I have WDW loving kids and camping may be a less expensive way to enjoy our favorite place. However, 2 of my children have cystic fibrosis. We would require electricity to do their twice daily breathing treatments and vest treatments. I think we can manage to sterilize neb cups by boiling water on a camp stove. I am really curious about details of tent camping at Fort Wilderness. There is really minimal info about it on the Disney website. Can someone fill me in on specifics?
Do you bring your own tent and supplies OR is the tent supplied?
I have noticed sites that say "premium hook ups" do all sites have electricity?
How far are the "comfort stations" on average? Is it a short walk or a drive?
How "secure" are the campsites? Do you pack your belongings up every day?
I think this could be a lot of fun - but with kids with chronic illness I have to have as much info as possible.
Have any of you camped with kids or adults with Cystic Fibrosis? How did it go?
Camping w/Cystic Fibrosis
in Camping with DisAbilities
Posted
Good Morning!
I have WDW loving kids and camping may be a less expensive way to enjoy our favorite place. However, 2 of my children have cystic fibrosis. We would require electricity to do their twice daily breathing treatments and vest treatments. I think we can manage to sterilize neb cups by boiling water on a camp stove. I am really curious about details of tent camping at Fort Wilderness. There is really minimal info about it on the Disney website. Can someone fill me in on specifics?
Do you bring your own tent and supplies OR is the tent supplied?
I have noticed sites that say "premium hook ups" do all sites have electricity?
How far are the "comfort stations" on average? Is it a short walk or a drive?
How "secure" are the campsites? Do you pack your belongings up every day?
I think this could be a lot of fun - but with kids with chronic illness I have to have as much info as possible.
Have any of you camped with kids or adults with Cystic Fibrosis? How did it go?
Thanks!