On Jan 3, 5:24 pm, RuthDol...@gmail.com wrote:
> > � Perhaps NEXT Year, the Yobs with New computers who have nothing
> > better to do with their time, will volunteer to help HealthGroups set
> > up REAL Websites, and take any medications their Doctor Prescribes for
> > them at the rate they suggest.
****************************************************************************
> > � That way they don't have to put up Junk like 5 posts overnight, that
> > are another set from the *one kid who changes his User ID each day --
[quoted text clipped - 12 lines]
>
> What does Yob mean?
*** Yob is a slang term (the reverse of 'boy', meaning someone who's
fooling around-- British I think), or in the case of my original post
he *did *not have epilepsy. The poster I was referring to did a
dozen? posts here (mass spams unrelated to living with seizures, or
knowing anyone who did).
The post that *my post referred to is described **above between the
****s and ////s .
My reply was posted following those (12) he did here (by robot),
and I stated the fact that his posts were already on
'uk.sci.astronomy', so he had his computer set to post same mass-
mailing on *all usenet groups, alphabetically, at least ones on Google
threads.
(I think his posts were a repeat of 'MI-5 keeping Alien Invasion of
Earth a Secret'-- a thread that repeats stuff posted on Science groups
since before 1998.)
Someone new, who did a 'reply to group' to one of his posts might
not notice the Reply put their address on the *other 4 groups he had
crossposted to, even if they weren't registered there.
That's why I started a fresh, single post. If you don't see his posts
(I replied on Separate thread, *following posts he did), then your
News Reader is discarding them--many news servers do not.
Typically someone posting disruptive posts like that put a 'chill'
on many of the former regulars or new posters, and interfered with the
purpose of the group.
We once had 20-30 'regulars', who posted here *every night, with
questions, workarounds or solutions that had worked for them. The
poster I was referring to did about 10-12 consecutive posts here, then
his computer program moved on to other groups. He was likely offline
within 6 hours of those posts I refer to, although the posts stay 'up'
on message threads, even after his ISP removes him.
The original 20? Regulars in about 11 timezones, have not been
active here since then. (His posts, and a second non-ep. poster, who
forged using other's 'email IDs', from active posters *here, at that
time, disrupted the 6-8 discussion threads that were active.) The
Valid posters have not posted since, if they're still reading this
group.
You can see how few valid posts have occurred since October, if you
have history threads going back that far-- down from 500+ per month.
I suspect many regulars unsubscribed or moved to one of the other
groups one of original founders (not I) posted last Sept or October. /
I am not a newbie to support groups. Are you
> saying
> that new people with epilepsy do not belong here. I feel sorry for
[quoted text clipped - 8 lines]
> not
> need to be babied.
** The message wasn't for you, or its intent was misunderstood.
A number of people responded 'reply to group' on **older crossposted
threads, without realizing (as above) their reply (and e-address) was
going to groups they weren't registered on. Then they'd spend next 10
days throwing out Junk Mails if they didn't have anti-viral /anti-spam
filters. I still get ~30 junk mails discarded each sign-on, even
though I think that post (Dec.31) was last time I posted here. That
number will be up tomorrow now.... //
Some people do need more help than others. You need
> to have a good attitude and be positive. Think about your attitude
> and empathy for other peoples feelings and what they are going through. At one time you were a newbie
Pass. I had a reply, but realized it might be a 'lecture', too.
I'm 63. This May will be 10 years szr. free/and here, after 5 years
onset to control that worked. That only matters since 1993 the Neuro
who did MRIs /EEGs told me to 'hope for' 2-3 szrs. per Month.
I was here originally as a Social Group, to exchange ideas w.
others using Tegretol, Frisium or who had Complex Partial /other szrs.
and Social issues wrt. seizures and attitudes of others.
If most of the regulars have left, Dave's site has collapsed. /
RuthDollar@gmail.com - 04 Jan 2008 07:41 GMT
> > > � Perhaps NEXT Year, the Yobs with New computers who have nothing
> > > better to do with their time, will volunteer to help HealthGroups set
[quoted text clipped - 108 lines]
>
> - Show quoted text -
You asked if I am a newbie. I belong to 3 support groups and learn
from
each other. I am sorry I sounded like it was a lecture. I did not mean
it
that way. I agree with the Social Group to exchange ideas. I have the
same
ideas that you do. I have not been seizure free since I was 6. When I
was
16 I had to decide whether or not to drive. At that time epileptics
could drive.
I thought about it. Then I decided not to drive because I might kill
myself
or someone else. I could not afford a car anyway. I take public
transportation.
Where I live, we have Dial-A-Ride. You call them and they pick you up
and
then you call them up when you want to go home. The price is not
expensive. It is cheaper than gas!!! I take the bus and walk to.
Your Friend Ruth