I have Relapsing Remitting ms (RRms) have had for a long time, twenty plus years. I do not know why I have it or how I got it. I do know it will never leave me no matter what I do or say. No, it is with me until the day I die. I am not happy about that but I believe I accept this. I still get upset about it at times, even shed a tear in frustration. But it is a big but, this is my and probably your situation. I might humbly suggest that “YOU” accept this, come to terms with it and shed your tears, when “YOU” are able to wipe your face, lift your head look yourself in the mirror. Say,”ok this is my lot in this life and I am still going to live it. I am going to live it to the best of my ability, and when I get there I am going to do it better and better”
Do not let weakness into your thoughts or into your life. A tear every now and again frustration are both okay. Weakness is never a solution, it is a trap. Do not be trapped, always move forward, this illness only beats “YOU” when “YOU” stop moving forward.
As these are my words and thoughts I will offer “YOU” my hand and invite “YOU” to walk with me a little way until “YOU” find your feet and can walk yourself. No strings attached, just a fellow companion on our long ms walk together.
My writing, my thoughts, my rules. “YOU” are my ms family. Welcome my sisters and brothers, welcome.
Royce
It is okay this is a doable illness nd together we can do it
