@wheelrunconflux 

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wheelrunconflux

Plegridy: False Horror Stories.

Diagnosed in 2019, I've now been on plegridy for close to 3 months and although I've had some side effects they were nothing in comparison to the horror stories I read online. The 1st time I felt like I had been beaten up, and at one point I had some problems with breathlessness but that's it. When I self inject, its very simple and there's never anything more than site reactions (which don't hurt at all) or at worst a small bit of blood if I screw up where the needle hits. It's a lot less interesting, writing about something that isn't a horror story but when I was looking for reviews of plegridy before it would have helped me to have someone say that it can be fine. Because it can be fine, it has become just another thing I take and all anxiety of self injection has passed, the actual process of administration is incredibly easy and tbh getting on, getting used to and then maintaining the dosing has had little to no impact on the way I live my life.
@Stumbler

@wheelrunconflux , Dr. Google isn't very beneficial to us, are they? You're right, there is a lack of good reports. Unfortunately, that is human nature. 99 out of 100 will shout about a bad experience, whilst 1 out of 100 relates a good experience. So, thanks for being in that 1%. I suppose that being presently undiagnosed, you are fortunate to be prescribed a Disease Modifying Therapy (DMT). Not many Neuros are that proactive in cases of CIS. So keep on, keeping on.

@BeatnikSpirit

@wheelrunconflux Thanks for that. I need to decide whether to accept the offer of Plegridy or Copaxone. Your post is the first thing I've come across that hasn't put me off one or other of them.