Life Moves Pretty Fast

Last month there was a big ceremony at my former high school in Oak Park, Illinois. Four alumni were awarded the annual Tradition of Excellence, a recognition of work that is representative of the Oak Park River Forest High School ideals and mission. I was fortunate to be one of the recipients, based on a nomination from one of my classmates. As my ALS progresses, travel has become very difficult, and I wasn’t able to attend and speak directly to the 3000 students who piled in to the auditorium for two different presentations. Instead, I made a video, and my parents and two of my best friends went on my behalf.

That morning, I was agitated and I couldn’t figure out why. I suppose I was wondering if my words would land in a meaningful way on this audience. A big part of me was disappointed that I couldn’t be there, and I was anxiously awaiting feedback. I shouldn’t have worried. The events went beautifully, and the Student Council representative who introduced me and my video did an excellent job. Afterward, I received photos of my friends standing next to the wall where my photo would eventually be hung, alongside people who have made much grander contributions to society. It was extremely humbling.

But the best part came a few weeks later, when an OPRF senior sent me a message. Her business class finishes every semester with a group project that benefits a charitable organization of their choosing. Hannah had written to tell me that her group had chosen #whatwouldyougive and the ALS Therapy Development Institute. They made T-shirts using our logo and you can see and purchase them here.
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Redemption Song

I miss my handwriting. I miss doodling on the margins of a page and filling in the answers to a crossword puzzle and sending a thank you note and making lists. I miss dancing and real hugs and opening doors and swinging my legs over the side of the bed and putting my feet on the ground.

Last night Scarlett was in my lap reading herself a book. Her hair is down to the middle of her back and it ends in rings of gold. All I could do was look at that glittery hair against her little brown back. My hands won’t even rise high enough to touch her. It is heartbreak. I want to hold her so much that my stomach hurts and I feel a quickening in my chest. I have shed enough tears over this to generate my own weather pattern, and still my body won’t accept the fact that it can’t reach for this person it created.

I am becoming increasingly breathless, and my tongue is twitching inside my mouth as if electrified. It is horrifying to watch, just one more muscle growing weaker and caving in, the whole thing looking like a worn down soccer field full of divots waiting to trap an ankle and snap it. I can still talk, still swallow. But my whole body is tired, and my brain races with ideas that I could never realize.

These are true things. But there are other true things that are significantly more uplifting. Read More>

When the Giving Gets Good

Who wants to talk about #whatwouldyougive?

Trick question! This is my blog, and we’re going to talk about whatever I want to talk about. And this particular post is long overdue. Part of the reason I haven’t been talking about the campaign is because there is almost too much to say. August was a huge success for us, and our incredible team members brought in 170K, a number I can barely believe. As many of you know, our goal is to raise 250K for research at the ALS Therapy Development Institute in Cambridge, Massachusetts. These brilliant folks have a  promising drug that can go to trial in 2018—but not without help.

What you may not know is that our campaign isn’t over yet. We launched the second wave of #whatwouldyougive this month, and it’s a big one. We are partnering with hundreds of social influencers (Bloggers, Tweeters, Instagrammers, and more) to raise further awareness about ALS and our efforts to find and fund treatments and a cure.

How does this work? Read More>