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I got quotes today at the start at $40/hr for Companion Care. This is the minimum price for over 8 hours a day. 4 hours a day is $60/hr. I don’t think Medicare pays for this?

I am going on medicare in December and I have been paying $10.00 for my Revlimid because I have medical coverage through my employer . On Medicare its$1700 per month( give or take). I do not qualify for assistance with Healthwell . I make just over the amount for assistance . With part D ,I have to spend over $6000 in order to exit the medical , then I was told it will be $894 per month. Does anyone know how to get a lower cost?or how to navigate a better plan with medicare?

My husband was just diagnosed with MM and it's in his bones, stage 2. Please tell me what all the CD numbers you are talking about mean? The doctor is rushing him into treatment and I do not feel good about this. What should we be asking about the CD numbers? How can I find out how high his natural killer cells are? Please, any advice is needed. Please tell me where to start.

In 7th week of MM treatment. Numbers are falling fast. Side effects are sucking my soul.. Looking for data on stem cell success and problems. Any insight out there? Thanks. Rich from simi valley.

Thank you. and we can beat this! Because of my condition, my family and I are looking for relief. I was wondering if the Myloma Foundation has grants? Georgia Power? or any other ideas would be appreciated.