I'm asking this in other places as well, and through the Cystic Fibrosis Foundation, but I thought I would toss it out here just in case, too.
My husband and I have long wished to move to New Zealand from the United States. However, our firstborn has surprised us by being born with cystic fibrosis. This life-shortening medical condition varies widely in its health impact, and one of the biggest factors is getting regular and appropriate medical care for the condition throughout one's life.
Does anyone know anything about the quality of care for cystic fibrosis in New Zealand?
Also, does anyone know whether having a baby with major medical needs would cause the authorities to deny an application for immigration? We are otherwise pretty good on the grading scale used (advanced degrees, needed job skills, etc.)
My husband and I have long wished to move to New Zealand from the United States. However, our firstborn has surprised us by being born with cystic fibrosis. This life-shortening medical condition varies widely in its health impact, and one of the biggest factors is getting regular and appropriate medical care for the condition throughout one's life.
Does anyone know anything about the quality of care for cystic fibrosis in New Zealand?
Also, does anyone know whether having a baby with major medical needs would cause the authorities to deny an application for immigration? We are otherwise pretty good on the grading scale used (advanced degrees, needed job skills, etc.)






