mother and child hugging in front of doctor

To the Parents Seeking Experimental Treatment for Their Children

1. Curing a mouse in the lab does not equal a cure for humans. Unfortunately, science does not always translate immediately, or ever from a murine model to human patients. There are countless mice who have regenerated motor function or been completely cured while children have not. This is due to many reasons ranging from how the mouse model was created to the differences in brain size, life expectancy and metabolism of mice and human children. It’s definitely a step in the right direction and cause for celebration, but don’t pack your bags just yet. There is still a lot of work to be done between curing or helping mice in the lab and using the same technology to help our children. I’m not trying to be negative or dash anyone’s hope, this is just a realistic assessment I have seen after 18 years of experience.

2. “One to two years” to trial rarely happens. Prepare for disappointment and delays. No matter how promising and exciting the progress in the lab may seem, as soon as you hear the words, “we’re about one to two years away from a human trial,” just ignore the timeframe and try to find out what, if anything, you as a parent can do to help move things along more quickly. I’m not saying this never happens, but there are so many unforeseen complications, that there is often no way to really have a reliable timeframe until your trial is well into the review process.

3. Ask for support from anyone who might be able to help you, but don’t expect it. Whether it’s increasing awareness or raising money, sometimes the people you assume will be gung ho to help are not, and often times help will come from the most unlikely places. Take whatever help you can find, and don’t waste time worrying about the people who don’t become involved with your mission. Focus on the people who are by your side and forgive the people who aren’t. You have enough to worry about without getting upset over things you can’t control.

4. Don’t shoot the messenger. If you decide you want to take the uphill path and try to get your child into a clinical or safety trial, you need to know most research for extremely rare diseases is parent-driven. This means that possibly before your child was even born, there have been families raising private funds to convince a researcher to work on some unheard of disease, discover the gene responsible for causing it, support the gathering of preclinical data, meet with hundreds of people, and basically do everything necessary to get to the point where you come into the picture.

Most of the charitable organizations trying to help find cures were started by parents of sick children. The goal is always to find a cure, but sometimes we must first develop medical interventions that can slow or halt progression of a degenerative disease in order to buy time for our kids. This is agonizing because we have to wait, and worse than waiting, we have to raise money. When new families ask me what is being done and why it’s taking so long I tell them because we need more money, tons more money — whatever we have is never enough. We need government money, biotech money, and we will always need privately raised funds. It’s unfortunate, but sadly if you want your child to receive some type of experimental treatment and you want it sooner than later, you might need to help raise money.

You absolutely do not have to help. You don’t have to do anything. But if you choose not to help, then often you will be relying on others to determine the fate of your child. If you choose to help and decide to join forces with other families who share your goals, then don’t be shocked or upset when the issue of fundraising comes up, again and again. And remember this is always your choice.

5. Know exactly where the money you raise is going. If you decide to become involved in raising money for a cure, you’ll probably find several places to send your money. This can be tricky, because if you want the money you have raised to go directly to research, or to a specific researcher, then you need to ask the important questions and fact-check. Ask the person who controls the money how and if you can earmark it for a specific purpose. Most organizations have a way to collect money from families who wish to help, but they might not be financially supporting the researcher who is working on the cure for your child’s disease every single year. Or they might not have a way to earmark funds in that way. It’s not always as simple as sending in a check and writing a researcher’s name in the memo — that almost never works unless you have made proper arrangements in advance. If you send money to an organization, there is a good chance that those funds can be used to support the organization and not the research you want. Unless you are the director of a charitable organization, those are questions you might want to ask. Oftentimes you have an option to support the research team directly. This way you have control of the funds and can dictate exactly what they are to be used for. When in doubt, ask a lot of questions and check online because finances are all public record.

6. Securing medical treatment for your child can become a full-time job. Often with no pay and sometimes with a ton of out-of-pocket expenses. There can be lots of travel, uncovered medical bills, and even a loss of work due to surgeries and follow up testing. It is a great deal of work and can go on for months or even years, but sometimes there is no other way to save your child’s life.

7. Research and become an expert on your child’s disease. If you are planning to search the world for something to help your child, then learn more about the disease than any average person should know. Study everything being done that concerns the disease. Become familiar with every known vector, stem cell, and animal model. Study everything, because when you speak to the team who is doing the work, you will need a medical background to understand them. Yes, you should always speak directly to the researchers yourself if humanly possible. Don’t be afraid to become overly involved in the process. I might have been the most annoying parent ever, but my son has had gene therapy twice, so I have no guilt or shame about the extreme measure I had to employ. If you need to start your own foundation to get things done, then do it.

8. Pray for a miracle, but don’t expect one. This road is paved with delay, disappointment and tears. Set high expectations, but don’t fall apart if things take too long, or the cure seems impossible. This requires thick skin, and it can hurt more than anything you thought possible to watch your baby deteriorate while it feels like you are standing helplessly by. Just keep working towards your mission, and hopefully treatments, and one day a cure will come. There is no guarantee. My son had his second gene therapy almost 15 years ago and no new trials have materialized since then. But I’m never going to give up. He’s not cured, but he’s still here and sometimes that’s all we can hope for. I’m still working towards discovering the cure and praying for a miracle.

9. If you are lucky enough to get your child enrolled in a trial, please know exactly what you’re getting into. I can vividly remember one of the doctors saying to me, “you do know you might just be extending his life, right?” It was exactly what I wanted. I never dreamed that my son would be about to celebrate his 19th birthday. He is still profoundly disabled and requires full-time care. He is and will probably always be 100 percent dependent on me for his survival. I knew exactly what I was getting into.

If you have a child who is like my son, please look ahead and be absolutely certain participating in a trial would work for you, before you take drastic measures to medically extend his or her life without really curing them. This can and does happen, because with such outstanding care comes a longer life. These cute little babies and kids will grow into adults, adults that love you and need you for their physical and emotional wellbeing. My son will have a place in my home until he takes his last breath. He’s thriving, smart and happy, and he is the love of my life. This is exactly why I fought to keep him alive. However, because each parent has a different outlook, it is beneficial to bring to light a topic people sometimes overlook or don’t want to think about. So, just know what you’re getting into.

10. Don’t ever give up hope. Sometimes hope is the only thing we have. If you don’t cling to hope, then you won’t keep pushing towards your goal of saving your child. I’m not saying this always works, because I’ve seen too many children lose their battles way too early in life. But if you dream of a cure, just keep hoping and working towards it, and maybe one day it will happen. I know my son will most likely never be cured, but he’s been helped and I hope that my continued efforts to help him will one day result in the cure for Canavan disease.


Why I Won't Keep Quiet About Researching a Cure for Canavan Disease

An open letter to families affected by Canavan disease:

ilyce holding her son up, smiling
Ilyce with her son, Max.

Canavan Research Illinois (CRI) is funding more research to treat and cure Canavan disease than any other charitable organization in the world. This didn’t happen by accident; it’s taken me 18 years to get to this point. My son Max was and still is the motivation behind my work and mission: to discover treatments that can help children diagnosed with Canavan disease. This is my personal choice and my personal mission. I want to make sure no other parent of a child with Canavan should ever feel like they need to do what I’m doing, join my efforts, or even support CRI.

I realize I am extremely prolific in writing about the success of our research and promoting my organization through social media. I have excitedly shared our breakthroughs with other families in parent groups. This is my way of sharing the fruits of our research and letting people know about things they can do, if they choose, to potentially help their child’s health and quality of life.

My mission is to work towards helping affected children by funding research. Sometimes people may not have the opportunity to learn about those advances, so I like to share that information with other parents. This should in no way make a parent feel guilty for not joining me, or feel shame because they don’t want to give their children experimental medication. My goal is to make the information available to other parents, so they have the choice I never had when my son was a baby.

When I talk about my own son it is because he is 18 and a half years old, and still here. He’s still doing well and he has been taking and testing many of the things that can offer help to other children. I am not comparing him to anyone else’s child, but trying to offer hope to families who are still being told there is nothing they can do, and that most kids die between 2 and 4 years of age. This is not usually the case, and no one should have all their hope shattered without seeing the other side of this disease.

I share my story with other families to help show some of the positive things. I share my story with our donors and supporters to let them know we are making progress because of their help. I share my story to let people know what it is I’m doing with the hard earned money they choose to donate. But, I do not share my story to ask, urge or shame any other affected family into joining me or giving their child the same medicine I give my son. I share my story in order to share information, and let people know there are choices and options available to them.

I didn’t get to where I am today by being quiet; that’s not my personality. This was all my choice, and my own sacrifices to make. I would never ask anyone else to do what I am doing. Canavan Research Illinois never has and never will rely on money from families raising children born with Canavan disease to financially support research. Instead, we have a large and loyal donor base. Of course there are many families who choose to do a fundraising event, or donate money in honor or in memory of a loved one. That is wonderful and appreciated because everything helps! But, I do not urge or force anyone to do this — it’s a very personal choice. I have chosen to not raise any money for my own son’s medical bills; many people have, and that is also a personal choice. I feel as the president of a public charity doing so could be confusing. So, I only raise money for CRI — my personal choice. I am not wealthy. We live in a small, modest ranch home with no basement. My two boys share a room so I can work from home and enable CRI to have an office in the third bedroom.

I am sharing with other affected families my true goal and intent as to why I post about my organization and my own son. I realize sometimes intent can be misinterpreted, because writing doesn’t always communicate the author’s tone. I would not try to force or shame anyone into joining me on my mission, make anyone think they should be doing more (or doing anything), or try to make people think that by sharing information about my son’s progress is to make him seem better than another child.

I share these things so people who are interested can access the information to have options and a choice if they want to pursue anything else that perhaps they didn’t even know existed.

Please contact me at [email protected], if you have any questions or would like more information about Canavan Research Illinois. We encourage sharing information with each other, without feeling obligated to do anything, join anything, or agree with anything. Our children share a diagnosis, and even though we are not all on the same path, we are all in this together.

The Mighty is asking the following: What is a part of your or a loved one’s disease, disability or mental illness that no one is aware of? Why is it time to start talking about it? If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

When I Was Told There Was Nothing I Could Do to Save My Child

When my 4-month-old baby, Max, was diagnosed with a fatal brain disease, I was told by doctors to “not become attached to him” and to look for a pediatric nursing home instead.

In desperation I contacted the largest organization I could find that had anything to do with Canavan disease. I was so excited to have some hope after initially hearing there was absolutely nothing I could do to save my precious child. But my hopes were dashed again when the woman on the phone told me about the wonderful grief counseling available, support groups and once-a-year family conference.

I just kept asking about treatment or anything I could do to help my baby. Unfortunately, the only thing they had to offer was emotional support and a family reference guide to help connect affected families. These things seemed wonderful and absolutely essential — for someone else, but not me.

young boy with walker
Ilyce’s son, Max, when he was young.

I didn’t want support or comfort. All I wanted was to save my baby. That’s it, that’s what I wanted. I wanted someone to do something to save my Max. I was determined to be the exception. I didn’t care what anyone said. I absolutely refused to lose my child, and my stubborn refusal to accept the diagnosis has grown into the largest organization in the world dedicated solely to curing Canavan disease.

No matter what else happens in my life, I know my child has become an adult, and I was able to set in motion treatment options for children diagnosed since his birth. The path I chose has oftentimes been lonely and met with resentment and even hostility. But I always knew in my heart if I absolutely refused to lose Max, I could choose to dedicate my life to saving him. This wasn’t the standard course. It was a grueling uphill battle of parent-driven research and experimental medicine. Max is still here, and I will fight with every fiber of my being to keep him here as long as possible.

No one should ever take away your hope.

The Mighty is asking the following: What’s one unexpected source of comfort when it comes to your (or a loved one’s) disability and/or disease? If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

How I Always Say Goodnight to My Son With a Life-Limiting Illness

Anyone who knows me knows about my son Maxie and his lifelong battle with Canavan disease. I have the obvious challenges associated with raising a son with a life-limiting illness, but our life is happy. Max is thriving at 18 years of age.

The charitable organization I founded has grown into the largest financial supporter of research to help children born with Canavan disease. I don’t think it’s helpful or productive to share too much about the pain this disease often brings to my life. But with that said, I would like to share something that could potentially affect anyone. And that is a simple kiss goodnight and making sure our kids’ — all kids’ — last feeling upon falling asleep is knowing they are loved and cherished.

When raising a child with a life-limiting illness, we as parents know the risks of our kids getting very sick and passing away at any time. We feel that even though they are living with a fatal illness, we would get to say goodbye. Sadly, this is not always the case. I have known a few children living with Canavan disease who went to bed happy and healthy and for whatever reason never woke up.

blonde woman kissing her smiling son
Ilyce giving Max a kiss.

I know this seems like a peaceful way to go, and it may be. But that is an important lesson I have learned. Just because my child has a fatal disease and could die from a common illness does not mean I will be by his side holding his hand as he leaves this world. This is how I’ve always imagined his last moments would be. I thought I would have the luxury of being there to comfort him as he took his last breath. That’s until last year, when a healthy child with Canavan disease passed away during the night. Then it happened again, and again. It’s probably been happening well before I was aware a child with a disease like Canavan could go to sleep happy and healthy and never wake up.

I now see that wanting to be there may actually be selfish because it would mean Max might pass due to a bad illness or seizure. Yes, I’d be there trying to comfort him, and smell him, and hold him until the last second of his life. But with the warning might come some illness and suffering.

So I kiss Max goodnight every night like I’ll never see him again, and my other son Alex, too. Is this healthy? Who knows, but that’s why I feel agony when I kiss Maxie goodnight, and joy because if something did happen then this kiss would be my last memory of him. A happy smiling boy giving his mommy a kiss goodnight.

Let’s all try to go to sleep feeling loved and happy. If that happens to be our last memory of someone, there is no way to go back and change it.

Kiss your kids too much, hold them too tightly and for too long. They will go to sleep feeling your love all night. Tomorrow is never promised!

boy lying down and boy next to bed smiling
Max (left) and his brother Alex.

The Mighty is asking the following: What’s one unexpected source of comfort when it comes to your (or a loved one’s) disability and/or disease? If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

3 Tips for Dealing With Roommates When You Have Autism

Chances are, at some point in your life you are going to live with a roommate. If you have autism, here some tips on making it the best experience possible.

If you have any ideas for videos you’d like to see, please send me an e-mail to [email protected].

To the Little Girl With Apert Syndrome Who Feels Like She's All Alone

Apert syndrome. Not many people know what it is, and no one would expect 7-year-olds to figure it out on the spot, either. No one seemed to understand how a child could be born to look so remarkably different than the rest — not even the one the disorder is affecting.

The closest definition a 7-year-old with Apert syndrome would be able to come up with is it’s something that causes the kids around her to shy away from her. It’s something that gives grief and loneliness and makes her feel as if she has to sit by herself at a lunch table because she feels too awkward and nervous to approach anyone because of how they react to her. It’s something that makes her constantly ask herself, “Why me?”

This is for the 7-year-old me. This is for the girl who spends all her recesses on the playground, walking around by herself because everyone else has drifted off into groups and wouldn’t invite you to play with them. Be patient. You’ll soon surround yourself with a bunch of friends, ones who will love you unconditionally no matter what, and they will be there for you through every obstacle you come across. They will never leave just because you look a bit different from them and had to have many trips to the hospital for surgeries.

I speak to the girl who was often scolded by her mother for not being on the same level of maturity as the rest of her peers (as mature as grade school children can be, at least). You’re going to grow and carry a specific type of wisdom not many people will be able to see with anyone else. It’s the wisdom to judge people on their character, whether they have a beautiful personality more than a beautiful appearance. It’s the wisdom to always hold out a hand to someone in need, no matter where they come from, how they look and how they live. Before you know it, you’ll be right there with your peers, proving your maturity.

vivi zhang

I speak to the girl who grew up living a life of struggles, doubt and judgment. Who didn’t think she would go far in life because no one properly welcomed how she looked compared to the others around her. Don’t give up. Because one day, you will find happiness. One day, you will find confidence just being yourself no matter what society thinks of your Apert syndrome. One day, you’ll find yourself surrounded with friends who will love you the way you are no matter how you look or what you do.

Don’t give up. 

One day you won’t be the lonely girl on the playground.

The Mighty is asking the following: Write a letter to yourself on the day of the diagnosis. If you’d like to participate, please send a blog post to [email protected] Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.

Real People. Real Stories.

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We face disability, disease and mental illness together.