> > My name is Ken and I have been diagnosed with EC last month. I just
> > found this group today and joined so that I may find out more about
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>
> - Show quoted text -
> > > My name is Ken and I have been diagnosed with EC last month. I just
> > > found this group today and joined so that I may find out more about
[quoted text clipped - 30 lines]
> tests they require but I am scared to death that it has spread and
> they will not be able to get it all.
Hi Ken,
Thank you for answering my question.
You just missed Richard, from UK
He was diagnosed on Dec 5th and had already seen his surgeon, before arriving
here.
His next move, I believe, was the scans and seeing the oncologist.
Very positive thinker - got married and bought an inclining bed.
wants to be on the cutting edge of science.
I think he already is - they're giving him 3 rounds of chemo
( ECX - epirubicine, cisplatin and Capecitabane, (5FU in
Tablet form).) before the surgery and 3 rounds after the surgery.
First I've heard of that and I've been here quite a few years.
(question for the oncologist?)
The tests he's having are:
a fitness test, a PET Scan, laparoscopy and gastroscopy the following week.
No Ultrasound as the surgeon is satisfied that it is T2 or T3.
(TNM Staging) http://www.cancerhelp.org.uk/help/default.asp?page=4492
I can't see in your body (obviously), but the way you describe how you were
diagnosed (and what you have not mentioned) leans me to think yours has been
caught early enough for cure.
Here's types of esophageal cancer.
http://www.cancerhelp.org.uk/help/default.asp?page=4487
Do what you think best about the hospital.
I hear you that you're alone.
I realize it's not the same, but we're here for you.
I'm also putting you in touch with the largest collection of people who've had
or have esophageal cancer at the ACOR mail list - over 2,000 people.
http://www.acor.org/mailing.html
Click on E, then on EC-GROUP to join. I hope you'll stay in touch with us as
well.
The EC cafe has lots of information - please pay attention to the meal and
recipe tips on the right side.
http://www.eccafe.org/cnt/index.html
Hopefully, your team will also provide you with support from a nutritionist.
I've tried to not overwhelm you with too many links. Take stock (of what you
think you might need at home). Take some notes. - not too many- the EC Group
might already have one they'll send to you. If not start your own.
We'll be here, if you have more thoughts and//or questions. I don't want to
interrupt you as you work through what's best for you for the tests and think
about what's on these webpages, but we're here, anytime.
Take care and please stay in touch and stay positive.
Questions? Ask away.
I'd send you some puppy hugs, but I'm not a puppy.
You'll have to take care of that from your end. <smile>
J
Ken - 07 Jan 2008 02:36 GMT
> > > > My name is Ken and I have been diagnosed with EC last month. I just
> > > > found this group today and joined so that I may find out more about
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>
> - Show quoted text -
Thanks J, joined the ec chat tonight and have been doing a lot of
research though ACOR and Cathy's EC-Cafe. Have met some wonderful
people, survivors and those caring for them as well as some who are
still fighting the fight. I really appreciate all of you...
Ken
J - 07 Jan 2008 23:01 GMT
> > > > > My name is Ken and I have been diagnosed with EC last month. I just
> > > > > found this group today and joined so that I may find out more about
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>
> Ken
Best of luck, Ken.
I do hope you'll share your news here, from time to time.
J