Hi J
> I just posted about Prednisone which has a warning on it about
Sounds like what I've been having - Dexamethasone. 3 or 4 days supply,
tapered dose, start of each regime fortnight.
> This is of interest to me for a number of reasons. Dad was a partial
> paraplegic but we never knew the reason.
There are a number of straines of polio virus. Its possible to have
the benign ones and pass it off as 'flu, with little or no after
effects.
> Also I had a friend in school who had polio, he had a pretty rough time
> but 30 years later at a school reunion he looked spiffy and rarely had to
> use his wheelchair. Some years later I heard he'd battled cancer (forgot
> which), yet had succumbed to polio. This had baffled me.
Polio destroys the ability of a motor nerve cell to pass messages from
brain to muscle. During recovery, some OK cells regenerate links to
the "lost" muscle fibres. This regenerated nerve tissue has a 30 to 40
yr life span. Also, healthy nerve cells in the path tend to be
overloaded which shortens their life as well. Both bad news but after
45 years I had no problems (polio at 21).
> I've seen posts on other newsgroups about postpolio syndrome -
> reactivation of polio. (I think)
PPS is not fully understood yet but the bad news above is one symptom.
Right - history if you're still here ;)
Colon cancer removed March '03 (transverse colectomy). Couple of areas
in liver noted. Modified de Gramont regime started June '03 via pic
line+pump every fortnight. Effects bearable :/ October '03 - nasty
bits stabilised - not good enuf so changed to hic line and new chemo
mix and was warned side effects not fully known but _may_ affect
nervous system. Oh Boy! Understatement. Stopped Jan '04. Ultra sound,
CT and MRI scans can't tell difference now between scar tissue and the
bad stuff. So - down for a PET scan soon.
> This Acrobat file might mention some of that
> http://www.health.qld.gov.au/polio/gp/GP_Manual.pdf
Imustavacheck :)
> I haven't read it all - but will try later.
> J
Alf