I was finally diagnosed with RRMS in June this year and was given a list of DMT’s to review. Lemtrada wasn’t on the list and when I enquired about it, the Neurologist said it wasn’t on the list because they don’t offer Lemtrada in my hospital, but as I meet the criteria for Lemtrada they could refer me to Bristol so that I would be able to be assessed for the DMT there.
Long story short, they lost my referal paperwork, then were delayed in submitting it, and finally I have had confirmation that a referral has gone through on 17th August (2 weeks ago), and I’ve been signed off the MS team at my local hospital.
I haven’t heard anything from Bristol yet , and have no contact details to chase my referral. Does anyone have any ideas on how I can get in contact with Bristol so I can encourage things along a bit?