ASF Walk - Bennington, VT

Registration for the 2022 ASF Walk is now open! Join us in May at over 50 locations.
Close to 2,000 people registered on opening day! We’re excited to be in-person again in 2022!
www.angelman.org/walk

ASF's MyMarathon Registration is OPEN - and it's FREE! Watch this!
https://fb.watch/88z8Q926Ew/
Want Swag? You just need to fundraise! check out fundraising incentive levels at https://www.angelman.org/events/mymarathon/
Get Healthy! Look Great! Make a Difference for all AS individuals! That's a Win-Win-WIN!

Spread the Health this October! Sign up for MyMarathon today -- it's free and the fundraising SWAG is kinda cool!
Make a healthy impact for yourself and all individuals with AS!
https://www.angelman.org/events/mymarathon/

ASF My Marathon – Angelman Syndrome Foundation ASF My Marathon October 1 - 31 October is a perfect time to take the challenge! The Angelman Syndrome Foundation is challenging you to get healthy and make October your My Marathon Month! Get in shape before the holidays, raise awareness for Angelman syndrome and fundraise for a cure! We will use an...

Dust off your red cape and metallic b***y shorts! It’s time to raise some awareness in a Super Big way!

On ASF Walk Day, Saturday, May 15, show us how you’re celebrating and honoring our loved ones with AS, our everyday superheroes!

Post your videos/pics with and your team could win a Safety Sleeper by Abram's Nation!

Please support Team Gabriel for ASF21! As we are a virtual walk again this year you can walk at anytime for us and as little or as much as you would like.

As you know, Angelman syndrome has had a daily effect on our lives for some time. While each day has gotten a little easier, we still wish more than anything that Gabriel—despite his amazing attitude and smile—could do everything his friends can.
As many of you already know, our son Gabriel was diagnosed with Angelman’s February 2020. He has seen countless doctors and therapists and continues to endure a staggering number of medical visits. We are fortunate enough that Gabriel is not on a lot of medications at this time but we are pushing for a CURE.
Gabriel has had a global delay since a very young age. After countless visits with doctors and therapists that we still see on a regular basis we saw a Genetic doctor that ordered a MRI and blood draw that gave us his diagnosis of Angelman’s. It has been a long journey to get where we are today with him. He just had his 3rd birthday this past July. Gabriel is a very happy boy that is always full of energy. We celebrate each milestone no matter how big or how small. He is walking mostly now on his own. Speech is still our biggest obstacle to conquer but we are determined to succeed.
Angelman’s syndrome is a neurological genetic disorder that may be misunderstood and is often misdiagnosed. My family is committed to improving the lives of individuals and other families affected by Angelman’s by ensuring that funding for research, clinics, and family services is available.
And we are only one of the thousands of families who feel the same.
Thankfully, more and more treatments are being discovered and improving Gabriel’s quality of life. That means more sleep, less seizures and better balance!
But that momentum will quickly vanish if we quit raising funds for Gabriel and others. Please donate to help us reach our goal of $1,000 for the Angelman Syndrome Foundation Walk! Your contribution will help make more groundbreaking Angelman syndrome research and daily family support services possible.
Keep the positive energy alive and help our cause by clicking here: VT, Bennington: https://secure.e2rm.com/p2p/location/351268/en-CA

I am supporting the 2021 ASF Walk Join me and other heroes in making a difference for Angelman syndrome!

It’s time to join the ASF Walk Virtual 10K Challenge! Get the MoveSpring app and enter code asf21. You’ll be able to track your steps, unlock milestones and chat with friends and teammates. The 10K challenge goes live on Saturday and you have until May 15 to complete the 10K! See you there!

🤩 The ASF Walk Online Auction is now OPEN!

Don’t plan your summer vacation without checking this out! All proceeds benefit the ASF Walk, so bid high and often! Check it out here:
www.angelman.org/walk/online-auctions

Order yard signs today to guarantee arrival before May 15!

Neighbors and friends walk by and stop when they see the pic of your loved one with AS. A quick scan of the QR code and the donations roll in!

https://tinyurl.com/yardsigns21

DEADLINE TO SIGN UP IS TODAY!! DON'T MISS OUT!

Support ASF while giving the Super Mom in your life the gift of a fun evening! She'll join other moms across the country as she sips a beverage and paints with love. Perfect gift for Mother's Day!

$60 includes a 16x20 canvas and supplies shipped to her door. All proceeds benefit the ASF Walk.
Sign up here: https://www.paintingwithatwist.com/studio/la-grange/event/2716664

Get your team registered for Trivia Night on Saturday, May 15! ASF Walk registrants play for free. Non-registrants are only $10. Winning team will win cash prizes and an Abram's Nation Bed! 🎉
Get details and register here: https://tinyurl.com/asf-trivia

This is going to be fun and interactive!! Sign up today!

Support ASF while giving the Super Mom in your life the gift of a fun evening! She'll join other moms across the country as she sips a beverage and paints with love. Perfect gift for Mother's Day!
DEADLINE TO SIGN UP: Monday, April 26th. $60 includes a 16x20 canvas and supplies shipped to her door. All proceeds benefit the ASF Walk.
Sign up here: https://www.paintingwithatwist.com/studio/la-grange/event/2716664

As you know, Angelman syndrome has had a daily effect on our lives for some time. While each day has gotten a little easier, we still wish more than anything that Gabriel—despite his amazing attitude and smile—could do everything his friends can.

As many of you already know, our son Gabriel was diagnosed with Angelman’s February 2020. He has seen countless doctors and therapists and continues to endure a staggering number of medical visits. We are fortunate enough that Gabriel is not on a lot of medications at this time but we are pushing for a CURE.
Gabriel has had a global delay since a very young age. After countless visits with doctors and therapists that we still see on a regular basis we saw a Genetic doctor that ordered a MRI and blood draw that gave us his diagnosis of Angelman’s. It has been a long journey to get where we are today with him. He just had his 3rd birthday this past July. Gabriel is a very happy boy that is always full of energy. We celebrate each milestone no matter how big or how small. He is walking mostly now on his own. Speech is still our biggest obstacle to conquer but we are determined to succeed.
Angelman’s syndrome is a neurological genetic disorder that may be misunderstood and is often misdiagnosed. My family is committed to improving the lives of individuals and other families affected by Angelman’s by ensuring that funding for research, clinics, and family services is available.
And we are only one of the thousands of families who feel the same.

Thankfully, more and more treatments are being discovered and improving Gabriel’s quality of life. That means more sleep, less seizures and better balance!

But that momentum will quickly vanish if we quit raising funds for Gabriel and others. Please donate to help us reach our goal of $1,000 for the Angelman Syndrome Foundation Walk! Your contribution will help make more groundbreaking Angelman syndrome research and daily family support services possible.

Keep the positive energy alive and help our cause by clicking here: VT, Bennington: https://secure.e2rm.com/p2p/location/351268/en-CA

I am supporting the 2021 ASF Walk Join me and other heroes in making a difference for Angelman syndrome!

Easy fundraising and awareness raising with ASF Walk Yard Signs!

“This turned out great! Meghan is well known and loved in our neighborhood. Many friends stop when they see her photo. A quick scan of the QR code and the donations are coming in!”
- Gretchen, Meghan’s Mom

Order your custom yard sign today! secure.e2rm.com/registrant/startup.aspx?eventid=355805

The ASF is looking for donations of vacation homes, airline miles, designer handbags, sports memorabilia or other items to add to our online auction benefiting the ASF Walk. Contact Kitty Murphy at [email protected] to learn more or donate!

Check out some of the great items going live on May 1st here:
www.biddingforgood.com/auction/auctionhome.action?auctionId=341697733

So many ways to connect and have fun safely during our ASF Walk Week. Don't miss out - get registered today!! Late registrants will still receive a "Heroes Unite!" Walk t-shirt in the mail (after May 15th). Another thing you don't want to miss out on!

Don’t miss out on the SUPER events planned for the ASF Walk. There’s something special for mom, a chance to chat with AS clinicians and Trivia Night for the whole team! Since we can’t be in-person, these events will be interactive, casual and FUN!

Find details and sign up for the events you want to attend on our website. Register for the ASF Walk to receive priority and free registration for Trivia Night! www.angelman.org/walk

TODAY is the T-SHIRT DEADLINE for the 2021 ASF Walk. This means that today is the last day to be guaranteed to receive your t-shirt by ASF Walk Day - May 15. Plus you’ll receive priority and free Trivia Night entry for the virtual events. Register today!
www.angelman.org/walk

The 2021 ASF Walk is Virtual, but we have a lot of SUPER events planned to Unite our Heroes!. Those registered for the ASF Walk will get their t-shirt mailed to their home, priority and free entry for Trivia Night, Zoom with clinicians and more! Find out details on our website: www.angelman.org/walk

Don’t miss out on the Early Bird Fee for the ASF Walk. On April 1, it’s going up - and that’s no joke! The t-shirt deadline is April 5. Register today and you’ll be able to participate in all the ASF Walk Week virtual events and receive your t-shirt before May 15. www.angelman.org/walk

"I want to bring awareness to my community for my son and others with Angelman Syndrome."
-- AS Avenger and Walk Coordinator, Whitney Olin

Sorry for the delay! Registration is now Open! Let’s Unite to conquer AS at the 2021 ASF Walk on May 15 (at most of the 50+ locations). Registration is open AND fees are discounted TODAY!

Register here: https://secure.e2rm.com/p2p/event/349779/en-CA

🤩 ASF Walk Registration opens on Monday! 🦸‍♂️ 🦸‍♀️
Please note: The ASF Walk will be held on May 15, either in-person or virtually, depending on CDC Guidelines. Either way, we are SUPER excited to Unite and honor our loved ones with AS. Find 2021 locations and more information on our website: angelman.org/walk

Hi Everyone- myself and my fiance Don live in Bennington with our 3 year old son Gabriel with Angelman's. This is my first year coordinating a walk event for Angelman's and it's a very exciting time! Feel free to reach out if you have any questions or would like to help out in anyway. You can mesaags me on Facebook, e-mail me at [email protected] or text 802.282.8282. I can't wait to get together for this event to meet and see everyone!