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Many would say this is too good to be true, I must say this real quick that it is very good and very true how Dr Madida Sam on UA-cam cured my Parkinson Disease with their PD treatment protocol🌱🌱🌱…

That's amazing. I've been looking at DBS info for a while. It's incredible to see this technology at work. I'm happy that this has helped you so much.

I am patient of yopd , good on medicine since two years Your video is very promising and hopeful to see myself in near future Thanks for sharing ❤

Don’t care

I am using my husbands account here, but It is amazing to see what good DBS does! I was diagnosed at 32 with yopd. Six years in, I am now being evaluated on if I am a good candidate. I just did my psych test today. Your video amazed me <3

Hi Jasmine. Finally got my Dbs😊

Another false narrative that nicotine is “brain poison”?

Thanks for this video.

Ive been sexually violated by 2 different doctors. Anytime im "REQUIRED" to disrobe, I go into fight or flight. Usually both. I am a mess.

That was pretty dramatic

After switching on the pace maker for first time can person have dyskinesia?

Ive done aloy of research on dbs. As an athlete, I hope that I can push it to current maximum. If not....I will be not happy lol. For me stiffness, slowness and rigidity when off.

I am going for a dbs assesment on the 27th, 14hrs with no meds...gonna be tough

I wonder if the nicotine vape you were using six years ago has been helpful, cause you look a lot better now in comparison. My brother has Parkinson's too and is trying to cope like all. All the best to you and your efforts.

Never forget you have friends, life with Parkinson's is never dull. I still don't believe I'm still living with Parkinson's since "You have all the classic symptoms of Parkinson's, but you are too young to have an old Person's disease. That was in 1983. Forty years later, still here, still doing my best to keep up with my boxing classes and yoga.

Please give your Facebook link

She is a brave young woman. As a man with Dystonia since 1978 and a recipient of DBS surgery in 2012 you'd have to fight me to turnoff my device. 😂

Amazing ❤

You give me hope. They keep postponing my Dbs surgery Perth au

Hi Jasmine! I hope you are well, happy Valentine’s Day to you ! I think you may have the same Medtronic device as mine , at least judging by the patient programmer you had in a prior video. I have had mine 4 years. Have you ever tried tweaking your pulse width or other settings ? of corse working with your dr. to find a “sweeter spot”? I’m wondering if I am taking advantage of all the capabilities of my DBS. I’m 63 and have had Parkinson’s about 8 years

You are very brave. Thank you. I'm looking forward to getting dbs

Hey Girl! Missed you tons!!! Happy to see your beautiful smile. Let’s catch up soon!

Jasmine. Hi. Glad you’re well and back 😊. I’m having DBS soon and am hoping that it improves my sleep. Did you have sleep issues and did your DBS improve it much? Thanks

🕊

Happy your feeling good and are back. Yes, the pandemic has been really hard on us Parkies, the added stress exacerbates our symptoms. I was hoping for a silver lining in the covid cloud, but it just is not to be. Keep us up with postings please and take care of yourself..

It is lovely to see and hear you. Happy Birthday, Jasmine!

Wow. How has this been working for you in the long run??

YAY for Mad Scientists!

So happy to see you back,

Happy Birthday

Soooo glad to see you Jasmine. So glad you have been busy.

Happy birthday Jaz!!!

Exciting for this medication for you! Sounds like it's definitely doing something!

Sooooo happy to see this video and your cute face!!! Missed you and really excited for your new adventures!!!!!

Thanks for Sharing 😊

I always enjoyed watching your videos, thanks for sharing ❤️

Thanks so much jasmine for posting this. Congratulations hope you are still doing well I'm on the waiting list for dbs but covif delayed it and then the surgeon stopped doing public surgery

I get constipated and i have parkinsons .

Jasmine are you still around with this channel?

You're such an inspiration! I am 27, was diagnosed with YOPD at 24 and with dystonia as a side affect. Your story inspires me and what a better way to turn pain into power by bringing spotlight to the subject! God bless you and so happy to see you doing well! I have the candidate appointment on July 29th for the DBS surgery! Hope I respond well

Thank you. Today I had a panic attack triggered by being given a prescription I didn't understand or agree with, and I felt so silly for all that happening "over a pill", even though I know the pill is not the cause only the trigger. Even you shared about your experience with signing your name, it really resonated with me, and helped me so much to feel less alone. Thank you for sharing <3

It's so weird to hear this information 2 yrs later. So many agree that there are very few memory markers to go by in the 2 yrs of Covid. For me as an older adult it was like losing everything I ever knew, like someone erased all the generations before the pandemic and we stepped into another world 🌍

Can you please share where you had your DBS done please, thank you 😊

This is an outstanding video of Kaizen Martial Arts owner Jody Hould at the start of her amazing Rock, Steady Boxing at Kaizen. I joined in 2017 and think the program amazing! Jody continues to enhance the program and keeps it fun and interesting. In addition to Jody, her son Zac is a now a RSB certified coach and adds much to the program. I cannot say enough positive things about Jody and Zac, supported by Jody's husband Tom. Except to say, "Thank you" for your innovation and dedication to the program even during Covid lockdown through daily Zoom classes!

Thank you for your contribution to a better world! You are a beautiful soul! We have OSDD and ASD and our story is absolutely heartbreaking. We feel we were left for dead. We were gaslit, abused and even raped in MULTIPLE MEDICAL FACILITIES because our ASD and OSDD prevented us from remembering the trauma or being able to express what happened. We thought about starting a movement in which ppl share their medical trauma stories, just like ppl shared sexual assault stories with #metoo. We’re thinking of calling it #leftfordead. . . What do u think!?!

i didn't realize how many others had this as well, i know many others that do but never realize so many people do. It should not be like this. Some days i would rather let something go really wrong and not get help for it than walk into another medical setting. I had a skull fusion in 2016, and since then it has been one trauma over another. And these simple things now - they terrify me. I am panic every time i even have a small appointment. I think our souls are just tired. we cant live without medical care when we are sick or permanently injured. at the same time we can't handle it anymore after a while. it is just one thing after the other. it is never ending. and i can not see a life and future full of this can continue. I feel for you so much as you are so young. mine happened when i was 39. we can not live with it , and we can not live without it. it has given me a nervous breakdown before, i can never find a day of peace because there will always be another shoe that drops. and then dealing with the pain and sickness on top of it. I understand wanting to be done with it. As long as you have people to help you , hang in there. THere are those of us who dont have anyone anymore, they are dead and gone, friends move on. We are doing this alone. utlize the xtra help as long as you have it and hopefully this stops for you

Please always share with us your videos because they motivate us a lot

After dbs do you still have gastroparesis?

Thanks a lot for sharing. Please tell us where did you do the operation?