[Note: While traveling my daughter and I will experiment with using this journal to communicate TO Patti through her visitors. MS symptoms impair Patti’s ability to use a personal computer. It’s all part of the adaptations involved in ‘living with 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.
Sunday, August 15, 2004
Subscribe to:
Post Comments (Atom)
Blog Archive
-
▼
2004
(230)
-
▼
August
(29)
- Bush to picnic here
- secret source of sanity
- “Ensuring Your Future..."
- boogeyman of 24/7 care
- 'drop in' any time of night and day
- Devil’s Playground
- Redecorating
- On the Road Day 8: Death Valley to the East Coast
- On the Road Day 7: Mexico
- On the Road Day: 6 San Diego
- On the Road Day 5: Los Angeles
- On the Road Day 4: Los Angeles
- On the Road Day #3: Joshua Tree National Park
- On The Road Day #2: Rt 66
- On the Road Day 1: Las Vegas
- while traveling
- Medical power of attorney
- Friday the 13th
- "We Will Rock You"
- from Patti's Mom ...
- tough to be 16
- MS & Parenting
- a crack in the chrysalis
- South Beach Diet
- nothing special
- wheel chair ‘road rage’
- ,,, a couple days in the life
- New Studies on MS, Stress and Depression
- rose colored glasses
-
▼
August
(29)
No comments:
Post a Comment