As always a word of caution, entries in this journal share our story of living with Multiple Sclerosis as a family for two decades.
One person’s case cannot predict or forecast any other person’s specific course of MS.
Sharing the trial and error learned lessons of a MS spouse caregiver / carer about family, home care, and transition to the care facility era from 23 years of living with Multiple Sclerosis as a family ... a ‘warts and all’ picture of living with MS.
Wednesday, August 02, 2006
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2006
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August
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- Caregiving: bureaucracy & free thinkers
- Caregiving: Writes of Passage
- Caregiving: scootering
- Caregiving: financial competency test
- Caregiving: throwing stones
- Caregiving: ... family first
- Parenting: Part 1 - mustangs & shooting stars
- Parenting: Part 2 - hiking, falcons & deer
- Parenting: Part 3 - dinosaurs & detours
- Caregiving: ... makes you wonder?
- Caregiving: campus visit AM
- Caregiving: campus visit PM
- Caregiving: MS "teaching aid"
- Journal: word count
- Caregiving: parenting & the beach
- Caregiving: a word of caution
- Caregiving: Cognitive Dysfunction Part 2 of 2
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August
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good point, Patrick.
ReplyDelete(okay, got to ask, how are you doing with your word count goals?)
betty
well duh! sorry i just figured everyone would know that lol i need sleep. is it hot where you are its unbearable here
ReplyDeleteDeb
......................you are so right, I hate it when a doctor tries to fit somone in a box like the rest of his patients, and that does happen. I agree, since we are all dealing with some "dis-ease" of a sort or a caregiver we would know that no two snowflakes are alike!
ReplyDeleteI think people know this, we're all wonderful individuals, but it's good to know of your family in case something said can trigger a solution or help in a problem they've been experiencing. Rache
ReplyDelete