CLADRIBINE vs Natalizumab

Does anyone have a knowledge or experience of Cladribine? https://www.bbc.co.uk/news/articles/czxnp0ej81vo

And ALWAYS get multiple opinions. I had a follow up MRI, post cladribine, was told by the free government neuro, my brain was “a ticking time bomb” and the “ship had sailed” to prevent disability from the 20 new lesions in my brain. She also said “the MRIs don’t lie” Obviously that crushed me. But

I’m wondering if there’s anyone here with this personal experience and how it has affected work? I’m in my mid 30s, working in an Emergency Department. While I have my moments of GOD WHY (especially when walking into nights shifts) I generally enjoy work and feedback so far has been that I could do

Very curious what experiences/drugs/trials everyone else has had during their treatment path. My mother's has been very long and ever changing, far more than I initially expected when doing a lot of research right as she was diagnosed (I'm very science based so lots of google scholar articles etc)

38 y/o male, diagnosed 12/18/24 Initially showed as pancytopenia. **Symptoms pre-diagnosis:** - More fatigue than usual, was falling asleep on the couch more in the evenings. - Partner felt I had decreased appetite. At my routine physical after telling my doctor about these issues and how frequentl

Hi, I am a 44m, in pretty good shape. I had to see a Hematologist due to low platelet counts back in January, after a bit of testing and a bone marrow biopsy, HCL was confirmed. I just finished the cladribine treatment for Hairy Cell Leukemia this past week. It was 5 days straight. I now have a 4 we

Hi there, I've been diagnosed with MS in 2021 and have been taking Plegridy (an interferon beta 1a therapy) since 2022. My last scan unfortunately still showed new lesions, so my neurologist suggested I change my therapy. The options he gave me are: - Dimethylfumerat (Tecfidera) - Cladribin (Mavencl

Hello everyone. I'm from Ireland. I was diagnosed with multiple sclerosis last April and started my first round of Mavenclad treatment for it this past week. I also suffer from Obsessive Compulsive Disorder and have done so for the past 20 years. Unfortunately the OCD has been quite resistant to tre

Study this article is based on: https://jamanetwork.com/journals/jama/article-abstract/2720726 Source: https://www.zmescience.com/science/multiple-sclerosis-treatment-82534524/ The worst of multiple sclerosis can be avoided or delayed with early treatment LAST UPDATED ON JANUARY 19TH, 2019 AT 6:21 P

# [Results of 2b/3 clinical trial for Dupuytren’s Disease’ Being Presented Wednesday, December 1, 2021, at 3pm EST](https://ir.180lifesciences.com/news-events/press-releases/detail/49/180-life-sciences-corp-co-founder-prof-jagdeep-nanchahal) Top line data for Dupuytren's disease phase 2b/3 clinical

Hi everyone. I have recently had a PML scare, got the all clear this morning (yay!), and thought it may be of interest to people here who have worries about PML. I am based in the UK, and the neuro services for the county are provided by a different hospital Trust. I was diagnosed back in 2011. I tr

edit: article below says it's rare. far below there are actual numbers of incidents reported and more details. ​ FDA direct link: [https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm626264.htm](https://www.fda.gov/Safety/MedWatch/SafetyInformat

# [Results of 2b/3 clinical trial for Dupuytren’s Disease’ Being Presented Wednesday, December 1, 2021, at 3pm EST](https://ir.180lifesciences.com/news-events/press-releases/detail/49/180-life-sciences-corp-co-founder-prof-jagdeep-nanchahal) Top line data for Dupuytren's disease phase 2b/3 clinical

Hi all, First time poster here! Unfortunately I, (27/f), have joined the MS club, not a club I wanted to join, but I just wanted to say how grateful I am for this community. Makes me not feel so alone. I first got diagnosed after having optic neuritis in my left eye a month ago, my sight is slowly

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*(A bit long but worth it)* **People with multiple sclerosis (MS) have significantly more T-cells equipped with receptors that specifically recognize the Epstein-Barr virus (EBV) than do healthy individuals, a study revealed.** Notably, no such differences were detected for T-cells with receptors sp