CDH International

Very thankful for Dawn and the charity CDH International. After losing our beautiful daughter Juniper in 2020 we felt alone in our loss. Very thankful that there is so much effort and work being put into this disease and preventing further loss

It has been over 16 years since I lost my baby girl to CDH. The greatest thing is this organization is pushing forward. I raise awareness to total strangers and hope that they will remember who and what CDH is. I will always be grateful for everything that CDH did for me.

This charity was my first contact after learning my daughter had CDH. This charity is the backbone for support for families both caring for a survivor and those grieving the loss of a child.

My son is a survivor of CDH. He will turn 40 in a few days. Back when he was born, we had never heard about CDH until the day he was born. We got very little information and were terrified new parents. Since being a part of CHERUBS, we have learned so much about this condition. I cannot thank Dawn enough for all of her hard work and dedication. This wonderful group has given parents like myself who were basically clueless, information, support, resources and a place to share with others who had never even heard of CDH. It has been a blessing to parents, siblings and extended family as they navigate their way through their own personal journey with CDH.

CDH international is a wonderful charity run by the most dedicated people. My 13yo has been involved since birth. Dawn and everyone have been a wealth of knowledge tirelessly advocating to advance the treatment of CDH. As a pediatric medical provider, I am so thankful for all they do participating in research, providing families with up to date treatment. Truly the best charity.

I have been a member since before it hit international. I have done interviews, events and hospital angel. My son has a rcdh and 4x repair. Keith is a miracle. Dawn and cdh international are amazing!

As a CDH survivor family, we have a tremendous amount of gratitude for the chance at life with our girl. CDH International has helped us to feel like we are of some use in the fight against CDH. Maybe one day, no child will have to suffer with the effects of this birth defect. If that's ever the case, it will be largely due to the charity's efforts all these years.

CDH International has helped us through our hardest days in PICU. There was always someone to lean and listen when I needed them.
Volunteering at CDH International has helped us make a lot of new friendships and meet so many CDH families, at Charity events. I am very thankful to have found CDH International and for all the amazing volunteers they have.

My son was born with RCDH and we were fortunate to live close by an excellent Hospital experienced with his diagnosis. Then we moved and it was like falling into that hole of uncertainty leaving our familiar team of doctors behind. It was then when I started getting more involved with CDHi. We can come with all questions and discuss it with other parents. Having others in similar situations gave us pointers on what to check/ keep an eye on, when doctors were out of their comfort zone.

As a scientist myself I also highly value the impact CDHi has on CDH research. The patient registry is so thorough, I’m certain once enough patients participate, there will be answers.

It has been amazing to watch this charity grow from Cherubs via e-mail to CDH International and publishing research. Dawn has done a tremendous job leading the charity. I am forever grateful to her, Tracy and all the friends we have made at this charity over the years. I can't imagine going through CDH with our daughter without this group by our side.

My son was a teenager before we found this charity. I think it is wonderful that families have such a great resource now.

My first experience with CDH International was after our Daughter, Juniper died from complications of an undiagnosed, left-sided Congenital Diaphragmatic Hernia. She was only 5 months old and we didn't know what CDH was.

CDH International helped me understand what CDH even was, and has given me a place for some of the grief. I learned how rare it is for CDH to go undiagnosed, but also learned we were not alone. It's sad to know other families know this grief, but also comforting to know we are not alone. CDH International makes connections like this possible.

CDH International remembers Juniper on special days. They say her name, share her photo and help being awareness. I'm so very grateful for this.

I started Volunteering for CDH International because I noticed how much they care, how much they help the families, and I noticed how important their role is in research and awareness.

My Daughter went undiagnosed until her autopsy so research and awareness are very important to me. It's important so we can help other families who endure a Congenital Diaphragmatic Hernia. These big-little warriors and their families deserve a chance, they deserve hope and survival.

CDH International is vital to the future of Congenital Diaphragmatic Hernias.

I'm incredibly grateful I found CDH International. I support their mission and their global fight against Congenital Diaphragmatic Hernia.

Thank you CDH International, for all you do!

I discovered CDH International back in 2007 when the charity was called CHERUBS. This was several years after my son was born with an undiagnosed CDH. I finally had found the support I needed, a place to come and ask questions and to celebrate my son's milestones. In 2009, I took on a volunteer role on their card committee and helping with prayer requests, from there my volunteer roles expanded and eventually turned into a job for me. A job I wholeheartedly love and have passion for. I am currently the Support Department President, and it is my goal to provide support to all families affected by CDH. To not walk this journey alone is very important to me. At CDHi, we make sure no family has to walk this journey alone. I am a personal witness that we have helped 1000's of families walk this journey with CDH.

CDH International focuses diligently on continuing the push for CDH research by running the CDH Patient Registry, eventually accrediting hospitals and charities, publishing studies, lobbying for NIH funding for research, and funding research grants. By working with NIH, the WHO and other research entities, we are on the front line of research while still personally supporting patient families. We work with hospitals, surgeons, researchers, and other charities on a global initiative to stop Congenital Diaphragmatic Hernia. Together we can make a difference! I am honored to work for CDH International to provide a better future for all babies born with Congenital Diaphragmatic Hernia.

This is a great non-profit with a wonderful vision.

CDH International was founded by CEO Dawn Ireland in 1995. Although Dawn's only child, Shane Torrence, at 6 years old sadly passed away in 1999 from complications of CDH, she forged ahead and continued the charity. She was determined to provide much needed information and support to families who were affected by CDH. In addition, CDHi raises funds to contribute to research. CDHi has expanded immensely and presently has branches in numerous countries. I first became aware of CDHi when my grandaughter was born with LCDH 24 years ago. I would be amiss not to mention Tracy Meats, President. Her dedication and hard work has also been instrumental in CDHi's long tenure. I would highly recommend CDHi.

This charity has only and will continue to put the children first, I love volunteering/working here.

CDH international is an amazing charity who gave us light in the darkest moments of our journey. You’re not just a number, but are cared for like family!

CDH International is a great organization. When you reach out to them you become a part of the family. No parent or child is alone with CDHI behind them.

CDHi has been incredible since the day we found out about our daughter's condition. They have countless resources for parents to learn about CDH, a large community support system to help struggling parents, and amazing appearal and accessories to help raise awareness.

At the top of all of this, they spend the majority of their time and money assisting with the research to help end CDH. While doing all of that, the leaders of CDHi spend whatever free time they actually have left, following the unfortunately high number of CDH babies and their families and reach out to the parents and share their stories.

I could go on and on about this wonderful organization but I will end with this. You can not and will not find a better charitable organization than CDHi!

I have never seen a more dedicated group that does everything from helping a family throughout their experience to educating doctors in foreign lands that otherwise would never have access to medical info that others have discovered. There is no more caring organization !!!

I have been part of the CDH Community since May 2002 when my son was diagnosed in utero with Congenital Diaphragmatic Hernia. He only lived for 6 hours when he was born in September 2002. They were there for me during my pregnancy, after I lost my son, and still to this day, my son is remembered! As a grieving parent, having someone and many someones remember your lost child is comforting. I will never be alone in my grief.

One of the first places we found real hope when we found out our daughter had a left cdh at her 20 week scan. Amazing people doing amazing things for cherubs and their families!

Having a child with a birth defect plus many complications means that I have had experience with several different non profits over the years. There are NONE in my opinion that ever met the standards set by CDH International. Not only are the staff and volunteers at CDH I caring, compassionate, and knowledgeable, but the services provided, the awareness, research, and so much more are stellar. For a charity with such a small budget, they go above and beyond to help, making sure to use a minimal amount on overhead so as much money raised as possible goes where it really matters. From an app for families, doctors and hospitals, to volunteers all over the world, speakers and representation at numerous conferences, an annual telethon and when possible a CDH conference, supporting research, so much is done with nothing more than families and children at the heart. I wish I could give CDH International more than 5 stars, because they have surely earned it.

By far, the most knowledgeable group, interested purely in the children’s health and the families of those children. Reaching out to, literally thousands of parents- prenatal, survivors and angels, giving information and guidance so the parent can make informed decisions.

Cant say enough about CDH International or Dawn. From my baby’s diagnosis onward, I felt like I had a trusted community behind me every step of the way.

Such an amazing organization! CDH is all about the babies and families, dedicated to making progress and save lives. The research and programs are patient centric, led by stellar volunteers and advocates. The passion is real!

Dawn Ireland is a very dedicated advocate for CDH. Her selflessness and drive to create awareness for this childhood disease knows no time limit or distance. The many families that she has helped along the way it’s priceless.

CDHI has been there for my family since the day of my son's diagnosis. They are always reaching out and offering guidance and support. I absolutely love that they constantly share prayer requests and keep the public up to date on the current struggling families.

Very tight knit group. Founder still runs the charity and is very easy to reach. Not much is known about CDH, but we are learning more with every effort this charity makes to further our understanding of this condition. Truly a grassroots charity that continues growing 25 years after its founding.

As an adult with CDH, I have benefited from this charity by meeting others with the condition, having opportunities to participate in research that aims to further our understanding of CDH, and using my experiences to help others going through similar experiences.

If you are looking for a charity to support, this should be on your list. Your contributions will not go to waste. Maybe you will save a life!

CDHi is hands down the most efficiently run non-profit in existence. Everything done, every decision made, every dollar spent is with the babies and families in mind.

This organization is there when you get news you never knew existed. Parents like me need this kind of support.

Was born with severe left CDH back in July 1993, never was told by parents about my birth defect, I was aware of my 2 scars at a young age think ecmo one little more on neck, then few more issues had that are common for cdh kiddos. Final cdh repair was 13 years old, February 2007. I found CDH cherubs to now cdh international in 2016 at the age of 23, around 24th birthday. Used my baby book as the hints then family albums few I never seen before 5-6 month old me second cdh repair after pneumonia then RSV. This page community has helped me connect final pieces of CDH/ PH, over time I’ve helped fellow families and if there little ones get PH again like myself I help direct them to PH community not just cdh community ❤️

We have a 4 year old CDH kiddo and we actually didn't learn about CHERUBS or CDH international until about one year after she was born. I had no idea we actually had an organization who cares so much about our kids battles. We have done a few fundraisers and donated to CHERUBS and continue to do so with a Facebook group we created called "Allie's Project Matters". We recently attended tje CDH conference in Nashville and learned alot in our short stay. We look forward to helping out CDH international more in the future!

Cherubs is more than a charity ..its a "family " ..made of people who know exactly how you feel because they have been or are currently on that same journey as you are ..always a shoulder to lean on and an ear to listen ..no better support you can find

They are amazing when we found out that our son had CDH they sent us all the information about CDH we needed to know.

Full of information pertaining to all aspects of CDH as well as forums and groups for parents to meet other parents in the same situation. Active, concerned, and available pretty much 24/7 so no one ever feels out there by themself if they have a question or issue or need a prayer chain started or want to share a first day of school or graduation photo.

CDHi has been amazing for not only myself, but so many families! After I came home from having my CDHer, we recieved a care package from CDHi filled with so many goodies... it was so nice to have a community supporting us as we went through such a difficult time in our lives!! This organization is also my go to for any and all info I need regarding CDH, because I know all things on their site are facts and comes with data.

My daughter was born with CDH 8 years ago. She was diagnosed at my 20 week ultra sound and without having these non profit groups to give us the correct info on her diagnosis and the support we have received from them and other families we would have been so lost. We are all so appreciative & grateful to have them!

Our son was born back in 2004 and from the moment we found CHERUBS, now CDH International, it has been a great source for support, a source to learn about CDH research and help contribute to, a source for amazing CDH awareness and overall an amazing charity that a family can turn to and not walk the CDH journey alone. I help run the CHERUBS support division now and I know that we put every penny to good use and that we are making a difference in the CDH community. I couldn't have walked this journey with my son's CDH without this amazing support community and what they are doing in the research field is so much needed. #savethecherubs #cdhi

Dawn Ireland, the founder and president of CHERUBS, is amazing. Everything she does, she does for those affected with CDH and their families. She turned the loss of her son into something that has helped countless CDH families whether it was emotionally or financially. Her organization can back up where every penny goes and has some of the most impressively low overheads compared to better known charities. With CDHi and CHERUBS, you know where your money is going. Dawn has always been a wonderful support system and has provided me with more than one opportunity to share my son’s journey with CDH. I can not say enough positive things about this organization and it’s staff. #savethecherubs

The emotional support and world wide family that’s been created has been the utmost importance to our family. To know that we’re not doing this journey alone. To be brought together with others. To know that there’s research being done to support families. To try and save the babies.

When we learned that our son was going to be born with CDH, this was the only helpful resource available. In the years since, we've become helpers and supporters. They've been awesome!

CDHi has been there for us through the years. The support is fantastic, and you always know that there is someone who has been in your shoes.

Both my daughter and I were born with CDH. CDHi is so important to our family because more funding for research is greatly needed. I don’t want a 3rd generation of our family to be effected with this devastating birth defect.

One of the neonatologists told us about Cherubs after our son was diagnosed in utero. It was been a great resource not only with information but community. It is wonderful to meet other people whose children have had a similar diagnosis.

I am in a relationship with Morgan Nuchols who is a CDH long term survivor. I also encourage and sympathize with patients and their families online. I am a PH patient and understand from a patient view. The Association of Congenital Diaphragmatic Hernia Research is a very helpful and needed nonprofit to the CDH community.

I am a NICU nurse and I go to the SDU for deliveries of CDH, I also follow them thru out their hospital stay, because I am on the Surgical team. To see a organization that help parents have support beyond the hospital and that understandi life after having CHD enter into their lives. Priceless memories about courageous people ❤

December 29, 1992 my son Preston was born with CDH. Jan 1993 I met a couple in the waiting room with their son, Shane, also a CDH newborn. We shared many triumphs and disappointments together. We also shared the inability to research or find any answers of our own. Just a paragraph or two in a very large book written in a way very hard to understand. When my son Preston passed, I had no answers or understanding or support from others. Because of Dawn and her heart for others to be informed, supported and not be alone, Cherubs came to be. I have been there since the birth of this charity. I have seen the heart behind its growth and love. The ups and downs, the fighting for each and every cdh family. Cherubs is what true charities are and should be about. Dawn Ireland has displayed the most incredible dedication I have ever seen in anyone. Cherubs, our sons lives, will live on past our own. Helping others to live their's.

As a CDH survivor, I went the first 36 years of my life thinking I was an anomaly. Then I found CHERUBS. Now, eight years later I have met other survivors and grieving families who have become like family to me. Some of my best friends now are ones I met through CHERUBS. Now, at a volunteer, I have the chance to give back and give hope.

My daughter was diagnosed with a left-sided hernia while I was still pregnant with her. I had 15 weeks to research and find out everything I needed to know. CHERUBS had the most easy to understand information and support group. 7 years later and I am still in awe of this group of people and their commitment to CHERUBS!

This charity has helped me understand more of what I go through and let me feel like part of a family that will support you through anything. I was born with cdh 28 years ago and never knew what was wrong with me or how to take care of my health.

My son was born in 2004 with a left sided CDH! Cherubs was the only place we could find any information regarding our situation! The support during that time and even for years after helped us through the toughest time of our lives.

I am a CDH mom and I volunteer for CHERUBS. I am proud of the work being done at CHERUBS and the transparency of the charity. I know that I am helping people through their journey because others helped me through ours. Thank you CHERUBS for being such a great charity.

My son is a 22 yr old RCDH survivor, ECMO x 2 and we were like Dawn in the very beginning not having a place to go for information. I have supported Dawn's efforts since she began.
Please keep up the good work! She is amazing!!!

Wonderful nonprofit charity. They were extremely helpful in supporting affected family and creating awareness!!

Love them and the work they do fro CDH families! I have been blessed to see a local family helped with the CDH journey of their angel, who was here for 12 days.

I have a RCDH survivor who is 3 years old. Cherubs has been a awesome support for myself and my family so glad I have them!!

Cherubs has been an amazing support for us since getting our son's diagnosis of CDH!❤

CHERUBS has been a blessing to our 19 month old LCDH and ECMO survivor!

My son was born with CDH and this charity welcomed us and made us feel like we had answers, support and someone we could go to just to listen in a very tough time. They sent us a care kit with a handmade hat and adjusted baby's first book to explain the time he had in the nicu. It's thoughtful things like that that make this charity above all others!

When our son was first diagnosed with CDH in 2002 the Cherubs organization provided us with support and education. We are grateful for all that they do to spread the word about CDH. Providing a way to connect families has also been a blessing.

This charity supported my family and I through the loss of my son. It is filled with amazing supportive people. They have given us opportunities to raise awareness about a horrible birth defect that many do not know about as well as allow us to participate and be a part of the family.

I've not had a personal experience but I have a friend who's had to go through this. It's mentally exhausting and so scary for them. I believe this needs to be better known.

Without Cherubs this journey would be so much harder. I learned most of it I know today about CDH because of Cherubs.

CHERUBS has helped our family find out more about CDH when there was hardly any information online about it. Our son was born 10 years ago with CDH. We continue to support CHERUBS and network with other CDH families through them.

Cherubs has given me the opportunity to fulfill a promise to my daughter that I made to her as she was dying in my arms; the promise to continue to fight for her as I knew she couldn't fight anymore. They have paved the way to join a movement of strong brave courageous parents and children that live the unimaginable. I am deeply grateful for this organization and everything they do.

They have been so caring and supportive since our daughter was born with undiagnosed CDH. They sent a totebag with goodies for us and EK while she was in the hospital. The most in depth information I was able to find while after our daughter was born!

I'm a Nannie to a 2 yr old survivor who is still fighting!! Without CHERUBS we would have been LOST!! Love love love the SUPPORT they GIVE TO EACH FAMILY!! CDH is a VERY LONELEY DIAGNOSIS until you get contacted and supported by CHERUBS!! They are the BEST!!

The tote bag project is amazing for expectant mothers. Such a relief to have a community to connect with while going through pregnancy and life with a CDH child. We also received a financial grant that really helped with the cost of making a daily 200 mile commute to see our child.

Cherubs is a wonderful organization. We are forever grateful for them always being there to answer our questions.

I love CHERUBS and would be lost with out them! It's nice to connect with families that understand what you are going through and who can share their experience. I had never heard of CDH until the day my son was born and the NICU doctor told me he was born with this birth defect. I love that they are taking ACTION raising awareness and funds for more research. CHERUBS has made the scariest times of our life much easier with the volunteers support and love! We will be forever grateful!

Our son was diagnosed with CDH in 2001. Our high risk pregnancy specialist told us to go to the CHERUBS website for "anything CDH related. They will have the most up to date and accurate information." CHERUBS was our guiding light from day 1 and still are. We have connected with families on a personal level because of CHERUBS. We have participated in research studies and felt endless support from the charity. Our lives were forever changed for the better because of CHERUBS and it continues! What a blessing! We have a 13 year old survivor of CDH and we are so grateful for all the love, support and guidance we have had through our CDH journey.

I gave birth to an undiagnosed cdh child. I felt so alone because I knew no one who had a child with this condition. After I discovered Cherubs, I learned of many people and now have many cdh families for friends! It's nice having people who you can relate to.

Phenomenal organization. Compassionate, educational, supportive, dependable communication. Thank heavens they have been available for us.

The best charity I could have ever come across after my sons diagnosis. They were there before birth, during his life, and after his death. The President, Dawn Williamson and VP, Ashley Berry took the time to meet my son too. I owe them more than I can say!

When my grandson was born with cdh we were lost. CHERUBS stepped up with information and care that was amazing. It's been 8 years now and we still never feel alone. Their state reps and anyone in the organization is always there to help. We've never felt like we were unwanted or an inconvenience. We've only had wonderful interactions with everyone. Still today we are so impressed with them that we do every thing we can to bring awareness not only to the birth defect but to the organization.

My daughter is a 28 year old survivor and I wish we had ha CHERUBS when she was born. We were alone in our journey. When she had to have surgery several years ago for a vowel obstruction related to her CDH diagnosis, we found CHERUBS. This is not just a charity. This is a family where there is so much information, compassion, love and prayers for all. My daughter and I now volunteer for CHERUBS. I am just so thankful they are there so no family will ever walk this journey alone again.

My son Aaron was born 15 years ago with CDH. Cherubs has been there for us from the beginning. Through our repairs and recovery in recent years and still there through our hard times as well as our praises! We would be lost without them.

At my 20 week ultrasound my world was turned upside down. My fist child was diagnosed with a birth defect. This birth defect was Congenital Diaphragmatic Hernia and he was given 50% chance of surviving. I then googled information about CDH and found Cherubs. I signed up their forums and was instantly connected to support system that has helped me through my whole journey, expecting, birth, and grief, when we lost him. They have created a whole connected CDH community that is very supportive. They are very active in all aspects of raising funds for research and support and everything under sun in raising awareness. They help many families not feel alone and fight hard to get progress in helping CDH families and future CDH babies.

My wife and I felt so alone and helpless when our son was diagnosed with CDH. We were both so pleasantly surprised and comforted when we found CHERUBS. Such an absolutely phenomenal charity to help other CDH families connect for support and resources that surely helped us for information and comfort. God Bless CHERUBS!

I have a 24 year old survivour my daughter Angel I have been involved with CHERUBS from the beginning and this charity does all it can for kids and families that deal with CDH it is a long hard road that is made easier knowing that there are other families that you can connect with

I was born with congenital diaphragmatic hernia jn 1965. For almost 40 years I thought I was the only survivor. Thanks to the internet I found Cherubs, a thriving support group. Not only did I meet fellow cherubs online, but one parent came from Belgium to visit with me in The Netherlands. Cherubs has given me support like no other support group has. Contact with other Cherubs and parents is valuable. They know how I feel, they know what it's like to live with the limitations that CDH brings. And when I needed more information about a possible reherniation, there were people who provided the much needed information. Cherubs provides support and knowledge. I am very thankful that this group exists and try to give back as much as I can.

Our family can not say enough good things about Cherubs! The information, support, and most importantly the hope they provided to is when one of our twins was diagnosed with CDH was one of the main things that helped us get through such a tough time. Our daughter Emily is a 14m old fighter and we our so blessed.

I am a mother to a angel cherub just in 2014. I have lots to thank for helping me keep my sanity, but Cherubs was the first place every doctor referred me to in reference to this birth defect. They offered comfort and answers when things were so confusing. I can't say they do everything right, but for a one woman show with volunteers they do accomplish a lot. Many thanks to being there for me and my family.

Gave us a ray of hope and comfort when my son was born.

Absolutely love cherubs!! I joined as soon as I found out my baby had CDH and it prepared me in many ways for his birth. Unfortunately baby Brody didn't make it but I've continued to visit this site for support and everyone is just that... supportive!! I've even decided to volunteer as much as I can. We need to get the word out about this group and CDH in general!!! Thank you CHERUBS for all of the help along the way.

I became a member of cherubs a few months ago, I love the support and love you receive from everyone in this page, reading other families journeys and knowing that your not alone in this difficult road is a true blessing!!

My daughter was born with CDH. The doctor had no idea why she couldn't breath on her own, only knew her lungs wern't developed. She passed away 4 and a half hours later. I got home, started researching the symptoms and CDH was the first thing to pop up. The only real indepth page I could find was Cherubs. They were very helpful in helping me to understand what happened. I'm currently wearing the awareness wristband they sent me with the huge amount of documentation they sent me on the condition. I'd have been completely alone if it wern't for them.

I love CHERUBS. My daughter has CDH and when I found out I was pregnant I immediately started the research. I really had to look no farther than CHERUBS. They sent me my tote and in it was all about what I was getting ready to go through what to expect. I am also part of the forums and this organization has become my new found family. Anytime I have had a question or needed advise, or even just someone to talk to CHERUBS has been there. I do not like CDH but I can say that out of a terrible defect I and my daughter Moriah have gained a new family. This family loves, supports but above all understands what I am going through as a parent and what she will go through as a survivor. Moriah will always be fighting CDH but at least with CHERUBS she will not be fighting alone. GO TEAM MORIAH! GO TEAM CDH! GO TEAM CHERUBS!!!!! Thank you all so much for everything. Our love always, Patricia and Moriah

I was born with CDH in 1976 and until I came across Cherubs several years ago I did not know much about CDH. Cherubs has been the most caring and personable charity I have come across. I am so happy that families affected today have a place to get the knowledge and support my family did not have access to years ago. Cherubs is amazing charity filled with wonderful people.

Wish I'd found CHERUBS when my son was here! Great people doing an amazing job simply because it needs done and they love doing it! Everyone has one goal; helping CDH families. Wait; make that two goals. We also want to put CDH on the map, like breast cancer and autism. We want the recognition, the awareness, and the research!

My daughter was born with LCDH. I wish I would have found the support then I see now on cherubs. They are amazing! Always bringing awareness and supporting all the family's with positive messages.

CHERUBS has been at the forefront of spreading CDH awareness since I found them over sixteen years ago when my son was born with R sided CDH. They were the only information available on the web back then and it was so comforting to find a group and forum that I could relate to and knew what I was going through. Dawn has tirelessly and passionately kept up this charity for all these years and has brought awareness and support to countless families.

After losing our precious grandson, Liam Anthony Hunt after 33 days to right-sided CDH, our family found CHERUBS. What a wonderful, compassionate organization filled with fabulous people who are knowledgeable, know what your going through, and are always always there for you. There are not enough words to describe this organization or express my sincerest gratitude. When my grief even 2 years later gets too much, I know I can always blog on CHERUBS and I know that I will always get responses that comfort me.

I volunteer for CHERUBS as a Hospital Angel. I am very proud to give back to them as I am eternally grateful for all they have done for me & my family in the last 3-1/2 years!

CHERUBS is more than just a group to me, they are truly like a second family. After my son Jayden died I was so devastated I locked myself away and was on the verge of wanting to end everything, but just when I was at my worst, my mom showed me CHERUBS. Once I saw what they were about and got to know some of the AMAZING people who not only TRULY knew my pain and wanted to help me in my time of need and beyond, I found that because of the support and LOVE of these selfless, caring, open, and understanding people I had truly found a renewed sense of purpose and reason to live!

Now because of finding this WONDERFUL community I now have a passion and drive for life and have met some of the most amazing, wonderful, and close friends I have EVER had that I NEVER would have met would it not have been for CHERUBS! I also now have a new mission and goal in my life to help other families like us and let them know they are not alone, and we will be there for them in ANY way they may want/need just like all the amazing families before me did for my family in this wonderful group.

My biggest hope and goal for this charity is to raise enough money and awareness to put to more research to help us someday find the answers, and in return find an end so no more babies die or suffer... pure and simple.

Thank you for listening and THANK YOU TO CHERUBS FOR ALWAYS BEING THERE AND HELPING TO SAVE MY LIFE WHEN IT COUNTED MOST .

This is the most professional and kindest charity I have met on my CDH journey. They are very focused on helping CDH families and being the best charity possible. I am proud to be a part of this charity and watch it grow.

I have known Dawn for many years and I second everything her husband said about her. She is a lady. When people sling mud at her she protects CDH families and doesn't throw it back. She makes it into pies and serves them with a smile. This woman is my hero.

I wasn't aware of the huge wages that the president was taking. After looking on guidestar I feel decived that this wasnt previously mentioned on fb. When I donate I want it to go to helping babies not into someones pocket. Taking 1/3 of annual takings is not justifiyable in my mind. I really think this is needs re-thinking.
But at least I Guess they are trying to help.

I am the mom to an 8 year old CDH survivor. I have been a member of CHERUBS since she was born, started serving on committees approximately 5 years ago, and have been a member of the board for almost 3 years. I served as the Treasurer for CHERUBS for about 2 years, and then moved to the role of Vice-President about a year ago. Through volunteering in these roles, I have had an inside view of CHERUBS for many years and am aware of all facets of the charity- the volunteers, the members of all 3 boards, and the finances. I am proud to say that CHERUBS is run by a team of wonderfully dedicated volunteers led by the charity's sole employee, the President of CHERUBS, Dawn Williamson. It takes a lot of hours, and people from many areas of the world, and with many talents to serve the CDH community. All of the volunteers that I have come in contact with from State Representatives, to Hospital Angels, to those who work on the various committees, to the Parent Advisory Board, and the Executive Board serve dutifully with professionalism and respect to see that families get the help they need while working to raise awareness of CDH and money to further research that is so desperately needed. From my role as Treasurer, and with continued knowledge of the finances of the charity as an executive board member, I can assure you that every donated dollar is used to the best of its ability to help the cause. Meticulous care is taken to see that donations are spent only in the manner with which the donor specifies (research, family assistance, awareness, etc.), and that money is never wasted. I am proud to count myself as a member of the CHERUBS team.

In 2010 our Daughter, (Angel Cherub) Libby, was diagnosed with CDH at the 20 week scan. We came home and Googled CDH and thankfully found CHERUBS! Over the past 3 years we have received the most amazing support from people that we now regard as Family. We will be forever grateful for all the hard work that CHERUBS members do. We have made some great friends! I have recently decided to Volunteer in the hope to help other families and am really looking forward to working with so many kind and inspirational people xx

I have been a board member of CHERUBS for the past year and I continue to be moved and inspired by all of the good work done by our volunteers, our President, our parent advisory board and our executive board. I look forward to the future, continuing to support families, raise awareness and funding research.

Since finding CHERUBS aafter the passing of my son, Liam Anthony Hunt, I have been blessed to connect with a network of incredible people! Members of CHERUBS have reached out to me and my family in a number of ways and have inspired us to find positive ways to give back and reach out to others affected by CDH. This will be my second year as the Vermont State Representative and I hope to continue in this role for many years to come to not only honor the memory of my gorgeous Angel CHERUB, Liam, but to help to many families that are affected by this devastating defect in my home state and nationwide. It is my honor and priviledge to be apart of such an incredible organization!

I first learned about CDH when I met my wife, Dawn, who is the founder of CHERUBS. She lost her only child to CDH in 1999. My first experience with the charity was helping to plan a conference and ball in North Carolina. I was able to meet families and I am always impressed at the dedication and impact my wife has had with her work at CHERUBS. I taunt her about being a "CDH celebrity" because everyone knows her name and because of the internet attacks she deals with as if she wasn't a person. People around the world know her and she works with politicians and celebrities to help these kids. No one else has done that and I am very proud of her.

I attend events and I support Dawn and CHERUBS and I have seen it grow from a small charity into a global one in the 7 years we have been together. When we first got married baby items were all over our home. They were stacked in our guest room, in our children's closets, under their beds and filled our attic. After 2 years I made the decision that CHERUBS had to leave our home because there was not room and because Dawn needed time off of work. At the time she was working 2 full time jobs and we had no time with her. I asked her to make a choice between jobs and I asked that she choose her company to contribute to our family. She chose CHERUBS because she wouldn't abandon CDH families. Her Board took a risk and hired her rather than lose her 3 years ago. With an office and 1 job, Dawn has done more in 3 years than 15 years. Instead of congratulating her and CHERUBS on all their accomplishments, her salary is being put on the internet and people are shaming her. She does not make $40,000 but what if she did? Most NPO execs make over $60,000 a year. Most company execs who oversee 4000 people make well over $100,000. Dawn is paid pennies of what she is worth and she would still be volunteering if she had her say. If she is successfully running the charity she should be duly compensated. What she makes is no one's business but hers and the Boards. If you think she is greedy or after money then you have never met my wife. She would turn our home into a homeless shelter and give away everything we have if I let her.

In the 7 years we have been together I have seen the dark side of CDH. I have watched my wife cry for her son and visit his grave. I have sat beside her in court many times when she had to take out a restraining order against a "competitor". I was there at the entire trial and I have watched my wife and my family be a victim time and again simply because she choose to help CDH families. That woman looks at my Linked In page, she contacted Dawn's ex-husband, she even had IRS auditors in our home in front of our kids because she filed a false complaint to try to shut CHERUBS down. For 10 years she has tried to harm my wife and our family in any way possible. I have read the blogs she posts about our family, our finances and our life that are not only none of her business but not even close to true. The only person coming between her and my lawyer is my wife and this person should be very grateful. My wife has too much class to do the same to this person or her family and she should be very grateful for that as well. Because my wife started a charity out of the goodness of her heart in memory of our son it does not give anyone the right to pry into our private lives, to publicly slander my wife or to stalk our family.

I won't comment on what type of man I think the British man whose wife runs a charity for the things he's done to my wife. What type of man accosts a woman alone by herself in another country and then writes such trash for the world to see? She has a very soft heart and I know she was proud to help you as much as she could. To pay her back her kindness you've betrayed her and the charity. She is a good woman and you are no man. I will be more of a gentleman to your wife than you have been to mine and not name either of you so harm doesn't come to your reputations. You owe my wife an apology and gratitude.

For everyone that thinks my wife runs CHERUBS alone and makes all the decisions, you haven't seen the committee meetings she holds or the volunteers she has had in our home. You don't know the conference calls she takes late at night or e-mails she responds to all evening long. My wife is the most honest person I have ever known. If she says something it is true and she always has proof of everything she says. I know, I've tried arguing with her. She is also the hardest worker I have ever met and loyal to the extreme. She has tried to help every single person who started their own charities. Some took advantage of her and now attack her but she still acts like a lady. I have never seen anyone give more of themselves or have the dedication and passion she does for CHERUBS. Having a wife so involved in CDH and grief every day is not easy on our family. Having her attacked for her charity work makes me want to make her quit and find a job that pays more with less stress. She never will. I am proud of all she has done and proud to be married to such a beautiful woman inside and out. My only regret is not having the opportunity to meet Shane.

I have NEVER been involved with a more compassionate group of caring individuals as Cherubs. I have found many times that when I am in need of support or answers - Cherubs has been there for us -ALWAYS!

I do not personally know any of the people who run this charity yet I have found that I have a real family within Cherubs. From the board members to the CDH families I can ask a question, seek support, ask for guidance or even if I find myself falling apart, I always know that I will find the compassion, resources, support and love readily available at all times - day or night. Their sincerity and continual pledge to bring awareness is second to no other organization.

CDH is a heartbreaking journey and never could any of us have even remotely pulled through this journey without the support and compassion of Cherubs, Dawn, support staff and the many other CDH families that really rally around each and every parent.

I know we are not the only ones on this roller coast of emotions but it is the compassion that is so freely provided through Cherubs that allows us to continually know that in those dark quiet moments of despair we are not alone and that help is always very close. Whether we seek encouragement, hope or prayers, I am continually reassured that I am not EVER alone and have never felt let down.

We are not just one family, unfortunately we are one of 144 families born every 24 hours yet the Cherubs family rallies around each and every parent as if they are the only family. From early morning posts to very late night screams for help to care packages and most importantly of all - raising CDH Awareness – Cherubs is there and hope is always found within Cherubs.

Our family received your care package yesterday and we are overwhelmed with gratitude. There is so much information and love in this box. All the labels with all the children's names are so touching. Thank you for all you have done for us and for others. We feel more prepared and not alone. We can't tell you how much this means to us. Bless you all.

With my CDHer being my first child. I had never heard of CDH until she was officially diagnosed with it. It was great to find a charity that had so much support and love. They treat you like family and after being a part of the charity for the past 9 years they have become family. What a wonderful thing to be a part of!

CHERUBS has been a blessing to both me and thousands of other families. If CHERUBS had been around when I was born, my parents would have been able to relate to others going through the same situation as well as get answers to questions that the Dr's could not answer. The amount of support that each volunteer and member gives is overwhelming. I am honored to be a state rep and honored to pay it forward to each new member. CHERUBS also has the most kind hearted CEO. Dawn gives and gives. The love she has for her son carries over to the members of CHERUBS.

CHERUBS has been such a wonderful organization for not only myself, but my large family. Unlike most families, I was aware of what CDH was, as I lost my oldest brother to it in 1973. However, I did not know to the extent of just how critical this birth defect was. My 18 week ultrasound showed nothing wrong. I didn't find out my son was going to have CDH until 8 days before his birth. I found myself not sleeping and searching for anyone who would talk to me and understand what I was feeling and going through. All I kept seeing online was the negative side to CDH. Then, I came across CHERUBS. I met and had an instant bond to all these families who knew exactly that I was feeling and going through. I remember posting something brief on the FB page explaining that I was due any day and just had barely found out, and the next morning I had several friend requests instantly from members.

CHERUBS has given me support and has given me the opportunity to serve others in the CDH community. I'm very grateful for the service, love, support and friendship I find with CHERUBS. I'm grateful that I can now call myself an official HOSPITAL ANGEL volunteer for CHERUBS and visit other CHERUB (CDH) families in need.

I found out about my baby having CDH when I was 35 wks pregnant. I was devastated. Everything after that went so fast it was a blur. Then I found CHERUBS. I finally had a support team and someone to turn to. At CHERUBS I feel like I always have a friend who truly understands what I'm feeling and going through. I love what CHERUBS does so much that I became a state rep so I could help out people who have helpe me & be there for CDH families who need support. I want to do what has been done for me plus so much more. I can't think of a better group to be a part of! We are all CDH family and raise CDH awareness together as a team! And I LOVE IT!! Thank you Dawn and EVERYBODY that is apart of CHERUBS! Our members are truly amazing and inspirational!

Breath of Hope and Cherubs were both there for me when I was pregnant with our daughter. I tell everyone to go to them and Global CDH for support along with other groups on Facebook. The best way to get through a CDH pregnancy is support! The more the better!

This is my 2nd term as the Co-chair of the CHERUBS Parent Advisory Board. I am also the Illinois and Wisconsin State rep along with being on a number of other committees. As an extremely active volunteer, I can honestly say that CHERUBS is a team effort. A team that consists of 1 extremely overworked full time employee and countless other volunteers.

I unfortunately didn't get very involved in CHERUBS until after my 1st son came home after graduating from the NICU. He is my first miracle. We found out at 37 weeks that our son would have CDH, so we were sent into such a tailspin that I just couldn't even process all the information in time to reach out to CHERUBS before my son was born. However, once I officially joined. OMG, did I feel welcomed and understood. The family and friendships I gained were invaluable.

Now that my 2nd son (who also has CDH) is due in just over a month, I am overwhelmed once again by the support. I have worked so hard as a volunteer to provide support to others. Considering how devastated my wife and I were to find out we had to ride this roller coaster again, I am glad we don't have to do it alone...again.

I first learned about CHERUBS 3 years ago when my grand daughter was diagnosed with CDH. I had never heard of CDH before this. I called and spoke with Dawn and she was awesome at listening to all my concerns and fears. It was nice to have someone to talk to who had already embarked on this horrifying journey. Two days after Maddie was born my daughter received a tote bag of hope in the mail it was great and very generous. I decided to become the Nevada State Representative volunteer in January 2012. CHERUBS website is the most comprehensive site with information on CDH!

Hello my name is Josh Hensley and I am a proud volunteer for CHERUBS. My first two children were born with and taken from me by CDH. It wasn't until after our second daughter died that I found CHERUBS. The experience has been truly unbelievable. From instantly connecting to hundreds of people who understood my situation to helping new people affected by this awful defect. Because of CHERUBS I have met people who I now consider some of my greatest friends. I have been able to go to the hospital and support parents of other CDH babies. I have traveled to San Francisco and Boston to learn more about CDH and lend a helping hand to others affected by CDH. I traveled to Washington D.C. and lobbied on Capitol Hill for recognition of our babies.

CHERUBS has over 4400 members worldwide and is in the process of establishing chapters in Europe. With an organization of this size, it is impossible to please everyone and I understand there are probably some who feel they were wronged in some way by CHERUBS. This is regrettable, but rest assured, this is not the case. CHERUBS tries very hard to recognize every member and their children; from birthdays to angelversaries. The work done at CHERUBS is for the benefit of the entire CDH community, not just a select few who work with us. Our work on Capitol Hill does not have CHERUBS in the wording, it is for all CDH victims!

In the past year CHERUBS made $20,000 in donations to CDH Research projects, awarded two $1,000 scholarships, and shipped an immense number of H.O.P.E. (Help Other Parents Expecting) totebags to families of diagnosed or newborn CDH babies to let the family know there is someone who cares! This is only the beginning of what CHERUBS does for the CDH community!

I am beyond proud to call myself a member of CHERUBS and will continue to volunteer with them in any and every way I can. At the end of the day, I know there are people suffering with CDH and its many complications. I will not engage in slander or take the time to be negative toward individuals or other CDH groups, we should all be working for a common goal. I will help and support these people in any way I can and continue to fight for the CDH community!

Hello my name is Freedom Green and I’m a proud volunteer of CHERUBS. I have been doing so for 10 years. I serve on CHERUBS Parent Advisory Board - ( CPAB ) anyone can reach out to us by sending an e-mail to cpab@cherubs-cdh.org and we are happy to answer everyone’s questions, On-Call for Grieving Families, Facebook Admin. I also raise funds and CDH awareness through running marathons in Maryland for CHERUBS that goes towards the CDH Research fund. I’ve been able to attend 2 CHERUBS marches in DC to celebrate April 19th – Congenital Diaphragmatic Hernia Awareness month and happy to assist members old and new whenever I can. I love working with our large group of volunteer’s who are all ready and willing to help out members in timely manor. Looking forward to another exciting year in 2013 and watching CHERUBS grow to do bigger and better things.

Hello My name is Melissa Larrison and I am the fundraising coordinator as well as being on the CHERUBS Parent Advisory Board. We try our very best to support all parents and family members who come our way needing support. I found CHERUBS in 2008 and they have become my family. Anytime I'm down or needing a friend someone is there to help you. We are run by a multitude of wonderful volunteers not one person. Together, with all the groups in the ACDHO, are helping to fund CDH research. I personally lobbied in Washington D.C. for more funding for CDH research and we have come a long way, but there is still lots left to do. Lets all work together for this common goal.

I am the Louisiana state rep. When my son was born 10 years ago Cherubs was the only place to go for support. It was Dawn and a loving group of people that helped us through the worst. The same people whp rejoiced with us. We are blessed to be a part of the wonderful organization.
As far as donations go if you are looking for a thank you then you are giving for the wrong purpose. I don't give for acknowledgement fir a good deed I give to help the charity I love._I've always recieved a thank you by the way.

I found out about CDH and CHERUBS about 7 years ago. In those 7 years, I have seen this charity grow from a small informational group, to an international charity. CHERUBS is a charity without borders and they continue to grow, raising awareness one step at a time. I finally decided to become a volunteer when I saw that I could personally make a difference and do something that I enjoy, helping in anyway shape or form. CHERUBS is more than a charity it is an extended family.

When our first daughter Chloe was diagnosed with CDH in utero at our 20 week scan, we felt lost and alone. We had no idea what CDH was, didn't know a soul who had been affected by CDH. Through the wonders of google search I found Cherubs, and boy am I glad I did.

Dawn, Cherubs founder, has been a huge support for us ever since. She supported us through our pregnancy, delivery, through losing out previous daughter and she has continued to do so ever since. We since established our own foundation which she has supported and so for any body to believe Cherubs is the only charity she supports is rediculous. In my opinion, without Cherubs there would have been no support for us, Cherubs started it all and continues to do an amazing job.

Through Cherubs I have met lots of wonderful people (many I now consider to be good friends) who have been affected by CDH. I love Cherubs, Dawn and Cherubs will always hold a special place in my heart.

In 2006 we had a baby boy born undiagnosed with LCDH, I had never heard of it and felt so very alone. My son Jordan passed away after 21 days on ECMO, I found CHERUBS after doing some online searching and it was a life saver. I had another son in 2007 also born with LCDH, Caleb and he too was not meant for this earth, I received so much support even if it was just over the internet. I was so broken after having one, but two? I must be the only one? No, I have found that there are many families that went through the same heartache that my family and I have. I would not have made so many friends, so many "partners in pain" if it was not for CHERUBS. I am saddened by the reviews that state how they feel about Dawn, I have never had any run ins with her and if I did it would not change the way I feel about CHERUBS. It is not called "DAWN" for a reason! CHERUBS is an organization that is made up of families of survivers and non, of researchers, volunteers and just amazing people who want to bring about awareness! So my review on CHERUBS is that if you have ever been through this horrible heartbreak or you know someone who has, or you just want to bring awareness to CDH then this is a wonderful group to be a part of. Please I ask one thing, I have pictures of my sons on CHERUBS and they do wonderful things in my sons memory...if you have a problem with Dawn take it elsewhere, please don't slander this Organization that has done so many wonderful things for CDH families

This charity has been a miracle to my family since before my baby was even born. They have been kind and supportive. If it was not for this charity our children would not have any awareness or support. I have been in several CDH groups and CHERUBS is the only one that does not attack others and it is the only one that seems to be doing anything to really help. I am proud to a part of this group. Soon as my baby is home I will volunteer and do anything I can to give back. Thank you Dawn and everyone. God bless.

My name is Christina. I am on the CHERUBS Parent Advisory Board. I will not throughout any of my comments, emails, etc. Bash, Downgrade, Commit Libel or Slander directed towards ANY CDH Organization. I believe it truly takes a heart filled with anger and hatred to do something like that. I choose not to posses those traits and make the conscience decision to Believe in the Positive and Hope that one day All CDH Organizations will Work Together for THE COMMON CAUSE THAT BROUGHT US ALL HERE IN THE FIRST PLACE!!!!! Do you Remember how CDH was brought into your life, Do you remember why you chose to Volunteer to help raise Awareness of CDH and Funds for Research for CDH?? Instead of the insults I am seeing on this page (which are making me ill), why don't we try lifting each other up with Positive aspects of the Organizations. We are here for one purpose CDH and our children!!! Who Cares what Organization your with, Who cares WHO you support. JUST FOCUS ON SUPPORTING CDH RESEARCH AND AWARENESS!!!!!!! I found CHERUBS while doing Research on CDH, which like many of you, I had never heard of. I was supplied with a Plethora of information and support from the Forums, Before, during and After my Son was born. There were days I felt so alone in that NICU, I knew all I had to do was turn on my computer and go to those Forums and I could talk to someone else that was going through that too! After we got home and settled into a routine (the CDH kid routine) I decided I wanted to be there for those Mom's in my State, I never wanted any of them to feel alone or just feel the darkness creep up on them in that cave of a NICU room. I Chose to Support the Organization that was there for me, I stand by that decision to this day. I have met so many wonderful people throughout this time, many support several different CDH Orgs, The one thing these PARENTS that support several different orgs are doing is SUPPORTING CDH RESEARCH AND AWARENESS and in return receiving support from all different aspects of organizations. I sometimes wish I didn't know how all these organizations treat each other and could look at all Orgs with innocent eyes. All I know is this, CHERUBS was and Is there for me. I SUPPORT CDH AWARENESS AND RESEARCH and everyday, that is what CHERUBS does as well. Thank you for hearing me out and lets just try and be nice and respect each other.

My son was born with CDH in 2011. Our hospital gave us information on both CHERUBS and Breath Of Hope. I never once felt like I got support from CHERUBS. When I started a page for my son Dawn started bashing me. I felt it was petty and self serving on her part. My goal at the time had been to spread awareness and give emotional support to other families affected by CDH. After her childish behavior, I with drew from CHERUBS and no longer would post about them or tell my friends and family to donate to them. I felt it better that way. A year later Dawn started bashing me again. She bashed my CDH awareness page and my personal Boutique because of their logos and names. She told everyone on CHERUBS facebook page that I was trying to profit off CHERUBS name. I couldn't believe how childish she was being. She out right attacked me. Dawn condemns all other CDH organizations that are not attacked to CHERUBS. She condemns those who use a cherub as their logo or the word cherub in any form. Never have any of my logo's looked ANYTHING like theirs, I wouldn't want anyone to mistake anything I do as associated with CHERUBS, an "non-profit" with a president who attack you if your not with her. The board of directors needs to monitor their president more. Its public record that she doesn't follow guidelines in following the proper paperwork. Who wants to support a charity where the president pays herself more than she donates to Research or families. Go to Guidestar.org and you can view CHERUBS IRS paperwork for yourself. And in researching I came along this little blog http://deceitfulnessofcherubs.blogspot.com/search/label/Dawn%20Williamson Shame on you Dawn for attacking people. Just because you don't have good intentions doesn't mean you have to try and discredit those who actually try to make a difference.

**I am NOT a chapter president. Paperwork for becoming a chapter president hasn't even been filed. Officially I am just a general member of BOH and supporter of their work. If Dawn bothered to do her homework she would be able to tell via IRS and the state of CA that there is no CA chapter as of yet. I fully support BOH. They are mature about their workings and don't try and conceal the true fact about their charity. They are there for parents who need them, like me, when no one else is.

When a donation is given an acknowledgement is usually sent. Cherubs never sends a thank you. My mom's church sent a donation in my daughters name and never received a note of thanks. Same thing happened to me and several of my friends. Cherubs PAYS its CEO nearly $40.000 a year. Dawn should have plenty of time to send simple thank you notes. SHAME ON CHERUBS BOARD OF DIRECTORS FOR NOT MONITORING THEIR CEO!

First off thank you so much for threatening yet again with your lawyers. It seems you do threaten people with them when you are backed into corners. In FACT my mothers church DID donate to your organization and when I recently visited her house a couple of them were visiting. They ASKED me why they NEVER got an acknowledgement for the donation they made. I then informed them to NEVER donate to you again because it just goes to pay your salary Dawn. They were SHOCKED that you drew such a large salary and agreed CHERUBS would never again get a donation from them! I can in FACT get a COPY of the CHECK sent to Cherubs and post it online if you wish. So be careful who you call a liar.

Second I am NOT a volunteer at Breath of Hope. I have stated that I am a turquoise kool-aid advocate for Breath of Hope as you have referred to me. I just figured why not announce it to everyone on Facebook. Since you have me blocked on Facebook I wonder how you trolled to discover that out. Oh I know you used a vulnerable CDH parent to find out for you!

Third a person has to wonder why all the sudden Breath of Hope was getting false reviews on GreatNonProfits. Could the answer be that you have been pushing for reviews on your Cherubs facebook page???? Coincidence? I think NOT! You better hurry and delete them before people realize I'm right! Also why are all the negative reviews on BOH left anonymously? Probably because you wrote them and are a coward not to leave your name. As you may notice bad reviews left for Cherubs are from real people who leave real names.

Also check out this website: http://deceitfulnessofcherubs.blogspot.com/
Dawn is so deceitful! This site has proof of the drama Dawn continues to create and it also shows how she is deceitful with her finances.

I'm from England and when my son was born with CDH and we looked for help cherubs was there to offer us support and still gives us this 12 years down the line. I don't know how we would have found the information and understanding if it wasn't for cherubs

When our Jayden was diagnosed with CDH we looked all over for support and found CHERUBS just before delivery. Although we had great family support there was so much they could not relate to that our CHERUBS family could.

When we lost Jayden to CDH they again stepped up to the plate with comfort & support that you could feel across the miles. We are proud to part such a great group of folks and are looking forward to many more years supporting this GREAT organization!

Cherubs has been amazing over the last 14 years. My son was diagnosed before he was born and I had no clue what to expect. They were there for me, giving me information I couldn't find anywhere else. My son has been through many surgeries over the years and Dawn and other parents where there with me or just a phone call away.

CHERUBS are a wonderful organisation, i live in the UK and they have been a huge support to me, before i found CHERUBS i had no one who understood my journey with CDH, it is like a huge family ,always someone around to talk to, i'd be lost without them and the many friends i have made

Outstanding service and support from this charity. Always someone there to help, support, answer questions. We have just moved and Cherubs helped me find doctors and other cdh families. I have no criticism whatsover for this charity just admiration and appreciation!

When I found out my son was going to be born with CDH and I looked it up I also found this organization. I tried to apply for their forums and had to wait nearly a whole month to be accepted. then when I was trying to get cnn to do a story on CDH and use my son they tried to take over the comments for their own thing and never got anywhere. Then Dawn kept saying my mother-n-law was my sons mom after I told her I was his mom 3 times. I didnt really feel support. They also like to attack all other organizations when really they need to realize that its not about their selfish wants ITS ABOUT THE BABIES!!! They kick people out and get mad if people have fundraisers and dont give the money to CHERUBS.

We lost my grandson to congenital diaphragmatic hernia last week. I am on the board of a trust that will be making a donation to your foundation. I am very impressed with your work and professionalism and wish you continued success.

I live in the UK and chose to volunteer for Cherubs after receiving such wonderful support after the birth of my daughter with CDH. The previous Rep in the UK started her own charity up so I wanted to continue the good work that Cherubs do in the UK. It truly feels like a family. The fact everyone understands exactly the journey you are on helps enormously . Cherubs continue to give us support and it has been a journey that has had many ups and downs . Only a Cherubs member can explain to you how much they are needed and. Of the wonderful work they do in supporting families and Raising Awareness of CDH. Not just in 1 country but all over the world.

As the director of the Pediatric Surgical Research Laboratories at Massachusetts General Hospital (MGH) (Boston, MA) and the Principal Investigator of a research study entitled, Gene Mutations and Rescue in Human Diaphragmatic Hernia, (based at MGH and Boston Children’s Hospital) that aims to understand better the genetic causes of congenital diaphragmatic hernia and pulmonary hypoplasia, our group has been honored to work with the CHERUBS association for over 6 years. CHERUBS has provided enormous support to many of our local New England families, as well as to those we have recruited both nationally and internationally. We look forward to presenting our research and interacting with new and returning families at the annual CHERUBS conferences. Dawn Williamson’s professionalism in initiating and sheparding this dedicated group and their support of our genetic research has made an enormous impact on our efforts towards devising novel treatments for CDH and associated abnormalities of lung development.

I learned about CHERUBS in 2012, when we found out our unborn son (who is now almost 10 months and kicking CDH booty) had CDH. CHERUBS is amazing and a great support system.

2 of my 3 children were born with CDH, Cherubs has been a great place for me to find support, information and just talk with others who have been through what we have. They do amazing things to help educate people on CDH and families affected by it.

I have been involved with CHERUBS since my son was born in 2008. I did not know he was going to born with CDH and knew nothing about the birth defect. Too afraid to look for information while my son was in NICU, I learned everything I needed and wanted to know about my son's condition from the experienced parents at CHERUBS. Everyone is so helpful and friendly. CDH can be a lonely place and it's so comforting to know that I have a family to support me at CHERUBS. I have been able to connect with several families in person over the years as well. Amazing!

CHERUBS has helped me in so many ways. I didn't find them until after my son passed away, but when I did I was able to work through my grief with others in my position.

I want to give CHERUBS a HUGE shout out for all that they have been doing. Ever since I became a part of this heartfelt charity, I have seen CHERUBS grow by leaps and bounds. CHERUBS is like a FAMILY everyone treats you like you mean something to them, it does not matter HOW CDH has affected you. CHERUBS DOES NOT stand in front of you, or stand behind you, CHERUBS STANDS next you, holding your hand, giving a hug, sending positive thoughts, or praying for you. CHERUBS does not just go away if you lost your child to CDH or if your child is a survivor, they are there for LIFE. I am very excited to be a part of this AWESOME group as CHERUBS raises CDH awareness for the MONTH OF APRIL, but all year long.

How come this organization does not transmit to everyone how much its president takes out of the organization in monetary terms. In 2010 she took $4500.00 in wages or COMPENSATION as it is on the IRS form in 2011 she took $35,000 IN COMPENSATION yet when expenses for 2011 are put on its facebook page ther is NO mention of her $35,000 payment to her and in fact the figures quoted on the facebook donnot corespond with the IRS form.Why is that is she ASHAMED she is taking so much out if not she should be