Hello,
My husband and I are considering a year abroad (possible move) in Spain with our three sons. Our youngest has Cystic Fibrosis. We are in the very early stages of researching/planning, so really we are open to all information.
Our biggest question is, where would we find the best care for our son’s CF? This would definitely make the biggest difference in where we decide to move.
We do have family in Andalucia, so southern and close to the beach are high on our wishlist….but we are open to anything at this point.
If anyone has any advice, information, suggestions, it would be greatly appreciated!
Thanks!
M