The Past 18 Months

Friday Apr 3rd, 2015

The last 18 months have been a whirlwind. I knew 2 things for sure after Alyssa’s passing; I was NOT going to let her be forgotten, and that I was going to make her proud. In this last year and a half, we have been able to do some pretty amazing things. And in my heart of hearts, I know this is only the beginning. Some of my happiest times since then have come from giving.

The first thing I wanted to do was send someone to college since we wouldn’t be sending Alyssa anymore. With the help of my hometown of Erie, the community, family and friends we were able to fully fund a scholarship in Alyssa’s memory at the The Erie Community Foundation. We now have a part in awarding deserving nursing students a little extra for school. Last year we couldn’t narrow it down, and picked 3! And the best part? Long after we are gone, the scholarship will still be there. Still a tribute to Alyssa’s memory and legacy.

The next thing I wanted to do was to establish a fund so that we could give monies to other organizations that aligned with our advocacy, and mission. We have also (with your help) accomplished that.

My next mission is to fundraise so that I can purchase and distribute as many epilepsy monitors as I possibly can. Had we have had one of these devices for Alyssa, she may still be here today. They are LIFE SAVING and LIFE CHANGING!!!

Imagine being a teenager and wanting the freedoms that all teens want, but because of your epilepsy you have a worry wart mother (like myself) and have all sorts of restrictions! Now instead, you can strap on a watch (like SmartMonitor) and your mom can relax (does that really ever happen)

Imagine your young child starting school, playing outside, riding their bike, taking a shower, driving…. all with seizure activity. It’s enough to drive you insane as a parent.

Imagine knowing your loved one has sleep seizures, and the only thing you can do at night is either stay awake, sleep with them, and then suffer yourself because you can’t get a good nights sleep. Did you know they have a monitor for that too? (SAMi)

Technology is amazing. If any such devices were available when Alyssa was alive I either didn’t know about them, or they weren’t specific to her type of seizure (tonic-colonic). But technology is moving faster then we could have ever dreamed.

I don’t plan on stopping my mission(s) anytime soon, and I am sure that I will come up with even more ways to advocate, help, and spread awareness. In fact, I feel like I am just warming up!

We owe all the SUCCESS of this ‪#‎ajo‬ movement to Alyssa. It has always been, and will always be HER. She is the drive. She’s really something special.

Some people don’t understand our “success” in such a short amount of time. I use that term loosely because that success came with a VERY high price. My daughter’s life. And if you were lucky enough to know Alyssa personally, then you know what a loss her life was. If you didn’t know her personally, I try my best everyday to make strangers feel like they did. To bring you into our lives. Our victories, our defeats, our grief, and our celebrations. Sometimes all those feelings will come wrapped up in a big package.

There are so many people, business, organizations, strangers, friends, and foes that have helped us with our journey. I can’t even begin to explain my gratitude. Someday I will write out a big long thank you speech (and the music will start to play midway through, just like on the award shows).

But please know, that with every good deed, with every pay it forward, with every receipt with an #ajo attached YOU are helping! You keep this alive. Alyssa’s spirit alive. And just for that fact alone, even if we never raised another penny (I still plan on raising lots of pennies) that is enough.

On that note, I will say thank you. Alyssa Josephine O’Neill thanks you!

Post your comment


No one has commented on this page yet.

RSS feed for comments on this page | RSS feed for all comments