G'day my Relapsing remitting ms(RRms) family. I hope today is going very well for YOU. The sun is shining and that furry family member is being loving and kind. Mine is still lying in bed, but he will be there for hours with she who must be obeyed.
l leads me to a thought. This all leads me to a thought. Do not regardless of your RRms. demands of YOU. All sorts of things, far too many to number and they are often changing. What YOU could do when first diagnosed it is not what YOU can do 1 year 5 years 10 years later. Do not fret, do not panic. This is normal, it is the progression of our disease. YOU are taking your chosen ms Disease-Modifying Therapy )DMT), YOU are eating cleanly, YOU are exercising. YOU, my Sister and Brother, are doing RRms. You will have losses, that is the price we ALL pay no matter what we do in this disease. Live your best life no matter what it may be, and be content with yourself. Do not judge yourself against others, not even on this site. We are all different, and RRms affects us all differently. Stay true to your individual RRms path and keep moving forward.
It is ok ,YOU will be ok, YOU can do this.
Royce
your ms writer
