A Stem Cell-Based Therapy for Retinitis Pigmentosa
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- Опубликовано: 15 фев 2015
- (Visit: www.uctv.tv/) Retinitis pigmentosa (RP) is a genetic disease that gradually destroys the light sensing nerve cells, called photoreceptors, located in the retina at the back of the eye. UC Irvine professor Henry Klassen describes a CIRM-funded project that aims to begin a stem cell-based clinical trial for RP in early 2015. Rosalinda and German Barrero also speak about the devastating impact of RP on their lives and their excitement about the trial. Series: "California Institute for Regenerative Medicine" [Health and Medicine] [Science] [Show ID: 29233]
Five years have passed, where did this research arrive? Please save us from blindness
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
I have RP, and have since birth - a gift from my late father. :) I'm tremendously excited about this prospect.
I do too, however I've been told mine is a different type. I've also had it since birth... I would do anything to see like a normal person
JPzEyes BUY THIS ON AMAZON Insight compound and occudyne 2
Did you have stem cell therapy .
@@moubak Not available where I live, and I can't afford to fly overseas and pay for it out of pocket. So, no.
@@JPCorwyn where do you live ?
Can’t wait! Almost there!!
Dr your presentation was very informative. I'm sorry that u had such disrespectful audience. I believe the people who was there "listening" was really unconsidered when making that much noise using their utensils. Guys just take a break, eat your lunch, and then pay attention. I can see in the Dr face how annoyed is he with the noise. I think these are " educated" individuals...the ones seated in that room...come on...really? Thanks for recording this...i hope you schedule better the lunch time for future presentations.
My name is Ruby Bautista from Philippines. My daugther Christina is a case Rp and arachnoid cyst. Right now her eye sight is slowly deteriorating want to bring her to some medical institution but with the life condition we have...its really impossible for us to bring her into such institution..Any help you can extend her is highly appreciated. To God always be Glory.
Ct Bautista BUY THIS ON AMAZON Insight compound and occudyne 2
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
Who wants to come in group for regular updation regarding this horrible problem ..
I want to join
Hey there.. I want to join group
Insta @rizwan_rits
Hello I want to join group
I want to join i am 60 year old and suffering Rp since child hood.
Plz add me on mahkamsum@outlook. Com
Hi, my name is James. I’m a 17 year old boy with RP caused by Bardet-Biedl Syndrome. I have night blindness, and my acuity is 20-50 in my right eye, and 20-70 in my left eye. I will be graduating high school in May of 2019. It’s been several years since this video has been published. I want to know what advances have been made with these ‘proretinalgenerative’ stem cells.
James Geiger BUY THIS ON AMAZON Insight compound and occudyne 2
I am suffering with night blindness is well
@@sandeepdhir3906 brother
@@robertappiahwellness how this work?
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
Dear Sir I am RP patient, I am 22 years old,, I am currently seeing 6/9 with glasses,, Sir is there any treatment to cure RP disease? Or is there any treatment to get night vision and peripheral vision back?
Hello I have RP from last birth can I have the contact info to discuss my stuation .tq
I also want to know .. from where are you
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
I have retinitis pigmentosa and I would like information on the clinical trials also. I would also like to know if there are any risk involved in having to try it. This will be life-changing.
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
@@danielfckSir where are you doing treatment and what is the cost
@@user-pg9oq9id5w my cost was about USD2000
Hello
This is Phanindra Kopparthi.
I am suffering from RP,there is any reliable treatment is available now
Try ayurvedic eye treatment at sreedhareeyam eye Kerala. I'm also planning to go to Kerala iam 8522811803
@@syedjaveed2288 hv u tried dt
Phanindra Kopparthi Your PK world BUY THIS ON AMAZON Insight compound and occudyne 2
What are the methods
i have rp am 74 yrs old live alone life keeps getting rougher a little more every day along withe the chronic pain from spine and ra.dont have a lot of money 1,273.00 a month income any help seems out of reach
Diar sir my son is both eye retina pigmentosa stemcells treatment (child hood) aveylable please replay
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
I have 2 sisters with retinitis pigmentosa...who can help me
BUY THIS ON AMAZON Insight compound and occudyne 2
@@robertappiahwellness what is it
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
May i know the current status of this stem cell project
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
Can you send me contact and clinical trial info. We have a family friend with Retinitis Pigmentosa. Id like to steer him in the right direction. Thank You.
+lucabrazi36 - The clinical trial information is given on JCyte's website (see this link to the relevant trial on clinicaltrials.gov):
www.clinicaltrials.gov/ct2/show/NCT02320812?term=jCell&rank=1
I would love to be involved in this trial as myself and my two sisters have RP and this research sounds really promising, however we live in the UK so sadly this is not feasible
@@nanamaplazmaboom hii my mom has this problem .., plssssss can u give me your WhatsApp contact number or email id , I am from India , and it is difficult to understand me this whole report please could u help us , my Mumma please sirr , , u can message me on kalia.radhika1989@gmail.com thq
@@dipikasharma4613 I'm searching very seriously about this kind of problem, got good result at sreedhareeyam eye care at Kerala, and 2nd one is prakash netralaya Jaipur, share ur opinions with me, iam 8522811803
lucabrazi36 BUY THIS ON AMAZON Insight compound and occudyne 2
How much is the treatment?
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
My son 22 years is suffering from Retinitis pigmentosa due to gene prom 1 .kindly help
I was diagnosed with RP back in 2018 and ever since then i have been looking for solutions to recover from my impending blindness.
early of this year, i finally found 2 methods of which both i have tried and it helps my eyes to recover from a light perception to counting fingers vision.
i hope to continue to work on both methods to slowly and steadily recover my eyesights again😊
BUY THIS ON AMAZON Insight compound and occudyne 2
Hello hope you respond do you have retinitis if so did u ever take the medication you recommend and if so did it ever help with night blindness
I am sending this comment from India I am suffering from retinitis pigmentosa problem of I it can be cured in future please help
Me too
Insta @rizwan_rits
I am present of rp
damaged optic nerve any treament in age of 23 years?
Hello friends
Ateeq Sherazi BUY THIS ON AMAZON Insight compound and occudyne 2
Damn everyone was starving I guess. All you hear are forks. Smh.
hersheythebody *Wooden forks!*
J
So this was 4+ years ago. I guess it didn’t work? 👎🏽
From what I've heard it has worked for people. It isn't a cure but it's at least a huge step in the right direction.