Cellcept vs Endoxan

[Voeltjie]

Hi i have been on cellcept 1g x2 day, they changed it to Endoxan , does anyone have experience with endoxan.

[lupus-support1 Administrator]

Welcome to LUpus Patients Understanding & Support (LUPUS) at HealthUnlocked!

You do not say precisely why you have changed to Cyclophosphamide (“cyclo” or “endoxan”) - is this for lupus nephritis?

We do have another website where you can find more information about Cyclophosphamide (“cyclo” or “endoxan”). You can also post questions and talk with other people. All you need to do is to register or open an account and then Search for information/

I have sent you a private message with details.

If you want to talk further, either post here again or email me roz [at] [lupus-support] [dot] [org] [dot] [uk]

With good wishes,

Ros

[Freckle1000 Volunteer in reply to lupus-support1]

Dear Ros.

I'm experiencing lupus nephritis and treatment/medication problems.

I was wondering whether you could tell me about you're other website, etc. that you recommended for voeltjie

: )

[lupus-support1 Administrator in reply to Freckle1000]

I have sent you a private message and will repeat it here.

If you have any problems, please email me at: roz [at] [lupus-support] [dot] [org] [dot] [uk]

We have another website called the LuPUS Message Board where you can also post questions and talk to other people. Registration is FREE and we offer free information and free online psychological support. We specialise in psychological support with our own counsellor/psychotherapist available.

By becoming a Member, you will have access to the private forums and because they are private, only Members have access and even bots and search engines are forbidden.

When you register, please use the following format for entering your date of birth: nn-nn-nnnn where n=number. Please use the "-" separator and not "/".

Finally, please go to: lupus-support.org/LuPUSMB and Sign Up.

I look forward to talking with you more!

Sometimes we need to talk to people who understand and who are not family or friends.

With good wishes!

Ros

Disclaimer: No attempt is made to diagnose or to make any medical judgement. You are advised to seek the advice from your own physician. LUpus Patients Understanding & Support (LUPUS) is not a substitute for your own doctor.

[Freckle1000 Volunteer in reply to lupus-support1]

Thankyou for that Ros. It sounds like a really excellent set up. I'll definately have a go at participating.

Again,

Many thanks.

[lupus-support1 Administrator in reply to Freckle1000]

I look forward to speaking with you again!

Best wishes,

Ros

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May I request the same, please? I was told Myco may not be strong enough..the next one..With C. I get to hear about bad side effects