Hey, don’t beat yourself up about not wanting to do the injections, who in their right mind would? When it was clear that the Tysabri wasn’t working for me I was absolutely dreading seeing the neurologist, because when I started the Tysabri last year the other 2 treatment options were both injections.
Thankfully, what I was offered this year, please note, offered, was different infusions or tablets. They can’t make you take any drug, they’re not legally allowed to do that. They can strongly advise you as to what they feel would be best for you, but they can’t force a treatment on you. So if you want to switch to Tecfidera, go ahead and ask, and good luck with it!
See as stress is a big contributor towards worse symptoms and relapses, I can’t see why your consultant would have a problem with you moving away from auto-injecting Unless they’re a butthole of course…are they a butthole?