Terris list ping
Good to see that the family has the financial means to continue treatment.
Dear Heavenly Father, please grant this family a miracle and destroy this so-called law. In Jesus’ Holy and Healing Name, Amen
About forty years ago my wife’s niece had a premature baby with lots of problems. The Drs said to “pull the plug” as the child had no chance of survival.
They refused and worked and worried with her for years.
Today that child has done well, worked and performed on Broadway, worked for a major Talent agency in NYC and today teaches Performing arts at a major University in OKC.
So much for “no chance”.
Mild Ebstein anomaly might never need treatment; there seem to be standardized surgical procedures to treat severe cases, even in infants.
Is the hospital saying the defect is so bad as to be inoperable? What would preclude putting her on a transplant list? Does the baby have other medical problems, brain injury or a chromosomal abnormality?
My cousin’s child has Down syndrome and was born with tetralogy of Fallot defect; they had to let her grow a few months until her heart was “as big as a walnut” before surgery to correct.
No one should take their child anywhere near this Nazi hospital.
I am praying this little person can be moved to a safe medical facility, where the doctors will care and be successful...
Honestly, we desperately need a new national organization, and centralized facilities in every state, that are absolutely committed to saving every life possible!
The “10-day rule” isn’t really a big factor in this case...Tinslee has been on life support in the ICU for 9 months.
https://childrenshha.com/services/
https://hhs.texas.gov/services/health/palliative-care/supportive-palliative-care
Hospital press release:
https://www.cookchildrens.org/SiteCollectionDocuments/about/release/Cook-Childrens-Statement-Patient.pdf
But hospitals are for treatment, not long term care.
It all boils down to the money.