High praise for Dr. Claire Henchcliffe for their patient in Parkinson’s. I do want inform her that this might be the first time in the USA, but she should reach out to stem cell clinics in Ukraine. I know one that has been treating Parkinson’s for years in patients with stem cells, and they do R&D and clinical trials for years before applying it to their patients. Also, instead of drilling into their head they have been doing intrathecal injections.
This was also the first thought that crossed my mind. Unless the cause has been determined and eliminated, wouldn’t the newly transplanted cells/neurons eventually die off as well?
Slowed up by the rigid clinacal trials rules. Yet many Drs says the trials rules need to change for Parkinsons research. Many trials don't get off the ground because of the trials rules are too rigid.
I am 7 plus years into my battle with Parkinson’s. 25 sinimet per day. Brutal. My dbs surgery was cancelled a few months ago because I was in pre op for 16hrs.
using cells to treat instead of medications -- as said in video -- is future for all medicine -- to fix a broken part a cell u must use a part a cell not use chemicals medications to try to drive a living part a cell in a direction leadin to side effects ... using cells to treat instead of medications is future for all medicine using cells to treat instead of medications -- as said in video -- is future for all medicine
Any idea yet whether or not a person who has had focused ultrasound for tremors can be treated with this stem cell procedure? How about a person who has had DBS?
My mom has DBS, and we were told it is very easy to remove if there are new treatments in the future. I have no idea how that would work with a stem cell procedure.
I watched a different podcast where they are doing a similar clinical trial and they said the target site is different to DBS and the DBS won't need removing for the stem cell treatment.
It is being aimed at people at 10 years since diagnosis. 50 to 70 years old. Mu diagnoses was slowed by covid by at least 2 years. I would act out my dreams sometimes but since having my sleep apnea treated with a CPAP machine I dont act out my dreams anymore and I wonder if the sleep apnea contributed to my parkinsons because I believe went undiagnosed for over a decade.
@@tootalljones77 I understand now. Untreated sleep apnea increases the risk of Parkinson's that is what made me wonder. I would have been treated earlier for the sleep apnea if I was sent 5 years or more earlier to a sleep clinic for a full sleep study instead to my local hospital where I wore a devise with wire that went up my nose and down my throat. The wire had sensors on it. A very crude way to diagnose sleep apnea and they said I didn't have sleep apnea when I did. It was until I had a sleep study that I was diagnosed severe sleep apnea. I do think it played a role in me developing Parkinson's with the lack of oxygen. I started falling asleep on my pc in the morning about 10 years before my diagnoses. I have lost 3 stone in weight and my sleep apnea has improved to wear I hardly snore anymore. Still use the CPAP machine every night though.
Stem cells these days are generally from the afterbirth (placenta, umbilical cord), which is usually discarded after the baby is born as medical waste.
God bless you and your team Doctor. Keep up the great work! ❤
Who do we contact in order to be considered for this treatment?
All Great ,moving forward .
Where do I sign up for testing
S.Biomedics in Korea is doing the similar approach for PD cure with ESCs. Their phase 1 trial results will be reported in late May or June.
High praise for Dr. Claire Henchcliffe for their patient in Parkinson’s. I do want inform her that this might be the first time in the USA, but she should reach out to stem cell clinics in Ukraine. I know one that has been treating Parkinson’s for years in patients with stem cells, and they do R&D and clinical trials for years before applying it to their patients. Also, instead of drilling into their head they have been doing intrathecal injections.
Could you tell me what the name of this blessed clinic is? I'm willing to leave Brazil to try.
@@Dc-jz9rfI recall responding to you. Did you get the information. I am going there this summer.
What about people with TBI associated dopaminergic demage ? What about people with RLS?
So has someone found difinitively what causes it? Everything i read says resolving health issues is always dependent on finding the cause first!
TCE, pesticides, chemicals, ...
This was also the first thought that crossed my mind. Unless the cause has been determined and eliminated, wouldn’t the newly transplanted cells/neurons eventually die off as well?
Slowed up by the rigid clinacal trials rules. Yet many Drs says the trials rules need to change for Parkinsons research. Many trials don't get off the ground because of the trials rules are too rigid.
It's all a load of crap.
Our government is totally controlled by big pharma and their lobbyist. Too much $$$ at stake
I am 7 plus years into my battle with Parkinson’s. 25 sinimet per day. Brutal. My dbs surgery was cancelled a few months ago because I was in pre op for 16hrs.
using cells to treat instead of medications -- as said in video -- is future for all medicine -- to fix a broken part a cell u must use a part a cell not use chemicals medications to try to drive a living part a cell in a direction leadin to side effects ... using cells to treat instead of medications is future for all medicine using cells to treat instead of medications -- as said in video -- is future for all medicine
Where can I find the symptoms. I think I have most of them
Can this work for other neurological damage?
Who ever the person is who got the transplant is like winning the lottery. Even though it is not a cure but will treat the movement symptoms.
Any idea yet whether or not a person who has had focused ultrasound for tremors can be treated with this stem cell procedure? How about a person who has had DBS?
My mom has DBS, and we were told it is very easy to remove if there are new treatments in the future. I have no idea how that would work with a stem cell procedure.
Thanks@@greyeyed123
I watched a different podcast where they are doing a similar clinical trial and they said the target site is different to DBS and the DBS won't need removing for the stem cell treatment.
what kind of surgrty plesae
do you take the immu therapy life long ... seems to have little change in symptoms?
It is being aimed at people at 10 years since diagnosis. 50 to 70 years old. Mu diagnoses was slowed by covid by at least 2 years. I would act out my dreams sometimes but since having my sleep apnea treated with a CPAP machine I dont act out my dreams anymore and I wonder if the sleep apnea contributed to my parkinsons because I believe went undiagnosed for over a decade.
What about the delivery focused ultra sound could be the way forward here with out the brain surgery check it out
I never used mycap. And I'm 100% convinced that because I chose not to use it, this contributed to the progression of the disease
@tootalljones267 Why would a CPAP machine that keeps you breathing at night make Parkinson’s progress quicker?
@@michaeloconnor9465
My decision NOT to use the cpap, deprivation and the lack of oxygen Sorry
@@tootalljones77 I understand now. Untreated sleep apnea increases the risk of Parkinson's that is what made me wonder. I would have been treated earlier for the sleep apnea if I was sent 5 years or more earlier to a sleep clinic for a full sleep study instead to my local hospital where I wore a devise with wire that went up my nose and down my throat. The wire had sensors on it. A very crude way to diagnose sleep apnea and they said I didn't have sleep apnea when I did. It was until I had a sleep study that I was diagnosed severe sleep apnea. I do think it played a role in me developing Parkinson's with the lack of oxygen. I started falling asleep on my pc in the morning about 10 years before my diagnoses. I have lost 3 stone in weight and my sleep apnea has improved to wear I hardly snore anymore. Still use the CPAP machine every night though.
If magnesium supplements can get past the brain barrier, then why not drugs ❤
They don't want it too
I believe there is a cure, we just have to find it...;)
Are these originally from adults or aborted babies?
No entiendo igles
I don’t have any desire to live off of others’ deaths so, if these are embryonic stem cells, no thanks.
Stem cells these days are generally from the afterbirth (placenta, umbilical cord), which is usually discarded after the baby is born as medical waste.