tag:blogger.com,1999:blog-21421591.post7829806331529034250..comments2023-10-11T04:24:16.671-04:00Comments on Multiple Sclerosis Blog: TheDisabilityShow 0001Charles-A. Rovirahttp://www.blogger.com/profile/16533985064280992874noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-21421591.post-20727557334075251622009-01-28T23:35:00.000-05:002009-01-28T23:35:00.000-05:00Hi Charles,Breaking news today...The Health Centra...Hi Charles,<BR/><BR/>Breaking news today...<BR/><BR/>The Health Central Network has purchased Wellsphere.<BR/><BR/>http://www.thehealthcentralnetwork.com/news/20090128.html<BR/><BR/>LisaLisa Emrichhttps://www.blogger.com/profile/10862232056342347990noreply@blogger.comtag:blogger.com,1999:blog-21421591.post-86148685534638155482009-01-27T12:51:00.000-05:002009-01-27T12:51:00.000-05:00Amen PB. Amen."Feelings, nothing more than feeling...Amen PB. Amen.<BR/><BR/>"<I><B>Feelings, nothing more than feelings...</B></I><BR/><BR/>Somehow, I don't think MS is quite what "<I>Dobie Gray</I>" had in mind when the song was written ... but with MS, half of the effects of the disease <B><I>are</I></B>, uh, felt there.<BR/><BR/>The other half is of course spasticity; which is what screws up our coordination (and makes us need special shoes, canes, wheel chairs, etcetera.)<BR/><BR/>Are you listening to the podcast or are you just reading the show (here or on msb.libsyn.com, or on MSBPodcast.com [and soon to be on the website of St. Peter's College http://pauwwow.com/ ? ])Charles-A. Rovirahttps://www.blogger.com/profile/16533985064280992874noreply@blogger.comtag:blogger.com,1999:blog-21421591.post-51984538478053925582009-01-27T11:05:00.000-05:002009-01-27T11:05:00.000-05:00Yahoo! Let no one believe what they feel, for fee...Yahoo! Let no one believe what they feel, for feelings are not facts.<BR/><BR/>When the disability hits, that may be only for a day, or for a lifetime, but it doesn't mean we can't try.<BR/><BR/>Doctors told me I would be in a wheelchair. They may still be right, but it hasn't happened yet, even though I am constantly told (nag, nag, nag) that my MS is progressive and progressing.<BR/><BR/>So I use the walking stick, or cane, or hold onto the walls and railings, but I keep going.<BR/><BR/>Ain't nobody gonna slow me down till I'm gone.<BR/><BR/>Great show!pbhttps://www.blogger.com/profile/11568681879593734160noreply@blogger.com