Experiences with

Ciloxan eye drops

has anyone declined cytoxan and had success with cellcept in treating kidney injury? My son has had Eculizumab and Rituximab with no success and is now declining rapidly with kidney function.

Here’s what they gave me: [i]Ciloxan drops, Flucloxacillian 500mg and Otomise spray but I won’t use that I’m positive that’s how I got T in the first place. [/i] I’m not sure what I’m asking for or if I’m just ranting lol

I was diagnosed last fall with limited GPA (in my ears). Was on methotrexate and low dose prednisone until a few weeks ago. Diagnosed with breast cancer in may so taken off the methotrexate when I started chemo last week. One of my chemo drugs is cytoxan. My question is, has anyone else had this

Been dealing with KD for 1.5 years. My doctor has me on a variety of meds that includes-BP, Chol, Lasix,Farxiga,Eliquis, Cytoxan and Prednisone-plus a few more. Always tired. My current EGFR-49, my creatinine level is-1.47, and my urine/protein-14.34. I am suppose to start Rituximab Infusion as

I just wanted to report in. My CA 125 has been kept nicely low via Avastin infusions every six weeks. Over the last few months I noticed a trend of it slowly creeping up, Ie, a two point increase each time. I knew that this was odd and my oncologist agreed. I have started 50 mg oral cytotoxin once a

Has anyone been on oral Cytoxan 50 mg daily to stop tumor growth? If so, what has your experience been? Thank you.

Dear friends, After 1.5 years on Ibrance/Fulvestrant and a very short time in NED status (great while it lasted...) my cancer reappeared this spring. I've just had an axillary lymph node dissection, removing all the known cancerous spots, and now the question is what will be my meds going forward.

Hi all you wonderful women/lovely ladies. Have any of you ever had a chemo called Topotican (sp?) or Gemzar? The Avastin and cytoxan doesn't seem to be working. I go for another cat scan next week to see what's going on. My CA 125 keeps rising and I'm starting to feel bloated and achy. I don't know what's

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

😊 thank you

Hello everyone. My father was diagnosed with metastatic stage 4 PCa in another country (2017). He immediately had bi-lateral orchiectomy, and thereafter when the PSA began to rise, he was prescribed Xtandi (lasted ~6 months) and subsequently had some radiotherapy to the pelvis and spine (pain management

Hello to everyone out there! I’m new to the group - seeking advice from those who have undergone the Euro Lupus Protocol? This is cytoxan (cyclophosphamide) treatments by IV every other week. I understand infusion treatment takes approximately 6 hrs. Sounds very looong to me! What does one do all

The annual American Society of Clinical Oncology (ASCO) conference encompasses multiple types of cancer, and this year many abstracts were submitted about MBC. I’ve reviewed the abstracts and taken the liberty of pasting information about those that were not previously in my book, “The Insider’s Guide

Well I had an appetite today for the first time in 12 days! Food sucks but edible. I think I ate too much even though I still didn’t eat much... For some reason they didn’t start my chemo until super late last night so now it won’t be done until late Friday night. I was very lucky to have visitors

Hi, I am so glad I've found this site as I am just at the start of my vasculitis journey and from what I read, seen and heard I will need all the help I can get. I suspect my immune system got triggered when I donated blood in August 2018 - I got really sick during the process. Nothing unusual, it happens

Hello I was diagnosed in 2006 with BC in the right breast stage 11, lymph node involvement 4. Treatment lumpectomy, 6 cycles every 3 weeks of a cocktail of Taxotere and Adriamycin/Cytoxan (AC) followed by 30 days of radiation. Was 53 yrs old and did really well. Was able to work full time except for

Hello! Everyone I'm going to my initial treatment tomorrow jan. 2, 2019 Happy New Year! 😊😁😂Any advice what to do after getting the infusion. Thanks all. I'm schedule to work the next day but my supervisor give me time to rest very thankful she's very supportive.

For fellow Gleason 10 diagnoses. I found that when I was diagnosed I found it difficult to find any information about what I could expect. I know that none of us have the same reactions to the same medication but still I’ll list what I’ve be through so they might see what could transpire. I was diagnosed

Hi I have been on Cytoxan/Avastin for awhile now I get Avastin IV every 2 wks and take the Oral Pill every day. I have been noticing bad aches and pains. I guess it’s muscle/joint and even bone pain. Anyone else get this. It seems to be worse now . It’s mostly my hips and thigh. I’m also very stiff

On 50 milligrams prednisone until 3 weeks ago. I had to take that amount but it made me feel horrible. I have been decreasing 10 mg weekly for the past 3 weeks. As of two days ago I am now on 20 mg a day with cytoxan every other month daily. When will I feel the decreased effect of taking prednisone