Interesting feed, I'm hooked, thanks to the author
@isaiahelliott8191 Жыл бұрын
seen vid for school
@janemike34902 жыл бұрын
#drojeabacha
@janemike34902 жыл бұрын
Permanent cure to IBS with Dr Oje Abacha in less than 2 weeks no side effect.
@stingsting11322 жыл бұрын
Am permanently cured with Dr iyaremoses herbal medicine on KZfaq #driyaremoses channel.
@charlottestallion75132 жыл бұрын
I know exactly what you going through, My mom was able to beat Huntington’s disease completely with the help of Dr Isibor a great herbalist with his Alternative Herbal supplement
@gunterliam74112 жыл бұрын
all thanks to doctor stanley for curing my from huntington disease i am forever grateful sir..
@gunterliam74112 жыл бұрын
all thanks to doctor stanley for curing my from huntington disease i am forever grateful sir
@wesleywilliams31502 жыл бұрын
My Huntington’s Disease story begins like most people in the HD community. With a family history. about a year ago I was diagnosed with having the defective Huntington’s gene. Yes, it is hard - and some days are much harder than others - but there are many positive noises coming from the Huntington’s experts about new research and treatments and that fills me with real hope. Have a look into gene silencing, it’s like something out of a science fiction movie, but it could be ground breaking! It was obviously gutting to have my fears confirmed but I at least know what I am up against and I know that it’s unlikely I’ll experience symptoms earlier due to having a similar CAG count. (A CAG count. Huntington's Disease is a devastatingly aggressing disease, I have known that neurological disorders were aggressive. As I learnt more about Huntington’s I wanted to do something positive in what was a negative situation. I know it’s hard at times but you should try not to focus on the negatives. Try to turn them into positives. I was hopeful that a cure will be found as science is really doing all they can. We took part in a research project which involves a two day trip to Florida to the Huntington’s Disease Centre, We were opportunity to meet with Dr Odia, A highly recommend herbalism with scientific medicine. There are lot to say about Dr Odia, I really want to thank God that this man was used to end my sorrow, All my pains and tears turn to joy from the day I came in contact with Dr Odia, We were educated more about the use of herbs and few purchase the herbs which I used for two month and three week's. To my greatness surprise it did work out for me. There is no need for anyone to have a date stamped on their forehead when they’re diagnosed with Huntington’s Disease. I would encourage anyone to seek a second opinion especially if they’ve been told there’s no hope. It’s also crucial to learn as much as you can about your diagnosis. Seek options. Find out about what’s out there that could help. Contact Dr Odia via( Dr Odia Herbalist Home on Facebook) or email: [email protected]).
@wesleywilliams31502 жыл бұрын
My Huntington’s Disease story begins like most people in the HD community. With a family history. about a year ago I was diagnosed with having the defective Huntington’s gene. Yes, it is hard - and some days are much harder than others - but there are many positive noises coming from the Huntington’s experts about new research and treatments and that fills me with real hope. Have a look into gene silencing, it’s like something out of a science fiction movie, but it could be ground breaking! It was obviously gutting to have my fears confirmed but I at least know what I am up against and I know that it’s unlikely I’ll experience symptoms earlier due to having a similar CAG count. (A CAG count. Huntington's Disease is a devastatingly aggressing disease, I have known that neurological disorders were aggressive. As I learnt more about Huntington’s I wanted to do something positive in what was a negative situation. I know it’s hard at times but you should try not to focus on the negatives. Try to turn them into positives. I was hopeful that a cure will be found as science is really doing all they can. We took part in a research project which involves a two day trip to Florida to the Huntington’s Disease Centre, We were opportunity to meet with Dr Odia, A highly recommend herbalism with scientific medicine. There are lot to say about Dr Odia, I really want to thank God that this man was used to end my sorrow, All my pains and tears turn to joy from the day I came in contact with Dr Odia, We were educated more about the use of herbs and few purchase the herbs which I used for two month and three week's. To my greatness surprise it did work out for me. There is no need for anyone to have a date stamped on their forehead when they’re diagnosed with Huntington’s Disease. I would encourage anyone to seek a second opinion especially if they’ve been told there’s no hope. It’s also crucial to learn as much as you can about your diagnosis. Seek options. Find out about what’s out there that could help. Contact Dr Odia via( Dr Odia Herbalist Home on Facebook) or email: [email protected]).
@channelsharon56213 жыл бұрын
I wan to use this medium to say a very big thank to dr Ehimare on youtube who was able to cure and reverse my mother in_law from this Huntingtons disease and God will bless you continiously sir🙏. You can also contact dr Ehimare on his youtube channel or what +2349027349748....
@tommylatonia25503 жыл бұрын
Read carefully, it's said that Huntington disease has no cure, yes with the western medication but not with herbal medicine, my daughter's situation made me to realize that with doctor Bharat herbal medicine it can be cured. In 2014 she experienced difficulty in concentrating, memory lapses and depression, at first I taught it was stressed from her place of work until I took her to hospital and the doctor made me to understand that it's juvenile Huntington disease because she is still in her late 20s, which she inherited from my late husband that died of the same disease, the doctor told me it has no cure, but gave her some medicine which I noticed that it has side effects, my daughter situation got worst each day that passes, she was the best at her place of work, now a shadow of her self because of this deadly disease, she speaks to herself often, she was really going insane, I do not want to lose my daughter the same way I lost her father, in 2018 I carried out research on internet and bumped into a comment of a lady that got cured of Huntington disease, without wasting time I contacted doctor Bharat whose name was mentioned in the comment, now is been 3 years my daughter is living her best life again, for those that have the disease or have any love one suffering from Huntington disease, contact doctor Bharat via [email protected].
@esthergabi41303 жыл бұрын
My name is Esther from Los Angeles USA, i want to share my testimony because I know it will help some people out there. My husband Charles was diagnosed with Huntington's disease in 2017, I watch my husband living like a mad person sometimes i shed tears. After several failed attempts to make him well again, I searched on the internet for a cure but there was none, in 2019 I bump into a comment on youtube on how Dr. Bharat cured a woman who also suffered from Huntington's for 6 years with his herbal medicine. Without wasting time I contacted him and he asked me a few questions which I answered then he prepared the medication and sent them to me here in LA with a prescription on how to use attached to it. I administered it to my husband as prescribed, within 2 months i start seeing improvements in his health and he was totally healed in 6 months, now my husband is living his best life again. You can contact Dr. Bharat via [email protected] you will come back to testify...
@valen24584 жыл бұрын
This is low key a fir vid droppin a sub
@cloudrain31864 жыл бұрын
The first cure of Huntington`s disease was in 1973. It took 22 months. The proceeding is documented in the book “Orthomolecular Medicine For Everyone”, written by Abram Hoffer, MD, PhD, and Andrew W. Saul, PhD. Abram Hoffer was asked, if a treatment with a meagavitamin therapy might slow the rate of deterioration. He and his patient understood that there had to be no expectations of recovery on anyone´s part. Relating to the start of the treatment the Patient remained well at its end.
@enyax3816 жыл бұрын
My mum and papa have it
@user-hn9nm1it3z2 жыл бұрын
كيف حالك الان
@Spaurtacus6 жыл бұрын
Change the video to 1.25x speed so you don't fall asleep.
@nai506nai67 жыл бұрын
I also will find the cure. Looking outside the box, the sea of infomation is daunting so lets see the hitchhiker on the 4th chrome take leave. What attracts the hitchhiker to the 4th? not the other 22, is the cure lying there... new ideas keep it flowing. My thoughts always go back to the hitchhiker, what is the hitchhiker dna?
@VoidHalo7 жыл бұрын
Is the chorea in HD caused by a restless sensation? That is to say, is it sort of voluntary in that the restless sensation builds up to the point where the person needs to move in order to relieve it? Or is it a completely involuntary thing like some sort of convulsion or I suppose severe spasm? I've also wondered the same with Parkinson's disease, if the excessive movements are the result of restless sensations and moving in such a way relieves it. The reason I ask is because I suffer from akathisia almost constantly, and I often wondered if such motion disorders had to do with akathisia at all. Which seems to relate to a deficiency in dopamine, so Parkinson's comes to mind. Mind you I would expect symptoms of such disease to be far worse than what I experience. Which frankly, is absolutely terrifying.
@VoidHalo7 жыл бұрын
Well after doing some reading on HD it seems it's entirely involuntary. But I would still be curious to know if Parkinson's is also entirely involuntary or more like a severe form of akathisia. Cuz to be honest, when I look at the motions people with Parkinson's make, they're eerily similar to some of the motions myself, or other sufferers of akathisia I've seen. I'm not saying I have Parkinson's or anything. I'm just wondering if it's similar, but more severe. edit: I also found out that HD is actually characterized by an excess of dopamine, rather than a deficiency of it. So I found that really interesting. It also causes a decrease in GABA. All of which leads to excitotoxicity.
@luciemcgovern61527 жыл бұрын
I'm twelve and my gramps has it and my mum doesn't know if she has it so I'm at a 25% risk
@obbytrycesiamusowa73557 жыл бұрын
the explanation is clearly illustrated.. thank u mam
@midnightcasanova73107 жыл бұрын
First it steals my dad away from me and then it will take me as well
@midnightcasanova73107 жыл бұрын
Great
@toomii9977 жыл бұрын
Very helpful, thanks a lot!
@DoDo-bw1dj7 жыл бұрын
My sister in law's dad has HD,but I don't think any of them want to get screened for it.I just wish there was something regular Joes like myself could DO about it.Like maybe be assistants in a lab or something.I would volunteer in a heartbeat if there was an opportunity.I pray all the time that there will SOON be a cure for this horrible disease.
@arisvera7717 жыл бұрын
my uncle has it
@Chiara244477 жыл бұрын
My mum has this 😔
@musimax18787 жыл бұрын
Chiararose Hale I wish her the best of luck
@Chiara244477 жыл бұрын
Max Muscrøft thanks she's had a brain scan and stuff so 💓
@musimax18787 жыл бұрын
Chiararose Hale how'd it go?
@dublindave78257 жыл бұрын
God's gay. Jk I don't care if he's straight or gay If he exists, I hate him either way.
@yousra68147 жыл бұрын
Whos here cuz of that dead in bed book?
@jakepierson62087 жыл бұрын
crispir may stop it
@lindamann26237 жыл бұрын
Please help Huntington's Disease survivor. Read and share. www.gofundme.com/SarasHDfund
@roxcyn8 жыл бұрын
Is this related to Alzheimer's/dementia? Many of the symptoms are the same.
@mouazchikhani78038 жыл бұрын
the music does not fit the topic at all
@mouazchikhani78038 жыл бұрын
13
@amymorris23108 жыл бұрын
My mom has this, she's 54 and lives in a mental health care home, me and my brother will have a 50/50 chance of getting it unfortuantly.I'm only 14 and I'm in care due to my mom and my dad fighting when I was younger because of the kickstart of her illness.
@darcysanders66298 жыл бұрын
SOOOOOOOOOOOOOOOOOOOO BORING. Can't understand it because I feel like falling asleep watching this.
@michalismichael82438 жыл бұрын
omg i might have the disease :( after some years i have noticed that i have problems with conversations and i cant make up sentences properly or understand and remember what other people say
@LateTrender7 жыл бұрын
Maybe you just haven't been learning in school lately
@michalismichael82437 жыл бұрын
Late Trender im fucking 16 years old man, and it progresses year after year
@michalismichael82437 жыл бұрын
Late Trender plus english is not my native language
@LateTrender7 жыл бұрын
Damn... is it official though? That you have it? Or you just think you have it?
@michalismichael82437 жыл бұрын
Late Trender i think i have it or something similar and god help me that i dont have it
@Shlepy20188 жыл бұрын
My dad has huntingtons so this video helps alot.
@Shlepy20188 жыл бұрын
My dad has huntingtons so this video helps alot.
@Tata-iu3fy8 жыл бұрын
does it make people lie all the time?
@loveamericanslife60038 жыл бұрын
i Yong and am doing this but i have never gotten my blood drawn how bad is it im scared.pleas help
@daniellehowser8 жыл бұрын
my dad has HD :(
@Zeaton6668 жыл бұрын
For M2K! RIP friend of M2K. I send my condolences!