So my MS nurse made contact with me this morning. Arranged to meet me in a couple of weeks to discuss everything at length, treatments and any questions I had etc…
I then get a call of this afternoon and she said after speaking to my Neuro, after he had meetings to discuss my MRI and symptoms with other experts, they are of the opinion I will need the Lemtrada DMD. This all depends on my LP and other blood tests which will be done in the coming month.
What are others experiences of Lemtrada? Am I lucky to be given this DMD? I have read nothing but good things about it for controlling MS minus the potential side effects and some people not fitting the criteria.
I don’t know if I should be relieved or what, this has been the most bizzare few weeks of my life and it all seems to be whizzing along now which is what I wanted, but still all this to take in in the space of a few hours and it doesn’t seem real.