January to
date:
Happy New year, everyone! It’s a brand new year of advocating, fund-raising, and racing to help improve the lives of people living with neurofibromatosis!
I’ve been working with a trainer/physical therapist and am optimistic my knee will be strong enough to handle our race schedule.
Our spring
2024 events:
New York
City Half Marathon—Sunday, March 17
Our fall
2024 events:
New Haven
Road Race Half Marathon—Monday, September 2
Feel free to donate here to kick off our 2024 fund-raising for the Children’s Tumor Foundation!
NF Update:
Late last
year I joined another effort to help find a cure for NF. I became a patient representative for REiNS,
Response Evaluation in Neurofibromatosis and Schwannomatosis (https://ccrod.cancer.gov/confluence/display/REINS/Home).
The REiNS
group is a collaboration between NF researchers, patients, and other members of
the NF community to establish standards for how to evaluate new NF
treatments. Without agreed-upon standards
for evaluating, say, how a new medication affects a neurofibroma, it can be
hard to compare treatments. For a simple
example, if one study showed that Medicine X reduced the size of a tumor, but
another study showed that Medicine Y reduced how often a tumor needed surgery,
it’s difficult to tell which treatment is better.
This is from the REiNS website:
I’m
looking forward to learning and contributing!
Jane Update:
The big
news this week: Jane got her driver’s
permit! She’ll be starting Driver’s Ed next
week. In Connecticut, once you pass the
permit test you have to attend 30 hours of classroom instruction and have at
least 40 hours of behind-the-wheel, on-the-road training before you can
take the road test to get your license.
Jane’s going to be busy!
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