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Cyclophosphamide
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Chemo in Tablet Form
I have been offered chemo in tablet form called
Cyclophosphamide
and wondered if anyone is on this or has been on this and might have positive feedback. Many thanks xx
I have been offered chemo in tablet form called
Cyclophosphamide
and wondered if anyone is on this or has been on this and might have positive feedback. Many thanks xx
Flute_7
in
My Ovacome
3 months ago
insurance issue
doctor recommended the below medications : Paclitaxel +
cyclophosphamide
+ phesgo+ zolodronic acid . I have corporate insurance in new India insurance with mediassist. These people are not approving phesgo which is targeted therapy telling that it is as immunotherapy instead of targeted .
doctor recommended the below medications : Paclitaxel +
cyclophosphamide
+ phesgo+ zolodronic acid . I have corporate insurance in new India insurance with mediassist. These people are not approving phesgo which is targeted therapy telling that it is as immunotherapy instead of targeted .
Srikalakm
in
Breast Cancer India
3 months ago
Lupkinis plus MMF most effective in lupus nephritis; tacrolimus safest
Most studies compared the effectiveness of MMF versus intravenous (into the vein, IV)
cyclophosphamide
or IV
cyclophosphamide
versus tacrolimus. Two studies compared Lupkinis, given in combination with MMF, with MMF alone.
Most studies compared the effectiveness of MMF versus intravenous (into the vein, IV)
cyclophosphamide
or IV
cyclophosphamide
versus tacrolimus. Two studies compared Lupkinis, given in combination with MMF, with MMF alone.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 months ago
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From high hopes to not a lot of hope in one gruelling morning.
To add insult to injury Dr Google says
cyclophosphamide
can actually cause ILD and pulmonary fibrosis so I won't be consulting that again.
To add insult to injury Dr Google says
cyclophosphamide
can actually cause ILD and pulmonary fibrosis so I won't be consulting that again.
DaveLister
in
Lung Conditions Community Forum
4 months ago
Re-introduction
I was diagnosed with GPA in 2012, which made a hole in my nose, and after treatment with
cyclophosphamide
, azathioprine, and then rituximab, I have now been in remission for several years. The hole in my nose is filled with a silicone prosthesis.
I was diagnosed with GPA in 2012, which made a hole in my nose, and after treatment with
cyclophosphamide
, azathioprine, and then rituximab, I have now been in remission for several years. The hole in my nose is filled with a silicone prosthesis.
suffolkgirl
in
Vasculitis UK
6 months ago
anyone with Churg Strauss come off all medication?
I initially had
cyclophosphamide
and have been on high doses of steroids but reduced over time Thank you
I initially had
cyclophosphamide
and have been on high doses of steroids but reduced over time Thank you
Katie18
in
Vasculitis UK
4 months ago
Hearing loss/pain/tinnitus
I was diagnosed with EGPA in December 2020, following intensive treatment including
cyclophosphamide
infusions I went into remission the following April. Since then I am on a drug regime that includes Azathioprine and Prednisolone. I am currently tapering down the latter with a view to stopping.
I was diagnosed with EGPA in December 2020, following intensive treatment including
cyclophosphamide
infusions I went into remission the following April. Since then I am on a drug regime that includes Azathioprine and Prednisolone. I am currently tapering down the latter with a view to stopping.
MIK65
in
Vasculitis UK
4 days ago
Quite the CLL journey
O (Obinutuzumab) CHOP (DOXORUBICIN (Adiamycin), vinCristine (Oncovin),
cyclophosphamide
(Cytoxan), Prednisone) plus Neulasta ejections. April-May 2024 3 cycles of O CHOP until BMT in Later June. BMT donor 10/10 match June 17.
O (Obinutuzumab) CHOP (DOXORUBICIN (Adiamycin), vinCristine (Oncovin),
cyclophosphamide
(Cytoxan), Prednisone) plus Neulasta ejections. April-May 2024 3 cycles of O CHOP until BMT in Later June. BMT donor 10/10 match June 17.
FiArt12X
in
CLL Support
5 days ago
Help me! behcet syndrome with tuberculosis
I have tried all the medical treatments for Behcet's disease such as: cyclosporine,
cyclophosphamide
, infliximab, adalimumab, colchicine, azathioprine, and methotrexate, and every time after taking these drugs, the heartburn worsens and I get perianal fistula.
I have tried all the medical treatments for Behcet's disease such as: cyclosporine,
cyclophosphamide
, infliximab, adalimumab, colchicine, azathioprine, and methotrexate, and every time after taking these drugs, the heartburn worsens and I get perianal fistula.
Hulusi
in
Behçet's UK
4 months ago
Avacopan (Tavneos®) is accepted for use within NHSScotland.
Full details posted here: https://www.scottishmedicines.org.uk/media/7938/avacopan-tavneos-final-oct-2023-for-website.pdf Indication under review: In combination with a rituximab or
cyclophosphamide
regimen, for the treatment of adult patients with severe, active granulomatosis with polyangiitis (GPA
Full details posted here: https://www.scottishmedicines.org.uk/media/7938/avacopan-tavneos-final-oct-2023-for-website.pdf Indication under review: In combination with a rituximab or
cyclophosphamide
regimen, for the treatment of adult patients with severe, active granulomatosis with polyangiitis (GPA
JaneLE
Administrator
in
Vasculitis UK
7 months ago
Rituximab- my experience.
I had Rituximab + dexamethasone+
cyclophosphamide
after that for 12 cycles over 10 months. (I had bad nausea with the
cyclophosphamide
for up to a week after each infusion). Remission again only lasted around 3 months.
I had Rituximab + dexamethasone+
cyclophosphamide
after that for 12 cycles over 10 months. (I had bad nausea with the
cyclophosphamide
for up to a week after each infusion). Remission again only lasted around 3 months.
Hidden
in
CLL Support
9 months ago
Behcet and very bad mouth ulcers in throat and esopshagus
Now suddenly I am on prednisolone,
Cyclophosphamide
6x therapies, little time i had chlorocine. I feel that my immune system is falling apart. 4 times i was in hospital from may I was that bad. Now they say in the future i will take Adalimumab injections for some period.
Now suddenly I am on prednisolone,
Cyclophosphamide
6x therapies, little time i had chlorocine. I feel that my immune system is falling apart. 4 times i was in hospital from may I was that bad. Now they say in the future i will take Adalimumab injections for some period.
Enyce
in
Behçet's UK
8 months ago
Transformation of Richter's Transformation Treatment to combination targeted therapy - tislelizumab +zanubrutinib (ASH 2023)
Richter's transformation" [/i] [i] [/i] Here's the paper from German CLL study group authors at the University of Cologne [i]https://www.nature.com/articles/s41591-023-02722-9[/i] [i] [/i] *R-CHOP is a combination of; R = Rituximab, an anti-CD20 monoclonal antibody, the 'R' in FCR, BR, VR, etc C =
Cyclophosphamide
Richter's transformation" [/i] [i] [/i] Here's the paper from German CLL study group authors at the University of Cologne [i]https://www.nature.com/articles/s41591-023-02722-9[/i] [i] [/i] *R-CHOP is a combination of; R = Rituximab, an anti-CD20 monoclonal antibody, the 'R' in FCR, BR, VR, etc C =
Cyclophosphamide
AussieNeil
Partner
in
CLL Support
6 months ago
CLL then long remission and now Myeloma
I was treated with Chemotherapy again (Bortezimib,
Cyclophosphamide
,Dexamethazone) I achieved a good partial remission and now having a bone strengthener infusion called Zonedronic acid once a month. Apparently Myeloma is a cancer of the blood plasma cell which is also linked to the B cell.
I was treated with Chemotherapy again (Bortezimib,
Cyclophosphamide
,Dexamethazone) I achieved a good partial remission and now having a bone strengthener infusion called Zonedronic acid once a month. Apparently Myeloma is a cancer of the blood plasma cell which is also linked to the B cell.
keepfit123
in
CLL Support
11 months ago
Anyone been prescribed cyclophosphamide as a steroid sparer?
They have just changed his methotrexate to
cyclophosphamide
- I have not read anyone on here that has been prescribed this. Feel for them as they have zero experience of anyone ever being ill and it is a lot.
They have just changed his methotrexate to
cyclophosphamide
- I have not read anyone on here that has been prescribed this. Feel for them as they have zero experience of anyone ever being ill and it is a lot.
Sophiestree
in
PMRGCAuk
9 months ago
CLL survival times ARE improving, thanks to BTK and BCL-2 inhibitors
Those older chemoimmunotherapy treatments, typically Bendamustine + Rituximab (BR) or Fludarabine +
Cyclophosphamide
+ Rituximab (FCR), selected for tougher to treat sub-clones, which they cause through inducing DNA damage that will hopefully trigger apoptosis [u]if[/u] the TP53 gene isn't mutated or
Those older chemoimmunotherapy treatments, typically Bendamustine + Rituximab (BR) or Fludarabine +
Cyclophosphamide
+ Rituximab (FCR), selected for tougher to treat sub-clones, which they cause through inducing DNA damage that will hopefully trigger apoptosis [u]if[/u] the TP53 gene isn't mutated or
AussieNeil
Partner
in
CLL Support
2 months ago
Physiotherapy
I was diagnosed in October last year and treatment (
cyclophosphamide
) was going well. No symptoms. I have finished that course and am now on mycophenolate tablets. I have severe lower back pain and am getting no where trying to get a physio referral.
I was diagnosed in October last year and treatment (
cyclophosphamide
) was going well. No symptoms. I have finished that course and am now on mycophenolate tablets. I have severe lower back pain and am getting no where trying to get a physio referral.
CotswoldOx
in
Myositis UK
3 months ago
PICC LINE CATHETER FOR SYSTEMIC SCLEROSIS
Recently, my doctors planned to prescribe intravenous
cyclophosphamide
and methylprednisolone to help manage my condition. However, due to the vasculitis affecting my veins, medical professionals are facing challenges accessing my veins for the required treatments.
Recently, my doctors planned to prescribe intravenous
cyclophosphamide
and methylprednisolone to help manage my condition. However, due to the vasculitis affecting my veins, medical professionals are facing challenges accessing my veins for the required treatments.
Lo1234
in
Scleroderma & Raynaud's UK (SRUK)
10 months ago
lymphocytes/neutrophils
After 5 of 6 of fludarabine
cyclophosphamide
rituximab I went into semi remission and now after many hospitalizations with infection have IVIG once a month that works quite well at keeping me out of the hospital.
After 5 of 6 of fludarabine
cyclophosphamide
rituximab I went into semi remission and now after many hospitalizations with infection have IVIG once a month that works quite well at keeping me out of the hospital.
Kimsome
in
CLL Support
9 months ago
Antineutrophilic cytoplasmic antibody (ANCA) Vasculitis
Treatment for vasculitis includes using steroids along with other medication the suppress the immune system, such as
cyclophosphamide
or rituximab. I am not coughing up blood like one of the symptoms. But I cough a lot, very thick clear mucus.
Treatment for vasculitis includes using steroids along with other medication the suppress the immune system, such as
cyclophosphamide
or rituximab. I am not coughing up blood like one of the symptoms. But I cough a lot, very thick clear mucus.
EllaNore
in
Pernicious Anaemia Society
1 year ago
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