Jameson’s Cranio Club

I want to introduce to you what I am calling Jameson’s Cranio Club!  When Jameson’s meme surfaced it was a fellow cranio mom that brought the meme to my attention.  Within minutes, and I literally mean minutes, there were hundreds of cranio families on Facebook who jumped into the fight.  I felt first hand how strong the cranio community is, and a fire inside me started to brew.  I have been inspired and am determined to continue to fight for our babies and raise awareness for the cranio world.  I have a long list of ideas that I hope to accomplish.  But, there is one thing I know, and that is I wouldn’t be doing this without the love and support so many have shown along the way.

My husband and I are so thankful to the support we have gotten, and we would love to see Jameson’s Cranio Club grow over the years!  We will do what we can virtually, but we have plans to set up cranio events here in San Antonio and bring this Cranio Club to life!  If you are interested or want more information please don’t hesitate to reach out!

Cranio Collage

This cranio collage represents over 100 cranio kids from all over the world, with all different types of cranio.  I had originally created this to bring to the taping of The Doctors, I gave it to them, but unfortunately it wasn’t one of the photos they featured.  This photo truly means so much to me, for many different reasons.  It shows the many types of cranio, and it shows cranio from all parts of the world.  For me, it’s a little more sentimental because it’s a physical representation of all the support that was given to our family.

Just to give you an idea, here is what this collage represents.

Types of cranio:

  • Apert syndrome
  • Beare Stevenson syndrome
  • Coronal craniosynostosis (right, left, and bicoronal)
  • Craniofrontonasal dysplasia
  • Crouzon syndrome
  • Frontosphenoidal craniosynostosis
  • Lamboid craniosynostosis
  • Metopic craniosynostosis
  • Muenke syndrome
  • Multi-suture craniosynostosis
  • Noonan syndrome
  • Pfeiffer syndrome
  • Plagiocephaly
  • Saethre-Chotzen syndrome
  • Saggital craniosynostosis


  • Australia
  • Chile
  • Canada
  • England
  • Germany
  • Greece
  • Alabama
  • Arizona
  • Arkansas
  • California
  • Florida
  • Georgia
  • Hawaii
  • Illinois
  • Iowa
  • Kentucky
  • Massachusetts
  • Michigan
  • Minnesota
  • Missouri
  • New Jersey
  • New York
  • North Carolina
  • Ohio
  • Oregon
  • Pennsylvania
  • Tennessee
  • Texas
  • Virginia
  • Washington
  • Wisconsin
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4 thoughts on “Jameson’s Cranio Club

  1. This is great! We are transplants to San Antonio from St. Louis. Our 32 year old daughter has CFNDS. We would love to help in any way.

  2. Hi! My name is Denise Christianson. I am not sure how I happened upon your blog just now, but I am blown away. We are a cranio family. Both my boys had metopic craniosynostosis. They each had surgery when they were 8 months old, here in Nashville, TN. Ultimately, my older son had 4 corrective surgeries, and my younger son had 3 corrective surgeries. I have some hateful memories burned into my head regarding how people treated my boys sometimes. My sons are now 20 and 17. I love what you are doing, and I love to talk with families who are dealing with some of these issues. Thanks for what you are doing!

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