CHROMOSOME 22 CENTRAL 
SUPPORT FOR
ALL CHROMOSOME 22 RELATED DISORDERS 

We are all about connecting! 
Click here for an online membership form to JOIN US!
 
Registered members receive our newsletter and can choose to be listed in our parent registry.

C22C is a parent driven group with more than 1000 members in 45+ countries. 

HOME | EVENTS | RESEARCH | NEWS | LINKS | PRIVACY POLICY | DISCLAIMER


Join our main support list

Subscribe to c22c

Powered by health.groups.yahoo.com


CLICK HERE FOR MORE E-MAIL LISTS (choose from, c22cnews only, infant/pregnancy loss, caregivers of adults, Spanish

MESSAGE BOARDS

FAMILY STORIES

FACEBOOK GROUP

MEMBERSHIP FORM

C22C INTERNATIONAL PARENT CONTACTS

LEARN ABOUT

 NEWSLETTERS

DOWNLOAD A .PDF COPY OF OUR BROCHURE - SPREAD THE WORD!

Chromosome 22 Central Inc. is a registered Canadian Non-Profit Organization 
and Registered Charity BN# 86009 3665 RR0001, and a Registered US Corporation with Non-Profit Status

Mei'ling

DOB: 06/08/03

14/22 translocation


Mom Tina

My daughter was born with so many medical problems that completely surprised us because I had such a normal pregnancy. My daughter Mei'Ling was born with cardio problems, ASD, VSD, and PDA, in other words 3 holes in her heart, the ASD is closed now, but the VSD and PDA are still open and may have to have a coil inserted for the PDA to close the hole. I'm keeping my fingers crossed that the next time we go for her echocardiogram it will be closed. She was also born with very high jaundice, her biliruben level was very high. They did a liver biopsy when she was a month old and found that her bile duct was very small and not allowing anything to pass through and was put on Actigall. Happy to say she is fine now and no longer on the medication. Mei'Ling was also born with a tethered spinal cord. Mei'Ling was born with a dimple on her back called a spina bifida occult mark, they did an MRI and CT and found that she had a tethered spinal cord, meaning her cord was connected to fatty tissue at the end of the cord. She had surgery this past February and it was a success-very tiny scar. She had the surgery at A.I. Dupont Children's Hospital in Wilmington, Delaware. She is now seeing an Ophthalmologist there because she has a lazy left eye and is patched 2 hours a day and just recently found she has some hearing loss in her right ear. The Geneticist at Dupont believes all her problems could stem from her chromosome deficiency but we really don't know and really don't know what to expect in the future. If you were to look at her she looks healthy and is very strong, but has delays in her developmental areas. She just started to roll once from back to front, but that is about it. She cannot sit or crawl and cannot grab food to feed herself. She eats fine when fed and has very strong legs. She will begin therapy soon through Easter Seals, so hopefully that will help.

Tina


 Use Paypal to pay MEMBERSHIP DUES, or for Canadian or International Donations ONLY.

USA members for DONATIONS Please forward a cheque or money order to our US HEAD OFFICE so that you can obtain a tax receipt.

HEAD OFFICE - for ALL inquiries: Chromosome 22 Central, c/o Stephanie St-Pierre, 237 Kent Avenue, Timmins, Ontario, Canada P4N 3C2 tel/fax: (705) 268-3099, EMAIL:  steph.stpierre@gmail.com

  US Head Office - for US donations: Chromosome 22 Central, c/o Murney Rinholm, 7108 Partinwood Drive, Fuquay-Varina, North Carolina, 27526  USA, tel (919) 567-8167, EMAIL: bgr@nc.rr.com

  Latin America / Spanish inquiries - Laura Munoz, Robinson Crusoe 1209, Las Condes - Santiago, Chile tel: 02-3251262 EMAIL: lauramuno@hotmail.com