If you had 10 million dollars to spend on... - Cure Parkinson's

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If you had 10 million dollars to spend on your Parkinson's treatment...

Alock2020 profile image
21 Replies

If you had $ 10 million to spend on your Parkinson's treatment, what specifically would you spend it on?

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Alock2020 profile image
Alock2020
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21 Replies
LagLag37 profile image
LagLag37

I just met with a friend yesterday that had DBS on Valentine’s Day and she said it was the best thing ever. It changed her life. She works out at Rock Steady Boxing headquarters and she asked at least 10 other PwP’s that has DBS the same question and everyone but one said the same thing…..It changed their lives. 🥊

I think insurance takes care of it so I don’t believe you would have to pay the $10,000,000 on it but it sounds like a winner.

theAfrican profile image
theAfrican

there is no cure . Send some money for research

Bennorca profile image
Bennorca in reply totheAfrican

Many people have been cured

Check out pdrecovery org

Rupa88 profile image
Rupa88 in reply toBennorca

I wish it was true

Fake news

LearningAllICan profile image
LearningAllICan in reply toBennorca

have you tried the protocol on pdrecovery.org?

LagLag37 profile image
LagLag37 in reply toLearningAllICan

I just listened to the video on PDrecovery and you should NOT try it if you have been on any Parkinson’s meds for more than 3 weeks. 🥊

JohnPepper profile image
JohnPepper

I'd pocket the ten million and immediately start doing FAST WALKING and actually start getting better. Then I'd tour the world and walk through every area of interest, until my final day on earth and die with a smile on my face!

Rupa88 profile image
Rupa88 in reply toJohnPepper

i did fast walking for a month and nothing happened

JohnPepper profile image
JohnPepper in reply toRupa88

Tell me exactly what you did in that month?

Did you walk every day?

Were you out of breath when walking as fast as you could?

What distance did you walk on each walk, at the beginning?

JohnPepper profile image
JohnPepper in reply toRupa88

Tell me more! How often did you walk and at what speed? You have to do this for the rest of your life! It is not a cure it is a treatment that works. I starte the walking in 1994 and by 1997 I was a great deal better and carried on walking ruight up till now.

Mechjack profile image
Mechjack

Quit my job. Fund my children’s education. Set up a health savings plan for my wife and I. Spend plenty of time living the good, healthy life with my family. Volunteer time to help PWP. Never stop moving to the best of my ability.

SilentEchoes profile image
SilentEchoes

If only..... I'd fund unbiased research on causation and then sue Bayer/Monsanto into oblivion with class action lawsuits from the 10 million worldwide AD/PD/ALS victims.

Rupa88 profile image
Rupa88 in reply toSilentEchoes

why Bayer?

SilentEchoes profile image
SilentEchoes in reply toRupa88

Bayer bought Monsanto, they make Roundup.

tandolino profile image
tandolino

I would spend money to obtain the vibrating gloves from Standford University, if they do not work I would go with the DBS. It seems like they are close to having these ready. It seems like they should be tried before the more invasive DBS?

Esperanto profile image
Esperanto

Unfortunately, our world looks like this these days, we'd rather consume $10 million for ourselves, than share with PD patients who can't afford even basic treatment C/L. 2018 Research in the Sub-Saharan Africa (SSA) region shows that these monthly costs of about 33 US dollars (USD) in Tanzania, 10.5 USD in Ethiopia and 48.2 USD in Kenya are for many insurmountable. Taking into account inflation and a small quantity discount of Sinemet, an average of around 500 USD per year. So if I'm right, with $10 million you can help about 20,000 fellow citizens manage their PD symptoms for 1 year. 

N=1 vs N=20,000  The choice doesn't seem very difficult…. 🍀

ncbi.nlm.nih.gov/pmc/articl...

They can use 10.000.000 $
MarionP profile image
MarionP

I think there is not much point to this question.

Massage therapy including swedish, reflexology and Thai massage. A new house with an indoor and outdoor swimming pool. Quit my job and travel.

LagLag37 profile image
LagLag37 in reply toBythejerseyborder

Have you tried Reflexology for your PD? I haven’t wanted to but never have. 🥊

Bythejerseyborder profile image
Bythejerseyborder in reply toLagLag37

I went to one of those foot rub places. Not real reflexology, but pretty good . They're not as expensive as the real thing, and it did help to relax my muscles. They also did some neck massages and massaged my arms and hands too .

crewmanwhite profile image
crewmanwhite

I would invest a large amount if it on research to more clearly define both causes (which we already know) and recovery pathways which are available but need refining.

This amount of money would enable excellent studies that are more likely to be published in widely-read journals.

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