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Emanuel Syndrome

and the 11/22 Translocation

  • Emanuel Syndrome
    • What is Emanuel Syndrome?
    • Receiving the diagnosis
    • History of Emanuel Syndrome and C22C
    • Emanuel Syndrome Development
    • Care and Treatment
    • Life Stages
    • Medical Issues
      • Cardiovascular
      • Craniofacial
      • Ears and Hearing
      • Gastrointestinal/Feeding Issues and the Digestive System
      • Genital/Reproductive
      • Immunity
      • Musculoskeletal/Orthopedic
      • Neurological
      • Oral and Dental
      • Prenatal
      • Respiratory
      • Seizures
      • Skin
      • Vision
      • Urinary
    • History of Emanuel Syndrome and C22C
    • Commonly Asked Questions
  • The 11/22 Translocation
  • Resources
    • Articles on Emanuel Syndrome and the 11/22 translocation
    • Emanuel Syndrome Guidebook
    • Facebook Group for Families and Caregivers – Emanuel Syndrome Support Group
    • List of References up to January 2022
  • Blog
  • Contact
    • Meet the Team
Emanuel Syndrome
Emanuel Syndrome Awareness
AdvocacyAwarenessEmanuel Syndrome
March 24, 2023 c22central

Emanuel Syndrome Awareness

We chose the 11th month and 22nd day for our Emanuel Syndrome Awareness Day, to represent chromosomes 11 & 22

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Parents with their daughter who is diagnosed with Emanuel Syndrome.
AdvocacyAwarenessEmanuel Syndrome
March 13, 2023 c22central

Advocacy and Becoming Your Childs Advocate

When you have a child who has extra needs, you might not always have everything you need to help them

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Raising the Goddess of Spring
11/22 TranslocationAdvocacyAwarenessEmanuel Syndrome
March 13, 2023 c22central

Raising the Goddess of Spring

In 2021, Stephanie Rese, founder of C22C, along with Dr. Melissa Carter and Murney Rinholm, published Raising the Goddess of

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AwarenessEmanuel Syndrome
March 13, 2023 c22central

Emanuel Syndrome Guide for Familes & Caregivers

The content of this guidebook is not a substitute for medical advice and intended for informational purposes only. You should

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Emanuel SyndromeResearch
March 13, 2023 c22central

Research

Many of our members have been very interested in supporting researchers to advance our understanding of Emanuel Syndrome and the

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11/22 TranslocationAdvocacyEmanuel Syndrome
March 13, 2023 c22central

Contribute

How can I help? Here are some ways people have helped our group in the past: Why contribute? C22C does

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A group of children with Emanuel Syndrome gather in an outdoor setting.
11/22 TranslocationConnectEmanuel Syndrome
March 13, 2023 c22central

Connect with Us

Now that you are part of the family, there are a few ways you can connect with us. Or email

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  • Facebook
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  • Instagram
  • YouTube
  • LinkedIn

DISCLAIMER

Chromosome 22 Central is a volunteer based organization. Every effort has been made to ensure the accuracy of the information provided on this website.

Links to other resources are provided solely as a means of further information, and C22C Inc. does not endorse any such resources.

Any information provided to members or the general public is provided for educational purposes only, and is not intended to replace professional advice from doctors or therapists. C22C Inc. representatives, members or board members DO NOT under any circumstances offer medical advice. Our group's purpose is to strictly offer support and basic information. We are run by a group of caring parents and are not trained to offer medical advice. The site contents were developed by Stephanie Rese, Melissa Carter, Murney Rinholm, and Joanna Holmes - Meet the Team. All information we provide is strictly on an information basis only, and should be shared with your own medical professionals.  

It is important to understand that when reading facts about specific disorders, that not all people affected will be the same. As with any disorder, there are degrees of severity, and it is important for parents to understand these facts. It is recommended that any information you receive from C22C or it's members be shared with professionals for comments or advice.

Our site does not accept any form of advertising. Any items, books, other websites etc. are posted with the interest of our membership in mind and no monetary benefit is gained from sharing such items.

Any concerns regarding the content of our website can be directed to Stephanie Rese, c22central@gmail.com

Effective date: July 9, 2003

© Chromosome 22 Central, Inc. 2011| Last Modified, July 2023
Chromosome 22 Central Inc. is a Registered US Corporation with 501 (c) (3) Status.

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