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Cladribine
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Cladribine
I'd appreciate hearing the views and feedback from others who've taken this
Cladribine
drug
I'd appreciate hearing the views and feedback from others who've taken this
Cladribine
drug
max011
in
My MSAA Community
4 months ago
Cladribine for MS
I have started
Cladribine
injection recently. I have change from Ocrelizumab.I would like to know the positive effect of
cladribine
on my mobility.
I have started
Cladribine
injection recently. I have change from Ocrelizumab.I would like to know the positive effect of
cladribine
on my mobility.
Sanoosh
in
My MSAA Community
1 year ago
What insurance for Mavenclad
He is taking Mavenclad (
Cladribine
), 7 tablets in August, 7 more in September. He has a few days left to find insurance on healthcare.gov. He’s in Texas. I am helping him with some research. On the healthcare.gov site I can filter for policies which include his doctor and Mavenclad.
He is taking Mavenclad (
Cladribine
), 7 tablets in August, 7 more in September. He has a few days left to find insurance on healthcare.gov. He’s in Texas. I am helping him with some research. On the healthcare.gov site I can filter for policies which include his doctor and Mavenclad.
JustAGuy
in
My MSAA Community
1 year ago
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Newly Released Real World Mavenclad Study
This study gives me pause because it states: “Moreover, we identified better outcomes in patients exposed to a lower number of previous DMTs, suggesting that
cladribine
might be more effective when placed as an early treatment along the treatment algorithm.” I’ll be talking to my neuro about this.
This study gives me pause because it states: “Moreover, we identified better outcomes in patients exposed to a lower number of previous DMTs, suggesting that
cladribine
might be more effective when placed as an early treatment along the treatment algorithm.” I’ll be talking to my neuro about this.
Raingrrl
in
My MSAA Community
2 years ago
Hairy cell leukaemia - 3 months after chemo
Looking back to April when I was in hospital for 2 separate weeks with sepsis, then had my subcutaneous
cladribine
treatment in May, now it feels like I'm a different person.
Looking back to April when I was in hospital for 2 separate weeks with sepsis, then had my subcutaneous
cladribine
treatment in May, now it feels like I'm a different person.
frankmok
in
Leukaemia CARE
3 years ago
Hairy cell - 3 weeks after chemo
So here I am 3 weeks after my
cladribine
subcutaneous chemo finished. Am having weekly blood tests, had a phone chat with my haematologist this morning who is happy the way my platelets and neutrophiles are recovering - plats up to 138 and neuts 0.6, both doubled from a week ago.
So here I am 3 weeks after my
cladribine
subcutaneous chemo finished. Am having weekly blood tests, had a phone chat with my haematologist this morning who is happy the way my platelets and neutrophiles are recovering - plats up to 138 and neuts 0.6, both doubled from a week ago.
frankmok
in
Leukaemia CARE
3 years ago
Hairy cell leukaemia - treatment update
My background is I was diagnosed with the hairies back in 2003 and treated with a
cladribine
drip, so I've had a good 17 year run before needing more chemo though in retrospect I probably should have had chemo 3 or 4 years ago. I'm now 72.
My background is I was diagnosed with the hairies back in 2003 and treated with a
cladribine
drip, so I've had a good 17 year run before needing more chemo though in retrospect I probably should have had chemo 3 or 4 years ago. I'm now 72.
frankmok
in
Leukaemia CARE
3 years ago
Post Treatment and Perimenopause
I am 49 years old and had
Cladribine
last January 2020. Whilst recovering at home and them shielding for almost 14 months, I have now returned back to work on a phased return.
I am 49 years old and had
Cladribine
last January 2020. Whilst recovering at home and them shielding for almost 14 months, I have now returned back to work on a phased return.
TM1972
in
Leukaemia CARE
3 years ago
Insomnia or return of HCL
I had chemotherapy(
Cladribine
) in January. Not due a blood test until October, recently started to feel breathless and fatigued. I suffer with insomnia.. Should I contact my consultant and ask for a blood test?
I had chemotherapy(
Cladribine
) in January. Not due a blood test until October, recently started to feel breathless and fatigued. I suffer with insomnia.. Should I contact my consultant and ask for a blood test?
TM1972
in
Leukaemia CARE
4 years ago
Latent TB Start of treatment
I had the test as I have RRMS and I was due to start second year of a drug called
cladribine
which is an immunosupressant. As it turns out second year has been cancelled anyway because of covid 19. I have never had any symptoms and chest x ray was clear. I am on day 3 of 112 of rifampicin.
I had the test as I have RRMS and I was due to start second year of a drug called
cladribine
which is an immunosupressant. As it turns out second year has been cancelled anyway because of covid 19. I have never had any symptoms and chest x ray was clear. I am on day 3 of 112 of rifampicin.
Octavia1968
in
TB Alert
4 years ago
Are they faking this serious illness?
So just did radiation..they are taking
Cladribine
, but isnt that for chemo patients? They say nurses come and pick them up for apt's. But on medical insurance. And to top it off they want to take a year off of treatment. None of this makes sense. Am I wrong??? Please leave some insight
So just did radiation..they are taking
Cladribine
, but isnt that for chemo patients? They say nurses come and pick them up for apt's. But on medical insurance. And to top it off they want to take a year off of treatment. None of this makes sense. Am I wrong??? Please leave some insight
Justwantanswers
in
Leukaemia CARE
5 years ago
Hairy Cell Leukaemia
I was treated with
cladribine
. I gained partial remission in December 2018. After a bone marrow biopsy in March 2019 my leukaemia is growing again and I need further treatment. I’m would like to talk to anyone who is having a similar journey Thank you in advance
I was treated with
cladribine
. I gained partial remission in December 2018. After a bone marrow biopsy in March 2019 my leukaemia is growing again and I need further treatment. I’m would like to talk to anyone who is having a similar journey Thank you in advance
Sajsingers
in
Leukaemia CARE
5 years ago
Another MSAA News Update - FDA Approves Mavenclad® (Cladribine) Tablets
I just wanted to share the latest news update that MSAA has posted on their website about the FDA approval of Mavenclad® (
cladribine
) tablets: https://mymsaa.org/mavenclad-approved-fda/ Thank you! Emily
I just wanted to share the latest news update that MSAA has posted on their website about the FDA approval of Mavenclad® (
cladribine
) tablets: https://mymsaa.org/mavenclad-approved-fda/ Thank you! Emily
MSAA_Staff
in
My MSAA Community
5 years ago
VIT B12 deficiency
I had treatment 5 years ago with
Cladribine
. I'm seeing GP on Wednesday following a blood test which said I was low in VIt B12 so just curious and want to go informed! Thank you
I had treatment 5 years ago with
Cladribine
. I'm seeing GP on Wednesday following a blood test which said I was low in VIt B12 so just curious and want to go informed! Thank you
emmieb-UK
in
Leukaemia CARE
5 years ago
MSAA News Update - FDA Accepts Application for Cladribine Tablets
I just wanted to share the latest news update that MSAA posted on their website about the FDA application for
cladribine
tablets: https://mymsaa.org/news/fda-accepts-application-for-
cladribine
-tablets/ Thank you! Emily
I just wanted to share the latest news update that MSAA posted on their website about the FDA application for
cladribine
tablets: https://mymsaa.org/news/fda-accepts-application-for-
cladribine
-tablets/ Thank you! Emily
MSAA_Staff
in
My MSAA Community
6 years ago
Hairy cell leukaemia
It now looks very likely that I will have a course of
cladribine
chemo in the next month or so. My key blood counts have declined, and I have experienced a couple of infections recently - night sweats, weight loss, fatigue etc.
It now looks very likely that I will have a course of
cladribine
chemo in the next month or so. My key blood counts have declined, and I have experienced a couple of infections recently - night sweats, weight loss, fatigue etc.
frankmok
in
Leukaemia CARE
8 years ago
Hairy Cell Leukaemia
I was diagnosed with HCL a year ago yesterday (4/12/2015) and had
cladribine
January this year. Have felt like I was on a conveyor belt and told a number of times if I was to get Leaukemia this was the one to get .... Err no ! Any type is awful to have.
I was diagnosed with HCL a year ago yesterday (4/12/2015) and had
cladribine
January this year. Have felt like I was on a conveyor belt and told a number of times if I was to get Leaukemia this was the one to get .... Err no ! Any type is awful to have.
Dustina8
in
Leukaemia CARE
8 years ago
COPING STRATEGIES for living better with CLL - Part 3 - some extra tips for making good use of "Watch and "Wait"
Fludarabine (FCR) (FR) Bendamustine (BR) probably Pentastatin (PCR.. used at the Mayo)
Cladribine
, not used much anymore If anyone can find changes to this recommendation from any authoratative primary source, like blood service etc. , then I would like to see them.
Fludarabine (FCR) (FR) Bendamustine (BR) probably Pentastatin (PCR.. used at the Mayo)
Cladribine
, not used much anymore If anyone can find changes to this recommendation from any authoratative primary source, like blood service etc. , then I would like to see them.
PaulaS
Volunteer
in
CLL Support
9 years ago
Original Coping strategies for Living with CLL - Part 1- Making good use of "Watch and Wait". Please read new version!
It should list all medications you're on, mention your immuno-compromised status, and if you’ve ever had treatment with one of the "purine analogue" medications (eg Fludarabine (part of FCR treatment), FCR, pentostatin,
cladribine
or bendamustine/rituxan,, it should explain that any blood transfusion
It should list all medications you're on, mention your immuno-compromised status, and if you’ve ever had treatment with one of the "purine analogue" medications (eg Fludarabine (part of FCR treatment), FCR, pentostatin,
cladribine
or bendamustine/rituxan,, it should explain that any blood transfusion
PaulaS
Volunteer
in
CLL Support
9 years ago
Had Fludarabine? You can only have irradiated blood...for life.
'Patients treated with purine analogue drugs (fludarabine,
cladribine
and deoxycoformicin) should receive irradiated blood components indefinitely (1B).
'Patients treated with purine analogue drugs (fludarabine,
cladribine
and deoxycoformicin) should receive irradiated blood components indefinitely (1B).
Cllcanada
Top Poster CURE Hero
in
CLL Support
11 years ago
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