hi I am 11 and have had cerebral palsy all my life and believe it or not I habe only just learnt the truth about my disability thank you emma for helping me
Really good for you, I'm starting to learn all that stuff at 29 since I'm stubborn. About 6 years ago I had a neurologist tell me that I have a lot of issues that point to a mild form of CP but it was so mild it wasn't affecting me then at least that's what I thought. I should probably investigate this more though since now I'm off work due to a load of health issues from pushing it past its limit over and over.
Hi Emma, Wanted to reach out. I have cerebral palsy, and I found this video very informative. However, there are several things I should emphasize: Though I'm in a wheelchair, that level of confinement isn't necessarily "severe". In fact, it's mild; I can talk with ease and have fluid upper-body movement. The movement in my legs is restricted, but that doesn't mean I can't move at all. The most important point to stress here is that the spectrum of CP is far from linear. There are some who can walk, but may experience great difficulty with balance and speech. On the other hand, there may also be some in wheelchairs who have very little difficulty with them. A few other points to be noted: Cerebral palsy is neither hereditary, nor is it a disease, and it is completely separate from paralysis or mental retardation. Anyway, just thought I'd offer my two cents. Great video overall!
It's no surprise, and I don't blame you. The main thing is that it's made out to be so much more than it actually is. While there is all this "if maybe possibly" talk about a disease, it's not in any way. This is an environmental condition, more of an accidental occurrence. Think of it this way, just because you broke your arm at some point, doesn't mean your baby will be born with one, neither will their baby, just saying :)
Weak posture, spasticity in the muscles (really depends on the severity), difficulty talking, all having to do with movement. Another thing you should know is that everything "down there" functions absolutely fine regardless, and everyone who has it is otherwise totally healthy by nature.
Hi Rohan, not necessarily. Those who were born premature with CP may experience some seizures when first being born (like I did), but as far as I know, full-on epilepsy doesn't come as "part of the package", if you know what I mean.
I have mild cerebral palsy and it was caused by the umbilical cord around my neck causing the loss of oxygen. I’m really surprised that it’s only like 10% of cases because I thought this way of getting it was one of the most common
I got pretty much diagnosed with a mild case of cerebral palsy and didn't even think much of it at the time since all of my symptoms were so mild that I didn't even notice lol. The problem is now since my anxiety is way out of control, I'm starting to really notice all of the symptoms I've been having since I'm born. I'm just one hell of a stubborn idiot that I'm off work at the moment. I have poor muscle control and balance but really good reflexes to make up for it lol. It's not falling or tripping if you could always stop yourself from falling in my head lol. I keep my muscles active all the time so maybe that's why I never usually notice alot of the symptoms don't know.
Reason #2401847 why I love Khan Academy. The subject matter Khan covers is so vast. I use Khan videos to study (in prenursing). But the most awesome thing is that I have been dealing with a possible CP diagnosis in my family for the past couple of years and you guys explain it elegantly in 10 mins. As for the periventricular leukomalacia, it’s also referred to as white matter hyper intensity or WMHI. Frustratingly, it’s considered a “non-specific” finding so it doesn’t come with an easy explanation about what other problems and diseases it can lend to... and there are many.
Coming from someone who has CP and is in a wheelchair, there are different types of "server" I can function normally. I just can't walk and need some help with daily things such as bathing and getting dress and getting in out of bed but other than that I can function on my own pretty well and i just want to point out. it is not genetic nor a disease.
wow, i was always afraid of CP... after this video and the subsequent one explaining types. i thank God i have understood at last. thanks for making it ridicolously easy.
Very well explained. Again, I have learned more here in this short video; then doctors have told me throughout my whole 2 year battle with my son; in which they caused this Postnatal CP; but are trying to call is PVL. Hmmm...
Yes, although doctors are often loath to admit it. However, with improved fetal monitoring, the increase in the rate of cesareans and advances in the treatment of oxygen loss, I suspect this cause is becoming increasingly rare.
hi I am 11 and have had cerebral palsy all my life and believe it or not I habe only just learnt the truth about my disability thank you emma for helping me
My 2 year old son has CP. Nice to meet you. I hope you are well. Many blessings to you.
Really good for you, I'm starting to learn all that stuff at 29 since I'm stubborn. About 6 years ago I had a neurologist tell me that I have a lot of issues that point to a mild form of CP but it was so mild it wasn't affecting me then at least that's what I thought. I should probably investigate this more though since now I'm off work due to a load of health issues from pushing it past its limit over and over.
My younger brother who is 30 years old has moderate hemiplegic cerebral palsy and migraines
Hi Emma,
Wanted to reach out. I have cerebral palsy, and I found this video very informative. However, there are several things I should emphasize:
Though I'm in a wheelchair, that level of confinement isn't necessarily "severe". In fact, it's mild; I can talk with ease and have fluid upper-body movement. The movement in my legs is restricted, but that doesn't mean I can't move at all.
The most important point to stress here is that the spectrum of CP is far from linear. There are some who can walk, but may experience great difficulty with balance and speech. On the other hand, there may also be some in wheelchairs who have very little difficulty with them.
A few other points to be noted: Cerebral palsy is neither hereditary, nor is it a disease, and it is completely separate from paralysis or mental retardation.
Anyway, just thought I'd offer my two cents. Great video overall!
+Jake Kussmaul thank you so much . I always thought it was genetic
It's no surprise, and I don't blame you. The main thing is that it's made out to be so much more than it actually is.
While there is all this "if maybe possibly" talk about a disease, it's not in any way. This is an environmental condition, more of an accidental occurrence.
Think of it this way, just because you broke your arm at some point, doesn't mean your baby will be born with one, neither will their baby, just saying :)
What were the symptoms. .. i am currently a nursing student amd i am trying to get as much info..if its any trouble to you
Weak posture, spasticity in the muscles (really depends on the severity), difficulty talking, all having to do with movement. Another thing you should know is that everything "down there" functions absolutely fine regardless, and everyone who has it is otherwise totally healthy by nature.
Hi Rohan, not necessarily. Those who were born premature with CP may experience some seizures when first being born (like I did), but as far as I know, full-on epilepsy doesn't come as "part of the package", if you know what I mean.
Hi. I am Travis Blair. I was born with Spastic Diplegic Cerebral Palsy. I found this video to be very informative. Thank you.
I have mild cerebral palsy and it was caused by the umbilical cord around my neck causing the loss of oxygen. I’m really surprised that it’s only like 10% of cases because I thought this way of getting it was one of the most common
I got pretty much diagnosed with a mild case of cerebral palsy and didn't even think much of it at the time since all of my symptoms were so mild that I didn't even notice lol. The problem is now since my anxiety is way out of control, I'm starting to really notice all of the symptoms I've been having since I'm born. I'm just one hell of a stubborn idiot that I'm off work at the moment. I have poor muscle control and balance but really good reflexes to make up for it lol. It's not falling or tripping if you could always stop yourself from falling in my head lol. I keep my muscles active all the time so maybe that's why I never usually notice alot of the symptoms don't know.
Thank you for this video and the others. I have a relative with CP so I have seen what a warrior he is!
Reason #2401847 why I love Khan Academy. The subject matter Khan covers is so vast. I use Khan videos to study (in prenursing). But the most awesome thing is that I have been dealing with a possible CP diagnosis in my family for the past couple of years and you guys explain it elegantly in 10 mins.
As for the periventricular leukomalacia, it’s also referred to as white matter hyper intensity or WMHI. Frustratingly, it’s considered a “non-specific” finding so it doesn’t come with an easy explanation about what other problems and diseases it can lend to... and there are many.
Coming from someone who has CP and is in a wheelchair, there are different types of "server" I can function normally. I just can't walk and need some help with daily things such as bathing and getting dress and getting in out of bed but other than that I can function on my own pretty well and i just want to point out. it is not genetic nor a disease.
Great video, if you could do more on different pediatric diagnosis into adulthood, it be helpful!
Amen. Same. I would love this information as well.
I would love 💕 to see the same thing
wow, i was always afraid of CP... after this video and the subsequent one explaining types. i thank God i have understood at last. thanks for making it ridicolously easy.
Very well explained. Again, I have learned more here in this short video; then doctors have told me throughout my whole 2 year battle with my son; in which they caused this Postnatal CP; but are trying to call is PVL. Hmmm...
Great video! Do you know when the other parts will be up? (I assume 2 more videos for 2 more types of CP)?
Awesome I have learned so much
thanks a lot.. this is very useful video
Is there a connection between cerebral palsy and bladder leakage, because I have cerebral palsy and my bladder leaks while I'm sleeping
Thank you so much 🙏🙏🙏
do you have to take any special medications and how was it like living with it..
Fantastic job!
Great explanation! Thanks
thank you so much
Very informative information :)
Tq
I have cp due to lack of oxygen at birth. I was also premature. mine is mild, spastic
I have spastic CP too!
Me to
my 9 year old have cerebral palsy its affects it walking only..
My 2 year old son has CP.
I know you are a great mom. This is really hard to deal with.
do u get the desorder when u are born or not
Yes, although doctors are often loath to admit it. However, with improved fetal monitoring, the increase in the rate of cesareans and advances in the treatment of oxygen loss, I suspect this cause is becoming increasingly rare.
X
Thank you
whats up my cp fam :) i have cp
Hi. My 2 year old has CP.
She's too fast.
Slow down the video speed a notch.
Yeah, I had to slow it down to 0.75 -- still sounds like pretty natural speech. lol
STORCH