The Chelsea Hutchison Foundation
Rating: 4.98 stars 94 94 reviews 1,563
Post Office Box 630048 Littleton CO 80163-0048 USA
The Chelsea Hutchison Foundation grants comfort and hope to those affected by epilepsy through providing monitoring resources, vital information, and a safe haven for conversation and community. Our main goal is to raise awareness of SUDEP and to make a positive difference in the lives of individuals and families living with epilepsy. We raise funds to provide education about SUDEP and to provide seizure response dog grants and life-saving movement monitors that help to protect against SUDEP. We stay up-to-date on current trends in medical technology in order to be able to provide the most effective devices as they become available. We respect the value and quality of life of every person living with epilepsy. We are dedicated to providing opportunities that allow individuals and families greater independence, increased confidence, ability to enjoy social environments, and community understanding.
as of April, 2015, we have provided 69 grants for seizure-response dogs and over 275 movement monitors for those in need.
Anyone who lives with seizures.
Direct beneficiaries per year:
Geographic areas served:
We provide to help to all 50 States.
SUDEP Awareness, Seizure-Response Dog Grants, Emfit Monitors, SAMiAlert Monitors, SmartWatch Monitors.
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Reviews for The Chelsea Hutchison Foundation
The Chelsea Hutchison Foundation, Julie and Doug have made a great impact on our life. By providing a sleep moment monitor for my son, it has given my son more independence. They are dedicated to raising awareness . Through the foundation we were given the opportunity to go disneyland during the epilepsy awareness day. We meet so many people and now have life long friends all thanks to Julie and Doug.
The Luna Family
The Chelsea Hutchinson Foundation is a wonderful organization. I live in Indiana and found out about the organization through reading other families positive experiences on social media. My husband and I were ecstatic and felt a great peace of mind knowing The Chelsea Hutchinson Foundation can provide us with a SAMi monitor for our son who has Dravet Syndrome. We are beyond grateful!
This organization helped fund our SAMi alert system for my daughter with intractable epilepsy. We couldn't afford a system like this without this wonderful organization! After getting the system I was able to notify her doctor she was having hour long seizures during her sleep. Without this system we would have never known! Thanks so much Chelsea foundation!
The Chelsea Hutchison Foundation has been wonderful with helping on advice for our son Logan (9). They also were amazing with working a way for us to receive a SAMi video monitor. This has been an extreme help, not only did they assist with our costs involved, but more importantly helped with peace of mind and as parents we are able to sleep better at night, in the event Logan has a seizure. We are greatful for their assistance in memory of their daughter. Thankful for all they do!
This is a family-based foundation that was created after the loss of a beautiful girl (their daughter) named Chelsea. They have made it their mission and Chelsea's legacy to ensure no more lives are lost to SUDEP. During the time when I had recently given up my full-time employment (and bread-winner role in my household which made the medical bills that much more overwhelming) to care for our infant daughter with epilepsy, The Chelsea Hutchison Foundation subsidized the cost of Emfit, a movement monitor to detect seizures during my daughter's sleep. This not only took away from some financial stress, but provided an invaluable gift of peace of mind so I was able to sleep at night once again.
Julie is a selfless, empathetic, determined woman. She is my epilepsy hero.
1 person found this review helpful
As the single parent of four boys, even the barest of necessities are often seen as a luxury. My son has epilepsy, and faces many challenges as a result. I have always wanted to take my kids to Disney, but my income, coupled with concerns my child's health, made it a far off dream. I am a member of the Chelsea Hutchison Foundation's online community, and saw that they were offering an opportunity to attend Epilepsy Awareness Day in Disneyland. I contacted the foundation, shared with them my son's story, and my desire for him to meet others like him who understand his condition, and perhaps make a friend. To my utter disbelief, they awarded my family with the opportunity to participate in E Awareness day in Disneyland! They are REAL people, helping REAL people. I am so thankful for their dedication to the E community. They are an inspiration
1 person found this review helpful
Great organization!! Live the passion they have to bring awareness to others. The world is a better place because of CHF!
What an absolute amazing foundation! With the Sami cam we received we are blessed! This foundation served as many things including supplying life saving devices/resources. Helping families in many ways to learn more about epilepsy and even help with sending them to a once in a life time (for some) trip to epilepsy days at Disney! I can't say thank you ENOUGH.
I only found out about CHF a short time ago... But can already tell that it's an AMAZING resource of information and help! We have adopted a little girl with a severe seizure disorder (hundreds of petites a day along with multiple grand mals a day), cerebral palsy, autism, fetal alcohol syndrome and ADHD. Our greatest concerns are here seizures. I have not been able to find a good resource of information and support until stumbling across The Chelsea Hutchison Foundation. I have learned so much! And finally glad to feel like I'm NOT ALONE! Most of her GM's happen while she is asleep... So I have found out about special devices to look into that can help put me at ease. Thank You for EVERYTHING You Do for Every Child & Parent that you have touched!!!
I think the foundation is doing a wonderful of sharing information, Keep up the great work