Cytoxan(Cyclophosphamide: Hello to All... - Encephalitis Inte...

Encephalitis International

714 members521 posts

Cytoxan(Cyclophosphamide

NebraskaTexas profile image
5 Replies

Hello to All,

My husband had an appointment with his neurologist today. The latest MRI indicates he still has Encephalitis. With the latest cocktail of meds, (prednisone, mycophenolate and Rituxan) his doctor thought the encephalitis would show improvement or be totally gone by now.

His doctor is talking about taking him off mycophenolate and Rituxan and add infusions of Cytoxan.

I was wondering if anyone has had experience with Cytoxan.

On a brighter note, we have a new member to our family. Her name is Bella. Bella adds life and joy to our home and takes our minds off our problems. Our other dog a Rat Terrier named Little Bit and our 2 cats, Kitty and KitKat are adjusting slowly. I have included a picture of Bella.

Thanks again for everyone posting their experience on this sight. Your experiences helps me immensely as a caregiver.

Nebraska/Texas

Written by
NebraskaTexas profile image
NebraskaTexas
To view profiles and participate in discussions please or .
Read more about...
5 Replies
Gandalf2 profile image
Gandalf2

Hi Nebraska, I don't know if you have made any progress with Cytoxan information. I haven't been prescribed it but I am on a similar drug called 'prednisolone', - many side effects, it seems you can't take an immune suppressant without them.

Here is a reputable site that provides plenty of information on a complete range of drugs including Cytoxan, including reviews from various patients.

drugs.com/comments/cyclopho...

Good luck! :-)

NebraskaTexas profile image
NebraskaTexas in reply toGandalf2

Thanks Gandalf2 for your help. I did not know about this website. I found it very helpful.

Gandalf2 profile image
Gandalf2 in reply toNebraskaTexas

Hi Nebraska, thank you for getting back. I found the website very good too - more detailed than the leaflets that come with the medication and the reviews are very helpful. Good luck with your husband's recovery - it's a long road but things do improve and summer is on its way. Best Wishes G2

jujumello82 profile image
jujumello82

Hi there,

The Cytoxan was the only med that was able to control my partners autoimmune encephalitis. They tried everything… 2 weeks after the first treatment we started to see improvements. He had to do 3 rounds.

Best

J

NebraskaTexas profile image
NebraskaTexas in reply tojujumello82

Thanks Jujumello82. Thanks for letting me know your partner had this drug and it helped. My husband has been through all the other treatments and this will be the next and hopefully the last one. Regards,

Not what you're looking for?

You may also like...

Has anyone had viral encephalitis turn into autoimmune encephalitis??

My father is still in the new hospital we took him in for a second opinion his MRI showed small...
Catmom8727 profile image

Changing relationship with parents

My parents have been with me through this 17 year journey every step of the way. Over the years...
RED1224 profile image

Encephalitis from Covid

Hi, my dad is in icu from covid, he is not waking from the induced coma, it has now been 16 days...
Miltch profile image

Update.. My Dad is in John Radcliffe hospitol Oxford

Hello thank you for your replies, it helps to know there are others who have experience of...
Mouseling profile image

Autoimmune encephalitis

My husband was diagnosed with autoimmune limbic encephalitis in 2024 (age 52). Both GAD65 and LGI1...
Konemor profile image

Moderation team

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.