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How is anymore getting on with plegridy?

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 🥰

No response? Interested how you’re getting on a due to start myself in the next couple of weeks! X


I get on good with plegridy, i have less side affects in my stomach than if I inject in my legs though