22q Texas has been amazing for our family. They have been a huge help and wonderful support system to our family.
22Q Texas has been and is a tremendous support network for parents and family members with 22Q or DiGeorge syndrome. I highly recommend this organization to anyone seeking more information.
These guys are wonderful! I no longer live in Texas, but any time I reach out, they are still so good to help! They do so much for the 22q community! Their support of individuals with 22q and the families with a loved one with 22q are unlike anything I've had. I love how they bring awareness and love through their work! Truly an amazing organization!
We have been involved with this group for the past 10 years. My daughter has 22q deletion syndrome and we didn’t know any other child or family that had 22q for the first 8 years of her life. We finally met this wonderful group when she was 8 years old and it was such a relief to not be alone. We attend 22q at the zoo and the wonderful 22q camp they have had the past ten years. My Saugus 18 now and I am currently a board member at large for 22q Texas. We will continue to support this group emotionally and financially as we can and help all the newly diagnosed families not ever feel alone.
This is an awesome group that one I found them it made my family not feel alone. We attend the yearly zoo events and yearly retreats which benefits my daughter greatly. 22q is a very common genetic disorder that is under diagnosed. VCFS Texas spreads great awareness and is my second family!!
Review from Guidestar
This support group has brought so many friends and important resources into our lives!
22q Texas is a group of amazingly inspiring people, working hard to support individuals with 22q11.2 Chromosome differences and their families. They run an impactful, very well organized annual camp, during which families get to interact and share.
I can not even put into words what this organization has meant to our family. They provide resources and tons of information to families who have a 22Q individual but more then that they provide support. This is the greatest group of people!
They have provided so much support for our family. The retreat they put on each year has ministered to our families in ways we can’t even begin to express. My daughter has had the opportunity to meet other kids just like her and it gives her such a sense of belonging. As a parent I’m appreciative of getting to learn from other parents and from the great speaker that this organization brings in. This is life changing work that is being done here and I know it will only continue to grow!
22Q Texas is a wonderful organizations supporting families just like ours. The friendships we have made will be lifelong, and honestly, some of those friends are more like family than some of our family of origin
I am so thankful that 22Q Texas has been a part of our lives since our daughter was a newborn! This is such a wonderful organization, they are truly our second family. Each of us looks forward to seeing our 22Q Texas family, especially at camp! That is the highlight of our year. In 7 years, we have never missed a May zoo event and had a blast with everyone at Morgan's Wonderland these past 2 summers
This group works hard even during times of crisis to help the families who deal with 22q even if it is to give advice. They even have outreach info for the families who have not joined the group before and share resources.
This organization does so much for the 22q community. They provide as much help and advice as possible as well as plan get togethers for face to face support as well as online. They are more than a group thanks to them. This community is a family.
22q Texas has been so helpful for my daughter. Lovely people.
This charity helps families like mine connect with resources and their families. This can be an isolating diagnosis- without support. Thank you!
Great organization for our 22qt’s.... my 22q child has met many great families in this group.
22Q Texas has made a life changing impact on our family. We now know we are not alone and we have gotten to experience the gift of being connected and supported.
My daughter is a 22qtie, and we’re ever so blessed to have found this nonprofit in TX. We love the members and the board. They’re all our new 22q family!
Great Non-Profit! All donations go directly to supporting kids diagnosed with 22Q. I couldn’t ask for any better support, networking, and information in finding treatment that works to help our kids! I highly recommend this group to anyone looking for a cause to support!
This group is very supportive of anyone with questions, needing advice, or just someone to listen and commisurate with. I’ve learned a lot and know my family is not alone in this. Very active throughout the state.
Our family found this group 9 years ago. These are the best people. The yearly family retreat is such a blessing for every member of the family. The feeling of family lets you know you are not alone. Nothing but love.
My daughter was DX in 2003, found this group 9 years ago, and I must say we are like family. The biggest event every year is our family retreat. You meet so many new families. There are speakers they also have family breakout sessions where you are both learning and teach either. It is amazing.
Our daughter was diagnosed with 22q deletion syndrome and we felt alone, discouraged and frustrated. We battled this on our own for a year before we found 22qTexas. It was here we found support, others who understand and direction of places to go to find the medical support we needed. It was our lifeline. We have enjoyed meeting with other families several times a year. We have a forum on line where we can ask questions and receive support from other families that have been there. It is here that our daughter can meet other kiddos with the same challenges she has had to face. It's a family. Our life's challenges are more manageable with the support we have found with 22qTexas.
Our son who is now 8 was first diagnosed with 22Q11.2 deletion at the age of 3. The day we took him in for genetic testing he had a full blown seizure on my shoulders and I knew something at that time wasn’t right. You see for years my wife suspected something was wrong with Sage but I was the dad who thought nothing was wrong with him it’s just part of him going through his childhood years. When he was diagnosed my wife immediately started doing research and I still thought nothing was wrong with him. Well one day my wife was on Facebook and saw a group about 22Q families and started reaching out to us. One of the first to donso was Suzi Beall Shaw who invited us to a retreat for 22Q families. I quite frankly didn’t want to go because it cost too much and still I thought Sage was normal. We went without my approval to this retreat. I will never forget the Saturday we were there walking down this ole dirt road to check on my daughter because we didn’t know any of these people. As I rounded a turn in the road I heard a lot of kids laughing and talking and when I saw those kids that’s when it hit me. All those kids looked just like Sage. Sage to us touches the lives of people he comes in contact with. He is a special gift from God and without this group we would’ve never made it. We are one huge 22Q family.
As a father I always thought my son was going through the typical fit throwing that a (3 year old) at the time goes through. My wife always thought there was something different about him but I was the one in denial who said nothing is wrong with him. Well after genetic testing and a full blown seizure in my arms we found out that he had DiGeorge syndrome or 22Q11.2deletion. We had no idea what that was or what it meant for him and so my wife found the 22Q Texas group on facebook. They were having a retreat up north of McKinney for all the families whose kids had the same syndrome. I did not want to go because my kid was normal and because we did not have the extra money to go. Well we went and all it took for me was one long walk down a dirt trail to see all these kids who looked just like our son and at that time it hit me like a ton of bricks. I knew at that time what he had and has gone through he cannot help. This group means the world to me. We have all laughed and cried together. It seems as though we continue to learn about this syndrome more and more everyday and the 22Q group is necessary in information sharing as well as we all consider ourselves one big family.
We love this organization. They are completely volunteer run and provide support for people and families of people with 22q. We love the camp they put on every year.
My daughter and I really enjoy the camp this group puts on every year. They have also been very helpful for us finding local resources that have knowledge of the syndrome.
This non-profit truly made the difference for our family when our son was diagnosed with 22q11.2 deletion syndrome. I am continually impressed with how much they do for all of us, being a group of VOLUNTEER 22q moms! They are a life changing support group that really helped us find the positive energy to accept an enexpected and scary diagnosis.
When I found out my son had 22Q, this rare syndrome I had never heard of, I was terrified and devastated. This nonprofit was a god send when I found it. There was resources, information, and support. I got excited about the community we had found and started to have a better idea of what this was and how to handle it all.
This organization is so helpful with information and events for 22q
This group is amazing at providing information and support for families with a child diagnosed with 22q. The annual retreat brings families together for education and fun!
This group has been a lifeline for our family since my granddaughter was diagnosed. The information, support and resources we have received have been essential in helping our family navigate the many hills and valleys of having a 22q child. Giving us opportunities to meet each other at retreats and 22q at the zoo is amazing!
Awesome organization that we are thrilled to be a part of!!
This is by far the best organization for children with 22q. The board members go above and beyond to help you any way they can.
22q Texas has been a life saver for my family. We were lost once our daughter was diagnosed with 22q. We felt all alone and lost. It was not until we found the organization that we began to gain knowledge, support and most of all love. We have know gained another family. We value this group so much and hope that we can can give another family the same.
Our daughter Abi was diagnosed at age 4 after years of doctors not knowing that all her issues were connected. We were given information to 22texas and our lives have not been the same. This group is not only for information this is a connection to a family. One that understands what we struggle with. A family that supports each other and makes you realize you are not alone. We love being part of this group! We look forward to our retreat because it's the one time a year you don't worry about anything! Just being loved and supported by your family!!!
This organization has opened their arms to my family after finding out my son was diagnosed with 22q deletion. They’ve answered every question and assisted in every way. I’m so very thankful for finding them!
Since my son was diagnosed 3 years ago at the age of 7 I have turned to this group so much for answers. The group is so supportive and quickly call to action when help is needed. This is a chromosome abnormality that needs more recognition in the community so these kids/adults are helped with daily needs.
Just when we felt so lost so many unanswered questions we found this organization! We immediately were welcomed and began networking to find the proper and knowledgeable care for our daughter. This organization is lead by a great group of people whom dedicate their time to help families like mine! It’s been 3 years since my family has been a part of this group and we continue to grow closer.
The experiences that my family shares with this group are priceless. No where else is my 22q kiddo deemed normal. No where else am I surrounded by people who understand the path and trials of having a special needs kiddo. No where else can we feel so at home. We will keep doing what we are doing thanks to the support we receive!!
I was so overwhelmed and looking for help in any way when this group found me about 6 years ago. My daughter was diagnosed at 3 wks but she had never met another person dealing with the same diagnosis until the first zoo event. We have found so many new relationships through this organization & I am beyond proud to serve on the board now. It is truly amazing to see the lives that have changed thanks to the work done by this group. It's very exciting to see!! Looking forward to see what the future holds.
22q Texas supports families in Texas and beyond affected by the second most common genetic disorder - 22q11.2 deletion syndrome (also known as DiGeorge or Velocardiofacial syndrome). It provides information, resources and support so that families can achieve the best possible outcomes! 22q Texas has let our child know that he is loved and supported beyond his own family and he and we are not alone.
I found this organization by chance and have been blessed ever since. The leaders are always available to answer any questions and always provide news and resources as they learn about them. Thank you 22QTexas
I was going through a divorce just months after my infant was officially diagnosed with two genetic disorders, one being 22Q. My world was in a tailspin. I spent months researching my little one's diagnoses. I came across international zoo day and began to cry because I had missed it by a couple of days. I felt so alone. I had been off social media for almost a year when one day I just searched for 22q. I found VCFS Texas/22Q Texas. I was immediately welcomed with warmth and encouragement. I missed the following international zoo day due to inclement weather. I was disappointed. I finally had the opportunity to meet members for this support group at the annual 22Q camp. We loved it! I get emotional now just thinking about the love and support I felt. This organization is wonderful. The organizers are personable, passionate, knowledgeable, and so supportive. I am now a single mom but the support I get from this organization is priceless.
~More than appreciative Mama
Review from Guidestar
Such a special network of supportive families. We cry together, lift each other up and learn from each other. Invaluable!
This group has been absolutely incredible. The support we have received continuously blows us away.
22q Texas has saved me. The group of men and women behind this group will never know the depths of my love for them. We are about 6 months into the journey with 22q as my daughter was diagnosed at the beginning of the year. I have made many friendships, learned from veteran families/ shared stories, tears & heartache with so many of these beautiful people. I can honestly say that life will never/ would have never been the same without 22q Texas.
Thank you for everything you do. ❤️
Review from Guidestar
This group has helped my wife and step daughter find support and to help me be more informed
This is a really great group that ya actually grown outside of Texas. We have found that those families had no support in their areas.
At the scariest time in my life when all of a sudden I had no idea what my sons future would look like, this nonprofit group gave me support that I desperately needed. I had people who knew what I was going through, and could answer questions no one else could. They also gave me a purpose of good from one of the worst things a parent could go through. I realized if I was involved in this great community I could have an avenue to help others and raise awareness for a genetic syndrome that desperately needs to gain attention so other children will not go through their lives undiagnosed.
This group is amazing my daughter is 10 and she just met this group at 22q at the zoo she has since started advocating for other people with 22q.
When your child receives a the diagnosis of a life-long, complex genetic disorder you've never heard of , it's impossible to not be overwhelmed. When your pediatrician has never heard of that disorder either, it's more than a little frightening and frustrating. You feel lost. When you find an online support group made up of families who have the same diagnosis and understand everything you are feeling, you realize you are not alone. When you have the opportunity to meet these families in person, talk, hug and play together, you know you have a new family! That is what 22Q Texas is. Not just a community. A FAMILY. Families living with 22Q who lean on each other, cheer for each other & love on each other
After an emergency c-section, our beautiful son was born. We learned on the second day of his life that he had congenital heart defects and at 2 months old, he had open heart surgery. Because the cardiologist ordered genetic testing in the operating room (thankfully), at 4 months old, he was diagnosed with DiGeorge Syndrome. When I looked that up on the internet, I found published medical articles about schizophrenia and immune system problems. I only figured out years later that the syndrome was also called Velocardiofacial syndrome or 22q11.2 deletion syndrome. With new terms, I found more resources and people who were going through the same journey - of unawareness in the medical and educational communities. I helped found this group of families dedicated to improving the lives of all people affected by 22q11.2 in Texas and beyond. We will connect you with resources, share our stories and support you in your own journeys. We are all in this together and we will make a difference!
I have seen hundreds of people benefit from the services and events coordinated by 22q Texas/VCFS. This organization is run by and for the 22q community. A most excellent group, making the 22q journey one that needn't be traveled alone here in Texas! ⭐️⭐️⭐️⭐️⭐️
I am one of the founders of 22Q Texas! Our daughter was born with and diagnosed at 5 months old. We needed support and families that understood what we were going through! This nonprofit does all of that for our family. We have contact info so you can call a parent looking for help and support!