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Cyclophosphamide
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Unrelenting pain post chemo dose
Commenced on 3 weekly epirubicin and
cyclophosphamide
. I'm on my 2nd cycle but during the 2 cycles I have the most horrendous, unrelenting pain in my upper back area which is also very tender. I have 15mg slow release morphine and more for breakthrough but despite this the pain continues.
Commenced on 3 weekly epirubicin and
cyclophosphamide
. I'm on my 2nd cycle but during the 2 cycles I have the most horrendous, unrelenting pain in my upper back area which is also very tender. I have 15mg slow release morphine and more for breakthrough but despite this the pain continues.
Cazdf
in
SHARE Metastatic Breast Cancer
1 year ago
UK NICE Approves Ibrutinib +Venetoclax for First Line treatment for ALL Patients from today
[/i] [i]
A: During scoping consultation, a consultee highlighted an urgent need for access to novel treatments for younger, fitter patients with chronic lymphocytic leukaemia as currently only fludarabine,
and rituximab (FCR) or venetoclax plus obinutuzumab via the Cancer Drugs
[/i] [i]
A: During scoping consultation, a consultee highlighted an urgent need for access to novel treatments for younger, fitter patients with chronic lymphocytic leukaemia as currently only fludarabine,
and rituximab (FCR) or venetoclax plus obinutuzumab via the Cancer Drugs
Jm954
Administrator
in
CLL Support
1 year ago
tapering off azathioprine
Initially had
cyclophosphamide
infusions and have been maintained on azathioprine since, Last rituximab was 2 yrs ago, been in remission for 2 yrs now.
Initially had
cyclophosphamide
infusions and have been maintained on azathioprine since, Last rituximab was 2 yrs ago, been in remission for 2 yrs now.
stuc
in
Vasculitis UK
1 year ago
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Cyclophosphamide & Niraparib
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Hidden
in
OvaCare
1 year ago
Cyclophosphamide & Niraparib
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Cyclophosphamide
& Niraparib Has anyone any experience with either? I’ve never even heard of
Cyclophosphamide
as a chemo infusion. Anne
Hidden
in
My Ovacome
1 year ago
cyclophosphamide
She is trying me on
Cyclophosphamide
, please let me know of any successes with this drug. Thank you. Xxx
She is trying me on
Cyclophosphamide
, please let me know of any successes with this drug. Thank you. Xxx
Clipper15
in
My Ovacome
1 year ago
Relative risk for secondary bone marrow cancer within 5 years after initial CLL chemoimmunotherapy treatment (typically BR or FCR)
In countries where targeted therapies ('brutinibs, venetoclax, obinutuzumab/rituximab) are now available, the remaining reason that FCR (Fludarabine+
Cyclophosphamide
+Rituximab) is still sometimes recommended for the treatment of CLL is that it can be curative* about 55% of the time - but [u]
only[
In countries where targeted therapies ('brutinibs, venetoclax, obinutuzumab/rituximab) are now available, the remaining reason that FCR (Fludarabine+
Cyclophosphamide
+Rituximab) is still sometimes recommended for the treatment of CLL is that it can be curative* about 55% of the time - but [u]
only[
AussieNeil
Administrator
in
CLL Support
9 months ago
IFN-1 levels before treatment may be biomarker of SLE activity: Study
Organ damage also was associated with the use of methylprednisolone pulse therapy or intravenous (into-the-vein)
cyclophosphamide
(IVCY) pulse therapy.
Organ damage also was associated with the use of methylprednisolone pulse therapy or intravenous (into-the-vein)
cyclophosphamide
(IVCY) pulse therapy.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 year ago
Systemic sclerosis and mycofit
I was on pulse therapy with
cyclophosphamide
infusion but the cycle of
cyclophosphamide
has been already finished so I have been prescribed mycofit by my doctor but this medicine cause some intestinal bowl problem and also some potential side effects like vomiting, nausea also increase the risk of skin
I was on pulse therapy with
cyclophosphamide
infusion but the cycle of
cyclophosphamide
has been already finished so I have been prescribed mycofit by my doctor but this medicine cause some intestinal bowl problem and also some potential side effects like vomiting, nausea also increase the risk of skin
Lo1234
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Living with Cll
But because I heard that the treatment was sometimes worse than watch and wait I procrastinated, when I started treatment I had WBC 270 , hemaglobin 10 and platelets 84 , I started to look weak and gray and had to drag my left leg because of pain of swollen lymph nodes , at first I had two cycles of
cyclophosphamide
But because I heard that the treatment was sometimes worse than watch and wait I procrastinated, when I started treatment I had WBC 270 , hemaglobin 10 and platelets 84 , I started to look weak and gray and had to drag my left leg because of pain of swollen lymph nodes , at first I had two cycles of
cyclophosphamide
starlifter
in
CLL Support
1 year ago
SUDDEN Rise in ESR - Pt. 3
As methotrexate, now discontinued, caused frequent vomiting and diarrhea, extreme fatigue, and almost total hair loss,
cyclophosphamide
is not being considered due its higher occurrence of side effects. Long term high dose steroids, being continued, have produced Cushing's Syndrome.
As methotrexate, now discontinued, caused frequent vomiting and diarrhea, extreme fatigue, and almost total hair loss,
cyclophosphamide
is not being considered due its higher occurrence of side effects. Long term high dose steroids, being continued, have produced Cushing's Syndrome.
irishponies
in
PMRGCAuk
1 year ago
SUDDEN Rise in ESR Pt. 3
As methotrexate, now discontinued, caused frequent vomiting and diarrhea, extreme fatigue, and almost total hair loss,
cyclophosphamide
is not being considered due its higher occurrence of side effects. Long term high dose steroids, being continued, have produced Cushing's Syndrome.
As methotrexate, now discontinued, caused frequent vomiting and diarrhea, extreme fatigue, and almost total hair loss,
cyclophosphamide
is not being considered due its higher occurrence of side effects. Long term high dose steroids, being continued, have produced Cushing's Syndrome.
irishponies
in
Vasculitis UK
1 year ago
Reply to issues with Spleen
Hi, I agree with most of these comments on here that the enlargement of your spleen is an indication perhaps that you are ready for some form of treatment, not removal. I had chemotherapy in 2020 and my spleen was massive. After a treatment cycle of FCR for 6 months and neutropenia sepsis for 10
Hi, I agree with most of these comments on here that the enlargement of your spleen is an indication perhaps that you are ready for some form of treatment, not removal. I had chemotherapy in 2020 and my spleen was massive. After a treatment cycle of FCR for 6 months and neutropenia sepsis for 10
Roseneath69
in
CLL Support
12 days ago
Recently started Acalabrutinib
Hi everyone, My father has recently started Acalabrutinib 5 days ago. He was diagnosed with CLL in 2007 and has received FCR (twice) and Benda-Ritux once. His CLL only went into partial remission on benda-ritux and has come back after one year since his last cycle of BR. I am worried regarding the
Hi everyone, My father has recently started Acalabrutinib 5 days ago. He was diagnosed with CLL in 2007 and has received FCR (twice) and Benda-Ritux once. His CLL only went into partial remission on benda-ritux and has come back after one year since his last cycle of BR. I am worried regarding the
Healthgiddy
in
CLL Support
18 days ago
uMRD 6
I have been living for the one year point on V plus O to get the clonal sequence uMRD6 bone marrow test done so I could decide if I wanted to continue with a Venetaclax. Technically, I consider myself partially treated rather than relapsed or refractory, because I only received three of the six cycles
I have been living for the one year point on V plus O to get the clonal sequence uMRD6 bone marrow test done so I could decide if I wanted to continue with a Venetaclax. Technically, I consider myself partially treated rather than relapsed or refractory, because I only received three of the six cycles
skipro
in
CLL Support
1 month ago
Wife getting MMR vaccine booster - isolate or not?
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
xpro3
in
CLL Support
2 months ago
Solutions needed to manage nerve pains ( Post herpetic neuralgia ) after shingles .
I was diagnosed of CLL in 2021. Had FCR as first line treatment. Was on remission for about a year before relapse. Currently on Ibrutinib since 5 months now. I had shingles on my left leg about 3 months ago. Was treated with Acyclovir. The sores and blisters have gone but the nerve pains( especially
I was diagnosed of CLL in 2021. Had FCR as first line treatment. Was on remission for about a year before relapse. Currently on Ibrutinib since 5 months now. I had shingles on my left leg about 3 months ago. Was treated with Acyclovir. The sores and blisters have gone but the nerve pains( especially
Oldscores1
in
CLL Support
2 months ago
Epithelial Haemangiendothelioma - has anyone else been diagnosed with this rare cancer please?
Hello, Having been diagnosed with CLL back in February 2002 (age 50) I was successfully treated with FCR from August 2009 to February 2010 and remain MRD negative as at present. Breast cancer followed in April 2016, then bowel cancer in September 2018. A five year surveillance period followed the
Hello, Having been diagnosed with CLL back in February 2002 (age 50) I was successfully treated with FCR from August 2009 to February 2010 and remain MRD negative as at present. Breast cancer followed in April 2016, then bowel cancer in September 2018. A five year surveillance period followed the
alipali
in
CLL Support
2 months ago
Shingrix side effects
just wondered what people’s experiences are with side effects after Shingrix? I had the first vaccine and was ill the next day with headaches, chills and feeling awful. However after the second vaccine the side effects have been worse, add in : headaches, unable to concentrate, weakness and wave upon
just wondered what people’s experiences are with side effects after Shingrix? I had the first vaccine and was ill the next day with headaches, chills and feeling awful. However after the second vaccine the side effects have been worse, add in : headaches, unable to concentrate, weakness and wave upon
Mandy56
in
CLL Support
2 months ago
splashsplash
UK based, CLL for 15 years, Treatments: FC, FCR, Ibrutinib, Venetoclax for 2.5 years, 6 month break now back on Venetoclax
UK based, CLL for 15 years, Treatments: FC, FCR, Ibrutinib, Venetoclax for 2.5 years, 6 month break now back on Venetoclax
splashsplash
in
CLL Support
4 months ago
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