Cure AHC is a much deserved leader in the AHC Community.
They not only provide much needed financial support for those seeking a cure for AHC they also provide much needed mentoring and a community that ensures our child (and us as caregivers) do not have to do it alone.
Since our daughter was diagnosed Cure AHC has assisted us with gaining a better understanding of our daughters condition as well as being an advocate in helping us navigate the hurdles associated with caring for someone with AHC. They have provided mentorship and support for our clinicians and have served as a conduit for them to share information with their peers. They are a truly amazing organization and fill a very critical role in the care for those with AHC.
Thank you Cure AHC for leading the way to a cure, for being our voice, and for making sure our families are provided the knowledge and tools to provide our Heroes the best possible care.
My son was diagnosed with this very rare disorder and I reached out to this organization just trying to find a place to start. I was overwhelmed with support, help in answering questions and people who understood the path we were on. Especially for people with such a rare disease, organizations like these are so important. There truly is no information available in other places. Even most doctors are unfamiliar with AHC, so this organization is such a support and help. Thank you for the bear and for the outpouring of support and help!
When our child was diagnosed with AHC, it was overwhelming trying to navigate information, doctors and treatments. Cure AHC was a great resource for all of the above along with having someone to meet with and talk to while we visit the multiplanary clinic at Duke. Ive had panicked questions answered, help with appointments and letters for equipment. Cure AHC and the research they fund, makes this journey less lonely, less difficult, and offers hope.
I first connected with Cure AHC through my granddaughter whose friend in Iceland, Sunna Valdís Sigurðardóttir (see her beautiful photo below), is the only person in Iceland with AHC. AHC helped fund and create Águsta Fanney's AHC documentary, "Human Timebombs," which has raised worldwide awareness of AHC.
Cure AHC has created a global community of families dealing with AHC, raising awareness and research funds for this rare disease at institutions like Duke University.
Through Amazon's "smile.amazon" program, I continue to donate to Cure AHC -- for every purchase I make from Amazon by opening the "smile.amazon.com" page and ordering from there, Amazon donates to my charity of choice -- "Cure AHC Foundation" -- at no cost to me: (https://smile.amazon.com/gp/chpf/about/ref=smi_se_abtpo_r_about_smi).
Cure AHC is among the foremost charities dedicated to finding a cure for Alternating Hemiplegia of Childhood, and they do a fantastic job for children and families dealing with this pernicious and debilitating disease.
I see how active this charity is in the lives of all the families dealing with AHC. Their care, and availability is unfounded. The research they have been able to accomplish towards a cure for this rare disease, and their commitment is amazing. I see a bright future for these kids because of this charity's tenacity.
I could not ask for a better organization like CureAHC. They are like my family. The amount of time they put in and love they share for all our kids with AHC is magnificent!! The hard work they put in day in and day out to help make the lives of all who suffer from this diesease is incredible and without them the Duke AHC Clinic would not be here. Thank you CureAHC for everything you have and still do for a Cure for AHC and all the AHC Families. We love you!!!!!!
Cure AHC is one of those rare foundations that has the ability to see each child and their family with individuality and great empathy. The manner in which they provide support to those dealing with this horrible condition while at the same time continuing the quest to find a cure is nothing short of amazing. I am honored to be connected with them.
This is a great charity that creates a community "family" - frequently sharing pictures, birthdays, stories, and prayers for each other. Love being a tiny part of this great group!
What a wonderful group to be a part of. Just being able to have questions answered from other parents with the same problems is so helpful and reasuring. If I didn't have this organization I would be lost for what to do with my daughter Gayle Jane! ❤
This Charity is amazing at keep families together to learn about the twist and turns of AHC. The information is immediate and honest.
What a great nonprofit to volunteer for! A great sense of community and friendships that make me want to volunteer again!
This disease has taught me so much.. My granddaughter Molly Marshall has AHC and all of the people that are wonderful and will do anything to help to understand the disease more.. they are learning more each day and hopefully one day will find a cure..
Thank you so much for your kind words! We at Cure AHC love dear sweet Molly! She inspires us to greatness daily!
This is a great organization. I have volunteered for Cure AHC for over 3 years.
Thank you Sandy , we are grateful for all that you do to help us raise awareness and funds to get to the Cure!
I have had privilege to work on projects with Cure AHC , as well as benefit from the vast resources they have available for families, professionals, etc. I am impressed with the dedication of the organization's staff and volunteers. They truly care about making a real difference in the lives of people that are affected by this disorder.
Cure AHC is a wonderful inspirational charity that provides all of us with information that without this charity we would have little or non advice/ support at all
Thank you so much for your testimonial to our hard work!
I'm a professor of medicine at Vanderbilt, and first became aware of Cure AHC a few years ago as they were organizing some of their first genetic work.
It's a rare disease, which makes it hard to study, but these guys are doing everything right. Unlocking the genetic origins of disease is a first step to finding a cure.
Thanks James for your support!
Cure AHC is an amazing resource and support for families of children who have been recently diagnosed with AHC. It was a relief to know we are not alone. Their tireless involvement makes a difference in the lives of many!
Cure AHC is a great group. They have put forth great effort in organizing events. They have made it possible for families to go to Duke University and get countless analysis and medical advice in the effort to collect data to further understand this disease.Their most recent was a great success bringing together families who are affected and doctors who are currently trying to find a solution. The gathering was very informative and is a great step for future success in this battle.
Hi:) Cure AHC is a wonderful organization who is extremely dedicated to helping children all over the world. Last year when my family hosted a fundraiser, I chose to donate to Cure AHC because I like the work they are doing for all the kids. I was called out by different organizations as to why I chose them, (which quite frankly I didn't need that extra stress), but I bluntly informed them that I chose Cure AHC because as far as I'm conserned they are the ones doing the work. Even though my daughter who sufferes from AHC and I live in Canada, I felt Cure AHC was the choice for us to help with what we could. Sometimes it takes a study of a few kids to figure out any kind of loophole in this horrifying desease, and that's exactly what Cure AHC is doing to benifit all the children. They have a wonderful team trying their best and I applaud their hard dedicated work:)
I just want to thank you for your constant drive to help our kids. As a single mother with a whole bunch of responsibility it's nice to know people are out there fighting to make all our dreams come true.
Cure AHC provides a much needed resource to families whose lives are changed with the diagnosis of Alternating Hemiplegia of Childhood. While physicians and researchers work hard for a cure, it is this group where families find comfort and support. As we wait for a cure, it is through this group we connect with one another to ask questions, get ideas and gain insights into our affected loved ones. Questions answered in this group are often more helpful than answers we find through our physicians. We are the experts in this disorder. We live it every day. Having this group for discussion and networking, alleviates some of the frustration that comes with living with a rare disease. That is a blessing.
CureAHC is a great nonprofit that provides vital support and services to families who have nowhere else to turn. Rare conditions like AHC don't get the backing that the more commonly known conditions get, so supporting CureAHC is a way to make a huge impact on people that need it. I've seen the impact CureAHC has had on families that were desperate for help. They give hope and are THE driving force for medical advances and a cure.
Cure ahc has been a fantastic resource for me since my daughter annya was diagnosed with ahc last year. It has allowed me to be in touch with other families all over the world which, although far away feels like im not alone in this! Thankyou to jeff for his devotion to the cause! Jx
Such an amazing organization run by people who truly care and put their heart and soul into this. They have brought so much awareness and help families wherever they can.
Cure ahc has been a life line I so desperately searched for after our diagnosis. The endless support given from all over the globe is truly amazing, me and my son are so grateful for this amazing group & all the other parents/ahc champions :)
CureAHC has been a miracle worker in our lives!! My son Tanner is 14 months old, diagnosed with Alternating Hemiplegia at 8 months old. I was thrown 3 papers from his doctor with his diagnosis and she left, leaving us with countless numbers of questions, worries, fears, struggles, unknowns. Cure AHC is there for me and my family whenever we need questions answered, advice given, ears to listen, and peace of mind that we are never alone. The amount of time dedicated to the families is unimaginable, and I am forever grateful for this organization!!!! Thank you, beyond words, to all!!! Brittany Rosebrook
This is a group made of primarily of parents whose children have been impacted by this devastating disease. It is extremely rare and much in need of good, consistent research. This organization reaches out to parents and professionals worldwide. Their efforts are non-stop and far-reaching. These children, who suffer from occasional bouts of non-stop seizures, heart problems, balance issues and the ongoing fear of head trauma, desperately need all our support.
Our son was diagnosed with AHC in August 2015. He was only 9 months old and we had never heard of AHC. We spent 9 hours that day at the doctor and looking back I didn't hear much after the diagnosis. Quickly, we looked for online support and found Jeff with Cure AHC. We realized at that moment we were not alone. We received information we would have not otherwise been privy to. Cure AHC has been available to answer our questions 24/7....and have put us in contact with the doctors and staff at Duke University so our lil one can be evaluated. Cure AHC and the entire AHC community have become our family. We are thankful to all the hard work and dedication they have to all of our families!!!
Cure AHC is great!
When my little nephew got diagnosed with AHC and we didn't really found the information we needed, I contacted Jeff and I got an answer on a lot of questions.
I know, when needed, we can count on Jeff and Cure AHC. An for that, we are really grateful!
Our daughter was diagnosed with AHC in the spring. Cureahc and its members have been supporting our family through many things since that very day. They have helped us better understand certain symptoms and problems, helped with ideas of new things to try, connected us with the expert physicians and most importantly, made us feel not so alone. We are thrilled that Ahc is becoming known by more people and are so thankful to cureahc for raising awareness and funds for research.
Like many I had never heard of AHC until a friends daughter had this. I made it a point in my life to make sure the word got out so people can know about AHC. I then did a softball tournament for CURE AHC. IT IS NOW MY MISSION. TO GET THE WORD OUT!!! Jeff is a truly amazing person and so are all the families!!!! My team and I all got shirts and we wear them with pride and in the hopes of someone asking us about AHC!!! I will continue to get the word out there and direct people to the website to learn more and donate!!! Love Cure AHC and I will continue to pray and help in anyway possible!!!!
Jeff and AHC helped me understand my daughter condition. This group offer a lot of emotional and profesional support. Brings families that is going thru the same together we can share our experience and questions. They have a great tram working hard to find a cure for AHC. I am glad I found this organization and I would like to thank everyone and specialy Jeff for all their help!
Like many people, I had never heard of Alternating Hemiplegia of Childhood before becoming Matthew Wuchich's nurse in 2013. I needed information so that I would know how to provide the best care for Matthew and be a support for his parents. I found the Wuchichs and the CureAHC foundation were both excellent sources of information on this debilitating disease. Honestly, I have never seen such hardworking individuals as Jeff and Renee Wuchich for CureAHC. Their involvement with other families goes far beyond the call as they visit with families at the hospital, host them in their home when they visit the Duke Clinic, and involve themselves in fundraising for research. They are constantly working at raising community and international awareness. Thank you for all you do to help alleviate AHC.
I love CureAHC! I had never heard of it or AHC until I was matched up with my AHC Champion thru the irun4 program. My little buddy's mom told me all about AHC and my new buddy and the first thing she told me to do was go check out CureAHC. I'm so glad I did. I've learned so much. Its a great organization and so thankful they are here to help spread the word about AHC and one day hopefully help find a cure. Thanks CureAHC and Jeff for all you do!
Cure AHC has helped our family tremendously! Our 6 year old son has been diagnosed with AHC 3 years ago, and Cure AHC has been a great help and comfort to families. It is reassuring to know what other parents and children are dealing with and the newest research for a cure on this disorder. Parents are able to communicate with others to research what works or doesn't. Triggers or how episodes affect our children . The newest research and duke university group all the work they do for our kids . Awareness and helping families deal with this rare disorder, has been a stepping stone in research and proving the best for our son to make his life the best it can be. It provides an outlet for parents to bounce off ideas and concepts that help with the care of our amazing hero children.
I found this group when my daughter was diagnosed august 1st 2013 and it has been a God send. Jeff and Renee have been super informative about AHC and also very welcoming. I don't know how we would have found Dr Mikati if it hadn't been for Renee. This group has helped me get my daughter to the AHC and have also been there be it bringing me dinner or just giving me a moment to shower while Lexi was in the hospital August 20 2014 to September 4 2014. Cure AHC is a blessing and I would recommend any family affected with AHC or anyone wanting to learn more about AHC visit the website it's very informative and if you have more questions then one message to Jeff or Renee and you will have an answer.
This organization is crucial in spreading awareness of AHC and establishing the first AHC clinic. They also work tirelessly to raise money for research of AHC. They also provide support to families with children affected with AHC.
CURE AHC has been a blessing to me and my daughter. When we were told that she may have AHC I couldn't find hardly anything about it until I found CURE AHC. They have helped us with any question that I had and with information to help understand what my daughter is going through and also they have lent an ear for me when I needed to vent,I don't know that many people that would take time out of their own lives and being busy themselves that would seat and listen to you babble on in circles but I do know that CURE AHC did and will every time I need help or don't know how to go about something I simply ask Cure AHC And they help me I am so grateful to this organization for everything thank you
CureAHC has gone above and beyond our expectations in guiding our family through the first steps after our daughter was diagnosed with AHC. We received advise, support, and insight. We were so full of questions and scared upon diagnosis, and having CureAHC there for us made such a huge impact.
We are very grateful for all of the hard & tireless work that CureAHC does. Our daughter was diagnosed with AHC in July 2009.
Jeff & Renee Wuchich are inspirational.
The aim of CureAHC is to support and educate families both of which they do wonderful.
Cure AHC is the best thing that has ever happen to me. I have a daughter who suffers with AHC and it has been a very difficult journey for my daughter and I until I met Matthew and his parents. They have been such a great support with guiding me through this journey. They have been there for me when I needed advice and also directed me with getting help with my daughter Kaylin. I'm truly blessed to have Wuchich's family in my life and to be involved in such a great organization.
I was introduced to Cure AHC when I met Matthew and his family! They are such an amazing family that are now mentors in my life. I have worked with the special needs population through most of my life but had never heard of AHC until being introduced to this family. Through Cure AHC and Matthew and his family I have learned so much about what AHC is and now have found an interest in working with these individuals. Matthew and is family are so inspirational as they find a way to give Matthew the most normal life possible. Cure AHC is a great organization that allows individuals who have never heard of AHC an opportunity to learn more about it. The people of this organization work so hard to find ways to help each and every family they are introduced to as well as educating the public and giving their own son an amazing life!!
AHC is a great group of people who work very hard for their cause. Working with them and for them has been a great experience.
I had never heard of AHC until I was introduced to Matthew and his parents. His parents are truly amazing and so loving to try to offer their child a "normal" childhood. However Matthew is not a "normal" child, he is a child with a special need. There needs to be much more research done and it can be done through awareness and contributions and support - even what you would consider small will help so much.
AHC is a rare neurological disorder with attacks that cause mild weakness to complete paralysis. It is sometimes misdiagnosed as epilepsy, because of the similar symptoms. Since there is no diagnostic test for the disorder; it can continue to go misdiagnosed for up to 2 years. Because of this, it is possible that it is not as rare as we think. The cause is unknown and so is the cure. Matthew and others deserve the opportunity to do things that others take for granted.
Like so many people I had never heard of AHC until I met and became friends with Jeff Wuchich, and was introduced to Matthew. As a parent myself it is difficult to see children, and the parents and family members who love them, deal with such a challenging health problem that does not have a "high profile". Jeff, Renee, and all the other wonderful people I've met since getting involved with Cure AHC are inspiring. They have embarked on a life long mission of love to help other children and families who suffer and to eventually find the cure. I look forward to being a continuing part of that effort.
With having the pleasure of knowing Matthew since his birth, I have also witnessed the amazing devotion of his parents. With their creation of Cure AHC, I continued to be amazed. Through their efforts, they have been able to engage Duke University. This amazing partnership has led to Duke discovering the gene and creating an AHC clinic in their Children's Hospital. Because of the drive and dedication of Cure AHC, I truly believe they will be pivotal in finding the cure.
I am so proud to be associated with them via donating and volunteering. This group fully has their vision on finding the cure and that type of dedication is what every Charity needs.
With the drive of the volunteers (all families of those affected by AHC), they work tirelessly to bring awareness about this debilitating disease and fund continued research to find a cure. They are making a difference ... every dollar raised, every speaking engagement or attendance at a community event, everything they do is just one step closer. The entire group is focused on their mission in everything they do, every day they do it.
My words are inadequate to describe the importance of Cure AHC to bring hope to families that are affected by this debilitating disorder, enabling resources for proper diagnosis and treatment, continuing research to find a way to stop this disease.
My friend's son is affected by AHC and so I support and keep up with all the efforts this group undertakes. For a little known disease with small numbers of affected individuals, little press and no powerhouse type sponsors, I am amazed on an almost daily basis on how much they do and how much care and comfort they bring to the community that lives with AHC every day. The resources, information, and support they provide seems priceless and as they have grown the ability to effect positive change in the medical and scientific arena seems equally phenomenal.
Cure AHC is the best thing to happen to my family. In April of 2013 our daughter Madison was diagnosed with AHC at Duke. There Dr. Mikati suggested we get in touch with Jeff Wuchich to help us understand everything and learn more about everything more. Jeff and his wife Renee were a blessing to us. Through them we learned more about our daughters condition while having the support of them and other families going through the same thing. They also helped us get a very expensive out of country medication that is not easy to get. Their whole objective is to help other AHC families and be there for you when it's the toughest. I stand behind them 100% and hope to help raise the awareness of their misson to find a cure :)
This organization has helped my family tremendously. The resources and support has been amazing
I just wanted to say how much our family appreciates you guys. My grand daughter Alexis Harding has gone without being diagnosed for almost 4 years , now we know what her health issues are and how to deal with this. you guys have been very supportive of my daughter and Granddaughter. You guys rock and have all of our support.
Thank you so very much