Good morning MS community 🤗. I was diagnosed in July with relapsing ms and have had it for four years before diagnosis. I am due to start my injections once the nurse has visited to show me correctly how to do the injection. I had worries about medication (family all have died of liver cancer or pancreas cancer) plus i have two autistic sons 24/7 at home with me plegridy can possibly cause suicide thoughts)....been reassured by my ms nurse. I just wondered how you all get on with the medication 🥰