What is Cerebral Palsy
Cerebral palsy or CP is the most common childhood physical disability. It is a permanent physical condition that affects movement. A new international consensus definition has been...
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Cerebral palsy or CP is the most common childhood physical disability. It is a permanent physical condition that affects movement. A new international consensus definition has been...

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Alone with CP **Please read!**
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Hi Everyone,
Thanks for taking the time to read this. I have grown up with mild CP. My whole life I was told I was normal, but then at the same time treated "special" by my mother. This has caused me to feel ashamed and embarrassed to mention my CP to anyone, even doctors, because every time I tried to say "I can't do that because of my CP." She would be right behind me telling me I was making excuses. When I would go to PT or horseback riding she would say "See those kids in chairs and stuff, they are disabled ... not you." I now think she was trying to convince herself but it has really damaged me as a person. All of my life I have dated non-disabled people. But at the end of the day, I never truly felt UNDERSTOOD. So again I felt embarrassed about my CP. Sometimes I would tell people that I got in an accident years ago and that is why I walk with a limp. I've tried to get to know others with CP but I felt like they had nothing in common with me because they were very involved with CP. Every time I mention that I have a disability, I always say "But only a little bit, so not really." Because they always say "You're kidding, I had no idea you were disabled." .... like I need to be in a wheelchair or something for them to believe me. I've been a part of a disabled dating site for a few years called www.whispers4u.com I think it is a fantastic site. I've made tons of great friends on there and I feel really understood. Because of this, I've stayed a part of that site even while in relationships. I have come to realize that I've never left Whispers because I've always thought it ideal to meet someone with mild CP like myself. And now I have. I met him very recently .... and things are becoming obvious that we are interested in each other. I have let him know that I am seeing someone, and let my boyfriend know that I am chatting to this new fellow. There is no deciet here. I have tried on many occasions to talk to my current boyfriend about my CP, but he says things like "You just need to work out, it's not your CP." or "You aren't disabled." One time he even said "Well, if you didn't walk like that (with a limp), then you wouldn't have all the back problems and stuff that you have." I have never had anyone say "Yeah, I understand how you feel..." So, it's very nice. My current boyfriend thinks that I am making a big deal out of this guy having CP. He doesn't understand how important it is or was for me to meet someone with CP as mild as mine. He thinks that I don't give him the benefit of the doubt for trying to understand. It's just not the same as understanding it in the first place. When I talk to my new friend, I feel like I'm a whole person, and that a big part of my life isn't awkward or off limits anymore. That I can truly be myself, someone with mild CP. It's liberating. My boyfriend thinks that I'm flawed because I think this way. He said "African American people don't think they need to date other people of their same race just because they have had similar struggles." I said, "No, because they are allowed to date and marry who they please. I had a deaf friend of mine tell me that if he could only find hearing girls to date, and stumbled upon a deaf girl, that it would be the best thing in the world to him... but that he knows both many deaf and hearing girls so he does not have a preference." My other disabled friends agree with me and my feelings. My boyfriend asked me to talk to my mom or her boyfriend about it. I did. And they agree with him and think I am crazy. I'm not sure what to feel. Many of my GBLT friends told me they felt similar when they realized their sexual orientation for the first time and/or came out. Why do I feel as if everyone thinks I'm wrong all of a sudden for feeling the way I feel (excited) about the fact that for the first time in my entire life I have someone who I can relate and be ME around? And why do all of my disabled friends agree with me, but all of my able bodied friends and family do not? Posted on 05/08/09, 06:05 pm |
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It would be nice to be all friends together. It doesn't matter how bad one has CP, the main issue for me and I hope for others is that we are all the same inside, we just struggle in different ways on the outside.
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Hello!, I am 34 and was diagnosed last week after a two year battle of seeing neuros and orthopedist. I was born at 28 weeks, and the right side was obviously smaller than the left, with my right eye being lazy. Somehow at that point I went undiagnosed. I think my parents believed it was all due to being a preemie. Later I developed severe progressive scoliosis and have have three surgeries there, two years ago i was diagnosed with Secondary Progressive Multiple Sclerosis but the neuros could not agree or figure out what was really going on. Last week I was diagnosed with Cerebral Palsy with Intractable pain and clonus.. So this is all new but I identify so much with you folks! It appears that I may finally have answers that to questions I have had for years..
Sorry so long winded there, but I totally understand that most healthy people do not understand and believe that if we just ate better, exercised more, etc that it would all go away. It is very frustrating when family and friends have had for years still dont understand why I cant just go to theme parks, or places that require a lot of walking, noise, or heat! Because of the three things combined the fatigue is so extreme that after 2pm i am pretty antisocial, so depending on how I am that day I seem to flake out often. I am happy to meet you all and look forward to knowing you better.
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Hey Heather,
I know exactly how you feel .sometimes you want someone to relate to u. And thats ok. u have cp and everybody has an opinion, but until walka mile in our shoes do u they really know? If you find a mate with CP or not- Jesus is looking out for us- trust him
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they don't understand what you are going through they will never understand they don't have a disability but t you shoiuldn't be embarrassed because they don't understand either
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IM now 50 in my 49th year i foundout the reason my leggs dont work right and my left arm is i have mild CP. WOW I was always told i had strokes at birth. Anyway it seems to me your really unhappy because no one is really listening to you. All but the guy on the site. Now where is he at? there is alot to think about with on line friendships. But do you really want to be with a man who doesnt believe you????OMG. Maybe he needs to go with you to the doc sometime. Dont settle please Heather you have along lift ahead.Think long and hard about this.
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Hello Heather,
I can't begin to tell you that I understand but what I can say is that I do have empathy. I recently lost my son who had CP. He was high muscel tone, could not walk or talk and was constantly having surgery to fix something that could not be fixed. I wish I would have taken the time to join a support group while he was alive. But time is the only thing that we can't get back. So no more wishing. What I can say to you is embrace who you're, do what makes you feel good as long as you're not hurting anyone and keep god first things will work out find. And I also want to say that it
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I also dont feel understood. I have had spastice diaplegia (form of C.P.) all of my life. I was married for 17 yrs and when that ended she told me she was tired of not being able to live life. I then met and was engaged to another but that ended when she met someone else that as she said "they just had more in common" (she enjoyed walks and I am not able to take long walks) my last relationship well long story and wounds still a little fresh. so Yes I understand!
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