[Mybabe4me]

Lorriane,
I am waiting hoping se will talk to one of us. We you and me both have been through so much with this congenital defect. And it goes undiagnosed so often. I have pmed her about our group we are in maybe she will join. Where we do not allow bashing it sometimes helps when that isn't happening. We both know how hard it is to take care of these special needs babies and being bashed is the last thing you need in this time.
I am just hoping she will take our help. Oh I must add I have three kids and my husband works I take care of a lady that had a stroke free of charge. So there is only on income coming in here also. I am still paying babybear's bills. I dont' care if it takes my life time I at least know his neck will not break again.
Oh yes i said check my avaitor well that is baby in a wheel chair trying to learn to walk again after surgery. like 6 months out post op this is what you will deal with if he breaks his neck unless you are one of the lucky ones like Lorriane and your baby walks again. We have many pups on our group Lorriane and I are on that are AAI/AAS survivers and they are running and playing like normal babies. I want to see this for you.