@hkittypink 

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hkittypink

So confused

I was diagnosed last August/September. Maybe it's just been head in the sand for me. But here's where I'm at - I'm scarred for the future - home, work and HATE doing betaferon with avengence. Wish I could turn back and not go to the GP, not tell people at work. I would still be me...
@gpeps

Hi hkittypink, I'm really sorry to hear you're having such a rough time. Firstly, I think it's completely normal not to face up to things straight away - I certainly didn't! Please don't think about things too far in the future, there are so many unknowns in this world (whether you have MS or not) that I think it's best to focus on what's going on now and making the best of it. MS does change things, however this isn't all for the bad - I promise I'm not just saying that. It makes you realise what's important to you. I can't imagine anyone likes the thought of injecting regularly. However, as lots of people on this site will tell you, it definitely becomes easier!

@gpeps

p.s. You are definitely still you! Sure, MS is an inconvenience, but don't let it get the better of you! x