Running Update:
9/10/2014
|
9.1
mi
|
1:24:10
|
9/12/2014
|
5.0
mi
|
44:04
|
9/14/2014
|
15.0
mi
|
2:26:10
|
Less
than a month until the Hartford Marathon!
I’ve got a 22 mile training run planned for next weekend and then I get
to taper.
Jane and NF Update:
Yesterday
was the 2nd Annual NF Walk in Putnam, CT! It was the first official NF event we’ve
attended as a family. Todd and the kids
always attend my running races, but usually I am the only person at these
events fund raising for the Children’s Tumor Foundation. The NF Walk was attended only by people supporting the Children’s Tumor Foundation! At first Jane seemed a little self-conscious. I don’t think she knew what to expect (nor did
I, for that matter…), but shortly after we arrived the walk’s organizer,
Rhianna Curotto, gave Jane a NF Hero cape and streamers, and she was off!
The
walk was an out-and-back stroll along the Quinebaug River, and our family
walked in the middle of the pack. When
we reached the turn-around point, Jane noticed that the parade was being led by
three kids holding a CTF banner. She
asked, “How come they get to be up
front?” I told her there was no
particular reason, that she could walk up front if she wanted. Before I knew it she had gone up to the trio
and asked if she could help carry the banner, too!
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| Face painting |
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| Showing off her butterfly |
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| By the Quinebaug River |
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| Aunt Anne came all the way from Boston to walk with us! |
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| Aunt Anne and Grandma Ag |
After
the walk we enjoyed a cookout and raffle.
Jane spent the rest of the event dressing up in the photo booth and
taking pictures with her new friends.
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| Dressing up for photos |
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| Each person at the walk who has neurofibromatosis was given a medal. Jane was happy to accept hers. |
Jane
won a basket of crafting items, including a small photo album. That night, after we were home, she put all
her photo strips in the album and carefully labelled them “NF Walk 9-13-14”. She pointed to the pictures and said, “This
girl had the tumor, too.” I think, in
her own way, Jane was very happy to finally have met other children affected by
NF.












































