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#lemtrada

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I’m struggling at the moment. As we went into lockdown, my partner of 11 years decided to tell me he effing hates living with me and dumped me, the same week as I had to have my 19 year old dog put to sleep. He knew from the outset of the relationship that I had ms and it is a degenerative disease...

I developed ITP (low platelets) and low white count 3 years after Round 2 of Lemtrada. It has been 7 months now and I am taking Promacta for my low platelet counts. My neutrophils are staying low and currently are 0.1. Has anyone else developed ITP or low white counts that lasted this long?

Having a flare up with all my old symptoms , been going on for the last month or so , have had 2 bouts of new symptoms since round 2 of lemtrada 15 months ago , no new lesions on my Last mri Just feeling pretty down about Feeling like I’m Getting worse and struggling doing simple things There are ...

Hi all, I need some advice. I had Lemtrada in 2016/17 and have had an awful time of it with ITP last year and Graves Disease this year. After speaking with the Endocrinologist today he has offered either Radioactive Iodine or the surgery. Has anyone had experiences with this? Please help.

Hi community, Does anyone have experience of neutropenia after Lemtrada? Horrid to have to deal with extra things on top of the MS. If anyone has I would love to hear if it’s reoccurred/needed treatment or went away naturally. Thanks, Sal

Today is a good day. Going to write some words to see how they're classified. Like Lemtrada...... It actually needs more text than this and we're going to make it content that talks about medical diagnosis of multiple sclerosis.

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune sys...

Testing this post out Lemtrada - whats happening?