Hi everybody! I’ve had my first relaps in February 2022 and got diagnosed in April and started taking Rebif in May. I’ve had flu-like symptoms the first couple of months, but not anymore. I do my blood analysis regularly and everything is great. But I just find it too difficult to get the injections. I can’t do it myself, I’m too afraid of it. And even though someone else is doing it, I still get terrified when I remember what day it is and that I need to get my medication that day. And I have to take it 3 times a week. I never know how painful it is going to be and it leaves me red patches and bruises. How is your experience with Rebif? I am seriously thinking about changing it, because it’s starting to get unbearable for me. I know it has very little side effects, which is why I liked it in the first place. I wouldn’t want to switch to a medication that has some horrible side effects and contraindications. What do you guys think?