<img src="https://res.cloudinary.com/hxn9dbuhd/image/upload/v1686084841/w5kzcjxi85szkbktuwki.jpg" style="width:319px;display:block;vertical-align:top;margin:5px auto;text-align:center;position:relative;max-width:100%;cursor:pointer;padding:0px 1px;user-select:none;box-sizing:inherit" /> This donation will help save children suffering from a horrible genetic brain disease. Canavan Disease is a destabilizing disease that makes it so children cannot talk, walk, or hold their heads up. They are mostly doomed to death by age 5 or 10.Without your support, they have no chance at life: With your donation, we'll be able to : - Support families who are struggling with resources, advice, and guidance - Power medical research into cures for the disease- Support gene therapy treatments of children with Canavan Disease, a destabilizing disease that makes it so that children cannot talk, walk, or hold their heads up  The Canavan Research Foundation spearheaded the first gene therapy in the world in 1998 in New Zealand. Since then, multiple children have been treated with gene therapy due to our important work.  Lindsay Karlin, treated with gene therapy three times, was predicted to die by age 10 and lived until 27 years old. These donations are also in memorial to that brave little girl.

Hello <span contenteditable="false" data-custom-variable="{{firstname}}" fr-original-class="fr-deletable styled-tag-chip " style="background-color:rgb(248, 248, 255);border:1px solid rgb(191, 191, 255);border-radius:4px;color:rgb(42, 42, 196);display:inline-block;margin:0px;padding:1px 8px;font-size:11px;line-height:16px;overflow-wrap:anywhere;user-select:none;box-sizing:inherit">First name <span contenteditable="false" data-custom-variable="{{lastname}}" fr-original-class="fr-deletable styled-tag-chip " style="background-color:rgb(248, 248, 255);border:1px solid rgb(191, 191, 255);border-radius:4px;color:rgb(42, 42, 196);display:inline-block;margin:0px;padding:1px 8px;font-size:11px;line-height:16px;overflow-wrap:anywhere;user-select:none;box-sizing:inherit">Last name, We thank you from the bottom of our hearts. This donation greatly helps to save the lives of those children who without you, wouldn't have a chance at life.  We will now be able to:power medical research into curing Canavan Diseasesupport gene therapy treatments of individual childrengive guidance, resources, and support to families who are suffering The Canavan Research Foundation is a 501c3 nonprofit, and your donation is fully tax-deductible. CRF has not provided any goods or services, in whole or in part, to you in consideration for this voluntary cash contribution. If you wish to claim the tax deductibility of this gift in the U.S., please retain this acknowledgment letter for your files. CRF’s EIN number is 06-1579083. If you would like to contribute further, contact us to become a volunteer, to apply to join the board, or spread awareness of genetic diseases like Canavan.  In particular, if you are of Ashkenazi Jewish origin, there is a 1/35 chance that you are a carrier for Canavan Disease. We encourage you to ask your OBGYN for the full panel of Jewish genetic diseases, and ensure that they include Canavan. This applies even if your partner is not of Ashkenazi Jewish descent.  Thank you again for your support.  Samantha KarlinBoard of Directorsinfo@canavan.org

<img src="https://res.cloudinary.com/hxn9dbuhd/image/upload/v1686084841/w5kzcjxi85szkbktuwki.jpg" style="width:319px;display:block;vertical-align:top;margin:5px auto;text-align:center;position:relative;cursor:pointer;padding:0px 1px;user-select:none;box-sizing:inherit;max-width:100%" /> This donation will help save children suffering from a horrible genetic brain disease. Canavan Disease is a destabilizing disease that makes it so children cannot talk, walk, or hold their heads up. They are mostly doomed to death by age 5 or 10.Without your support, they have no chance at life: With your donation, we'll be able to : - Support families who are struggling with resources, advice, and guidance - Power medical research into cures for the disease- Support gene therapy treatments of children with Canavan Disease, a destabilizing disease that makes it so that children cannot talk, walk, or hold their heads up  The Canavan Research Foundation spearheaded the first gene therapy in the world in 1998 in New Zealand. Since then, multiple children have been treated with gene therapy due to our important work.  Lindsay Karlin, treated with gene therapy three times, was predicted to die by age 10 and lived until 27 years old. These donations are also in memorial to that brave little girl.

www.canavan.org

Donate to save the lives of Canavan Children

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