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Cyclophosphamide
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cyclophosphamide?
So I was just wondering whether anyone else on here is having
cyclophosphamide
as treatment? if so how are you coping with it?
So I was just wondering whether anyone else on here is having
cyclophosphamide
as treatment? if so how are you coping with it?
Priya_S
in
LUPUS UK
10 years ago
I have cerebral vasculitis and also pmr, I finished a second course of cyclophosphamide Mid march, I was ok until about three weeks ago when
I had a chest infection, since both vasculitis and pmr have flared, any idea,s if this could be due to chest infection have had a course on antibiotics.?
I had a chest infection, since both vasculitis and pmr have flared, any idea,s if this could be due to chest infection have had a course on antibiotics.?
Louzoejf29
in
Vasculitis UK
10 years ago
Low platelet count. How long before this recovers ?
I started my first course of FC(without R for the first course) six weeks ago. WBC down from 139.3 to 14.4 which seems a good start. However, my platelet count is now 68 and my consultant wants this to recover before my next FCR and has put me on Folic acid tablets. Does anyone know how long this
I started my first course of FC(without R for the first course) six weeks ago. WBC down from 139.3 to 14.4 which seems a good start. However, my platelet count is now 68 and my consultant wants this to recover before my next FCR and has put me on Folic acid tablets. Does anyone know how long this
Haileybury
in
CLL Support
10 years ago
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Who's on what anti-sickness drugs?
Hi guys, I have just finished FCR chemo 4 of 6. Every chemo has knocked me sideways on the 5 days i take "c+r" but the sickness has just got worse and worse. It was thought i would only have 4 sessions as treatment has gone so well but they now want me to complete the 6 as its hoped it will make me MRD
Hi guys, I have just finished FCR chemo 4 of 6. Every chemo has knocked me sideways on the 5 days i take "c+r" but the sickness has just got worse and worse. It was thought i would only have 4 sessions as treatment has gone so well but they now want me to complete the 6 as its hoped it will make me MRD
grizzlebear
in
CLL Support
10 years ago
On FCR and mum has shingles
The title says it all ! Im on round 4 and have a little neutropenia after my chemo's. My mum has shingles which she gets a lot. How long should i stay away for? she had it 2 weeks ago and her rash has just gone. I dont want to risk anything as i believe shingles is bad if your on Chemo.
The title says it all ! Im on round 4 and have a little neutropenia after my chemo's. My mum has shingles which she gets a lot. How long should i stay away for? she had it 2 weeks ago and her rash has just gone. I dont want to risk anything as i believe shingles is bad if your on Chemo.
grizzlebear
in
CLL Support
10 years ago
Rehearsing being 'In Remission'
Hello all, I just wanted to say: "I've finished chemo and I'm in remission". It's as if I need to practice saying that to remind me that there was an endpoint to the treatment, and that I can now use the word 'remission' to describe my CLL status. Another new word (and world) to learn to inhabit.
Hello all, I just wanted to say: "I've finished chemo and I'm in remission". It's as if I need to practice saying that to remind me that there was an endpoint to the treatment, and that I can now use the word 'remission' to describe my CLL status. Another new word (and world) to learn to inhabit.
jibs60
in
CLL Support
10 years ago
Hello everyone just joined.
On steroids, and
Cyclophosphamide
to try to slow down my deterioration. What I wanted to ask is I have had all the tests done and sent off to Newcastle and am awaiting a call to visit them for a consultation re Lung Transplant.
On steroids, and
Cyclophosphamide
to try to slow down my deterioration. What I wanted to ask is I have had all the tests done and sent off to Newcastle and am awaiting a call to visit them for a consultation re Lung Transplant.
suemaz
in
Lung Conditions Community Forum
10 years ago
Anybody out there had 7 cycles of FCR treatment for CLL rather than the usual 6?
I have had 4 treatments but have concerns, shared by my consultant, that I will still have lumps in my neck after the 6th and final treatment. Wondering what other options there might be rather than just going back on watch and wait with lumps in my neck.
I have had 4 treatments but have concerns, shared by my consultant, that I will still have lumps in my neck after the 6th and final treatment. Wondering what other options there might be rather than just going back on watch and wait with lumps in my neck.
yorkie19
in
CLL Support
10 years ago
Is there anything that can be done if lumps in neck remain after 6 cycles of FCR treatment?
Due to have 5th cycle of FCR treatment next week and although lumps in neck are much reduced they are still significant in size : two of them about 2.5cm across, one on each side under the jaw line. Saw consultant yesterday and he agrees it is unlikely that the lumps will disappear even after the 6th
Due to have 5th cycle of FCR treatment next week and although lumps in neck are much reduced they are still significant in size : two of them about 2.5cm across, one on each side under the jaw line. Saw consultant yesterday and he agrees it is unlikely that the lumps will disappear even after the 6th
yorkie19
in
CLL Support
10 years ago
Pain in the bone at the injection side
My mother has completed her 3rd chemotherapy with adriamycin and
cyclophosphamide
on 9 April,2014.But today she is feeling pain in her hand and arm bones where she has has taken her injection , Is it serious ? What we will do ?
My mother has completed her 3rd chemotherapy with adriamycin and
cyclophosphamide
on 9 April,2014.But today she is feeling pain in her hand and arm bones where she has has taken her injection , Is it serious ? What we will do ?
pritompaul
in
Breast Cancer India
10 years ago
Had my first course of FCR with great blood results. Consultant tells me I have the 11Q variation. What will this mean in the future ? David
Haileybury
in
CLL Support
10 years ago
CLL Results - Blood - Full Blood Count - In order of significance
I have my blood test (taken at 7th May 2014) results. They are the first since my 2nd round of FCR on 17th April 2014. This intrigues me and I trust someone could enlighten me – Given that the consensus of contributors to this site is that the Absolute Lymphs merits exclusive attention, primarily – How
I have my blood test (taken at 7th May 2014) results. They are the first since my 2nd round of FCR on 17th April 2014. This intrigues me and I trust someone could enlighten me – Given that the consensus of contributors to this site is that the Absolute Lymphs merits exclusive attention, primarily – How
Bribin
in
CLL Support
10 years ago
Starting with FCR treatment tomorrow. Can I continue to enjoy a glass of red wine in the evenings .
Haileybury
in
CLL Support
10 years ago
Fertility after FCR
I am aware that most people with CLL are of an age where they are past thinking of having children but I was wondering if anyone with CLL who has had FCR has gone onto to have children naturally or with IVF? I have recently got married and having a baby 'was' our next dream until treatment of FCR was
I am aware that most people with CLL are of an age where they are past thinking of having children but I was wondering if anyone with CLL who has had FCR has gone onto to have children naturally or with IVF? I have recently got married and having a baby 'was' our next dream until treatment of FCR was
Fishface
in
CLL Support
10 years ago
Any CLL patients close to my age of 29?
I was diagnosed with CLL at the age of 27 in 2012 and have just commenced FCR April 2014. I was wondering if there are any CLL patients close to my age of 29 to share experiences as I am repeatedly told that I am very young to be diagnosed with CLL at this age as it is more commonly found in people in
I was diagnosed with CLL at the age of 27 in 2012 and have just commenced FCR April 2014. I was wondering if there are any CLL patients close to my age of 29 to share experiences as I am repeatedly told that I am very young to be diagnosed with CLL at this age as it is more commonly found in people in
Fishface
in
CLL Support
10 years ago
Treatment of My Father suffering from CLL with Endoxan (Cyclophosphamide) and Bendit--Bendamustine Hydrochloride.
He has started Chemotherapy with Endoxan (
Cyclophosphamide
) and did 06 Cycles of chemo (Each after 21-Days). After that we have performed test from Hospital as advised by the Doctor and %LYM values reduced / down to 53 % as per attached reports of CBC and B2M.
He has started Chemotherapy with Endoxan (
Cyclophosphamide
) and did 06 Cycles of chemo (Each after 21-Days). After that we have performed test from Hospital as advised by the Doctor and %LYM values reduced / down to 53 % as per attached reports of CBC and B2M.
nadeemnaz4190
in
CLL Support
10 years ago
daft question, but when taking Cyclophosphamide on an empty stomach - how soon can I have breakfast?
I should have asked the pharmacist or doc but keep forgetting until I take my 11 tablets then think "Oh beggar!"
I should have asked the pharmacist or doc but keep forgetting until I take my 11 tablets then think "Oh beggar!"
djgolding
in
CLL Support
10 years ago
My CLL journey with a bone marrow thingie and FCR thrown in.
Thursday morning, as instructed, I had to start my F= Fludarabine and C=
Cyclophosphamide
tablets. 16 pills between them plus an assortment of other tablets. Friday and Saturday same routine.
Thursday morning, as instructed, I had to start my F= Fludarabine and C=
Cyclophosphamide
tablets. 16 pills between them plus an assortment of other tablets. Friday and Saturday same routine.
Bribin
in
CLL Support
10 years ago
A shorter treatment plan???
Hi, I started FCR for cll earlier this year as my WBC was just rising so fast. Im only 45 so it was inevitable that i would need treatment at some point.Because i had lots of little masses my Onc thought it best to start a little early so they didnt become bulky. Also my submalinder glands were getting
Hi, I started FCR for cll earlier this year as my WBC was just rising so fast. Im only 45 so it was inevitable that i would need treatment at some point.Because i had lots of little masses my Onc thought it best to start a little early so they didnt become bulky. Also my submalinder glands were getting
grizzlebear
in
CLL Support
10 years ago
Fingers crossed!
Hi all .... just thought I would add my tuppenceworth and share my experience of CLL treatment. Diagnosed in Oct 2009 at age 47 with 'Watch & Wait' (lymphocyte count 16) ..... however by Jan 2011 my lymphocyte count was around 130 so was offered treatment on a Clinical Trial at Southampton General Hospital
Hi all .... just thought I would add my tuppenceworth and share my experience of CLL treatment. Diagnosed in Oct 2009 at age 47 with 'Watch & Wait' (lymphocyte count 16) ..... however by Jan 2011 my lymphocyte count was around 130 so was offered treatment on a Clinical Trial at Southampton General Hospital
Timobeanie
in
CLL Support
10 years ago
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