Has this ever happened to any of you? You get ?good news? and it feels more like reminder of how bad things really are? I know that I should be falling down grateful that A.?s infant spasms seem to have stopped with the help of the ACTH. What I thought were still the spasms are apparently a different type of seizure (who knew spasms are worse than siezures?!) So while I know I should be relieved, the whole thing seems more like semantics than I thought it would. I thought bringing the IS under control would sort of temporarily solve our issues. For the crazy money that this cure costs, I was thinking if it worked it could buy us a small stretch of smooth sailing. Not so I guess. At least weaning off of this set of drugs will hopefully make DD less irritable...
Re: When good news hurts?
oh, hugs.... it is rough sometimes isn't it.
I hate it when the geneticist brings up things that the regular pedi says not to worry about. It is just depressing that in a normal kid (pedis perspective) this would be no big deal but for DS (geneticist perspective) we need to be worried.
bah!
Hey NH
I wanted to mention, as you spoke a bit about the cost issues, that you can apply for Katie Beckett Medicaid in NH and your DS will probably be approved as long as it's a chronic condition. Katie Beckett (also known as Healthy Kids Gold) means you will have no copays at any doctors offices (including out of state docs) and you don't have to pay for prescriptions. They also cover costs associated with Early Intervention, which has been helpful for us.
ave you heard of the organization Partners in Health? Please let me know if you'd like more information. PiH can help with the application process and providing some financial relief for some things in the meantime.
Edit: DD not DS...sorry!