Wow.
Laura,
Wow. Losing your lifelong plans is about the hardest slap in the face I can think of. My heart and prayers go out to you and I hope you can find some peace and comfort, though there is precious little of that in this cruel world to begin with.
I certainly sympathize with you regarding rare and little known syndromes. My wife and my son each have a different very rare syndrome. But one thing I've learned over the years is that diagnoses (we've had ours changed many times) are nothing more than labels for insurance companies. No matter what they call it, you still have to learn to live with the effects, and I'm here to reassure you that you can learn to live with them. Maybe you will have to make some major adjustments to how you planned to live, but you can still be a valuable contributing member of society, just in a different way than you had planned. So take some time to grieve for your lost former life, and then make a plan for your new life and its new and different challenges. After all, you wouldn't really want a life free from hardship and challenge would you?
Again, you have my sympathy and prayers.
Spencer's Dad
11 year old boy with PMD Luekodystrophy
Nonambulatory, nonverbal, nonweight bearing
VRO and Pemberton hip reconstruction at age 5
Nissen fundo at at age 7
Subdermal spinal drug pump at age 9
Complete Spinal Fusion Jan. 9, 2007 at age 10.
118 degree curve before surgery - less than 25 after!!