My niece has Craniosynostosis. She had surgery 1 year ago. and the care package that they sent to her was awesome it let her parents know someone cared. I support Cranio Care Bears
Finding out your child had anything wrong with them especially at infant age I s devastating. Being able to find a support system, positive stories and information on this defect is everything. This non profit is able to provid all of that. We are so thankful for everything cranio Care Bears has done for us and does for many families dealing with their sweet cranio children.
When my daughter had to have a cranio surgery these wonderful ladies sent her a care package to help ease the thought off surgery. They go above and beyond to make many families feel so loved, such a wonderful non profit. Truly a blessing!
During such a hard time learning our child was going to need surgery for craniosynostosis ,it was so special to learn that there was a whole community of people who had been there, and were praying us through. We are beyond thankful for Cranio Care bears!
As soon as my baby was diagnosed with sagital cranyosinostosis I stated looking for information that would clear all the doubts I had. I came across cranio care bears an awesome organization. I found out that what they do apart from spreading awareness about the condition is to send a care package to families. Ours included things for me to bring to the hospital along with pijamas, blanket and toy for my baby which he loved. Receiving our package made me feel special knowing that someone is taking the time to do something this nice to try and make our difficult time more bearable. I really appreciate the prayer chain full of good thoughts for our family and the card we received sending prayers for my baby.
Great organization that provides care packages for free to families with a child undergoing craniosynostosis surgery. The packages have items for you and your baby to use while in the hospital and range from a blanket to toothpaste. So helpful when you’re overwhelmed with you child’s surgery and forget to pack something. By far the best was the prayer chain, we still have it hanging in our child’s room. Shelby & Summer are both very kind and responsive too!
When my son was diagnosed with Craniosynostosis at 1 month old my entire life came to a halt. I consumed myself with finding as much information regarding Craniosynostosis as possible when I came across Cranio Care Bears it gave me relief knowing that there are other people that have been through the same thing I was going through and that they wanted to send a care package to help my family and I during the difficult time. Shelby and Summer are both wonderful ladies that have helped our family in so many ways.
When I found out that my son had Sagittal Craniosynostosis I was overwhelmed. I found Cranio Care Bears and immediately felt so much love and support during this uncertain and scary time for our family. The Care package was so thoughtful for out little Jackson and they have such great products on their shop to support and show awareness for Craniosynostosis.
We found out that my daughter was going to be born with Craniosynostosis when I was 37 weeks along! Searching for support was on my first mind after finding this out. I came across cranio Care Bears and they have been great! We ordered a care package before her surgery at one month! What we got was astonishing! Anything I needed and it beat the hospitals stuff along with things for my daughter! A sleeper a blanket a few toys :-) we have since bought items to show how proud we are of our baby girl who has sagittal craniosynostosis! This group is amazing and has helped us through a tough time in our lives!
This is truly an amazing organization. They helped us get through a tough time. Thank you!
My grandson is afflicted with a rare form of craneosynostosis. I consider myself well educated, but I had never heard of this birth defect. Their information is enlightening and the help parents and caregivers receive is invaluable. This group is supportive and giving. I cannot thank them enough for the encouragement and support they have shown my daughter and her family as they navigate an unknown highway called Craneosynostosis.
My baby boy was diagnosed with sagittal and left coronal at birth as he was rather disfigured. The care package for his surgery was wonderful and uplifting, to think a charity in the US can send something to the UK for free is amazing. The items arrived when my friend was here and made her cry!! Thankyou for your support! Xx
Cranio Care Bears is a wonderful organization run by people who truly care about each "care bear" they serve. My nephew is a cranio kid and had his surgery several months ago. Cranio Care Bears sent my nephew, brother and sister-in-law some goodies and words of wisdom before his surgery. I know my brother and sister-in-law truly appreciated the support, advice and encouragement they received from this organization. Each child is treated with love and you can feel what an inclusive and warm family this organization creates. I love this organization and will be donating to them each year in my godson's honor. Thank you, Cranio Care Bears!!
Cranio Care Bears is by far the top resource moms like myself have for not just support for families with cranio kids but as a place to reach out and share experiences with other families. Before my daughter was diagnosed I had never heard of craniosyntosis. This organization was a life saver to me when I felt the most lost I had ever been in my lifetime. I can not imagine what I would of some without the wealth of information they provided and the love they share for all kids and families going thru this same process.
Carenio Care Bears is an organization dear to my hear...I thank them everyday being there for me every step of the way when i needed someone the most...my baby was diagnozed with saggital craniosynostosis at 2 months old and underwent surgery at 4 months...when we found out that she was diagnozed with craniosynostosis we had no idea what to expect thanks to cranio care bears and their support we were able to get through the surgery...their care packeges are amazing and brought nothing but warm and secure feelings to our heartsl...even after my baby's surgery cranio care bear was there for me to answer questions and just to make us feel better when i break down....thank you cranio care bears for everything you do and what you stand for.... the most amazing thing in their care packages is deffenatly the prayer chain....you hold a spacial place in my heart....thank you, from the Lopez Family from New Haven, CT
Genuinely caring people who like to help babies going through surgery for Craniosynostosis and their families. What an awesome organization.
My son had his surgery February 14,2012 and I found this group when my son was born in April 2011. These ladies have been so nice caring and supportive. I would not have gotten through this without them. I was very lucky to have Shelby with me this whole entire time we've been on this journey. I hope more people find this group and see how amazing these ladies really are and start donating to this amazing group. - Trine and Skyler