Then I met successful adults with disabilities and they have helped me to accept it, I started with the chair and now I would not want to still be able bodied, because I noticed cp has given me more than he had taken. Only instead of \\\”oh my God, the trees have leaves!\\\”, it \\\”oh my God, the world feels heavy!\\\”.. I’ve always wondered, like others, could only hop out of bed and into the bathroom without stumbling into a wall. June 2016, 9:02 PM hi, I was told, at the age of 30, I CP.I found out by a foot specialist. Moderators or the author, if you want to check it out, here is the link: Thank you Kyle for finally telling the world how it really is like with mild CP. September 2017 at 5:52 AM I have a Facebook page called DISABLED FRIENDS DISABLED I have CP, all of my life on crutches was walking with a walker and l later with the elbow, but after many years and many traps l to use an electric chair. My wife is able, with the help of your specs reply Delete Anonymous 6. (I swear grinds that the walls jumping at me) My leg behind me, until I was fully awake. We love you and we know that the care is for someone with a disability is probably just about as weird as you. I had no friends because I grew up in an environment where friends were just \\\”given\\\” and not made. Reply Delete Replies Anonymous 5. I’m doing my best to push through it; it is there, use it to help keep me mobile (this is rarely an easy task, but I do it anyway because if I don’t) think, I’m going to stagnate. I told my husband about 1 year into our relationship, I have a huge hang up with him, and I don’t know why
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July, 2015 at 7:07 PM hi,I am 63 years old, born with a mild cp that effects my right side,but I’ve achieved almost everything I wanted to do,very strong-willed.I’ve been married,raised 3 healthy sons by me,went to college,my job was working with the disabled adult as a Rehabilatation specialist,love my job since 20 years,now retired, with grandchildren and great-grandchildren,and the education of my 4 dogs,all of the busy that keeps me, and to be able to go,I do the exercise three times per week,that helps me a lot,all things are possible with God at your side. Answers Answers Linh Khanh 18 Delete. I stayed with a friend in Maryland, who like CP \\\”me\\\”, and it was during my time there I learned something about myself that changed my life I had no idea how to socialize, since I hardly spoken ever to anyone without disabilities. I can only walk on crutches, so that everyone could tell I was different, and sometimes people treat me like a 2 year old. I didn’t know the world was hard up to the day, and I didn’t know the heavy feeling was actually chronic pain. October, 2015, 9:58 PM Infinite thanks Ellen for the opportunity to have a blog-link here.
- I suspect that my parents, the intention was to place me in a special nursery, to me, the feeling that a disability was normal, but that didn’t stop me from noticing there were other people very obviously don’t like me, even if these people were.
- July, 2015 at 3:43 PM Feels amazing response Paulette Parker 3 Delete.
- I have mild affect hemiplegic cp and has never been treated for, or told that I was disabled (at least by anyone with any) and I have never considered myself as such.
- If you saw me on the street you would probably never know that I was different, and that is something that is not to say many people with CP can.
September 2016 at 2:38 PM dear Ila, I have a daughter 12 years old and she has mild CP. Reply Keri Vandongen, 7 Delete. Reply Delete sensitive Sara 3. July, 2015, 2:36 PM This is a great post with a ton of great insights in mild CP that not even I was aware of how the chronic pain Problem. Reply Delete Anonymous 2. Delete, reply, RJ.Confiant April 1, 2017 at 5:13 PM I have a mild spastic diplegia and hemiplegia (in the form of uncontrollable tremors in the hands and arm, especially when you are under stress), CP.. Reply Delete Anonymous 26. September 2017 at 5:09 PM My husband has the effect of cp and he’s 55 now, to his legs, he will not go to the drs every thing that’s not suggesting I want to help, to see him suffer more, reply Delete Add comment Load more. I relate to this, on the whole, but the opposite school of education experience had, because I was systematically according to the pre-school and was regularly in a public school, all the way from K-12. It is used as a generic term for a variety of disorders that manifest in different ways, in the rule caused by some kind of brain damage, either before, during or shortly after birth.
But it has. My little boy is almost 2, also with CP is mild, and I hope, one day, he is giving back to the community, as they are. (Holy Muscle Twitching, Batman!) Now I’m on the verge of tears, close to a tenth of a mile. Every, orthopedic surgery, know that when it rains, they are in pain their bones, sometimes in the affected area. Kyle is one of my best friends!) Reply Delete replies Ellen Seidman-June 30, 2015 at 11:57 AM you are a lucky man, Emily, Kyle as a friend. I’ve been very productive: Master’s degree, married, 12 years, and two little girls who are now old enough to be my hand to hold the foot of the stairs, so that I fall. After college, I was an internship at the United cerebral palsy (UCP)’s national office in Washington, DC.. No one told me that 35 years ago, resulting in my right leg, my bad leg would cause me issues. She laughed at me, gave me a pill and said: \\\”you do not take aspirin for the CP-pain, take this!\\\” So I did, and the feeling was, as always, your first pair of glasses that late in life. I used to be able to walk a mile and a half, no problems, until I sat down. Answer Tom Stafford may 25, 2017 at 2:14 PM This was a well thought out post and I have decided to have it in a blog post by me on the fabulous blog posts I read this week Delete