Anonymous wrote:OP, ignore the mean posters. DCUM is filled with miserable people who roam around looking for a fight and a chance to build their pathetic selves up by making someone else feel low. If you had written a post saying you were taking your daughter despite your other child's medical needs the same people would be piling on calling you neglectful.
In general the special needs board is better, but I think a lot of non special needs parents have been trolling there too lately because all the boards seem slower for the summer. But next time try posting there.
Your daughter does not need to go to Disney. My older son has never been because his younger brother doesn't have the physical stamina. It is not a "hardship". He is not "scarred". Only spoiled people think that way.
I'm sorry you have such a complicated life. It sounds stressful. I hope you can find a way to get some support.
Anonymous wrote:I'm a grown up SN sib, and I get the attention thing, but it's basically BS, just an excuse to get people who want to go to Disney to do it. I wouldn't send my kid and I wouldn't feel any guilt about it.
Anonymous wrote:Anonymous wrote:op: We discovered my 8 yo dd is peanut allergic a few months ago. Didn't know before.
So, she recently developed the peanut allergy? Or had she never had peanuts before? Did she break out in hives that cleared up with Benadryl? Or did she have full anaphylaxis from the peanut exposure?
The reason I'm asking is I can't figure out why your parents can't handle her peanut allergy. Obviously, they are flipped out by the idea of using an epi-pen but how severe could the allergy be if she didn't have it until she was 8?
Anonymous wrote:The drama class is private, once a week during the school year, and all summer at day camp. The day camp does swimming, crafts etc but the focus is theater. I believe it's a marketing approach by Disney to partner with theater schools in order to get families to travel to Disney.
Anonymous wrote:Anonymous wrote:Wow. Maybe it's just because I don't have much disposable income for a dance trip to Disney, but I just don't agree with the idea that this "opportunity" is so make or break, or that any good parent would find a way to make it work.
A child's epilepsy is a big deal. Seizures can do permanent damage. OP is an MD as s presumably knows how to manage it better than a layperson.
Sometimes kids have to hear no or at least not now. Life goes on. If your kids aren't spoiled they'll understand that they aren't entitled to everything money can buy.
This isn't about money. It's about the kid who doesn't have special needs getting the shaft because the kid with special needs requires all of Mom's attention, and Mom won't find another solution for her other kid.