I came across your video and I have to say that the level of care that you give your son is beyond words. I know personally by working with individuals who have autism and other developmental disabilities just how much love, dedication and effort goes into a single days work. Your videos definitely display this, and it's uplifting to see parents who go above and beyond in both caring and advocating. God bless you.
I never get over what a strong supportive family you guys are for Jamey. I am sure Jamey is less scared at home than he was at the group home. You guys are awesome
it is always hard trying to get a decent video while at the same time trying to keep those whom are fitting from falling and or injuring themselves.
Looking at this 'coldly' you have struck a nice balance, though I do realise it is more by luck than judgement especially in the early hours when something like this happens.
I started with nocturnal fits until I was around 40 and have had infrequent but injurious fits falling from my feet & landing on my head.
When will we man up as a race and realize that there is absolutely no point in severely retarded people existing. We should abort them as soon as they are diagnosed. They literally have no functional consciousness and cannot socialize. There is simply nothing in there, it is a flaw of our genetics and it simply a waste of one's lifetime to care for these people. It is also a huge burden on society. I hope we come to realize this and not let religious bs get in the way.
I have a mild form of autism and cerebal palsy that have brought about self injuriouse behavior. I know all about self injury, I've expierienced it first hand and believe me, it ain't pretty!!!!!!
I work with people who have autism, and in most cases seizures. I've thankfully never witnessed a seizure this long. I've seen them ''worse'' but they are only up to 2 min. I do what I must, but it still hurts me aswell, and I don't even have real relations to these people. So I can't even imagine what you and your family are going through when you see him in this condition. Much love, and good luck with your son.
what kind of medical professionals allow this to continue...you know what i would say to the doctors treating jamey "why don't you come and spend the night and see what we have to contend with". if they did the seizure activity would stop quickly it would force the doctors to get off their duffs and prescribe the correct meds and doses and provide any supplemential care that is necessary. in my opinion he should be in a qualified group home or have 24 hr care...i'm so mad at the dr's!
I had a range of emotions while watching this. I'm also in shock that CNA's can't give meds since where I live, most CNA's and many in-home mental health professionals receive training to become a certified residential medication aid. I just can't believe that you guys don't have that...LVN and LPN's are also much more expensive for the state since they are nurses compared to a certified nurses aid which gets paid much less. I hope that Jamey no longer has seizures like these,
hello my name is James I'm a college student studying social and human services i am doing a project about autism. your videos have truly touched me. my son is 4 and has aspergers. he doesn't live with me but i see him often enough to know he can be a handful. you are an inspiration to the world. god bless and good luck. my hart is with you.
I feel awful for Jamey. I dont know much about autism, but might be kknowing more, my son is being tested for it right now. i dont want any of my questions to sound stupid or rude, I would just really like to know. Is the self injury sort of a way to calm himself down? Are there certain tactics or getures that your family uses to calm him down?
We use a lot of different interventions to soothe him,,,you have to have a grab bag of things in case one flops, you can reach for the other intervention..ie..if massage fails, you grap a colored sensory egg or re-direct or put him in a warm aromatherapy bath, you just keep trying until you find out what will soothe and comfort him..sometimes it's just holding him tightly and hugging him..other times he's so self abusive we have to give him meds....but he is getting better...very slowly, .....
watching this is so scary. i know i have atypicalautism but, i dunno. if i knew i had to live my life like this id kill myself because autism affects people in so many ways. and its a dissability that not many people understand. And the fact that it cant be treated is unbearable. i cant even bring myself to watch anymore of this video.
Actually, yes it can be treated and we've made A LOT of progress...I show these videos also because it documents some of the most severe sides of autism yet, I know, believe and trust that my son is and will get better and there will be more and more positive videos to show....healing takes time in some cases, sometimes years before you see major progress...we just keep trying. never give up. never lose hope.
Because I'm tired of this willful apathy, ignorance and cowardice of others who can't handle reality of certain sides of autism...we are not hiding in the walls of our home anymore. We aren't going to be ashamed of what we or others go through. If you don't like, don't watch. Go watch Brittany Spears or Paris Hilton. Read the National Enquirer. Forget all about other people's pain and how you may bring awareness or hope to a tough situation....thanks for support
@DirectorKJK As graphic as the video is.. Its LIFE.. i have them and i wouldnt know what i go through during them without seeing video's.. so im thankful for the video's they help myself and the people who are around me during my seizures.
you are such a brave woman. i work in a school for autistic children and always panic when they have seizures. its so hard not to. especially when they are head banging. my thoughts are with you.
They cut your hrs, thats fucked up!! Arrrggg,, what are the state trying to do.. same here in our country.. its like they want people to go away and give up.. which some do,, I know you wont; that anger keeps you strong,, oh honey.. Has James got worse with age.. Im so watching your life here,, I wish I was your neighbour,, why do we live on the opposite side of the Atlantic...
What many people don't understand is just how much parents suffer too, perhaps even more, when their children are having difficulties. Anyone that would deny this family services is an evil bastard. Many autistic people suffer from these types of seizures and I believe this family is trying their best to bring this to light. Many parents would not have the internal strength to endure this and would simply wish their and their child's life away. I applaud you guys and hope an answer comes.
sorry for your son and thankx for his sister.
hakimpolice 3 months ago
I came across your video and I have to say that the level of care that you give your son is beyond words. I know personally by working with individuals who have autism and other developmental disabilities just how much love, dedication and effort goes into a single days work. Your videos definitely display this, and it's uplifting to see parents who go above and beyond in both caring and advocating. God bless you.
jennalah 4 months ago
I never get over what a strong supportive family you guys are for Jamey. I am sure Jamey is less scared at home than he was at the group home. You guys are awesome
DarkQuietWyattON 4 months ago
Hi CDFoakley,
it is always hard trying to get a decent video while at the same time trying to keep those whom are fitting from falling and or injuring themselves.
Looking at this 'coldly' you have struck a nice balance, though I do realise it is more by luck than judgement especially in the early hours when something like this happens.
I started with nocturnal fits until I was around 40 and have had infrequent but injurious fits falling from my feet & landing on my head.
My best wishes to you
mrbluenun 4 months ago
what causes self injury activities?
i wish your son and you and your family all the best. thats great that you are making videos and letting people know
zhenichka18 5 months ago
When will we man up as a race and realize that there is absolutely no point in severely retarded people existing. We should abort them as soon as they are diagnosed. They literally have no functional consciousness and cannot socialize. There is simply nothing in there, it is a flaw of our genetics and it simply a waste of one's lifetime to care for these people. It is also a huge burden on society. I hope we come to realize this and not let religious bs get in the way.
waljayo 5 months ago
i am so sorry you and your sons well be in my prayers
Covie11 7 months ago
I have a mild form of autism and cerebal palsy that have brought about self injuriouse behavior. I know all about self injury, I've expierienced it first hand and believe me, it ain't pretty!!!!!!
Champ675 8 months ago
I work with people who have autism, and in most cases seizures. I've thankfully never witnessed a seizure this long. I've seen them ''worse'' but they are only up to 2 min. I do what I must, but it still hurts me aswell, and I don't even have real relations to these people. So I can't even imagine what you and your family are going through when you see him in this condition. Much love, and good luck with your son.
Krygeryo 11 months ago
what kind of medical professionals allow this to continue...you know what i would say to the doctors treating jamey "why don't you come and spend the night and see what we have to contend with". if they did the seizure activity would stop quickly it would force the doctors to get off their duffs and prescribe the correct meds and doses and provide any supplemential care that is necessary. in my opinion he should be in a qualified group home or have 24 hr care...i'm so mad at the dr's!
Alprazolam 1 year ago 3
I have a cousin who has autism, but never this bad.
Seattlecarnut 1 year ago
Comment removed
krstcmjns 1 year ago
please tell me that girl with pink shorts is single
mrdimebreezy100 1 year ago
I had a range of emotions while watching this. I'm also in shock that CNA's can't give meds since where I live, most CNA's and many in-home mental health professionals receive training to become a certified residential medication aid. I just can't believe that you guys don't have that...LVN and LPN's are also much more expensive for the state since they are nurses compared to a certified nurses aid which gets paid much less. I hope that Jamey no longer has seizures like these,
Maesterofcool 1 year ago
hello my name is James I'm a college student studying social and human services i am doing a project about autism. your videos have truly touched me. my son is 4 and has aspergers. he doesn't live with me but i see him often enough to know he can be a handful. you are an inspiration to the world. god bless and good luck. my hart is with you.
moorsejames 1 year ago
what is tonic clonic?
dclark12553 1 year ago
Makes me feel so impotent. What others have to endure. Could not morphine or opium at least give him peace and calm ?
spiderboymax 1 year ago
Is he snoring or breathing seriously heavily?
xxxAlphaxxx5 1 year ago
You and Jamie are in my prayers..
lovlybrwneyedlyn 1 year ago
You are all amazing. You don't give up because you know he's totally in there.
mrefus 1 year ago
you said on the video your other son has seizures also i was wondering if he has them to the same extent James does ?
ShawnMichaelsNo1 1 year ago
I wish you all the patience and strength in the world. I wish I could transfer some of mine to you.
If there is a heaven, you deserve to be in it.
YTubeMoralAction 2 years ago
I feel awful for Jamey. I dont know much about autism, but might be kknowing more, my son is being tested for it right now. i dont want any of my questions to sound stupid or rude, I would just really like to know. Is the self injury sort of a way to calm himself down? Are there certain tactics or getures that your family uses to calm him down?
mizzamaya420 2 years ago
We use a lot of different interventions to soothe him,,,you have to have a grab bag of things in case one flops, you can reach for the other intervention..ie..if massage fails, you grap a colored sensory egg or re-direct or put him in a warm aromatherapy bath, you just keep trying until you find out what will soothe and comfort him..sometimes it's just holding him tightly and hugging him..other times he's so self abusive we have to give him meds....but he is getting better...very slowly, .....
CDFoakley 2 years ago 2
@CDFoakley
how old is he.
his autism looks very severe.
ps. is he wearing a diaper?
hunter7754 1 year ago
watching this is so scary. i know i have atypicalautism but, i dunno. if i knew i had to live my life like this id kill myself because autism affects people in so many ways. and its a dissability that not many people understand. And the fact that it cant be treated is unbearable. i cant even bring myself to watch anymore of this video.
themickeymouseband 2 years ago
Actually, yes it can be treated and we've made A LOT of progress...I show these videos also because it documents some of the most severe sides of autism yet, I know, believe and trust that my son is and will get better and there will be more and more positive videos to show....healing takes time in some cases, sometimes years before you see major progress...we just keep trying. never give up. never lose hope.
CDFoakley 2 years ago
why in the hell would someone record this. he looks like hes in so much pain
DirectorKJK 2 years ago
Because I'm tired of this willful apathy, ignorance and cowardice of others who can't handle reality of certain sides of autism...we are not hiding in the walls of our home anymore. We aren't going to be ashamed of what we or others go through. If you don't like, don't watch. Go watch Brittany Spears or Paris Hilton. Read the National Enquirer. Forget all about other people's pain and how you may bring awareness or hope to a tough situation....thanks for support
CDFoakley 2 years ago 14
@CDFoakley The Fowlers from Texas are 100% behind you. Thank you for posting these videos. There's a story going on that people are afraid to hear.
coach77060 1 year ago
@CDFoakley Well Said!!
My heart goes out to you and your family.
Poor Jamie. :-( xoxoxoxox
Gatecrasher12 1 year ago
@DirectorKJK As graphic as the video is.. Its LIFE.. i have them and i wouldnt know what i go through during them without seeing video's.. so im thankful for the video's they help myself and the people who are around me during my seizures.
lovlybrwneyedlyn 1 year ago
omg throughout the whole vid i just wanted to hug him and go, everythings ok kid :(
kaylinsvlog 2 years ago
how old is james
bunnyz324 2 years ago
@bunnyz324 i think his mom says in one of the vids that he is 20 and that hes had severe autism/ self injurious behavior since he was 2.
kaylinsvlog 2 years ago
Just wondering, how much sleep do you get at night usually?
smsorour 2 years ago
you are such a brave woman. i work in a school for autistic children and always panic when they have seizures. its so hard not to. especially when they are head banging. my thoughts are with you.
leelouballoo 2 years ago 5
They cut your hrs, thats fucked up!! Arrrggg,, what are the state trying to do.. same here in our country.. its like they want people to go away and give up.. which some do,, I know you wont; that anger keeps you strong,, oh honey.. Has James got worse with age.. Im so watching your life here,, I wish I was your neighbour,, why do we live on the opposite side of the Atlantic...
sammbah 2 years ago
Thank you for posting this! Your son is cute. I have seizures too. What a drag. I sure hope things improve for all of you. Best wishes.
allijxn 2 years ago
omg, he got a lot worst.... i wish theres something i can do
iamacoolkorean 2 years ago
What many people don't understand is just how much parents suffer too, perhaps even more, when their children are having difficulties. Anyone that would deny this family services is an evil bastard. Many autistic people suffer from these types of seizures and I believe this family is trying their best to bring this to light. Many parents would not have the internal strength to endure this and would simply wish their and their child's life away. I applaud you guys and hope an answer comes.
christschool 2 years ago 14