I am the caretaker for my husband who has PPMS. Does anyone else feel alone with no help or support from their family? My family is supportive, but my husband's family is not. I know it hard for them watching him die, but he just wants to spend some time with them now. His mother and daughter have both told me that they can't deal with this. Does anyone have any ideas how I can help them cope so that they can see my husband more now before it is too late?
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Hi all! This is for those of you that have or have had the same neurologist for 4 years or more. I have been with mine now since 2009. He is one of the best movement disorder secialists in the midwest. I know he is extremely busy on the lecture circuit now and in fact not taking new patients there is a huge waiting list for him. BUT.... I feel like my visits are not what they use to be. He...
theatre and I are there already. I'm having a very berry tea with crackers, cheese and cherry tomatoes and she's having a joint with some beer and we're both on really comfy recliners on thick pile carpet. we need some help with the decor if anyone is around??