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FMT into the Transverse colon only will cure it. Google fecal matter transplant.

Hope my CUE2 comes soon...been signed up for months! My friend Terry has one and swears by it...he's even in Charco's videos...somewhere!

Brilliant and informative as always!

Welp, that explains the small drool problem I've developed. I wasn't even sure it was a symptom, but I began to suspect. Man, this disease is just a hoot and a howl.

Another fantastic video. Really informative! Thank you for keeping up these videos Jodie.

I'll date ya

Very helpful video, demonstrating clearly how Parkinson's symptoms are unique to every individual patient.

Eat carnivore.

Say no to drugs that over time will not continue to work. And what are the side effects?

Jaw Tremor, nightmares......it went down hill from there.

Great video! So young for a PD diagnosis 🧡

How do they know it’s Parkinson’s Vs Dementia w Lewy Bodies?

Have you heard of Aminopyridine? A Naturopath said they have some success w this.. I am at my wit’s end w C/L - as it’s causing hallucinations and severe constipation w my HWP… Having a really tough time w HWP and not sure what to do.. The dilemna is: On C/L they get horrific REM disorder dreams/ Nightmares/ Paranoia- and even called 911 in middle of night saying there was truck coming through apartment. They have off C/L for a few days- and these horrible active nightmares where they sleepwalks have subsided.. HOWEVER, it seems like the Dopamine or missing C/L now they have less motivation to get themselves off bed, to physically walk themselves to the bathroom; constantly asking me to help pull them up, I am having more now to dress, put diapers on them ( as they also are having frequent urination) and had last few nights where they don’t know where bathroom is and we’ve traded the vivid nightmares w C/L for lack of motivation / w short term memory issues- and they aren’t having “the get up and go” as much to do daily tasks… Any thoughts? THANK YOU AND SENDING STRENGTH AND LOVE TO ALL OF YOU IN THIS BATTLE 🙏🏽🙏🏽🙏🏽🙏🏽

Love the jokes! I think it's great to lighten things up and be able to laugh at ourselves. In a round about way, you're helping people to understand/recognize Parkinson's through your comedy. Hope to see some updated videos on your YT page.

Good on ya mate ! Wishing you all the best in your future gigs. From a fellow shaky parky.

Superb. Very enjoyable.

The jar opener would be more helpful to someone with arthritis, with Parkinson’s it would be very difficult to even position the jar opener on the jar correctly.

Terrific content and well-presented!

Hi Team, we love your channel ! If you ever want to discuss light therapy for parkinson's, we would love to do something with you. You might have missed us at the WPC2023 in Barcelona last year, but our devices are CE and ARTG listed reduction of Parkinson's symptoms (motor and non motor). We have already completed clinical trials, and have another three currently underway.

Was just watching out of interest, my alteimers symptoms first showed after pregnancy but took many years and now I have joint pain etc. So many doctors dismiss that pregnancy can bring the first symptoms, even suggest more kids have the longevity increases. Will switch to woman doctor for albeit sympathy on how scary it is and my diet may only help albeit to live to see my grandkids

Absolutely fantastic video! Great to see how technology is developing. I've seen a few wearables now for PD and i'm really excited to see them become more refined in the future! Well done Jodie for getting out and delivering these videos!

Is it a sign of Parkinson's that music playing while I am trying to listen to people talking, like in this video, is irritating?

People should be cautious about ascribing a condition to Parkinsons....there is a lot of misdiagnosis as well as underdiagnosis.

my first symptom was the loss of my sense of smell, about 10-12 years before any termers started

I want you all to join me thank Dr Madida Sam on RUclips for helping me with their treatment plan to reverse and cure my Parkinson disease🤢 I have been suffering from for 12 years, it is amazing how this I want you all to join me thank Dr Madida Sam on RUclips for helping me with their treatment plan to reverse and cure my Parkinson disease🤢 I have been suffering from for 12 years, it is amazing how this treatment plan has changed my life for the better and I know that he can do same for you all too and that is the reason I am recommending him to you because his treatment works 100%✅✅✅...

Hi jodie. Thanks for the information. I just wanted to ask would you go for dbs maybe later on? Do you know if Michael j fox or muhammad ali (rip) had dbs?

My husband only eats once a day because any kind of food interacts with the levodopa. But in all honesty, it seems like in the Parkinson's forums that levadopa is pretty sensitive to foods, drinks and other medications. Seems like it's a hit or miss for everybody. In regards of timing and when to eat. If anybody else was curious about others experiences with levodopa and Parkinson's

Fabulously informative video as always! I'm so glad these are being made! Well done Jody! Keep it up.

Listening from Australia and I really appreciate the podcasts

I think we are closer than 30 yrs away from a cure. My gosh, that’s very long. Let’s hope that gene editing can help edit this out of the DNA chain either before birth or after. We have got to get more attention on getting Parkinson’s cured! Alzheimer’s gets alot more attention for some reason and it’s not fair! Parkinson’s is impossible to live with…very hard on patient and spouse, family, etc… so hard to live a normal life. God bless the patients.

Are you suggesting that the results could continue to improve after 5 years? And possibly last for 29 or more years? Thank you very much!

Hello, Would like to ask if Madopar can be taken 15minutes before and 15minutes after the prescribed time? Thanks.

I can’t find the name of the app or where to get it.

A small constant shake of my eyes... later it was my whole head.... other people noticed these,i did not.

15 YEARS I'VE BEEN ASKING VETERANS ADMINISTRATION DOCTORS WHY AFTER COMBAT I CAN'T DO THE FINGER TO THUMB THING yet i still work with my hands!? 15 YEARS!!!! NO ANSWER... thank you for sharing your story... it was the missing passage in mine.

I had a dead sinking leg in the pool... swam daily for years.... then my left leg would just drag me down and start sinking when swimming.

Sir, Should a Pakinson patient travel by plane?

I am waiting on an appointment at the Walton already have a dnet brain tumour, but if your left arm stops swinging when walking is this a sign I could have early parkinsons I am 53 and tried the pinch test and although I don't go slower I go smaller straight away I can't go back to that starting point distance between finger and thumb. I see the neurologist on the 18th but from what I have read so far I am thinking it's likely. I have an occasional small tremor which I notice when holding my phone or holding a spoon. I ask really because the lack of arm swing does seem a strong indicator from what I have read. Haven't got long to wait now so at least maybe able to get the help. Thanks for the work you do.

What a great video and app created by a fellow PwP to meet our needs. I went to the Apple App Store to get it and nearly dropped my iPhone whem I saw the price at $99.99! Why so much money when there are free apps out there?

Do trials involving stem cells appear to indicate a reversal of some symptpms or merely slowed progression?

Nicotine is not addictive, however, what they mixed in with it Pyrazine is !!!... After tobacco the next highest nicotine content plant is the egg plant !!! (Is the egg plant addictive !)... It's the nicotine that helps the Parkinson's disease sufferers !!!...

Oh man, I haven’t taken vacation with my wife for many years now after being diagnosed with Parkinson’s. It’s our 20th year anniversary in March. We use to go to Mexico every year. Now, I don’t know if I can handle it. 25 sinimet per day..

I'm 40 and one day, my right leg felt like I was walking in quick sand. I had just had heart surgery so my PCP brushed it off until a year later

See Johnathan sackler bernstaeins piece on no silver bullet.

I absolutely love the questions you ask in this video Jodie and really looking forward to the episode of movers and shakers.

and buntanetap in phase 3

Couldnt sign my signature at the bank

Wonderful podcast, I look forward eagerly to every episode, I can't overstate the good it does for me and the extended Parky community. Keep up the excellent work.

It is unfortunate that I am from a country having PD since 2014 where hardly 1% people heard about or know a little about the disease. There are many Neurologists, but I could not find any movement disorder specialist. My condition deteriorated even visiting three senior Neurologists. Finally, I went to another country (Thailand) and fortunate to get a good Doctor who is really a Movement disorder specialist trained in USA. Things started improving from that point and I have been under the same Doctor for last eight years. Can I join the Congress 2024? (Just fyi, I am going to US in April 2024. Regards, Shah Murshid

No symptoms until I got vaxxed and 1 week later I couldn't use that arm.