Can there be anything more aggravating than an organisation which buys
a small ISP primarily because of their "loyal customer base" then
proceeds
to make changes without notification - and when things go wrong seem
not to even bother trying to fix the problem?  We're all feeling a bit
like
"mushrooms" except there's no feeding of any kind going on.  I started
up
a Google group for Zetnet subscribers when Breathe took over, so that
we
had somewhere to go to keep in touch when things went wrong, and I
didn't
even realise just how "wrong" things were going to be... Subscribers
are
leaving Zetnet in droves, now.

I'm keeping in touch, via Facebook, with many friends and family who
have Facebook accounts,  Some others are kept informed via SMS
text messages, and one or two I call on the phone.  I'm encouraging
my daughter to  set up a blog, so that they can access that.  It all
takes time, and I have so much more to do at the business, since my
grand-daughter who is normally in charge there is spending a lot of
time with her mother - but the letters and quotes must still go out,
or
the business ceases to function, and we'll all be in the "deep and
smelly".

I'm about ready to.  I just can't waste time with an ISP that has, to
all
intents and purposes, ceased to function.  My son is in the process of
sorting email facilities from my own domain, but I'll need to sort out
something reliable for newsgroup access.  That's what's keeping me
sane - at the moment (although some times I wonder!) ;-)

Well, I've been around for what seems like a very long time...  <G>

The hospital staff were wonderful - and the Maggie's centre, well,
there is
no praise high enough for the helpers or the concept.  Every hospital
with
the facilities to treat cancer should have a Maggie's Centre...
http://www.maggiescentres.org/maggies/maggiescentres/home/centres/dundee/introdu
ction.html?gclid=CP2NqKmiuZsCFZgU4wodvBLUCQ

All seems to be well, today.  We'll see how things go for the next
week or so.
My daughter has an appointment to be measured for a wig - isn't the
NHS
wonderful!  How we would have coped if we had to pay for treatment, I
hate
to think...  I've had a diagnosis for a persistent rash on my calves -
it's
dermatitis.  Something I've never suffered from in all my 67 years!
Worry
can manifest itself in so many different ways, can't it.

Thank you J

--
AnneJ

I will be here, as long as the computer (and body) stay "humming". :)
Thanks for the info.

I see that zednet is making changes and having glitches.
When such happens with my ISP, there's often difficulties accessing and/or error messages.
There was also a message there about ZIMACS (which is in your headers).

Don't give up on them yet.
I see you're a Usenet pro. :)
I have a list of other resources (using newsreaders instead of Google) should the problems continue (some free).
It's important to (be able to) block certain posters here.
Since you weren't archiving, other Googlers may not see your posts.

No apologies necessary.  We understand you've other priorities.
How did things go at the hospital?
I'll watch for your updates.
Take care.
J

It's Adeno, or so she remembers from her first consulation
with her specialist.  They are giving her E C F, according to
my granddaughter who went with her when she was
admitted to the hospital today.

(Sorry about the delay in my reply - my news server appears
to have gone AWOL, and I'm having to post through Google.
Such a cumbersome procedure!)

I think we're in for a hectic six months or so...

--
AnneJ

Since you're in Scotland, here's the Scottish Intercollegiate Guidelines
http://www.sign.ac.uk/guidelines/published/numlist.html
Management of oesophageal and gastric cancer is # 87

I'm unsure whether your grand-daughter should read it.
Depends on her age and ability to cope with it.

It will be interestiing to hear which type (Squamous or Adeno) she has and
which chemo (or chemos) they'll be giving her.
Take care. Sounds like you'll be very busy.
J

Thank you Bobert.  There will not be any radiation.

The first specialist she saw said that they would do three courses
of chemotherapy, then a scan to see if the tumour had shrunk, then
possibly more chemo before removal, and then further chemo to
ensure that the lymphatic system was clear.  

Then she saw the oncologist, and removal of the tumour was never
mentioned.  They are going to do six courses of chemo, spaced
three-weeks apart, and see how it goes from there.  The cancer is
in the lymphatic system, they told her.

We are in the UK, by the way, so treatment is free on the NHS.

Anne,

J will be chiming in soon with info and web sites, so in the meantime
I'll try to suggest things that be in her future.  

If they attack with radiation, she will probably get a feeding tube
installed.  I had radiation to Lung Cancer tumor that was near my
esophagus. As the esophagus gets radiation, it will get radiation burns
that are described as like a sunburn in your throat.  Food will irritate
the throat and swallowing will be painful if not impossible.  I survived
on smoothies and milk shakes.  Soft scrambled eggs and yogurt were about
the only thing I could get down with a minimal pain.  Thus the feeding
tube will make it easier to get nutrition.  The important thing is to
keep her weight up.  Not eating will guarantee weight loss.  Lots of ice
cream was my solution.   Popsicles will help to cool and soothe throat
and hydrate her mouth.

Others here will have more info, but I just wanted to get you started
with some info.   Best wishes for your daughter.  

Bobert

She was diagnosed with cancer of the oesophagus
earlier this month.  It is stage 4.

She is 45 y.o. and I wondered if anyone here would
like to comment, or offer advice.