Yes, that was sarcasm but it really is not so bad. When people say "oh it could be worse it could be xyz disease" They really are right, it is only Relapsing Remitting ms (EEms) and that is a hassle but it really is not that big a deal. It is not so bad, honestly, it is not.
What do "YOU" have to look forward to this week? Is it physio, a really tasty meal or a good book. I had a really tasty cup of coffee this morning. It was no different than yesterdays, it was just rather tasty this morning. I wonder if I can make it again tomorrow morning, that is something to look forward to. Lots of good little things to put into my good memory vault. All of those good memories will give me strength one day. One day ms will make a demand on me that will try to break me, but I have my good memories there that I can draw on when the night is dark and lonely.
Build a huge bank balance of good thoughts and achievements. This is your strength, be strong, "YOU have this entire day a whole week full of opportunities to make yourself stronger. Take that opportunity, make your long ms life one in which "YOU" live well and are content with. This can be a very sneaky mischevious illness, but "YOU" most certainly "CAN" make it a "DOable" condition. "YOU" will bend and bend hard, but there is never ever a need to think that "YOU are broken. Believe in yourself, if I can do this so can "YOU"
Develop your good memories, your strengths. Accept that this is your mslife. Accept it and then slowly teach it to adapt to the way that "YOU" want to live. Be a bright shining star for those coming after us to follow. Do not just be a dull comet travelling alone and cold through deep dark space, we are together, we "WIL"L get through this together.
Royce
one part of the whole that is "US"
I have RRMS
26 Years RRMS 💪🏿💪🏿💪🏿💪🏿💪🏿💪🏿
Recently Diagnosed with RRMS
