Read true personal stories, chat & get advice, support and help from a group of 183 people who all say I Have Cerebral Palsy
6 posts. Updated a while ago 3 posts. Updated a while ago 1 post. Updated a while ago |
- What works for you?
- Describe to me your favorite pair of pants. Mine: jeggings with quite a few holes in them:)...
- Will you slap me for saying what I was thinking...ur ah..rather saying what came to me without thinking?
- Who wants to come and do my dishes, so that I can continue answering questions on E.P.?
These snippets show some of the most common themes mentioned in this experience's stories:
- "I have minor cerebral palsy due to a minute's lack of oxygen to the brain when I was born..."
- "There are a few different forms of CP and mine was diagnosed as spastic diplegia..."
42% of people who have this experience are in their teens, 32% are in their twenties, and 18% are in their thirties. 70% of people who have this experience are women.
Here are a few tips...
- Is to have to prove everyday you can do things other people think you can't.
- It like havent to work 5 times harder than the average person to get your brain and body to work together.
- I get kind of annoyed when folks treat CP as a 'life style' and only mix with other CP folks. Personally, I can't think anything more limiting. You don't have to wear your disability as a badge or act 'professionally disabled'. Be you first - CP second!
Other experience groups that have been combined into this group include: None yet.
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