To get the most from your Relapsing-Remitting ms(RRms) journey, I highly recommend asking questions and lots of them. Ask them no matter how silly or dumb "YOU" may think they are. Ask them one hundred times until somebody uses the words that suit "YOU" A lot of things can be said in a lot of different ways. Ask until "YOU" can make sense of something for "YOU" Because somebody says fight ms it is a demon. Does not mean that it will ever be to "YOU". I prefer to manage because that is something I can do. Why do I have it, I again prefer because, because I am human and humans get it. Maybe "YOU are not ready for that yet, maybe "YOU" feel that fighting is what "YOU" have to do. That is okay, this is a very long journey that we take. "YOU" might change your mind one day. Take your time find yourself. This is a longterm incurable condition, "YOU" and I will have it for a very long time. Sit back and take stock of what "YOU" have "YOU" might be surprised.
Try not be scared. Take a deep breath and when "YOU" are able take my hand and start walking your very long RRms journey. I will not let go until "YOU" decide "YOU" are ready. "YOU" are not alone.
Royce (the ms writer)
You are never alone, talk and if I or we can help we will try
