I am up to seven hours of sleep a night. So far it has been good sound sleep for four nights. The six hours was hard to get up from but seven seems to be good. Maybe in a few days I'll try to bump it up to eight hours and see how that goes.
Have been reading and watching news about MS and CCSVI. It is so disheartening. I don't know what to do to open the eyes of the powers that be. I watched a new report with the Alberta Health Minister stating that they have 6-7 million to put into CCSVI when it is proven safe and ethical. Really?!?!?!? What is not safe about angioplasty? It is preformed here everyday. Ethical??? Is it not ethical to treat people who are suffering and help relieve that suffering?? I feel like I'm banging my head against a wall and screaming at the top of my lungs and no one is listening.
Frustration runs high when you know and have felt firsthand the power of healing and others don't believe. Living proof is not enough.
Sorry for the rant! My fellow blogger Marc, a.k.a. the Wheelchair Kamikaze, stirs up my frustration when I read his blog and he shares the corrupt world of big Pharmacy. Read his blog but I warn you, you will be enraged and frustrated too!!
I have not read Marcs blog, but I do strongly feel that the lack of progress in getting CCSVI 'okayed' has a lot to do with big pharma and the money they give to govt and even the MS society. After working with the osteoporosis society and seeing how much they rely on funding from big pharma ... until a drug goes generic, then big pharma gives NO money ... if a non-drug treatment is successful ... well, you can see where I am going with that. I'm so pleased to read of your progress Joanne. good for you. Debbie Remeshylo
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