https://padlet.com/glovemia24/7uj8chvvpuvm out of my mind project en-us 2017-10-03 17:55:30 UTC 2025-11-13 06:16:36 UTC hello@padlet.com https://padlet-assets.s3.amazonaws.com/icons/Xmastree.png glovemia24 https://padlet.com/glovemia24/7uj8chvvpuvm/wish/200582419 1. The disability is called Cystic Fibrosis.
2. A person with cystic fibrosis would experience fatigue, chest burning, diarrhea, wheezing, shortness, delayed growth, salty sweat, weight loss, and nail deformity.
3. Cystic fibrosis is contracted by a mutation in chromosome 7, which is inherited from family genes. That chromosome mutation causes the thickening of sweat and mucus.
4. Cystic fibrosis can be prevented by most of the time and there are ways to ease the symptoms, but especially in severe cases, it can't be fully cured. A few ways to ease the symptoms is penicillin, cough medicine, postural drainage, and a chest wall oscillation. You can prevent getting cystic fibrosis by getting a pneumococcal vaccination.
5. People ages 0-40 are most commonly affected, and equally affects men and women, meaning no gender is affected more than the other. White people are more commonly affected by cystic fibrosis than any other race.
6. Cystic Fibrosis is actually quite rare.There is no chance of passing the disease from one person to another, but you could pass it to your child if the wife and husband both have the mutated gene. Until the 20th century, not many people with cystic fibrosis lived past their childhood, signaling that this is a very fatal disease.]]> 2017-10-25 19:05:17 UTC https://padlet.com/glovemia24/7uj8chvvpuvm/wish/200582419 glovemia24 https://padlet.com/glovemia24/7uj8chvvpuvm/wish/200947311 1: They wouldn't have to ride to school in anything extra, they just wouldn't be able to run or bike ride to school because they have trouble breathing, and they can't sweat effectively since the sweat is thick and sticky so they may overheat from not cooling effectively.
2. They are able to use their legs to get around school, so they would be able to get around school just like anyone else
3. The sticky mucus and sweat of someone with cystic fibrosis makes it hard for them to absorb fat, so they need a lot of extra fat and protein, which also helps since they have trouble growing. They would not have to have any help eating.
4. They would be able to write and complete assignments just like anyone else because they don't have anything wrong with their brain or body parts like fingers and arms.
5. They would not have any problem working with other people because cystic fibrosis only affects the mucus, lungs, and digestive system. 
 6. They have no problem with the ir memory like remembering information, so they can easily study, learn, and retain information.
7.  They could participate in any extracurricular activity that wouldn't make them to sweaty because their mucus membranes get easily clogged since their sweat is thick, and they couldn't do much physical activity for long because it would cause them lung problems. They could still participate in clubs and extracurricular activities that don't require much physical activity.
8. Someone with cystic fibrosis  could take a medication that helps them clear out their mucus membranes and keep their lungs healthy. It wouldn't completely cure the disease but it would ease the symptoms.]]> 2017-10-26 17:39:53 UTC https://padlet.com/glovemia24/7uj8chvvpuvm/wish/200947311 glovemia24 https://padlet.com/glovemia24/7uj8chvvpuvm/wish/202676845 1.]]> 2017-11-01 19:04:43 UTC https://padlet.com/glovemia24/7uj8chvvpuvm/wish/202676845