Nice to see new names on the board this morning. Not nice to see more people on the journey through ms life, just nice to see new family involvement. Who knows they may know things that I do not (VERY LIKELY) and also have experienced things that I have not (AGAIN VERY LIKELY) iand they might like to share it t is nice to be a part of a family. If they like they can continue being part of ours.
It is a nice coolish rainy day in my neck of the woods. Not much hot water as the sun is not shining on the solar panels and I am not a big fan of shaving in cold water. Must dee if I can talk mum into baking. Strangely I doubt it. Only one diabetic son and she is not to fond of baking me cakes anymore. Fat chance that I will do it as all I will do is make a huge mess. So it us a day of setups and listening to my Bill Bryson books.
Quiet and non eventful. Such is life with a chronic illness. I wonder what I can imagine? I could put on my yellow construction helmet and my hi vis vest and imagine the Tecfidera running through my head repairing ms damage. Diverting it and doing construction work. I must find “Bob the Builder” music online. Such are the games we play.
Have a nice day and remember all I have said to you. It might help “YOU” just a little today. Oh of course remember that ms is a doable disease and “YOU” should be taking your disease Modifying Therapy (DMT)
having a cold and rainy day