I had my fourth dose 3.5 years ago (was on the Campath trial), no letters re self isolation. The fact I have had four doses suggests I am “At risk”.
Yet I feel that I am forgotten…
Hiya I know the feeling. Everyone has very individual circumstances but we know ourselves best.my partner has just recovered from cancer. Best cancer you can have apparently. But the whole covid story started the day after OP. So we had to keep reaching out to NHS. For results advice wound management. They didn’t reply but we patiently pressed on because we had to. It took them 3 months. But you can’t give up because your loved and valued. My ms nurse is a joy! She advised me that email is your best route. It’s her first job of day. Patients 1st then trust stuff. If your sure you need specific advice you can email gp neurology. As long as you practice extreme social distancing your looking after yourself as best you can. I feel forgotten too but I won’t let it devalue me xxxx
So, my MS nurse phoned me and said the government has been out to individual neurologists. Mine put everyone who has had Lemtrada in the last 5 years (myself included) on the list. My GP also rang me to put me on their list, so I’m on the list, but no news from supermarkets about delivery slots which I know others have had. If I were you I’d ring the MS nurse and the GP