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Archive for August, 2012
Posted by 1987tc | Aug 23, 2012 @ 01:29 PM | 4,501 Views
Ray Mack one of the VPs of the Tulsa M.S. Society is going to be at the fly in with his family.
He is bringing a tent and table and will have MS materials at their table to hand out.
Lets all make them feel welcome and show our appreciation for their attendance.
And for all the good work the M.S. Society does for those of us with M.S.

Wes
Posted by 1987tc | Aug 15, 2012 @ 10:34 AM | 4,865 Views
We are updating the banners we put up each year for the fly in. One of them we have made a practice of listing the sponsors on.
So if you are thinking of donating or sponsoring any part of the event please contact me! We want to put you on the banner. It is 4'X8' And makes a good backdrop for pictures!
The clock IS ticking but there is still time to join us in helping find a cure for MS. Any and all donations are helpful and gratefully appreciated!
Wes
Posted by 1987tc | Aug 03, 2012 @ 08:45 AM | 4,588 Views
Well the fly in is getting closer!
There is still so much to do. Hobby King has stepped up again as title sponsor and has shipped prizes and other things for the fly in. And other sponsor has too.
I will start posting who has donated soon.

But there is a lot needed yet too. We need more prizes for the raffles. And we need bodies at the fly in to help manage and run the event.

And help contacting businesses and sponsors, And most importantly we need lots and lots of people to attend the event! After all it is the people that makes this event a success!
People to come and fly and have fun. People to buy raffle tickets and enjoy the prizes.

Keep in mind the real goal of the event is to help find a cure for Multiple Sclerosis. And to educate people about MS and about the greatest hobby there is!
So if you want to help in any way at all please do! It can be helping get donations. Sending emails or helping man the event. And of course just coming and taking part in all the fun helps a lot!

I wish everyone could have been there when I handed over the check to the MS Society . To hear the applause from the people there. To see the gratitude in the eyes and on the faces of the people there that deal with MS every day of their lives. It means a lot more then I can tell you to them and to me.

I have MS. And I want to help others like me to have hope for the future and a cure and end to MS.

You can help, You can make a real difference.

Wes