Hi, Been ages since I posted. Time for re cap since my diagnosis in January 2019. Have been on Tecfidera since the middle of April. All in all it has been okay. Number of flushes of varying degrees of severity but nothing drastic. Get used to that and the general nausea…tried all the hints to…

Hello, I am in the middle of trying to swap to a different medicine, I am currently on plegridy changing due to terrible side effects. I was advised by my ms nurse to change to ocrevus but my neurologist advised no and said the only options are Aubagio and Tecfidera. There are a lot of side effect…

Hi all So I went for my annual MRI in September. The previous one I have in September 2018 was stable, I didn’t have any new lesions. The results just came in for this MRI and there is one new patch. I started Tecfidera in September last year so was hopeful that it would be at least stable for a …

Hi everyone. After getting told everytime I ring my ms nurse that I am not having a relapse, I have just found out that infact I was having a relapse, which means tecfidera is not working and I need to change medication. They have given me the choice of gilenya or tysabri. They have chosen these as…

Evening lovely people, I haven’t been on for a while since I started tecfidera, which is working well for now. Just wondered if anyone had heard about the research and benefits of taking colostrum for your ms? I’m just looking into the research and looks pretty positive! Hope to here from you. …

I’ve been taking Tecfidera for nearly 2 weeks now and so far I have been fine, no side effects whatsoever. Until today – I’ve had horrible diarrhoea all day to the point even sipping water is making me need to rush to the loo. Is it normal for side effects to start after a couple of week…