Ok, friends! So on
November 3, 2013, Jen Devore is running in the NY ING Marathon in honor of my
dad and other friends of mine and people all over the world that cannot run
because of Dystonia. When doing this, though, the NY Marathon requires a
minimum fundraising goal of $2500 per entrant. We are currently at $945 and are
really anxious to raise the rest of the money! All the money is going to the
Dystonia Medical Research Foundation and their agenda to find a cure for
Dystonia! What Jen is doing for my dad
is something I cannot do, run a marathon, but I can surely help her raise
awareness and the funds to let her run on behalf of my dad and all the others
affected by this disorder.
Now,
your part is easy. All you need to do is commit to sponsoring Jen. Please
donate as generously as you can by sending in your check payable to the Dystonia
Medical Research Foundation to the address below or by going online and make
your donation online!
Dystonia Medical Research Foundation
Jen Devore Marathon
One East Wacker Drive, Suite 2810
Chicago, Illinois 60601-1905
Jen Devore Marathon
One East Wacker Drive, Suite 2810
Chicago, Illinois 60601-1905
Now
if all that isn’t reason enough to donate, I’ve come up with the top 10 reasons
to donate!
Top 10 Reasons to sponsor Jen
in the Boston Marathon
10.
You can sleep in late on November 3 while still funding Dystonia research,
while we are getting in to NYC early to work all day to help find a cure for Dystonia.
9.
You can transform my sneakers into a money machine as we raise almost $100/mile.
8.
Your donation is tax deductible.
7.
If you sponsor us, Jen has no excuse to walk or to crawl and will run the entire
26.2 miles.
6.
If we do not raise the total $2,500 we have to pay entry fee out of pocket, not
including the shame and blech feeling we will get from coming up short!
5.
The public can access comprehensive Dystonia information 24 hours a day, seven
days a week,
through
the DMRF’s web site (www.dystonia-foundation.org). During a time when so much health
information is available through the internet, much of which should be viewed
with caution, the Dystonia Medical Research Foundation is a dependable resource
for accurate, unbiased information.
4.
When I was in Alabama this summer, we weren’t sure if the Dystonia had taken
away my dad’s full ability to walk again – but it didn’t! Help us celebrate
that!!!
3.
You can help us make it back to Montoursville, PA where we plan on celebrating
the finish of the marathon! We plan to have chocolate - lots of chocolate, which will fuel those
last few miles!
2. Jen will have gone through 896 oz. of Gator Aid, 43 Power Bars, 5 pairs of running
shoes, a new pair of cross
country skis (for winter training) 53 lbs of ice for my knees, 2 bottles of
Alleve and all you need
to do is send in a check payable to the Dystonia Medical Research Foundation. **some of this bullet point might be an exaggeration to get our point across - LOL**
1.
The average diagnosis time for Dystonia patients is a few years! Help us raise
awareness to decrease the time of diagnosis and to end the disorder! Let’s put
the DMRF out of business by finding a cure!!!
Thanks to all of you for reading, for following my blog, for finding interest in my father's journey, but more importantly, for making even just a $5 donation! It means the world to me, my dad, and everyone else who can't run in the NY Marathon because of Dystonia.
with appreciation for you all!
Rebecca :)
Rebecca :)