®, Kymriah®, Tecartus™
These include: • Bruton tyrosine kinase (BTK) inhibitors, such as Imbruvica® (ibrutinib), Brukinsa® (zanubrutinib) and Calquence® (acalabrutinib) • Anti-CD20 antibody treatments, such as Rituxan® (
rituximab
) and Gazyva® (obinutuzumab) • CD-19 targeting CAR T-therapy (Breyanzi®, Kymriah®, Tecartus™
lankisterguy
Volunteer
in
CLL Support
1 year ago
Thinking of having a tattoo !!
My lupus is well controlled and I am on
Rituximab
and methotrexate.
My lupus is well controlled and I am on
Rituximab
and methotrexate.
littlemissp
in
LUpus Patients Understanding and Support
2 years ago
Post Splenectomy
Prednisone,,,dexamethasone.....IVIG.....
Rituximab
.....Revolade.......BUT lots of side effects. Seven months ago I had my spleen removed. Since then my platelets are hovering around 20 - 30 with no medications. I have not had any issues with bleeding or bruising. I am in my 70’s.
Prednisone,,,dexamethasone.....IVIG.....
Rituximab
.....Revolade.......BUT lots of side effects. Seven months ago I had my spleen removed. Since then my platelets are hovering around 20 - 30 with no medications. I have not had any issues with bleeding or bruising. I am in my 70’s.
Bradyella
in
ITP Support Association
2 years ago
My Covid experience.
I write this as only the facts. I don’t intend to make any political statement, nor want to argue. Just the facts: On 7/7/22 my wife and I hosted two young families for a cookout. By the end of the evening, I felt pretty tired but chalked it up to a day of hustling around smoking meats, husking corn
I write this as only the facts. I don’t intend to make any political statement, nor want to argue. Just the facts: On 7/7/22 my wife and I hosted two young families for a cookout. By the end of the evening, I felt pretty tired but chalked it up to a day of hustling around smoking meats, husking corn
fishnman
in
CLL Support
2 years ago
Venetoclax+Rituximab OR Acalabrutinib - What is the best choice?
I have had experience of
Rituximab
(with the FCR). I was wondering if anybody with experience of these therapies could comment on what would be the best second line treatment with the most positive outcome for a remission and probable/possible side effects. Thank you Richard
I have had experience of
Rituximab
(with the FCR). I was wondering if anybody with experience of these therapies could comment on what would be the best second line treatment with the most positive outcome for a remission and probable/possible side effects. Thank you Richard
Rich316
in
CLL Support
2 years ago
Has anyone had a brain MRI while on venetoclax or rituximib ?
I began to relapse CLL early 2021, started treatment on venetoclax Aug 2021 and then 6 X monthly rituximib infusions. In Mar 2022, a month after the last infusion ,( after a bit of nausea over the previous couple of months) I had BAD nausea in the night then two very brief faints/blackouts, then vomitting
I began to relapse CLL early 2021, started treatment on venetoclax Aug 2021 and then 6 X monthly rituximib infusions. In Mar 2022, a month after the last infusion ,( after a bit of nausea over the previous couple of months) I had BAD nausea in the night then two very brief faints/blackouts, then vomitting
Moggn
in
CLL Support
2 years ago
Venetoclax & fainting?
I am just on 8 months thru the program, of ramp up Venetoclaxfor a month, then 6 mths of monthly
Rituximab
infusion and continuing V for 2 years.
I am just on 8 months thru the program, of ramp up Venetoclaxfor a month, then 6 mths of monthly
Rituximab
infusion and continuing V for 2 years.
Moggn
in
CLL Support
2 years ago
3rd Rituximab Infusion One to Go!
I believe that the
Rituximab
infusions seem to be working. WBC back in normal range. RBC up but still a little low. My Haptoglobin has stayed the same at 14 which it has been for every test on record since September. I am wondering if anyone knows why that is and if I should be concerned.
I believe that the
Rituximab
infusions seem to be working. WBC back in normal range. RBC up but still a little low. My Haptoglobin has stayed the same at 14 which it has been for every test on record since September. I am wondering if anyone knows why that is and if I should be concerned.
SantaZia
in
CLL Support
2 years ago
Rituximab reaction?
Hi, I had my first infusion of
Rituximab
the 22/12, around New Year’s Eve I started to feel unwell , I had my second infusion due the 5/01/22 but the night before I had a bit of temperature, I rung them and they said if the temperature was below 38 to go, I went but feeling really weak , the pain all
Hi, I had my first infusion of
Rituximab
the 22/12, around New Year’s Eve I started to feel unwell , I had my second infusion due the 5/01/22 but the night before I had a bit of temperature, I rung them and they said if the temperature was below 38 to go, I went but feeling really weak , the pain all
Melaxx
in
LUPUS UK
2 years ago
Rituximab and fourth vaccine
I was hoping to push back my regular
Rituximab
infusion to give Omicron a chance to calm down. But the results of the latest blood test force me now to have it quite soon. I was also due my fourth vaccine. Does anyone know what the usual protocol is ?
I was hoping to push back my regular
Rituximab
infusion to give Omicron a chance to calm down. But the results of the latest blood test force me now to have it quite soon. I was also due my fourth vaccine. Does anyone know what the usual protocol is ?
Condensation
in
Vasculitis UK
2 years ago
Anyone thinking to postpone rituximab doses until Omicron wave is over?
I am on Venetoclax plus
rituximab
treatment and have already had 3 of the 6
Rituximab
doses. The 4th dose is due on January 3, but I am reluctant to visit hospital and remain there for so many hours coming into contact with several people of all sorts.
I am on Venetoclax plus
rituximab
treatment and have already had 3 of the 6
Rituximab
doses. The 4th dose is due on January 3, but I am reluctant to visit hospital and remain there for so many hours coming into contact with several people of all sorts.
RamsesII
in
CLL Support
2 years ago
Lupus Nephritis and Cyclophosphamide
They're hoping to move me onto mycophenolate or
rituximab
once I'm done with the chemotherapy. My self esteem and body image are rock bottom at this point 😪.
They're hoping to move me onto mycophenolate or
rituximab
once I'm done with the chemotherapy. My self esteem and body image are rock bottom at this point 😪.
CPower
in
LUPUS UK
2 years ago
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