I am very excited of these breaking therapy. I am also a care giver for my partner her development of Parkinson's is increasing daily. Help can only come asap. Thank you all for your work! The future population can now have some hope.
13 to 15 year development? We can create covid vaccine in one year and approve in a month but millions of people have wait over a decade for such treatment? It shows how little medicine has changed past 50 years
I would prefer to have slower development of any type of intervention that attempts to change rna . Otherwise we may have results like the ones we had with the COVID "vaccines". Vaccine is supposed to PREVENT a virus, not just make it milder. I'm not even convinced that it did that actually. When we have the hubris to think we can change outcomes of our messing around with nature, we make things worse ... and then refuse to admit or accept that we did so.
bless the animals that w/o volunteering, give out their lives to advance research aimed to humans. we do little to honor them. wish the best for this project.
I really hope everything turns out a success!🙏🏼 This was a miraculous discovery! Good job team!👍🏼👍🏼 In all that was discussed. I was wondering. Is anyone working on. Or discovered yet. How to recreate beta cells in Type 1 Diabetics? This discussion makes me think this can be done!🤔
This is amazing and then some, and I should be excited. Instead I'm heartbroken because of the time perspective. Parkinson's is destroying my 79-year-old dad NOW, and it's been progressing horrifyingly fast. He'll be moving to a nursing home soon. So instead of rejoicing, I find myself wishing that the scientists would throw most of their caution to the wind and start human trials immediately, risk of side effects be damned. I wish they would leave the question of how lasting the effect would be for later. I don't care whether the new neurons would be susceptible to the same degeneration as the old ones; just make new ones and deal with that problem later if it comes. PLEASE! ... You know? That "We need to know" list drove me crazy. I'm sorry. I know I'm being an a**hole about this. I'm just so desperate and afraid, about to burst with grief. I can think about nothing else, only my dad's suffering. The powerlessness - his and mine and my sisters' - is unbearable. The emotional pain is constant and devastating. We need help now.
Great discussion and news. PTB is a gatekeeper for regeneration and can be managed. Let’s hope so.Thank🍁you for your perseverance in pursuit of a cure for PD. And, Thank🍁you Sergy Brin.
So heartbreaking to realize that by the time this gets approval...if ever ( I don't trust the drug companies to get behind it and actually market it and they control way too much) my husband who was diagnosed with PD 7 years ago and is already 5th stage of PDD, will probably be gone but not before his care has bankrupted us.
My mother had PSP a Parkinsonian type of disease she died last December, unfortunately after she. Had called covid recovered.. bug one day felt not good with vomiting.. after going to hospital the hospital killed her
I got damaged by psychiatry in late 2006 as a comedy of errors. 30 grams of Lithium and Risperdal M-Tab cause Drug Induced Parkinson's. I got a social worker to pass me a note about the medication I was put on.
I believe my dad was also affected by drug induced parkinsons after being put on sodium valproate. Were you able to reverse the drug-induced parkinsons?
@@wendyolorga No not yet. Daily fatigue and mental slowness. High dose Thiamine is superficially helpful. There is a video about thiamine for Parkinson's. Anti-Crazy medications follow about the same time line as synthetic opioids. Over 100 billion synthetic opioids were distributed in the U.S., and promised to be safe and non-addictive with some feckless humor. I'm trying "Lairds Performance Mushrooms" now as well.
Hi. Please, let us pray together. Dear God who art in heaven hallow be thy name thy kingdom come thy will be done on earth as it is in heaven, give us this day our daily bread and forgive us our trespasses as we forgive those who trespass against us and lead us not into temptation but deliver us from evil for thine is the kingdom and the power and the glory forever in Jesus Christ's name we pray amen.
Think I would like to participate in testing something for this neuropathic mess I'm encountering..t9t10 spinal mess from defective hf10 Nevro device. Or surgery moving it. Sting is unreal yet I'm trying to beat it..walk..and be normal..was paralyzed right leg n side..its a living hell each day..
i hsve receny been diagnoist with parktnsons im 65 april 1 1958 is my birthday onhorably discharged cbs was my mos with 3 children and devored heard through y6outube that there might be a drug trial on turni ng gleial cells into neurons and want to get into a drug trial for This and looking to get a sugestion on this
Hello sir,,,my mother is suffering from Parkinson,,,her condition deteriorating day by day,,,,she is now 56,,,,i don't know what to do,,,,,i need your help sir,,,pls suggest me🙏🙏🙏🙏🙏🙏
I got parkinson now ill be 65 april.1 my syptons are getting harder to deal with quickly i have 3 children and devorced question what do you know about turning glieal cells of the brain into neurons human trials i was into cbs in my 4yr honorably dis charged duty at a young age 17 yrs Are glial cells. To nerons more common and easier to convert into nerons because of recent discovery
A 72 veteran was diagnosed with PD. He had blacked out many times over the past 5 years. He had the tremors and slow muscle movement. He is taking the 2 prescribed medications. But then he started taking alpha gpc and lipasomal vitamin C daily. After a week or so he is moving like he did when he was 40!! I l know this could just be a miracle but I think these supplements made the biggest difference. His mind is on point. Razor sharp focus and recall. He is a preacher. He had to stop preaching because he had the bad tremors and couldn't recite the scripture he had inside his mind. But now he's back in the pulpit running around like a young preacher. It's been 3 months and he's still saying the PD is over! I'm thinking the alpha gpc fixed a choline deficiency..who knows??
Still very surprises how all my symptoms of Parkinson’s disease just went aware after undergoing *MADIDAHERBALCENTER* treatment, but I am very much happy because I don’t longer have them anymore for like 9 months now.
Please let us know address of this center and share us more details of treatment you received during your stay starting to end so others can benefit from your experience.
This was 2021 - now, a year later, when could we think of human trials and how would one apply to be a part of any human trials UC is planning? How can one contact the people involved with this really fantastic and amazing discovery? You ask what can now be done and that IS the question and how can a person with early Parkinson's be a part of it?
A year ago I was diagnosed with dementia, now it's been updated to possibly Parkinson. I knew ten years ago something was wrong, as my fine motor, fingers was getting hard to manipulate small things. Today I have multiple symptoms that in my mind say's I have it.
I’m 32 and at 21, I was diagnosed with a VERY, VERY, VERY rare genetic condition called Friedrich’s Ataxia. Unfortunately it’s progressive. Essentially my body can’t produce frataxin anymore which causes many symptoms like neuropathy, lack of muscle coordination, etc. and increases the risk of heart disease and diabetes. As far as I know, there is not a lot of knowledge on what frataxin’s actually roll is but it’s involved in iron-sulfur clusters in mitochondria, what ever that means lol. Now fortunately for me my condition is progressing a lot slower then others who have this condition but this does not mitigate my future outcome. It has taken running, hockey, motorcycles, skiing/snowboarding and many others. Even other activities/hobbies that Ive never done and would love to try. On top of that it’s made it extremely difficult to go out and even enjoy simpler things like traveling, concerts etc. let’s just say everything that involves both your legs and balance simultaneously. I still walk (w/ a walking stick mostly), I still drive (even a stick), I still work and I still play guitar. Walking seems to be the only activity, right now, that I feel I’m holding on to by a thread, I feel it’s really only my lack of balance. Is really my biggest issue at this point. Guitar is really the only hobby and talent that I have left. If I loose that then there is not really anything for me to live for anymore since I’m single and don’t have children. I’m trying to hold on to that best I can. Holy crap I’m sorry this comment turned into a book. It was intended to be only a paragraph lol. If you read this entire rant thank you and ✋ to you! That being said, the only thing I wanted to say is this video seems very exciting and in my opinion and shows more promise than the CRISPR case9 stuff. Now CRISPR, from a medical context, looks great for near future applications but at the same time it makes me real nervous. I feel like it’s like watching a child run through a field of tall dry grass and tinder with a torch. Not sure if this is the best analogy lol. It’s the only one I can think of at the moment haha! In short I’m about 30/70 for it right now.
@@tomhennessy7276 Are you a neurologist? Have you heard about Omaveloxolone?Supposably it is FDA approved now for a treatment for FA but I’m not sure. It apparently had very positive results during the clinical trials with minimal side effects. I may be interested in trying but I want more info before I try it out.
@@tomhennessy7276 Thank you for the info. I read the vitamin E in mice study. I will try supplementing with vitamin E and see if it helps. Have you heard anything about diet helping?
@@tomhennessy7276 I’m a big believer in getting vitamins with food. I would eat more foods w/ vitamin E and supplement a little with for a bit and see if I felt a slight change. I definitely wont be stupid and go crazy with it.
I have a friend in Colombia who was just diagnosed - he studied here in the US in college with me years ago and we were good friends and recently began communicating - how can we contact you so he can participate in the study ? I am about 7:45 min Now , I will continue to watch
Amazing breakthrough. My Dad is 67 years old 10+ years suffering from this disease. The thing is Tidomet 25/250mg becoming so ineffective for him and I dont know what to do because other meds so expensive here in Phils.
What is his gut health like? Healthy gut means healthy brain, I would start there. Get him on good probiotics, magnesium, Q10, eliminate gluten and dairy, and see if there’s improvement
@@kathypr1051 These past few days it's getting harder, it's hard for him to eat and he doesn't like taking tidomet and rivotril anymore. He's having hallucination or saying something out of nowhere or nonsense, He can't get up from bed alone, He can't stand even within using his 4 legs Cane, His Dr. can't check him up because my Dad got this cough 4 weeks ago. I understand that the Dr. won't check him up due to covid. but I knew my dad don't have it and he got his vaccine as well. We don't know who to go from.
I think it's surprising that not much has changed regarding Parkinsons medication over the last 20 years. Once you get used to taking them they become less effective. I am watching my friend disappear as the months go by. Its frustrating that there dosent seem to be much progress.
If you follow the conventional treatment, don’t expect any positive results other than going downhill. I refuse to believe in the medical establishment , you are better off if you are seeking a cure from people with success stories.
