Hello I was diagnosed with MS in 1998 and have been on Copaxone for about ten years then Rebif and now on Tecfidera for about 5 years or so, I am thinking of changing to Mavenclad which recently got FDA approved in the US. I wanted to know from someone in the UK who tried the drug Mavenclad what th…

So many ask does the treatment work, and how are folks getting on after taking it? We’ll I’m a year into taking it and due my second dose in August but I’ve had a review today and the results of my scan from April. My last MRI on Feb last year showed 2 lesions on my brain which I …

Hi all, tomorrow will be the last dose of this year of mavenclad, so far so good. No significant side effects so far thank god. How you are all well. ☺

My wife is an RRMS patient, (32yo) diagnosed in 2012. She is a Bahraini national and I am British, born and raised in UK and now living and working in Dubai. I would very much like to take her to see a specialist in the UK – in London or Birmingham for a second opinion after her neurologist …

hi I’m currently on tysabri natiluzinab de past 3 yrs my JC virus test in the past has been zero negative awaiting result of this jc test this time my neuro wants me too consider coming off tysabri and going on mavenclad cladribine or lemtrada . I need advice as tysabri has giving me over 3 yrs w…

I started mavenclad last month and I’ve noticed my teeth/gums hurting. I’ve never had this issue before so thought it must be the medication. I spoke to the adveva nurse about it and he said he had never heard of this happening before but will log it anyway. I just wanted to know if any…