Dating Someone With Mild Cerebral Palsy

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dating someone with mild cerebral palsy

I had no friends because I grew up in an environment where friends were just "given" and not made. The one where we recognize bin "differently." This happens to each of us at different points in our lives, but it is the first step on the way of our acceptance of our disabilities. My wife is able, with the help of your specs reply Delete Anonymous 6. June 2016, 9:02 PM hi, I was told, at the age of 30, I CP.I found out by a foot specialist. I am now 55yo. My doctor believes I have osteoarthritis in the knee, but I have experienced chronic pain for most of my life with some days better than others, and Vice versa. Reply Keri Vandongen, 7 Delete. October, 2015, 9:58 PM Infinite thanks Ellen for the opportunity to have a blog-link here. 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. 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 remember he saw my limp and noticed that I was disabled, so I told him I had cerebral palsy. Reply Laura Damon October 20, 2016 at 10:52 PM Delete Hello, I was born at 26 weeks, so my mother always told me I was a miracle. I'm currently 28 and I have pain in my left ankle from holding my weight on him while I can. 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. I told my husband about 1 year into our relationship, I have a huge hang up with him, and I don't know why. I try to be as active as possible most days, but to be honest, this was not a fight - on Most days, I want to move, and I take short-cuts (such as transit, instead of walking). 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. Reply Delete sensitive Sara 3. July, 2015 at 3:43 PM Feels amazing response Paulette Parker 3 Delete. 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.

Only instead of "oh my God, the trees have leaves!", it "oh my God, the world feels heavy!". 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. 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 was on an outpatient basis life most of my,even though I have gone downhill in the last couple of years, because of the pain. When I was younger, have faith my parents to me, I would be able to go and run like the other kids, when I grew up, but obviously I could not so I felt as if there was something wrong with me. 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 Reply Delete Replies Anonymous 5. 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.

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. I often have the feeling my legs are stiff, especially when it's cold, but I don't know if I could call it pain, because I never knew anything else. 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. I wish I could just hop on my chair, instead of trying to get me to do xD I have a question for you: Was the pain very bad, if you are taking medications. We love you and we know that the care is for someone with a disability is probably just about as weird as you. 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 believe that exercise and a healthy body posture has, at least partially, prevented me from pain. 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. I've always wondered, like others, could only hop out of bed and into the bathroom without stumbling into a wall. (I swear grinds that the walls jumping at me) My leg behind me, until I was fully awake. 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.

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