Cladribine
Just wondered if anyone could share their experience of taking Cladribine? I’ve had RRMS for about 15 years with thankfully minor symptoms of numbness and fatigue with 4 relapses during this time , the last being this time last year. I’ve now been offered Cladribine which will the first drug I will have taken for RRMS and am slightly nervous so would welcome any advice. Thanks, Sara 😋
There was a new member on here the other day who had been on it a couple of yrs i think: @Precious20
I started Cladribine in April 2024, had my 2nd treatment this year, no real side effects and no relapse yet 🤞I 100% would recommend it, I just hope it continues to work for me, good luck with your decision