child care fusion
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Child Care Fusion

United States, EnglishFamily

"Let's dream a new child care society!" We want to have discussions with thriving parents of children with rare diseases to assist the parents of children recently diagnosed who are in survival mode. Be our guest, contact: teaguer@twlsnc24hr.com hostess, Rhonda Teague Supported by: Talk, Walk & Learn Center/SHIFTS Night Care Center 24 hour childcare http://www.twlsnc24hr.com Massimo DeAngelis "Child Care Mix"

On-Demand Episodes

01:10

Julie N. Jancius is the mom of Ellie, born with Noonan Syndrome. President/CEO of RASopathies Foundation and Noonan Syndrome Foundation branch. Julie discusses the rollercoaster journey of Noonan Syndrome and the gifts of... more
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00:48

Amanda Williams is a wife, mom, hairstylist, advocate for their son, Jayden, who has Angelman Syndrome, and resident of Ponchatoula, LA. http://www.angelman.org Angleman Syndrome Foundation, Inc.... more
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00:50

Vicki Ross- wife, SAHM of 3, KD advocate discusses and consultant for Thirty One Gifts. Colson, the youngest, is a KD survivor. Vicki will tell us terms as coronary aneurysms, GIANTS, true angina, true heart attack, beta blocker, blood... more
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00:39

Holli Meehan- wife, mother of a 4 year old Kawasaki Disease Survivor, advocate of Kawasaki Disease. 1000 blood donors create 1 treatment of IVIG which is crucial for children with Kawasaki Disease.
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00:46

Leah Bakshy Ruiz is a mom of a daughter- 2 time Kawasaki Disease, advocate of KD, maintains a blog- http://thegreyseeker.blogspot.com/p/desperately-seeking-kawasaki.html and runs... more
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00:43

James Dickniete, husband, parent, sibling, son, resident of Missouri. He, his son and 4 other members in his family have Cri Du Chat. James is also an advocate for children with special needs. He is employed in the electronics industry.
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00:46

Linda Danielle is an advocate of Kawasaki Disease, above that a wife and mom of 4, the youngest- Johnny, Jr has Kawasaki Disease. She tells of her familys journey with Kawasaki Disease- symptoms, doctors and encouragment.
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00:57

Scarlett Clay resides in Austin, TX. She is a wife and mother of 4, the youngest- Knox has Cockayne Syndrome. She has a blog Art is Medicine http://bluepurpleandscarlett.com Cockayne Syndrome support can be found on... more
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00:46

Carrie Champeau, resides in Victoria, Minnesota. She is a wife, a SAHM and a mother of 4 adult children. 2 of the adult (ages: 26 and 22 years old) children were diagnosed with Cohen Syndrome approximately 6 months ago. Carrie... more
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01:05

Felicia Copas- Wife and Mom of 2 boys and 17 years employed in a pharmacy and resides in Red Boiling Springs, TN. She is a strong, excited advocate of this extremely rare disease- her son, Brady Grey, is 41st of 42 in the WORLD!... more
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