If you have noticed, this blog provides a variety of information about the ongoing life of Hawaii ALS Support Group. This group meets every second Tuesday of the month at the Queen's Conference Center, at the corner of Beretania Street and Punchbowl in Honolulu. It started about 12 years ago, when Joyce Okahashi and I brought the need of organizing a group to the attention of then MDA Directpr Kathleen Hurtubise. Since then, the group has been meeting regularly, thanks to the unrelenting support of MDA.
One way to continue to help families with ALS everywhere is to provide a forum in which information about caregiving is offered and discussed. This blog will start a caregiver series, in which relevant topics are introduced and reflected upon. Comments are welcome; in fact, encouraged!
What do you think?
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