Wednesday, June 28, 2017

#ThankfulThursday; Alexa's Modesto, CA Dinner & Dance July 22 at 5:30PM

We are grateful this Thursday to Alexa Rast and her family. Read on to learn more about their exciting dinner and dance happening this summer.


Please join the Rast family for a dinner and dance to benefit CCA this July! The Rast family has been fundraising for CCA since 2007, after seeing the impact the Annual Family Retreat has on children and families with craniofacial conditions.

This July they are hosting a charity dinner and dance in Modesto, CA at Season's Event Center Saturday, July 22nd at 5:30PM.  We need you to recruit your friends and business associates to sign up to join in the fun. You can also contribute a silent auction, or raffle item to help benefit CCA. 

Denise Rast has come up with some amazing prizes and sponsors which will make the dinner one to remember. 


Monday, June 26, 2017

Big IGive Promotion: New Shoppers Earn CCA A $5 Bonus for CCA

$5 Member Referral


Summer shopping can help Childrens Craniofacial Association grow our donations. New members' summer shopping can help even more!

Every new member who joins to support your organization by July 15th and makes their first purchase by July 31st earns a $5 Bonus for Children's Craniofacial Association!

So, Tell-A-Friend about iGive today, and encourage all of your supporters to do the same! 

Spread the word by posting on Facebook or share on Twitter. Send an email! Use this join link in your social media posts and email messages.  https://www.iGive.com/ccakids. Word of mouth works, too!

Remember the referred member MUST be new to iGive. They must join iGive by July 15th AND make their first purchase by July 31st, 2017. New member must join by using your Tell A Friend or Cause JoinLink to qualify.

WeHealth, Raising Awareness About Rare Diseases

By Kara Jackman


WeHealth hopes to utilize the power of social media and personal connections to raise awareness, advocacy opportunities, and research with those who need it most: people living with rare diseases. 

How it works 
Social media is vital in the world of marketing today. The same tools, tips, and tricks can be used to help raise awareness about health conditions that are helping to sell products and influence people. WeHealth's technologically advance staff and developers help connect people with rare diseases wth medical professionals, other people who endure the same disease, and to high-quality medical information. WeHealth hopes to change the way the world views rare disease. They want to build a world of connections that only became possible thanks to today's social media sphere.  Awareness will improve the treatment of those affected by rare diseases, eventually leading to a cure. 

What You Receive In Return 
Through the advocacy and connections you create with WeHealth, you will earn a variety of cool incentives. Each campaign will have its own impressive set of prizes in return for your hard work online.

Current Campaign
The newest campaign focuses on Lipodystrophy, "degenerative conditions of the body's adipose tissue." Most people do not know they have this disease until later in their life. Signs and symptoms to look for are high cholesterol, no fat in the arms, legs, buttocks, and hips, pre-diabetic symptoms or diabetes, among others. 

How Can You Help
Follow WeHealth on Twitter and go to  the WeHealth website to join the existing campaign or find ways you can start beginning your own for a rare disease that touches your life. You can make an impact from the comfort of your home by finding a group of influencers that could improve the lives of thousands of people around the world. Sound like something you would like to be involved with, then check out the site and start leveraging social media for good. 

Thursday, June 22, 2017

Modesto, CA Alexa's Craniofacial Awareness Charity & Dance July 22nd at 5:30PM

If you live in, or near, Modesto, CA, save the date for Alexa's Craniofacial Awareness Charity Dinner. The event will take place on July 22nd at 5:30PM. There will be a silent auctions and new sponsors are being announced daily. Head over to the event website to learn more. 



Wednesday, June 21, 2017

Take Surveys, Raise Funds For CCA






Want to volunteer, but are busy with work, the commute, and the kids? No problem! There is a way for you to volunteer from anywhere at any time. Give back to CCA on your schedule by taking part in a  Opinions for Good survey. 

CCA has partnered with Opinions for Good, which delivers surveys to your computer to complete. Compensation for your time can be donated, in part or completely, to CCA.  Join other members from around the United States and be part of the "world's most innovative army of volunteers." All your help will benefit CCA in immeasurable ways. Every little bit counts. Participation is crucial for effective fundraising. 


#WonderWednesday: 'Wonder' Movie Trailer and A Few Words From CCA


Children’s Craniofacial Association is a proud supporter of the forthcoming film, Wonder. We are pleased and grateful that both the author of the book and movie production team consulted families, studied and worked with craniofacial children and formed connections with families on deep and meaningful levels. 

CCA is proud to endorse both the movie and the actors for their hard work to get the story right. We are so thrilled they created this film that tells our story with dignity, stunning accuracy, warmth, and sincerity.


Thursday, June 15, 2017

Family Spotlight: Wayne Family


This month's family spotlight focuses on the Wayne Family of Coatesville, Pennsylvania. Jennifer Wayne, mother of four kids, has her three youngest children living with her in, as she aptly puts it, "a small house full of craziness and love," which is their own "wonderful corner of the earth." 

Jennifer writes, "My parents (the kids' grandparents, a.k.a "Nan" and "Popsey") are incredibly present and involved in all of our lives. They live only a few minutes away.  I could not be doing this without their endless love and tireless support.  We live about an hour away from the most incredible hospital in the world:  CHOP! That is where we were introduced to CCA when Sammi was three by the one and only sweet, welcoming, sensitive, thoughtful, connected and concerned Patient Liaison, Diana Sweeney.  We are so excited to be heading to our sixth CCA Family Retreat in just a couple of weeks!"

The Wayne kids wrote their own updates. so keep reading to hear from each of these beautiful children.


Sammi (Today) 
Sammi,(Before 2008 Surgery)




















Hi.  My name is Sammi.  I am 14 years old and a Distinguished Honor Roll student.  I have Crouzon Syndrome and over the past year I have successfully worn my second halo (to move my mid face and forehead) and had a rhinoplasty (to straighten my nose and help me breathe better).  As of December 29, 2016 (the nose surgery) I am officially done with surgeries!  It has been a rocky road having all the procedures and even daily life, but I had to go through rough times to be where I am today.  I’m more confident and a happier person now and I can’t believe it’s all behind me!  Keep pushing if you are going through hard times, because it’s all worth it in the end!  Also, I recently was able to stop wearing my back brace after wearing it for three years for scoliosis and it helped me so much that I don’t have to have back surgery.  In my free time, I love to read and watch YouTube.  I also play in the school band and I am part of the Yearbook Committee.  I can’t wait for the CCA Retreat this summer.  Now that all of my procedures are over and I’ve learned so much from those experiences, I hope to one day help others with craniofacial differences! 

Cory and Zooey


My name is Cory.  I’m Samantha’s older brother and I’m 26 years old.  I have been living in Philadelphia while pursuing a science degree for a few years now and have been enjoying every moment of it.  I spend most of my free time with my five year old dog, Zoey, or travelling to any interesting locations I can get to. Besides my interest in space science, I love to bike and run as often as possible.  Getting outside and enjoying the outdoors is something I think everyone should get a chance to do regularly.  One day, I hope to be able to discover new and incredible things both on earth and outside our solar system.


I am Joey, son of Jennifer and brother of Cory, Sammi and Tommy Wayne.  Some things I enjoy are Boy Scouts, being outdoors and fixing and making things.  I enjoy hanging out with my friends.  We have known each other for at least six years.  We all have a lot in common and we love joking and laughing.  We all love to draw.  I am in the 6th grade and I love it!  I have gotten Distinguished Honor Roll for the first two marking periods.  I thoroughly enjoy using tools.  Just recently I made a sling shot out of wood from a fallen branch.



Joey and Tommy

My name is Tommy.  I am the youngest of four kids and in the 6th grade.  I am a Distinguished Honor Roll student and I thoroughly enjoy my time with friends.  My favorite academic class is math, but I really love Gym.  I am pretty intelligent and love athletics.  Lacrosse, football, and basketball are my favorite sports.  I also like swimming, driving golf balls, and shooting.  I want to be a Mathematician in the future.





Thank you, Wayne Family, for this awesome update and sharing your story with us. CCA is committed to fostering connections between our craniofacial families near and far. If you'd like to network with someone in your area, with a similar diagnosis, or in a specific age range, please reach out to us at Contact CCA@ CCAkids . com (no spaces!). 

#ThankfulThursday: Overview Talking to Your Child About Upcoming Surgery



Summer is upon us. For all of us this means more time in the sun, but for some of our kids this means time for surgery. Summer provides ample time to recover without missing any school. This time of year is a great time for families to review one of CCA's new overviews called "Talking To Your Child About Upcoming Surgery" You can also view images of the document below.

Additional overviews on craniofacial conditions and other useful medical information can be found at the CCA Kids website. All of these overviews are written by expert physicians and clinicians, featuring top-quality information about well over a dozen topics.

We are grateful to all those who contributed to these publications to help our families stay informed.





-By Kara Jackman 


Wednesday, June 14, 2017

#WonderWednesday: CCA Brings Wonder to Your School or Group

Happy #WonderWednesday everyone!

CCA can help you bring Wonder to your school. We have all the resources, curriculum, and fun additional swag for the kids to keep everyone interested and engaged about the important message delivered through R.J. Palacio's New York Time best-selling book. Learn more about these resources, curriculum packs, and more at our Wonder 4 Schools webpage. 

Check out the impact CCA's programming had in this short video.

Monday, June 12, 2017

On Seeing A Baby With An Unrepaired Cleft Lip


By Ashley Barbour


Ashley Barbour was born with a complete bilateral cleft lip and palate.  She works as a special education teacher and has recently started CleftLove, a Facebook page created to share her experiences growing up and living life as a cleft-affected woman.  

A couple of years ago while I was putting oranges in my shopping cart at Meijer, I looked over and saw a baby with an unrepaired cleft. Despite being in my late 20's, I had never seen an unrepaired cleft in person. I knew what my baby pictures looked like and I had seen others, but something about seeing this little one with my own eyes, impacted me in the most significant way. 

Amy Barbour


I experienced a flood of emotion. I hadn't had this thought consciously before, but I realized there was a part of me before that was almost nervous to see an unrepaired cleft. I was scared that I might be disgusted and what would that mean about how I see myself?

In that fruit section of the grocery store, I realized I had never seen anything more beautiful or perfect than this baby in all of my life. I went over, tears in my eyes, to tell the mother and grandmother how absolutely perfect this little one was.

From birth, and throughout our lives, those of us who are cleft-affected experience so many less than nice gazes: medical staff looking to fix us, strangers trying to figure out just what it is that looks different, and cruel kids on the playground pushing their nose flat with their pointer finger.

The moment I saw this baby boy, I felt compelled to look at him with pure, loving eyes, the way all babies and people should be seen. I thought that just maybe I could transmit enough positive energy that I might be able to counteract some of the negativity he has, and will, experience throughout his life.

Through my tears, I talked with his family and I could feel the hope that filled them as we spoke. In that moment I realized I might be able to offer something important to this community: the knowledge that your little ones will grow up and will be okay.  From this time on, I felt something growing inside of me, a need to share with families, a need to give a voice to those of us who are cleft-affected. 


For me, it was next to the apples on that sunny Saturday afternoon that I was finally able to see what has always been there: a beauty and perfection in myself. 

Saturday, June 10, 2017

CCA Car Raffle *Buy Your Tickets Today*











Children's Craniofacial Association is holding a car raffle and you could win your choice of a Jeep Wrangler, a Dodge Ram, or a Chrysler Pacifica! Only 1,000 tickets will be sold, so scroll down to the bottom of the page and BUY YOURS NOW! 

Thursday, June 8, 2017

#ThankfulThursday: 2nd Annual Wonder Picnic in California




Here are some great photos from the second annual Wonder Picnic in Chula Vista, CA. Families came together for games, food, and fun to celebrate Wonder and some wondrous kids. Thank you Dorina Watkins for this great event. These photos of these kindness warriors are a testament to what could be possible if we all treated each other with respect and an open heart. 




Wednesday, June 7, 2017

Wonder Movie Trailer Released *Video Inside*




The movie trailer for "Wonder," the movie based on R.J. Palacio's novel, about a child born with a facial difference, was released two weeks ago. I am sure most of your watched and shared the video many times over via social media. If you have not seen it, check out the trailer below. 

The movie features Julia Roberts, Owen Wilson, and Jacob Tremblay, playing Auggie Pullman, who goes to school for the first time after being homeschooled. We travel with Auggie and his family as he negotiates a world filled with everything from relentless bullies to inspiring teachers. 


Monday, June 5, 2017

Bullying and Craniofacial Disorders



By Marie Miguel

Marie Miguel is an avid internet researcher. She is fueled by her determination to answer the many questions she hasn't been able to find the answer to anywhere else. When she finds these answers she likes to spread the knowledge to others seeking help. She is always looking for outlets to share her information, therefore she occasionally has her content published on different websites and blogs, like Women for One, Finer Minds and Sisterhood Agenda. 




If you are an expectant parent or the parent of a child with a facial difference, you know how scary different procedures and surgeries can be for you and your child. You seek answers when you do not know what to do, and for many, it can be overwhelming.

Someone with a craniofacial disorder has face and/or head abnormalities. Several syndromes are within this umbrella of disorders, including the following:

   Facial cleft, or face cleft or palate;
   Types of dysplasia;
   Microtia/Atresia;
   Miller Syndrome;
   Pierre Robin Sequence;
   And more common, and rare forms, of craniofacial disorders.

While each craniofacial disorder has its own characteristics, one issue that could plaque individuals with these disorders is bullying. Whether you are being directly bullied, or a loved one with a craniofacial disorder is being bullied, it can have damaging effects that last your entire life. Here are some tips to teach your children (and adults) to not engage in bullying behaviors towards those with craniofacial disorders.

Have a conversation with your child.
If your child comes home and tells you about an instance of bullying, calmly ask him or her the details of the situation. Answer any questions and issues with kindness. If your child asks for specifics, try to return the favor with details. If your child mocks someone or engages in other negative behaviors, refrain from telling them to not do that behavior. Instead, explain why that behavior could hurt another child or adult. Engaging in two-way conversations instead of brushing issues under the rug is beneficial because you are able to help change the conversation.

Take action if someone else is bullying.
If your child tells you that he or she witnessed a bullying event, encourage your child to tell someone in charge, or other authority figure. If the event takes place at school, the person to talk to could be a teacher or principal. Tell your child to use the buddy system to prevent bullying of others from being bullied. Have a friend back them up when confronting the bully. Encourage your child to remain calm if they witness bullying. Overreacting or becoming combative will only make things worse.

Change their behaviors.
If your child is the bully, tell them that you will help them change their negative behaviors into more positive ones. If you have a younger child, he or she may not know that they are actually bullying another child. Let them know that is not acceptable behavior. Show and tell them what behaviors are acceptable.

If your child is older and displaying aggressive behavior (hitting, punching, name calling, gossiping or something else), you may want to seek therapy for your child from a licensed mental health professional. Bullying takes on many different characteristics, and a professional can help improve a child’s behavioral patterns and provide solutions.

Teach your children that everyone is unique and beautiful.
All of us are different in our own ways. Some differences are just more visible that others. Teaching your children respect and that uniqueness is what makes a person special will help children realize that they should treat others how they want to be treated.

If you need anti-bullying advice, seek out a licensed professional to talk with you about your situation. This advice can be found online. Good news: you do not have to leave your couch!  Talk with someone at your convenience — anywhere you are —at www.betterhelp.com.

Check out other useful resources below:

Resources

^ www.betterhelp.com. Accessed March 29, 2017.

^ Syndromes. Children’s Craniofacial Association. http://www.ccakids.com/syndromes.html. Accessed March 29, 2017.

^ Why Perspective Matters When Parenting a Child With a Craniofacial Disorder. Liz Anderson. https://themighty.com/2016/10/what-perspective-means-when-your-child-has-a-craniofacial-disorder/. Accessed March 29, 2017.

^ Five Ways to Bully-Proof Your Kid. KidsHealth. http://kidshealth.org/en/parents/bully-proof.html. Accessed March 29, 2017.


^ What To Do If Your Child Is A Bully. Stomp Out Bullying. http://www.stompoutbullying.org/index.php/information-and-resources/parents-page/what-do-if-your-child-bully/. Accessed March 29, 2017.