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Cure Sanfilippo Foundation

To advocate for and fund research directed towards a cure or treatment options for patients with Sanfilippo syndrome.

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Morgan Rachal está arrecadando fundos
Save Lydia
A parent's worse nightmare is losing their child. Our daughter Lydia is 3 years old. She is so full of life. She loves playing right along side with her big sister. But her little body is dying. Before her disease takes over her body and brain damage starts to occur, we have one chance to change her fate & it has to happen soon. What if money was the one thing that stands in the way of your child's chance to live? We need your help to save our sweet Lydia. **donations are tax deductible**

Our Story

When Lydia was born, we were so excited. Her big sister was so happy to have a forever best friend. Our hearts were so full. She had a perfect birth. The doctor said “she’s perfect”. We were so in love with her. We were so happy to have our new girl to take home with us. 18 months of our lives were just full of happiness. Until April 4, 2024, the day our lives changed forever.

Our sweet Lydia was diagnosed with a rare genetic disorder called Sanfilippo Syndrome type B, which is terminal. Life Expectancy not passed teenage years. Our hearts were shattered and it was a dark place I cannot even explain. How was our child slowly dying and we did not even know it?

In March, my mother sent me a TikTok of a little girl named Olivia with the TikTok account "Saving Liv". This little girl could have been my Lydia's twin. It was a gut punch when I saw the diagnosis of Olivia being a terminal illness. Of a disease I did not even know existed. So I started researching more of the disease, with symptoms that went along with it. I found frequent ear infections, sleep disturbances, distended belly, GI issues, and prominent thick eyebrows, which were all the symptoms Lydia had. The thick eyebrows were something I thought she inherited from my husband. Everyone always said "They look just alike". I knew then when I saw the symptoms, this was what my daughter had. My gut told me so but my heart told me there was absolutely no way (it is 1 in 70,000) that my baby who has met all milestones in her life and to me, was a healthy baby as I thought.

I took my concerns to our pediatrician in our hometown of Natchitoches, Louisiana. I showed him side by side pictures & the TikTok I had seen. He told me "I have never been asked this before, nor have I ever seen a child with it". He told me he would have to go do research himself and come back into the room. He came back into the room and tells me "I cannot come back in here & tell you she does not have it, so I will order you the genetic testing for it, but you will have to do it at another hospital because our town does not have that type of ability to test for it. I want you to assure you that this is very rare, and children come in all the time with issues not sleeping, constipation, and frequent ear infections still after tubes". I was so grateful that he listened to me, ordered us the testing, and did not make me feel crazy. We went to another hospital to have the testing done the very next day. It was a blood test and a urine test.

A week of anxiously waiting to "rule it out".... the following Thursday I pull up my patient portal to see POSITIVE MPS III (Sanfilippo Syndrome). That exact moment was the worst feeling of any day I have ever had on this earth. My heart sunk, I felt like I could not breathe. The instant feeling of "my baby is going to die".

This dark place my husband and I were in last for about 2 weeks. It was then, I was ready to fight for her. I contacted the Cure Sanfilippo Foundation to figure out what I could do as a mother to fight for her and the treatments available for her. There are no current treatments or cure approved by the FDA, only clinical trials. But there is HOPE. The clinical trials have a gene therapy treatment and an enzyme replacement therapy. In Sanfilippo Syndrome, Lydia's body is missing an enzyme that is used to breakdown sugar molecules. Without this enzyme, toxic waste build up in her body. This would explain her distended belly from an enlarged liver. That I thought was just from constipation. As the years go by and more toxic waste build up, it will start affecting her brain, causing damage, leading to her to lose or forget all of her abilities such as walking, talking, and feeding herself, everything she has already learned. This is why it is called Childhood Dementia. She will also eventually endure pain and suffering, and then die. This is 100% fatal.

Luckily, we were able to get diagnosed early because of TikTok and our pediatrician. The regression usually starts around age 3 and 4. But every child with this disease is different. This would mean we have about a year or less before brain damage begins & takes over. Fast forward 18 months after we got the diagnoses, THERE NOW IS A TREATMENT OPTION. We need 6 million to fund a treatment that could be available for her as early as this summer 2026. 3.8 million by December 1, 2025 & the rest by spring 2026. This is how you can help us Save Our Lydia. So one day, when my 6 year old daughter, Heidi, is able to understand, I will not have to explain to her that her little sister is going to die. The words I never want to hear is "I don't want my sister to die". After the diagnosis, that is the moment I am dreading. She is the best big sister to her. Her sister deserves a chance at life.

As a mother, feeling helpless and knowing this disease is out of my control.. the only thing I know to do is fight for her. Fighting for her in this case is making awareness of this disease, sharing her story, fundraising, and in hopes her story will reach the world. Hoping the world will help save her. We pray everyday for this. We will never stop fighting for her. Every dollar counts. We need a miracle and this world of a community could be our miracle. Along with all the other children and families suffering with this disease and heartbreak.

Our goal is to raise $6 million dollars to help fund treatments and give our Lydia a chance at growing up, a chance at life. We can't just sit back and accept that she is going to die with knowing there are treatments out there. Previous clinical trials done for Sanfilippo Syndrome have shown real promise. The treatments WORK. Our Lydia needs treatment!! This campaign for her LIFE is as urgent as it gets. It's now or never for Lydia. This is our last chance to save her life before brain damage begins. 3.8 million by December 1st.

This is truly our only hope. Her story has already reached millions. People Magazine, VT, Daily News, & News stations. Help us keep sharing her story. In hopes it will reach a celebrity or millionaire that will be these children's spokesperson and help fund for them. They deserve a chance at this life. A parent's love is like no other. If you are a parent, you understand.

There are three things we are asking you to do. A campaign like this can grow quickly if supported and if shared with great mass. We can reach this goal if it goes viral.

1. Please donate what you are able. All donations go to the 501c3 nonprofit Cure Sanfilippo Foundation (Tax ID: 46-4322131) to fund a clinical trial and are tax deductible.

2. Please take a few minutes and share our GoFundMe everywhere you can. It’s really easy to do. Just click the “Share” button and send it everywhere you can. Please help this reach the right people. I know if they see it, this can happen.

3. Please leverage any avenue you have to make this go viral.

Thank you for making it this far in our story. I hope you are able to help save our girl.

-Morgan & Kirk

Other ways to donate:

-- By check: Cure Sanfilippo Foundation, PO Box 6901, Columbia, SC 29260. Include “Save Lydia” in the memo.

-- Donate via Venmo, ACH, digital wallet or digital wallet, go to https://give.curesanfilippofoundation.org/save_lydia

-- Make a recurring donation, go to https://give.curesanfilippofoundation.org/give/630751/#!/donation/checkout?recurring=1

-- By stock gift, email [email redacted] for details.

Follow us

-- TikTok: https://www.tiktok.com/@hopeforlydia

-- Instagram: https://www.instagram.com/hopeforlydia/

-- Facebook: https://www.facebook.com/profile.php?id=61561244030850

For media

For additional information and photography for the media, please go to http://CureSanfilippoFoundation.org/Save_Lydia

Credits

Special thanks to Joe Lane of Anointed Media LLC (https://www.anointed.media) for lending his tremendous videography, video edit, music and audio editing skills, and passion to this project.
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24,5 mil apoiadores
Christin Ulrich está arrecadando fundos
Saving Veda
I'm Christin, Mom to Veda. When Veda was born, Jericho and I thought we had our fairytale life. That this was the beginning of our happily ever after. We never expected that our entire world would turn upside down in a matter of years. And that one TikTok video would change our lives forever.

When Veda was born, she seemed like a completely normal baby, aside from some breathing issues right at birth. Those first days, weeks, and years were just bliss. Counting fingers and toes, and dreaming about our family’s future.

Veda is one of those “big personalities,” filled with vibrance and joy. She is always smiling and loves to be goofy. And, I’ll admit, she’s definitely Daddy’s little girl, through and through. She has this second sense for when it’s time for Jericho to come home from work and she always waits for him to arrive. As soon as he walks in the door, she’s running to him, giving him hugs and kisses. The two of them together are something special.

But Veda began falling behind in meeting some developmental milestones and we became concerned. Like every parent, we went to the pediatrician in search of answers for her delayed speech and chronic ear and upper respiratory infections. Sadly, we were met with repeated assurances of “She’s fine.” and “She’ll catch up,” from doctors, despite having a growing list of concerns. We had to push relentlessly to be referred to specialists. We spent months trekking to appointments with specialists, who ran test after test, but they didn’t have answers either.

My mother’s intuition was telling me there was something wrong, something causing all these concerning symptoms in Veda. Despite all the assurances from doctors, I knew there was something going on and I had to find the answer.

I never imagined what I was going to find and how I would find it. Especially since I wasn’t even looking.

One night, I’m scrolling TikTok in bed after Jericho had already fallen asleep. I see a video of a mom talking about her daughter, Haidyn, who looks like Veda’s twin. In the video Haidyn’s mom is talking about how Haidyn has a disease called Sanfilippo Syndrome and so many of the symptoms sounded like what we were seeing in Veda.The realization Sanfilippo Syndrome could be the reason for all Veda’s symptoms hit me like a punch.

I immediately Googled “Sanfilippo Syndrome” and, as I started to read, the world came crashing down.

Sanfilippo Syndrome is like Alzheimer’s, but in children. It is a terminal, degenerative disease that causes children to lose all the skills they’ve gained, suffer seizures and movement disorders, experience pain and suffering, dementia, and then die usually in their teen years. It’s caused by a single gene defect which leads to lack of a necessary enzyme in the body. This lack of enzyme results in the build-up of toxic storage in every cell, and is especially harmful to the brain. This build-up causes a cascade of detrimental effects and ultimately death. Currently there is no FDA-approved treatment or cure for Sanfilippo Syndrome.

The fear racing through me was like nothing I had ever felt. I was so scared that I woke up Jericho, hoping he could convince me this couldn’t be true. We both prayed it wasn’t Sanfilippo. We couldn’t face the idea that our daughter has peaked in her development, that she would lose every single skill she’s ever gained, and that she will die in the coming years after years of extreme suffering.

In September 2022, genetic testing confirmed that Veda has Sanfilippo Syndrome. All those years of searching, begging doctors for help, and we finally had an answer. An answer that was worse than anything we could have ever imagined. We were completely crushed.

We spent the first few weeks after her diagnosis stricken with grief. But we decided we had to fight. We had to do our best, like any parent would, to save our child. We reached out to Cure Sanfilippo Foundation, for opportunities that might give Veda a chance.

But there is hope! A clinical trial for Sanfilippo Syndrome is in the preclinical stages (drug production, drug safety testing, efficacy testing, IND application process, etc.). With enough funding, this will become a clinical trial that begins treating multiple children. And we need it to start as soon as possible. Not just for Veda, but for all children with Sanfilippo.

It just needs funding, and a lot! Clinical trials for rare diseases are enormously expensive.

Large pharmaceutical companies often have little interest in rare diseases like Sanfilippo because there isn’t enough of a business incentive. Angel investors and federal grants are incredibly difficult to obtain. Which often leaves funding the research that could save our children to parent-led organizations like Cure Sanfilippo Foundation. Cure Sanfilippo Foundation works with the community of Sanfilippo families to rally kind-hearted people (like you!) willing to donate.

Your donation will help make the clinical trial happen!

Our goal is to raise $500,000 to help fund the clinical trial. Being part of a clinical trial will give Veda a chance at growing up, a chance at life. We can’t just sit back and accept that she’s going to fade away and die, not when there is something we can do to try to save her.

This is as urgent as it gets. It’s Veda’s only chance.

There is no guarantee Veda would be accepted into the trial. That decision is up to the clinicians running the trial. But it’s the only chance. We have to try. This is our only hope. And without funding for research and clinical trials, her future is certain: she will lose all of her abilities, suffer, and pass away, likely in her early teens. All right before our eyes.

We’ve had to let go of a lot of dreams, of things we thought our future held. We have one dream now, one desperate hope: Saving Veda.

Please, please help save our daughter.

There are three things we’re asking you to do. A campaign like this can grow quickly with your support. You are the key!

Please donate what you are able. All donations here go directly to the 501(c)3 nonprofit Cure Sanfilippo Foundation (Tax ID: 46-4322131) to help fund this clinical trial and are tax deductible.

Just as important, please share SavingVeda.com with everyone you know via social media and email so it keeps spreading.

Please leverage any avenue you have to make this go viral. Click 'contact' below to share any leads you might have with us.

Please help us give Veda a chance at life. It has to be now.

Our deepest thanks. We are so moved and humbled by your support,

Christin, Jericho, Elise (Veda’s older sister), and Veda

Follow the latest:

-- TikTok: Veda's TikTok

-- Instagram: https://www.instagram.com/savingveda

-- Facebook: https://www.facebook.com/SavingVeda

Donations can be tax-deductible.

Other ways to donate:

-- Donate via Venmo, PayPal, digital wallet, and ACH on this site. Simply click the “Donate” button and choose your preferred payment method at the bottom of the page.

-- www.CureSanfilippoFoundation.org (click “Donate” and put “Saving Veda” in the dedication)

-- By check: Cure Sanfilippo Foundation, PO Box 6901, Columbia, SC 29260. Include “Saving Veda” in the memo.

-- By stock gift, click Contact below and we can provide details.

Special thanks to the artists, who graciously dedicated their time and talent:

Video footage by Eva Philippe Petit and Quinn Michael Reeder

Video editing by Benjamin Von Wong

Photography by J Blanch Photography Inc, Benjamin Von Wong, and Amanda Joann Photography

Original music by KeithTim Anderson

Audio mastering by Andrew Kesler

***A special note of thanks***

We want to thank Haidyn, her mom Carrie, and her entire family for helping bring us to diagnosis earlier, for sharing their story on social media, and for choosing to be a part of this video and campaign. We love their family! Their courage is inspiring to us and to so many!

Information for the media: www.CureSanfilippoFoundation.org/SavingVeda

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A MESSAGE FROM CARRIE FOWLER, HAIDYN’S MOM

I support this project and want to see it succeed because it’s the only hope our children have. The only hope is to continue to push to fund clinical trials. Because without the trials, we don’t have a chance. We know that they could fail, they may not show the results hoped for, and they cost a ton of money. But if there’s a potential to save children’s lives, even a small number, in the Sanfilippo community, these innocent children deserve a chance.

I speak for myself and, I think, every other parent in the Sanfilippo community that our hearts break every time there is another child diagnosed with Sanfilippo Syndrome. Because we know what they are facing, what their future looks like, and that they’ve entered this world and nothing is ever going to be the same again.

This is why we really need to keep pushing to make clinical trials happen. To even, at least, find a treatment to make life just a little more comfortable for these children.

Part of Haidyn’s legacy will be saving other children. I want her story to be remembered, a child who led to further innovation in finding treatments and cure because we put her story out there. We put a lot of our own vulnerabilities and our realities out there in honor of her. Because we promised her that we would do everything we could to change the world for children like her, even if we weren’t able to save her.

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WHERE IS YOUR MONEY GOING?

Every dollar goes to Cure Sanfilippo Foundation, a 501(c)(3) nonprofit organization which funds research that can lead to a clinical trial for Sanfilippo Syndrome that could give Veda a chance at life. Donations are tax deductible. 100% of the funds raised here will go toward this clinical trial project. We are currently racing against time to fund this potentially life-saving new treatment. It could help Veda and so many other children have a chance at life, today and for generations to come. ***Any donations received above the goal will go directly to Cure Sanfilippo Foundation to continue funding the clinical trial costs and other research to help children. ***

WHY SO MUCH MONEY?

Getting a clinical trial up and running can cost millions of dollars. In rare diseases, large pharmaceutical companies often have little interest because they don’t see ways to make a profit. The truth is that it is left up to parents, patient-led organizations, and donors to drive and fund the research for treatments and a cure. This will help fund a clinical trial that can possibly help Veda and other children with Sanfilippo. Raising this amount of money may seem daunting, but it has been done before and research and clinical trials have happened as a result. It can for Veda too.

TIME IS OF THE ESSENCE

Sanfilippo Syndrome causes children’s cognitive and physical abilities to be completely taken away quickly once they begin regressing. In time, children regress back to an infantile state, likely never to return. This rapidly-progressive neurodegenerative disease will soon start taking over completely. Veda is 4 years old. We don't want to lose our daughter. This must happen now, and thank you for your compassion and generosity.
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332 apoiadores
Erin Stoop está arrecadando fundos
Saving Liv
Our daughter Olivia just turned three. She is energetic and loving. And she’s dying. We have one chance to change her fate and it has to happen soon. We need your help to save Liv’s life.

When Olivia was born, we were so excited! We couldn’t wait to start showing her the world and watching her experience life. Dance lessons, teaching her guitar, and baking together. All those things you envision for your child.

When Olivia was born, she passed all the newborn screening tests and was given a clean bill of health. However, in her first two years, she constantly had recurring ear and sinus infections and frequent loose stools. We pressed Liv’s pediatrician for answers at her two-year-old check up and began seeing a series of specialists, hoping for an answer. We were so scared the answer would be some type of chronic condition that she would have to live with her entire life. Little did we know that something even worse lay ahead.

In March 2022, our world came crashing down. Olivia was diagnosed with Sanfilippo Syndrome Type B, a genetic degenerative brain disorder in children caused by a single missing enzyme. It’s the worst disease you’ve probably never heard of. It’s like Alzheimer’s, but in children. It’s 100% fatal and there currently is no FDA-approved treatment or cure.

Because Liv lacks this single enzyme, toxic cellular waste material is building up in her brain every second and damaging it. As the degeneration rapidly progresses, Liv will stop walking, stop talking, stop being able to feed herself. She’ll develop movement disorders and seizures, suffer severe dementia, endure a lot of pain and suffering, and then she’ll die. All in the coming years.

Today, Liv loves playing waitress, helping take care of her baby brother Liam, and singing with us during bedtime snuggles. Without a cure, that will all go away and Liv will pass away in her teens.

But there is hope! There are promising forms of treatment that are already being investigated for Sanfilippo Syndrome. They just need funding to continue and reach the clinical trial stage.

Current promising research underway that could lead to clinical trials includes gene therapy, substrate reduction, and drugs already-approved for other diseases that could also help children with Sanfilippo. All of these focus on lessening the build up of the toxic cellular waste in children’s brains and bodies, which reduces neuroinflammation in the brain and prevents development of Sanfilippo’s many disease symptoms.

It just needs funding.

Large pharmaceutical companies have little interest in rare diseases like Sanfilippo because they don’t see ways to make a profit. Angel investors and federal grants are incredibly difficult to obtain. Which leaves funding the research that could save our children to parents, patient-led organizations (like Cure Sanfilippo Foundation), and kind-hearted people willing to donate.

We need your help to fund research so a clinical trial can happen.

Our goal is to raise $1 million dollars to fund the research that could lead to a clinical trial and give Liv a chance at growing up, a chance at life. We can’t just sit back and accept that she’s going to fade away and die, not when there is something we can do to try to save her.

This is as urgent as it gets. It’s Liv’s only chance.

There is no guarantee Olivia would be accepted into a trial. But it’s the only chance. And without funding for research and clinical trials, her future is certain. But we have to try. This is our only hope.

A parent’s love for their child is like no other. If you are a parent or simply love kids, you understand. Please, please help save our daughter.

There are three things we’re asking you to do. A campaign like this can grow quickly with your support. You are the key! We have faith and pray every day that your kindness, generosity, and compassion will help us make the difference for Liv.

1. Please donate what you are able. All donations go directly to the 501(c)3 nonprofit Cure Sanfilippo Foundation (Tax ID: 46-4322131) to fund research for Sanfilippo Type B and are tax deductible.

2. Most importantly, please share this page with everyone you know via social media and email by clicking share button or typing in SavingLiv.com.

3. Please leverage any avenue you have to make this go viral. Send leads or tips to us by clicking the Contact button at the bottom of this page.

Please help us give Olivia a chance at life. It has to be now.

Our deepest thanks. Words can’t even express how incredibly grateful we are.

Erin and Tyler Stoop

Follow the latest:

-- On Instagram: https://www.instagram.com/saving_liv/

-- On TikTok: @saving_liv

-- On Facebook: https://www.facebook.com/profile.php?id=100088622245570

Donations are tax-deductible.

Other ways to donate:

-- At Liv's campaign on Cure Sanfilippo website, donate via Venmo, PayPal, ACH, digital wallet at this site.

-- To make a recurring donation (monthly, weekly, quarterly, or annually), click here.

-- www.CureSanfilippoFoundation.org (click “Donate” and put “Saving Liv” in the dedication)

-- By check: Cure Sanfilippo Foundation, PO Box 6901, Columbia, SC 29260. Include “Saving Liv” in the memo.

-- By stock gift, message us and ask for details by clicking contact button at the bottom of this page.

-- By cryptocurrency at www.CureSanfilippoFoundation.org/crypto

Special thanks to the artists, who graciously dedicated their time and talent:

Video footage by Alex Sharon, Pilgrim Visual, LLC

Video editing by Benjamin Von Wong

Photography by Traci Stoop of Stoop Images, the Stoop Family, and Vanessa Wyler of Vanessa Wyler Photography

Original music by KeithTim Anderson

Audio mastering by Andrew Kesler

Information for the media: https://www.curesanfilippofoundation.org/SavingLiv

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WHERE IS YOUR MONEY GOING?

Every dollar goes to Cure Sanfilippo Foundation, a 501(c)(3) nonprofit organization which funds research that can lead to a clinical trial for Sanfilippo Syndrome Type B that could give Olivia a chance at life. Donations are tax deductible. 100% of the funds raised here will go toward the research. We are currently racing against time to fund this potentially life-saving research that could lead to a clinical trial. It will help Liv and so many other children have a chance at life, today and for generations to come. ***Any donations received above the goal will go directly to Cure Sanfilippo Foundation new research projects in need of funding***

WHY SO MUCH MONEY?

Getting a clinical trial up and running can cost millions of dollars. In rare diseases, large pharmaceutical companies have little interest because they don’t see ways to make a profit. The truth is that it is left up to parents, patient-led organizations, and donors to drive and fund the research for treatments and a cure. This will help fund research that could lead to a clinical trial that can possibly help Olivia and other children with Sanfilippo. Raising this amount of money may seem daunting, but it has been done before and research and clinical trials have happened as a result. It can for Liv too.

TIME IS OF THE ESSENCE

Sanfilippo Syndrome causes children’s cognitive and physical abilities to be completely taken away quickly once they begin regressing. In time, children regress back to an infantile state, likely never to return. This rapidly-progressive neurodegenerative disease will soon start taking over completely. Olivia is 3 years old. We don't want to lose our daughter. This must happen now.
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3,9 mil apoiadores
Minnie Lau está arrecadando fundos
Save Matthew
**12/20/25 UPDATE: The fundraiser goals for BOTH Phase I (Dec 1) and Phase II (early 2026) of the EAP have been met!! You helped our family raise over $831,000 since fundraising for the EAP began at the end of Oct ~ we are so grateful for our community's outpouring of love & generosity, and amazed by how God provided in such a short amount of time!

The work is far from finished though--over the next few weeks we will wait for details on the EAP which is projected to start in Q2 or Q3 of 2026 and may need to fundraise further for clinical administration costs (TBD). Meanwhile, any donations received after 12/05/25 will support these possible EAP costs and/or to other Sanfilippo Type B initiatives (gene therapy, research, etc.) for which there is always a need. Thank you!**

Follow Matthew's journey:

Instagram: Instagram.com/Cure.Matthew

Facebook: Facebook.com/CureMatthew/

We Need Your Help

Most parents imagine a bright future for their children--them growing up and meeting many milestones, going to school, making friends, getting a job one day, getting old... That will not be the case for Matthew unless we can get him a treatment soon. His brain and body are dying, and the condition he has will likely end his life before adulthood. We are fighting for his life and the one thing standing in the way is funding. We need your help to save Matthew.

Our Story

Our son Matthew is a sweet and playful kid, loving his family deeply. He adores his brother Nathan, saves treats for Mommy, requests piggyback rides from Daddy, and prays for his grandparents nightly. His big grin warms every heart, and he can be seen toting around his favorite Baymax pillow everywhere.

Matthew's life began with challenges due to multicystic dysplastic kidney syndrome, and at 2 years old, he started early intervention due to mild expressive speech delay. A few months later, impaired hearing and ear fluid led to genetic testing, from which we expected negative results. We could never have imagined what would follow.

A week later, the genetic results confirmed Sanfilippo Syndrome Type B, a rare, neurodegenerative and terminal disease caused by a missing enzyme needed to recycle waste in the cells. As a result, toxic material builds up in the brain and other organs, leading to progressive damage and eventual early death.

Our hearts were shattered. I cannot explain the unimaginable grief we felt, to know that our sweet and vibrant son who loves to sing, laugh, and play -- will soon lose the ability to think, talk, and move, dying after just a short time in our lives. This was the most difficult and daunting thing we have ever faced.

We have spent the past 1.5 years navigating the world of rare disease -- talking to doctors and researchers, going to appointments and therapies, fundraising, advocating, and searching far and wide for help. Any help.

We quickly learned that Sanfilippo Syndrome Type B has NO cure, NO treatment, and NOTHING accessible in the clinical trial stage. It seemed unlikely Matthew would receive any treatment before irreversible decline set in.

A Window of Opportunity

However, in just the past few weeks, a rare window of opportunity has opened up. For the first-time ever, a potential treatment for Sanfilippo Syndrome Type B is on the horizon and within reach. We realize this is a crucial, God-ordained moment, with a narrow window of opportunity to make a difference.

A company has agreed to create an expanded access program that would allow a number of Sanfilippo Syndrome Type B children to receive treatment before it obtains FDA approval, helping them stay healthy and potentially slowing or even preventing decline.

To move this treatment forward, $6 million total is needed, with $3.8 million required by Dec 1 to take the next critical step.

Our family has decided to step out in faith and partner with other Sanfilippo Type B families to fundraise for this cause -- because this is the only possible option available right now to save Matthew and other Sanfilippo Type B children.

We're asking you to walk with us. While we can't guarantee the outcome for Matthew and other children, we know we cannot miss this. This treatment could pave the way for dozens of children and redefine the future for families affected by this diagnosis. It's a chance to change what's possible for those who come next.

How You Can Help

Pray. Please intercede to God for all the children affected. Pray for wisdom, stamina, and God's provision in this endeavor

Be a voice. Share this page with your community. Text a friend. Post it online. Every share brings us closer to a breakthrough for kids with Sanfilippo Type B. One share could change everything

Give. Please consider donating to support this opportunity -- a gift of any size makes a difference

Follow Our Journey

Instagram: Instagram.com/Cure.Matthew

Facebook: Facebook.com/CureMatthew/

Other ways to donate without fees

Fidelity Charitable:

search for "National MPS Society" or "Cure Sanfilippo Foundation". Include "in honor of Matthew Lau" in the memo

Mail a check to:

National MPS Society

c/o Donations

PO Box 14686 Durham, NC 27709-4686

Include Memo: "in honor of Matthew Lau"

or

Cure Sanfilippo Foundation, P. O Box 6901, Columbia, SC 29260. Include "In honor of Matthew Lau" in the memo line

Don't forget to check if your company has a donation match! You can submit a tax receipt if you donated outside of your company's matching portal.

FAQ

Q: What does the expanded access program look like?

A: The expanded access program aims to provide treatment to 14 kids for 1 year via compassionate use (a pathway for patients with serious conditions to access investigational treatments when no other options are available and they can't join a clinical trial). This buys time for the kids, preventing regression while awaiting FDA approval.

Q: Where do your donations go?

A: Donations pass through the Foundation and Society, then the biotech company, to pay for manufacturing of the treatment. No fees are taken by the Foundation and Society or the biotech company. The manufactured treatment will be used in the expanded access program, with Matthew's potential participation in 2026

Q: Are we fundraising alone, or with others?

A: We're fundraising alongside 16+ families impacted by Sanfilippo Type B, as well as other Sanfilippo types families selflessly jumping on to support

Q: What is the fundraising goal?

A: About $6M with two phases of fundraising: $3.8M by Dec 1, followed by $2.2M by early 2026

Q: What happens if we don't reach our goals by the deadlines?

A: If the program doesn't move forward, all funds will go toward alternative Sanfilippo Type B treatments

Q: How is Matthew doing?

A: Matthew is continuing to develop with his favorite activities including scootering, fetching mail with mommy, baking cookies, and playing with big brother Nathan. But with Sanfilippo Type B, progression is unpredictable - skills like talking can vanish in a matter of weeks. We are racing against time to secure a treatment!
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Rachel Wood está arrecadando fundos
Save Oren
Last year, we learned that our 4 year old son Oren was dying, that there was no cure, no treatment, no fight to be won. But you can help him have a chance to live. *donations are tax deductible*

Our Story

Oren is an outgoing and joyful 6 year old boy who loves playing with his younger brother and sister and his cousins. He is expressive, has a contagious smile and laugh, and loves others unconditionally. When he was born, he had several minor complications which required surgery to correct. But according to doctors, the surgeries went well and there was nothing to be worried about going forward.

However, when Oren was 2 years old, we began to notice challenges: difficulty learning to talk, developmental delays, chronic bowel issues, and trouble sleeping. We immediately started him in speech therapy and enrolled him in a preschool program to support his development.

Despite early intervention, constant specialist visits, and our efforts at home, something still wasn't right. Not only was Oren not improving, his condition was worsening.

After two years of doctor visits, research, and questioning, we still had no answers, no clear path forward to help our son. Not until a family friend, who is a nurse, saw a video on TikTok with a child who had symptoms strikingly similar to Oren come across her feed. The child had Sanfilippo Syndrome. The more we learned, the more we knew this was what Oren was facing. We contacted our pediatrician asking for a referral to a geneticist so he could be tested for Sanfilippo Syndrome. We were quickly referred to the nearest children's hospital, where testing began. `

On July 31st, 2024, we learned that our 4 year old son Oren tested positive for MPS IIIB -Sanfilippo Syndrome Type B- a terminal disease with no cure and no available treatment. Commonly referred to as "Childhood Alzheimer's," Sanfilippo will take everything from him. He will lose his ability to speak the few precious words he knows, Oren will lose his ability to chase after his siblings and cousins, he will eventually forget all those he loves most. And then he will die.

But now there is HOPE.

Just over a year after his diagnosis, there is an actual treatment option available for children with Sanfilippo Type B. This is truly a medical breakthrough in the world of Sanfilippo/MPS III. We believe that you can help our Oren get his miracle. For months, we laid by Oren's bed, praying and crying out for his healing and for a cure, and we promised we would do whatever was in our power to fight for him, for a cure, for better quality of life. We didn't know if we had the faith it would take to believe for a miracle, but now there is a path that could lead to one. Our hope is that bringing awareness to this rare childhood disease could help Oren and other beautiful Sanfilippo children have the opportunity to share their lives with us a little longer.

Whether you can give financially or not, you can play a role in changing history.

How You Can Help

1. Pray 

Pray for the children impacted by Sanfilippo B. We believe that God is opening doors and that he is not finished with this story yet. Hope is rising. We have seen God moving in every step of our journey with Oren.

2. Give 

A gift of any size makes a difference.

Your gift doesn’t just help our family — it helps create access for many children battling this disease.

Other ways to donate:

--Donate on the Cure Sanfilippo Website (transaction fees apply; donors may opt to cover them): https://give.curesanfilippofoundation.org/campaign/653569/donate

--For gifts of $500 or more, checks may be made payable to:

Cure Sanfilippo Foundation

P.O. Box 6901

Columbia, SC 29260

3. Share

Awareness is key.

Share our GoFundMe. Just click the "share" button. Tell your community. Text it to a friend.

One share could be the one that changes everything.

Follow Us

Facebook: Save Oren (https://www.facebook.com/share/1DMYPnKtHk/?mibextid=wwXlfr)

Cure Sanfilippo Website: https://curesff.org/oren

Instagram: @saveoren
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144 apoiadores
Sarah Horne está arrecadando fundos
Give Hope: Support Research to Cure Sanfilippo
This Christmas our family is asking for donations to the Cure Sanfilippo Foundation. It is a devastating condition that has no cure or approved treatment. By giving money to research, we can give hope to families whose children are in desperate need for a cure. I can think of no better Christmas present.

As my thanks for supporting the Cure Sanfilippo Foundation, each individual who gives a minimum donation of $50 will receive a unique piece of craft jewelry of your choice until the fundraising goal is met. Keep it for yourself, or give it to a loved one this holiday!

'Tis the season of giving. Please consider contributing to this worthy cause.

Learn more about the foundation here: https://curesanfilippofoundation.org/
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John Wolfe está arrecadando fundos
JohnWolfe Fund-A-Thon Supporting Cure Sanfilippo Foundation
GoFundMe Fund-A-Thon X JohnWolfe

Supporting Cure Sanfilippo Foundation

Every parent dreams about their kid’s future and watching it unfold.

Sanfilippo Syndrome takes all that away, replacing it with pain and suffering. The child experiences severe dementia and dies in their mid-teens. All before their parents eyes. Cure Sanfilippo Foundation architects and funds cutting-edge research to accelerate discovery of a treatment or cure for Sanfilippo Syndrome so parents can dream of their children’s futures again.
88 apoiadores
Kristen Diamond está arrecadando fundos
Plunge for a Cure
The words Alzheimers and childhood should never have to be spoken in the same sentence, but did you know that 1 in 70,000 children suffer from Sanfilippo Syndrome, a disease referred to as childhood Alzheimers? Most do not. With your donation, a cure is possible.

Treatments for Sanfilippo are out there, though due to barriers in funding and policies, they remain unavailable. It will be years before they are released, but the children suffering from this disease now do not have years or even months to spare as their bodies, skills, and livelihood are being taken from them every moment. Awareness can help break down barriers to treatments for rare diseases like Sanfilippo.

For rare disease day 2023, many Sanfilippo families will be taking a cold plunge to raise awareness and much-needed funding for the research of treatments for this devastating disease. All funds will go directly to the Cure Sanfilippo Foundation. Join us in saving these children and fighting for their cure.

More information about Cure Sanfilippo Foundation: Cure Sanfilippo Foundation works to fund urgent research for treatments or a cure for Sanfilippo Syndrome. Sanfilippo syndrome is rapidly degenerative and fatal disease in children, currently with no FDA approved treatments or cure. More on the research the Foundation funds at www.curesff.org/research

More information on the #plungeforacure challenge can be found here.

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ABOUT US

We are The Diamond family and our son Noah was diagnosed with Sanfilippo Syndrome in December 2022. We are fighting to save his life and all children affected by this horrible disease.

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WHAT IS SANFILIPPO SYNDROME?

Sanfilippo Syndrome is caused by a single gene defect which leads to lack of a necessary enzyme in the body. This lack of enzyme results in the build-up of toxic storage in every cell, and is especially harmful to the brain.

This build-up causes a cascade of detrimental effects, such as increasing intellectual disability, loss of mobility, loss of the ability to eat, seizures, movement disorders, and eventually early death, often before the second decade of life.

Learn more at https://CureSanfilippoFoundation.org/What-is-Sanfilippo

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WHERE IS YOUR MONEY GOING?

Every dollar goes to Cure Sanfilippo Foundation, a 501(c)(3) nonprofit organization which funds research for Sanfilippo Syndrome that could give Noah a chance at life. Donations are tax deductible. 100% of the funds raised here will go toward the research. We are currently racing against time to fund potentially life-saving research that could lead to a clinical trial. It will help Noah and so many other children have a chance at life, today and for generations to come. ***Any donations received above the goal will go directly to Cure Sanfilippo Foundation new research projects in need of funding***

WHY SO MUCH MONEY?

Getting a clinical trial up and running can cost millions of dollars. In rare diseases, large pharmaceutical companies have little interest because they don’t see ways to make a profit. The truth is that it is left up to parents, patient-led organizations, and donors to drive and fund the research for treatments and a cure. This will help fund research that could lead to a clinical trial that can possibly help Noah and other children with Sanfilippo. Raising this amount of money may seem daunting, but it has been done before and research and clinical trials have happened as a result. It can again.

TIME IS OF THE ESSENCE

Sanfilippo Syndrome causes children’s cognitive and physical abilities to be completely taken away quickly once they begin regressing. In time, children regress back to an infantile state, likely never to return. Sanfilippo is a rapidly-progressive neurodegenerative disease that eventually takes over a child’s body completely.

Please note: This challenge was not created by Cure Sanfilippo Foundation. Participating is entirely your choice and at your own risk, so please assess your ability and safety before you participate. Cure Sanfilippo Foundation shall not be liable for any injury, damage or loss to you or your property that might occur as a result of your participation.

Cold Water Safety – General Guidance

· If you have underlying health conditions (i.e. heart disease, asthma, lung conditions) or any other medical conditions that might be affected by exposure to cold water, or if you are pregnant, then please seek appropriate medical advice before proceeding.

· Do not take part in the challenge under the influence of drugs or alcohol.

· Do not participate in this challenge if under the age of 18, unless supervised by an adult.

· Participation in this challenge is entirely at your own risk, so please assess your ability and safety before you participate. No person or entity shall not be liable for any injury, damage or loss to you or your property that might occur as a result of your participation.

· Let your friends / family know about your participation in this challenge.

· Do not undertake an open water swim unsupervised.

· Never go beyond your comfort zone.
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Charlene Aceto Smith está arrecadando fundos
My Pal Spencer #mpsIII

Update 2/15/18 The Wells Warriors wrestling team are raising awareness & crucial funding to find a cure for Spencer. We need a cure before time runs out.

We need your help today to SAVE Spencer, and other kids with Sanfilippo. Their only chance at life is a treatment in an experimental clinical trial. Clinical trials take millions to fund and we are hoping to raise $500,000 to help fund a clinical trial. The clock is ticking and due to the rapid degenerative nature of the disease, time is running out. Very soon, severe dementia could take away all of what Spencer has learned if a cure doesn't come in time. From there it gets much worse. This is TOO MUCH to bare. Please consider giving today and please share, to help save his life!

Our sweet Spencer has Sanfilippo Syndrome. It's known as the Children's Alzheimer's. But worse. Can you imagine? Neither could we.

Sanfilippo is a rare and fatal genetic disease that robs children of their brain function and gradually kills them. Starting often around age 3, Sanfilippo kids begin to lose critical skills. They stop talking. They become extremely hyperactive and can go days without sleep. They lose the ability to walk. They can lose their hearing and their eyesight. Eventually they suffer seizures and stop being able to swallow, meaning they need a feeding tube to survive.

Most kids with Sanfilippo die in their early teens.

And there is no cure.

In fact, there's not even any kind of treatment to help mitigate Sanfilippo's devastating effects.

Spencer already has significant hearing loss; he can't talk like normal 3-year-olds and communicates mostly through some sign language. We are in a race against time to try and save him from this horrible cruel disease.

Can you help?

There are some exciting possible treatments and a possible cure on the horizon -- especially in the realm of gene therapy. We need to fund this as soon as possible so that it can be adminstered to children like Spencer. It's their only chance at LIFE before this severe dementia sets in, followed by life.

Because Sanfilippo is a rare disease, it hasn't attracted interest from big pharmaceutical companies. That means it's up to the families of those suffering to fundraise for the clinical trials that could lead to a cure. With your generosity, we have a chance to help Spencer and other children suffering from Sanfilippo.

Please considering donating today. All funds raised go to the Cure Sanfilippo Foundation, a group of families across America helping to fundraise for these important clinical trials.

No donation amount is too small! All donations are tax-deductible.

Want to know more about Spencer? Follow him on Facebook at My Pal Spencer . And share our campaign!

In the Press
Congdon's After Dark
WGME 13
Bangor Daily News
Seacoast Online
‌Rare Disease Report
Journal Tribune
NESN
207 Maine
Portland Press Herald
WCSH6
York County Coast Star
WGAN News Radio
York County Coast Star
Rome Sentinel
Lexington Wicked Local

__________________________

Original Story

Like all toddlers, I love to splash in the pool with my daddy, dance in the yard with my mommy, and pet every puppy dog I can get my hands on. But unlike most boys and girls, I'm battling MPS-III, commonly known as Sanfilippo Syndrome.

Sanfilippo Syndrome is a genetic neurological disorder that can be easily understood as the childhood Alzheimer's. Both are a death sentence, but where Alzheimer’s strikes people toward the end of their lives, Sanfilippo attacks kids just as they have begun to learn to walk and talk. Also unlike Alzheimer’s, Sanfilippo is considered an "orphan disease," which means there isn’t enough incentive for drug companies to pursue a cure.

There are several teams of researchers around the world who are studying ways to treat Sanfilippo kids like me who lack an enzyme that breaks down complex chains of glucose. Sadly, some of the treatments already put through clinical trials have not panned out. What this means is that without more awareness of this terrible disease, and crucially, the money to fund more research, many kids with Sanfilippo will die as their peers head off to high school.

I don't want to be one of them.

I don't want to stop being able to walk. Or talk. And eventually, to swallow. All of which could begin happening, progressively, as early as the year I should be entering kindergarten.

I want to live.

I hope you will help me in this fight.

Follow me on Facebook (My Pal Spencer #mpsIII is Fighting to Cure Sanfilippo Syndrome). Please like and share my page!

All donations will go to the not-for-profit Cure Sanfilippo Foundation, a 501(c)3, and will be used for research to find a cure. Donations are tax-deductible tax ID (46-4322131).

I've been learning sign language since I got my hearing aids last summer. "Please" was one of the first signs I learned.

The Goldfish Photo. It's one of my dad's favorites of me! (credit: Dahlia Rin)

Told you I love puppy dogs!!!
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166 apoiadores
Glenn O'Neill está arrecadando fundos
Saving Eliza Continued
Every single dollar raised here has, and continues to go to Cure Sanfilippo Foundation, a 501c3 nonprofit (tax ID: 46-4322131). Donations are tax deductible. Cure Sanfilippo has a mission to advocate and fund research directed toward a cure or treatment options for children with Sanfilippo Syndrome. In short, we fund research to save children via treatments & clinical trials. No dollars ever go to or for any particular family or child. We tell individual stories, for the greater cause and mission....which is to cure this terrible fatal brain disease in little children, often referred to as a Childhood Alzheimer's. Our deepest and humble thanks for visiting this page and considering support. You are our hero! Glenn O'Neill (Dad, Donor and President of Cure Sanfilippo Foundation) [email redacted] (anytime)
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Thank you for visiting this new campaign to help us continue our efforts. Orginal Story is down below.

Happy 8th Birthday Eliza!!   A 10 day, $100,000 goal to help save and better the lives of innocent children. If the new goal set here is reached, we will do it!

You never stop fighting for your child. Ever. I'll be honest, I'm nervous this year. It's hard to know how many supporters are out there, still following...still fighting with us to help Cure Sanfilippo Syndrome. We have only a few more days to reach our Annual Drive goal to fund urgent research* for children, in honor of Eliza's 8th Birthday on Nov 16th.

We think Eliza is doing well overall, and can't believe our little girl will be 8 years old. She is happy most of the time. We cherish every second of time with her, and her loving big brother. The HOPE we have is thanks to your support!  A VIDEO update is below and we hope you'll take a few minutes to watch.

And after you do, would you be one of our $100 donors this year (although every amount helps)?

The truth is, we will need YOUR support to reach this goal. Literally, children's lives hang in the balance.

* There are 3 current projects in need of urgent funding, with a path to clinical trials for more children: 1) for enzyme replacement, 2) gene therapy, and 3) mesenchymal stem cell to repair the brain.

You can support here, or by sending a check made out to Cure Sanfilippo Foundation, PO Box 6901 Columbia, SC 29260.

Thank you for your kindness, compassion, and empathy. Our humble and deepest thanks is from all Sanfilippo families.

Glenn O'Neill (Eliza's Dad)
Cure Sanfilippo Foundation www.CureSFF.org
[email redacted] (anytime)
Latest Foundation update: www.CureSFF.org/update

#Happy8thEliza

1,000 supporters at $100 = GOAL REACHED! Will you be one?

SHARE SHARE SHARE

As always, all funds go toward the mission of our non-profit 501c3 Cure Sanfilippo Foundation (Tax ID: 46-4322131), which is to advocate for and fund research directed toward a cure or treatment options for children with Sanfilippo Syndrome.  Donations are tax deductible.

Our Story

It all started back in 2014, with this 3 minute video:

Now, we truly believe we are witnessing a miracle. What else can explain more than 36,000 people already donating more than $2 million dollars, over the past 2 years, to fund a chance at life for our daughter Eliza and other children. Diagnosed 3 years ago with Sanfilippo Syndrome —a terminal disease sometimes called “Childhood Alzheimer's”— Eliza has now become the first child in the world to have been given this new treatment! The second child has also been treated and in the coming months & through next year, a few handful more children around the world will be part of this groundbreaking gene therapy clinical trial that is already showing promising results.

The WORLD decided to rally around our little girl for this greater cause, and she’s become the face of this disease…a symbol for Sanfilippo parents everywhere not to give up HOPE.

And we’re not giving up on them either.

Many more children are still fighting, and we won’t stop until every last one of them is afforded a chance at life. There are more children that need this treatment than there are available spots in clinical trials, and these precious little ones can’t wait. Given the rapidly degenerative nature of Sanfilippo Syndrome, not receiving a treatment, and soon, is a death sentence. Can you imagine being one of these parents?

Since treatment, we see a new light in Eliza’s eyes— she is connecting with us in a way we thought was gone forever. She is working to regain the skills the disease stripped away in the 6 and half years it tore through her body. She is a fighter! Other Sanfilippo children deserve this chance too. At this stage, funding is one of the only things that will accelerate research to give these children a chance. Money doesn’t make the world go round, but it does bring medical treatments faster to children who are dying.

Our goal is to reach $4M here to help make this happen. Please donate TODAY to give these beautiful Sanfilippo children a rightful chance at life. Please share so the world can hear their collective voices.

Our hearts are forever thankful for giving our daughter Eliza and others a chance at life. We are reminded of one quote from a special supporter that has helped us through the hard days: “Keep the faith, and the faith will keep you”.  We believe!

Glenn, Cara, Beckham and Eliza (The O’Neill Family)

Learn more about Sanfilippo Syndrome here www.CureSFF.org/about-sanfilippo

Meet just some of the Sanfilippo families here: www.CureSFF.org/meet-the-families

Baby Sadie

Paisleigh and the Butler Family

Rowen and the Fernandez Family

Izzy and the Jurado Family

Keira and the Esposito Family

Parker and the Talbert Family

Abby Grace and the Ferguson family

All funds go toward the mission of our non-profit 501c3 Cure Sanfilippo Foundation (Tax ID: 46-4322131), which is to advocate for and fund research directed toward a cure or treatment options for children with Sanfilippo Syndrome. We are out to end this disease and help ensure treatments for as many children as possible along the way. We must reach our goal and mission before it is too late for these beautiful children. With a donation and a share, you can make the difference! Action saves lives. Action brings miracles. Our daughter Eliza is proof of that.

Donations are tax-deductible.

Other donation options:
-- www.CureSFF.org (click Donate)
--By check: Cure Sanfilippo Foundation, PO Box 6901, Columbia, SC 29260

Follow the latest at www.facebook.com/ElizaOStory

Special thanks to the artists, who worked free of charge to help us:
Video by the amazing Benjamin Von Wong
Photograpy by the talented Anna Tenne Photography
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439 apoiadores
Jill Wood está arrecadando fundos
The Final Countdown
Sanfilippo Syndrome have you ever heard of it?

Gene Therapy have you ever heard of it?

If No, than consider yourselves fortunate.

The children and families suffering from rare genetic diseases are not so fortunate. Parents of terminally ill children love their children everyday as if each day could be their last.

Sanfilippo Syndrome is a horrible genetic disease, caused by a gene mutation that stops a specific enzyme from doing it's job. Without the enzyme, children slowly loose all of their skills that they had learned from talking, walking, eating everything goes and they die.

Gene Therapy is a treatment that binds a virus to the missing enzyme. The virus delivers the missing enzyme to the children.

Sanfilippo Syndrome type C is ultra rare, occurring in 1 in 1.5 million births. Most drug companies don't see the financial value in producing and commercializing a drug for our dying children.

It's up to the parents of Sanfilippo children to fight their fate!

Ten years ago a group of foundations across the world found each other and banded together to find and then fund millions of dollars towards research and a treatment for Sanfilippo Syndrome type C. H.A.N.D.S.

Our scientists have proof of concept and we are now ready to manufacture our vector in large quantities so that we can conduct a clinical trial. For this we need your help in funding!

Be part of something that you can smile about. Help our Sanfilippo type C families fund the production of a drug that will halt this disease for many of our surviving children and save the lives of the next generation to come.

Translations: Spanish, German, French and Portuguese below video.

Spanish
Síndrome de Sanfilippo ¿has oído hablar de esta enfermedad?

Terapia génica ¿Has oído hablar de este tipo de terapia o tratamiento?

Si no, entonces considérate afortunado.

Los niños y las familias que padecen enfermedades genéticas raras (enfermedades huérfanas) no son tan afortunados. Los padres de niños con enfermedades terminales aman a sus hijos y cada día los tratan como si pudiera ser el último.

El síndrome de Sanfilippo es una enfermedad genética horrible, causada por una mutación genética que impide que una enzima específica haga su trabajo. Sin la enzima, los niños pierden lentamente todas sus habilidades aprendidas, como: hablar, caminar, comer, etc, hasta causarles la muerte.

La terapia génica es un tratamiento que une un virus a la enzima faltante. El virus entrega la enzima faltante a los niños.

El síndrome de Sanfilippo tipo C es extremadamente raro y ocurre en 1 de cada 1.5 millones de nacimientos. La mayoría de las compañías farmacéuticas no ven el valor financiero en la producción y comercialización de un medicamento para nuestros niños moribundos.

¡Depende de los padres de los niños con Sanfilippo luchar contra su destino!

Hace diez años, un grupo de fundaciones de todo el mundo se encontraron y se unieron para encontrar y luego financiar millones de dólares para la investigación y un tratamiento para el Síndrome de Sanfilippo tipo C. H.A.N.D.S.

Nuestros científicos tienen pruebas de concepto y ahora estamos listos para fabricar nuestro vector en grandes cantidades para que podamos llevar a cabo un ensayo clínico. Para esto necesitamos tu ayuda en la financiación!

Sé parte de algo sobre lo que puedas sonreír. Ayude a nuestras familias Sanfilippo tipo C a financiar la producción de un medicamento que detendrá esta enfermedad para muchos de nuestros niños sobrevivientes y salvará las vidas de la próxima generación.

German
Waren Sie schon einmal mit dem Sanfilippo Syndrom konfrontiert?

Haben Sie sich mit dem Thema Gentherapie auseinandersetzen müssen?

Wenn nicht, dann können Sie sich glücklich schätzen.

Familien, die von seltenen genetischen Erkrankungen betroffen sind, haben weniger Glück.
Eltern todkranker Kinder verbringen jeden Tag mit ihren Kindern, als könnte es der letzte sein.

Das Sanfilippo Syndrom ist eine folgenschwere genetische Erkrankung, die von einer Genmutation
verursacht wird. Diese hindert ein spezifisches Enzym daran, seine Aufgabe zu erfüllen. Ohne
dieses Enzym verlieren die Kinder langsam alle bereits erworbenen Fähigkeiten von der Sprache
über das Gehen bis hin zur Fähigkeit selbstständig zu essen. Am Ende steht der Tod.

Die Gentherapie ist eine Behandlungsmethode, bei der ein Virus durch einen Vektor an das
defekte Gen angebunden wird, der den Kindern das fehlende Enzym liefert.

Das Sanfilippo Syndrom Typ C ist extrem selten. Es kommt nur bei einer von 1,5 Millionen
Geburten vor. Die meisten Pharmafirmen sehen keinen wirtschaftlichen Nutzen darin, ein Heilmittel
für unsere sterbenden Kinder zu produzieren und zu vermarkten.

Es ist also an den Eltern der Kinder für ihr Schicksal zu kämpfen.

Vor zehn Jahren hat sich eine Gruppe von Stiftungen gefunden und zusammengeschlossen um
Millionen von Dollar für die Forschung zur Entwicklung eines Heilverfahrens für das Sanfilippo
Syndrom Typ C aufzubringen: H.A.N.D.S.

Unsere Wissenschaftler haben den Machbarkeitnachweis (Proof of Concept) erbracht und wir sind
jetzt bereit, den Vektor in größerer Anzahl herzustellen, um die klinischen Tests durchzuführen.
Dafür benötigen wir Ihre Hilfe.

Seien Sie Teil von etwas auf das sie stolz sein können. Helfen sie den Sanfilippo Typ C Familien
die Herstellung eines Heilmittels zu finanzieren, dass die Krankheit in den betroffenen Kindern
aufhalten und zukünftige Betroffene retten kann.

French

Le Syndrome de Sanfilippo En avez-vous entendu parler?

La Thérapie Génique En avez-vous entendu parler?

Si non, vous avez de la chance.

Les enfants et familles qui souffrent de maladies génétiques rares n'ont pas cette chance. Les parents d'enfants souffrants les aiment tous les jours comme si ça pouvait être leur dernier.

Le Syndrome de Sanfilippo est une maladie génétique horrible, causée par une mutation génétique qui empêche une enzyme spécifique de réaliser sa fonction. Sans cette enzyme, ces enfants perdent peu à peu leurs facultés telle la parole, la possibilité de marcher, de manger. Eventuellement c'est une perte motrice en chute libre qui se termine avec une mort prématurée.

La thérapie génique est un traitement qui attache un virus a l'enzyme en question. Ce virus permet à ces enfants de retrouver cette enzyme manquante.

Le syndrome de Sanfilippo de type C est une maladie très rare. Seulement 1 naissance sur 1,5 million. La plupart des compagnies pharmaceutiques ne voient pas d'intérêt financier à produire et commercializer un remède pour ces enfants.

C'est donc aux parents d'enfants Sanfilippo de se battre!

Il y a dix ans, plusieurs fondations à travers le monde se sont trouvées et réunies sous le nom de H.A.N.D.S. pour trouver et financer des millions de dollars de recherche pour trouver un traitement pour le syndrome de Sanfilippo de type C.

Nos scientifiques ont abouti leur recherche et nous sommes maintenant prêts à créer un vecteur en grandes quantités pour pouvoir passer aux essais cliniques. Pour ceci, nous avons besoin de votre soutien financier!

Faîtes partie de quelque chose de beau. Aidez nos famille Sanfilippo de type C a financer la production d'un remède qui puisse arrêter la progression de la maladie de leurs enfants, et sauvez les vies de la prochaine generation.

Portuguese
Já ouviu falar da Síndrome de Sanfilippo?

Já ouviu falar de Terapia Genética?

Se nunca ouviu falar em nenhum deles, considere-se uma pessoa com sorte.
As famílias e crianças que sofrem de doenças genéticas raras não são tão afortunadas. Pais de
crianças com doenças terminais olham para os seus filhos todos os dias, como se cada dia
fosse o último.

A Síndrome de Sanfilippo é uma doença genética terrível, causada por uma mutação num
gene, que impede uma enzima específica de degradar açúcares. Sem a enzima, as crianças
perdem lentamente todas as suas capacidades, desde falar, andar, comer, sendo a doença
fatal.
A terapia génica é um tratamento em que a enzima em falta é colocada num vírus ou vetor. O
vírus entrega a enzima que falta às crianças.
A síndrome de Sanfilippo tipo C é uma doença ultra rara, com incidência de 1 em 1,5 milhão de
nascimentos. A maioria das empresas farmacêuticas não tem interesse na produção e
comercialização de um medicamento para uma doença tão rara.
Cabe aos pais das crianças Sanfilippo lutar contra o seu destino!

Há dez anos atrás, um grupo de fundações de todo o mundo juntou esforços para angariar e
depois financiar milhões de dólares para desenvolver um tratamento para a Síndrome de
Sanfilippo tipo C. H.A.N.D.S.

Os nossos cientistas fizeram a investigação pré-clínica e agora estamos prontos para avançar
para a produção do nosso vetor em grandes quantidades, para que possamos realizar um
ensaio clínico. Para isso, precisamos da sua ajuda!

Faça parte de algo que o faça sorrir. Ajude as nossas famílias Sanfilippo tipo C a financiar a
produção de um tratamento que mudará o destino dos nossos filhos e salvará vidas nas
próximas gerações.

__________________________________________________________________________________________________________________________
More information about Cure Sanfilippo Foundation : Cure Sanfilippo Foundation works to fund urgent research for treatments or a cure for Sanfilippo Syndrome. Sanfilippo is rapidly degenerative.

Jonah's Just Begun (JJB), raises funds under Cure Sanfilippo Foundation (CSF) a 501c3 not-for-profit. JJB has terminated it's 501c3 status and joined forces with CSF. JJB Co-Founded: H.A.N.D.S., Mission Hide and Help and ConnectMPS.org

A big thanks to our scientists and their lab members that have stood by us and work everyday towards a treatment: Dr. Alexey Pshezhetsky and his lab at Sainte-Justines, Montreal, Dr. Brian Bigger and his lab at Manchester University, Dr. Patricia Dickson at WASU and Tsui-Fen Chao at LABiomed. Special mention to: Dr. Claire O'leary thank you for your dedication.

A special thanks to: CBS, Jonny Lee Miller and Kristine Johnson. Our families greatly appreciate all your help in fundraising and raising awareness. #CUREmps #CUREsanfilippo #CUREmpsIIIC
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Sobre Cure Sanfilippo Foundation

To advocate for and fund research directed towards a cure or treatment options for patients with Sanfilippo syndrome.

Encontre Cure Sanfilippo Foundation em

Causas

Diseases and conditions

Fundado

2014

Com verificação do GoFundMe

2025

ID fiscal

46-4322131

Código NTEE

Specifically Named Diseases Research

Cure Sanfilippo Foundation é uma instituição de caridade pública 501(c)(3), EIN 46-4322131. As doações são dedutíveis de impostos. O conteúdo selecionado é fornecido pela Candid.

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