Planning is already underway for the 2010 Relay for life
in the area of Fairfield. This year we participated as a
team, but for next year three of our lovely members
Sharon, Leanne and myself have joined the committee to
make a stronger impacked.(Don't get me wrong our team
will still be participating).

This year the event will be held at a later date (October
16th and 17th) and at a larger more equiped venue.
There will still be Relay Idol and Miss Relay and all
the other fun activities. Last year over 80,000 dollars
was made-this year I am sure will be even greater.

Anyone that wants to be part of this great event-either as
a sponsor, entertainer,make your own team etc...........let
us know and we will forward more information to you.
(fill in form at bottom of page)

Cancer is a very wide spread condition which isn't
sexist or concerned with age or race. Anyone
can get cancer and the sad reality is that you
don't know who or when it will hit.

Join us and help us make a difference in this
battle to defeat cancer. We will hand out any
promotional materials for any donating businesses
or individuals. So if you can't make it to the relay-your
business can still have a prescence.

This is a wonderful charity event to help defeat cancer (to raise funds for cancer research) The weekend is a festive style full of community spirit! It is not a marathon and you don't have to run, just walk around the oval-you can walk as many and as few as you like.

For those battling cancer, your not alone-A good friend of
mine has created a great site with forum in which is
highly recommended by us-


 

finally in remission, on the 17th of june I was told by my onc that things were good and I was in remission,9 months after transplant.
But I am going through some mild GVHD, dry eyes and mouth sores.
plus With some stomach problems and low iron leval and very low imunity.
other then that all is good.
Mark....

Please no advertising.
Contact all moderators for permission or suspension will accure.
your moderator ,Chemo.....

Its now 6 months following my second SCtransplant using my brothers cells this time.
Only just recently started getting some mild GVHD with Sore irritating eyes and very sore in the mouth and throat, and very tiered at times.
Continuing have constent blood tests every 3 weeks as the whites cells go up and down a bit, but all normal last week, except for some slight inflimation in the liver.But not to much concern.The docs want to keep me on 50mg Cyclosporin a day for a bit longer so the GVHD dont get to bad.they say that the medications could be upsetting the liver, but need to stay on them to servive.
Mark.....

Welcome to the new Moderator, Chemo to the forum.

ArtMark your Admin.

Hi Chemo,
Thanks for emailing me your details, glad to have you onboard.
I've been held up having treatment lately not able to maintain things on the forums, I hope you can manage the spammers for me.
I want this to be a clean forum for all ages and not have the wrong things being displayed in threads.
Artmark.

Hi Admin ,
I would like to become a moderator, I see you have had some Porn spamers and other spammers,I can help you rid of them with new mods.
Chemo/gassa