Parkinson Canada is the national voice of over 100,000 Canadians impacted by Parkinson’s. Thanks to the support of generous donors, we empower the Parkinson’s community through tailored programs & services, innovative research and raising the voice of all Canadians impacted by Parkinson’s.
Parkinson Canada est la voix nationale de plus de 100 000 Canadiens touchés par la maladie de Parkinson. Grâce au soutien de généreux donateurs, nous responsabilisons la communauté de la maladie de Parkinson grâce à des programmes et des services sur mesure, à des recherches novatrices et à la voix de tous les Canadiens touchés par la maladie de Parkinson.
I am the husband of the picture here and as a nurse I am so appalled at your add I saw on a billboard today.How dare you make fun of this disease. At least that's the way your add is making it look. This campaign needs to stop immediately.
Thank you for reaching out. At the heart of our efforts lies a deep commitment to those living with Parkinson’s, as exemplified in our latest advertising campaign. Throughout the process, we engaged extensively with individuals impacted by Parkinson’s and their families. What resonated consistently was their desire to be recognized first and foremost for who they are, beyond their symptoms or condition. While Parkinson’s presents undeniable challenges, our aim was to encourage individuals to redefine their lives in relation to their symptoms. Rather than portraying sadness and despair, our intention was to extend a welcoming hand to those experiencing these emotions, offering support and empowering them to live as fully as possible. Through this campaign, our goal is to inspire both individuals and the broader public to see beyond Parkinson’s, appreciating each person’s unique qualities, interests, and personality. We want everyone to understand that Parkinson’s is just one aspect of their narrative.
I found this Ad leaving me puzzled and confused. I didn't get the message. I checked the website which didn't answer anything due to its poor layout and lack of information. I had to do some searching on the website to eventually find info on symptoms. Is this ad raising awareness? How many viewers will go to the website? How many viewers will search the website to find the hard to access symtoms info? After reading the symptoms I feel that the ad campaign should of had different scenarios in seperate commercials that inform on what Parkinsons is. Yes it's upbeat. I was confused why a Beck song was used. Yes its catchy but does it help convey the message of what Parkinson's is?
Thank you for your message. Your perspective is important and our hope was to create an ad that supported the idea of people with Parkinson’s living boldly, unapologetically and proudly. In casting one person to be at the centre of the ad, we understood that it would be impossible to reflect, in a few seconds, the variation in experiences and symptoms. Along with the ‘find your swagger’ ad, we’ve created a web page that shows a few stories of living with Parkinson’s at www.findyourswagger.ca. We are also working on an improved website at the moment at www.parkinson.ca to ensure everyone can find information more easily. If you’d like to find support and resources for living with Parkinson’s, you can also contact our Information and Referral team via support@parkinson.ca
‘‘I am not only happy am alive but also glad that "#DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease (PD) 🦠🦠with their herbal treatment. My smile is so bright because I am happy 😊😊😊..’’
‘‘I am not only happy am alive but also glad that "#DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease (PD) 🦠🦠with their herbal treatment. My smile is so bright because I am happy 😊😊😊.’’
I never comment on RU-vid but I find this ad campaign incredibly tone deaf. You claim you worked alongside people with Parkinson's and that it's impossible to reflect everyone's experience, which is fair, but what this campaign does is diminish and trivialize the experience of those who have more advanced forms of Parkinson's. Parkinson's is not about "the wobbles, the wiggles and the wonky moments" as your website puts it, and trivializing it to that is pretty offensive. Parkinson's did not help my mother "find her swagger", but in fact took her swagger away. I hope you rethink this campaign and look for a different way to provide uplifting messages about living with Parkinson's without trivializing it.
Thank you for reaching out. We deeply empathize with the challenges your mother faced and recognize the importance of addressing them. Our focus is on putting individuals with Parkinson’s at the forefront of our efforts, which includes our latest ad campaign. Consistently, we heard that those with Parkinson’s wish to be acknowledged for who they are beyond their condition - not solely defined by their symptoms or struggles. While Parkinson’s presents undeniable challenges, our aim with our campaign was to encourage individuals to redefine their lives in relation to their symptoms. Rather than portraying sadness and despair, our goal is to welcome those experiencing such emotions into our community, providing support and promoting a fulfilling life to the fullest extent possible. Through this campaign, we aspire to inspire both individuals and the public to see each person's unique qualities - their charisma, interests, and personality - recognizing that Parkinson’s is just one aspect of their journey. Your perspective is valuable to us, and we understand that each person's experience is unique. If you would like to share more about your journey, we invite you to visit findyourswagger.ca to learn more.
We need to stop the stigma and not self isolate. Exercise and social contact is a must for quality of life for everyone especially those with PD. We know everyday can't be like this but try to seize the moment, if not the day.
Love this campaign! As someone who worked in the MS Community for years, it is a good thing to look beyond your diagnosis and provide levity. This in no way diminishes the disease or the struggle with the disease in my opinion. Great work!!!
Thank you for your message. We have not removed any comments, and are happy to engage with the community with both positive and negative feedback. It seems our 1 minute video here has received more comments than the 30 second video: ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-FhDgQLw_RBc.htmlfeature=shared We thank you again for your feedback!
I actually liked the video, it was upbeat and happy. Since being diagnosed in 2018 I have watched many videos of people with PD and most are depressing. I sometimes feel like a fraud, because my symptoms of PD have moved at a snail's pace over the last 6 years, most are symptoms you cannot see, except for my R-hand tremor. That is starting to get a lot more noticeable. I do not tell people I have PD because some have looked at me and stated, "but you do not look sick, or you do not look like someone who has PD." So learned most of the time to keep this disease to myself. My neurosurgeon says it is a good thing everything is moving so slow, and of course PD does not follow a concrete set of symptoms and that is one of the problems getting the public to understand. Would love that this could be included in a campaign, that everyone affected by PD do not have the same symptoms. Thanks.
Thank you for your message! We're so happy that the ad is meaningful to you. If you’d like to watch it again and learn more about ways to get involved, you can visit findyourswagger.ca.
good for u! i experienced that honeymoon period too and, while u may get lucky enough to ride this out , trust me (and im not trying to be cruel or a doom-saryer) but darker days are ahead. A lot of us PwP aren't in the "swagger"" stage of this horrendous disease. No amount of Beck's funkadelic tunes or flowers or smiles or Parkinson's Canada aaad-'agency promos will change that! All the smaev, I wish u well and thx for chiming in on the debate that is brewing with ur perspective!! ::)
I love this campaign! We all know parkinsons is a horrible disease but some days dont you just want to scream "yes i have parkinsons but parkinsons doesn’t have me!" I'd love a t-shirt that proudly proclaimed, "It's not Parkinsons...its swagger!
Thank you for your message. People with Parkinson’s are at the centre of our work, including our latest ad campaign. We spoke to many people living with Parkinson’s and their family members at every step of the way. What we heard consistently is that people with Parkinson’s want to be seen as themselves first, and not be defined only for their symptoms, their struggles, their Parkinson’s. So, while Parkinson’s undeniably creates challenges, we wanted to inspire people to redefine, as much as possible, their lives in relation to their symptoms. We could have created an ad that shows sadness and despair, but what we hope to achieve is to welcome people who are currently experiencing those feelings into our community, support them, and as much as possible, help them live well. With this ad, we hope to inspire individuals and the public in general to see the individual first - their charisma, their interests, their personality - and to know that Parkinson’s is only part of their story. Your perspective is welcome and valid, and we know that every journey is different. If you’d like to share more about your experience, we’d love to hear about it. You can visit findyourswagger.ca to learn more.
I like this video. I've been a member of the Parkie Club for 23 years now and enjoy a little levity to help set aside the complete suckage of PD for a moment. Well done mate
Thank you for your message. I’m so glad our new ad is meaningful to you. If you’d like to watch it again and learn more about ways to get involved, you can visit findyourswagger.ca There are many ways to join our community: - Participate in an event - Volunteer your time - Share your story - Donate to fund programs for people affected by Parkinson’s and to fuel groundbreaking research Learn more on our website: www.parkinson.ca/getinvolved
You have me befuddled with this one!! I wanted to like this ad - the catchy upbeat tune, the interaction between the man and the woman (his smile particularly) , the "swag" the character exudes that's all good! It's fun. It's humorous - and believe me living with the moniker imshakydad for the past 24+ years, I can appreciate the importance of humour in coping with PD! On the other hand, there's a part of me that makes me want to rage against it. Parkinson's is more - much much more - than a walk in the park, whistling a catchy tune, showing "swag" on the street. It suggests that Parkinson's is not that old , decrepit disease that has been with us for 200+ years but it's just "swagger". Get out on the streets all u PwP and strut your stuff. The ad feels like it belittles the disease. Yet, as I say, I'm divided on this one - I'd be curious to hear other voices.
Thank you for your message. Your perspective is important, and we recognize that no two journeys of living with Parkinson’s will be the same. We worked alongside many people with Parkinson’s in the development of this ad to ensure their perspectives were represented, but we know if would be impossible to reflect everyone’s experiences. We know the realities of living with Parkinson’s disease, and we hope that we can inspire people with Parkinson’s to connect with us for support, so they can live well. We also hope that this ad will challenge the stigma that many people with Parkinson’s face while navigating the world, and help the broader public think twice before rushing to judgment. Thank you again for your feedback. If you’d like to share your own personal experience of living with Parkinson’s, we’d love to hear it. You can share your story or find more ways to get involved at www.findyourswagger.ca . If you have any additional concerns, you can also reach out to us at communications@parkinson.ca
This ad is the best thing Parkinson’s Canada has done period. It hits home. As a person with Parkinson’s for 19 years, it’s always about reframing and one’s mindset. The website linked to this campaign, on the other hand, looks like it was done by an eight year old. Surely you could make it more professional looking.
Thanks for sharing your ambivalence. Yes, Parkinson's is much more than this one happy, upbeat moment. And, I don't think the video is claiming that this represents all of Parkinson's for all people. I imagine the goal of this video is to raise awareness, increase engagement and show that there can still be days, hours or moments of joy and connection for people living with these kinds of challenges. And, to highlight how important social connection is.
Agreed, but what struck me was , when he gave the flower to that woman ( so typical of that type) she seemed confused by the act of kindness and a sweet gesture! It took the whole ad for her to crack a smile. Great ad My Favorite Uncle had Parkinson's... Id redo the ad and put someone who can at least smile when given a kind gesture 🙌 🙏
My prayers are with you all and I know how you all feels, my Dad suffered same illness for 13 years until madida herbal center came to his aid and cured him with their natural PD herbal medicine, Click and search #DrMadida, and let your Parkinson Disease be taken care of and be cured just same way my Dad’s own was taken care of and cured👌👌..
I am not only happy am alive but also glad that "DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease(PD) with their herbal treatment. My smile is so bright because I am happy .’
I am not only happy am alive but also glad that "DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease(PD) with their herbal treatment. My smile is so bright because I am happy ‘.
Parkinson disease 🦠 🦠🦠is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine from Dr Madida that truly works that helped treat, cure and reversed all his symptoms…”My Dad is well a gain”.
Some people really need benzos to sleep. Doctors should not superimpose their own benzo experience onto the needs of their patients. We are all wired differently.
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine🌿 🌿🌿from Dr Madida that truly works that helped treat, cure and reversed all his symptoms. My Dad is well again.
My wife who had Parkinson's for 22 years died in 2022 in her instance she did quite well for 19 years then dementia came about and medicine for it did very little for her and she needed 24/7 nursing home care . After a bout with a skin disease ,Bulbous Permphigoid that spread into her mouth she quickly went in to a coma and died within a month. Her USA death certficate states she died of "Parkinsoniasm" . Recently I have heard of this skin disease becoming in some instances Parkinson related ,the Drs did cure her BP ,however she remained in the coma and soon lost her swallowing functions . She never knew she was dying and had no pain. So tragic and swift from conversational to death in 32 days.
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine from Dr Madida that truly works that helped treat, cure and reversed all his symptoms...My Dad is well again🔁
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine from Dr Madida that truly works that helped treat, cure and reversed all his symptoms...My Dad is well again🔁
Great things Dr Madida on RU-vid has being doing for mankind, I undergo his Parkinson disease treatment plan for weeks and my Parkinson Disease🦠 was completely reversed..
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms.. My Dad is completely okay and healthy now.
I hav lived with extreme PAIN FOR 3 YEARS NOW! Is this from my Parkinson’s diagnosed In 2017?!.? or is it from the broken vertebra that I suffered ?? In I am prescribed HYDROMORPH ABOUT 12 g a day It doesn’t seem to relieve the pain for very long! They would like to prescribe METHODONE WITH YHE PAIN MANAGEMENT CENTRE IN MONTREAL PIERRE BOUCHER HOSPITAL COULD YOU SHARE YOUR EXPERT OPINION WITH ME!
I manipulate my own dopamine system with Cannabis and ONLY Cannabis!! I’d love for an M.D. such as this Doctor to discuss my protocol versus the atypical protocol of Dopamine Antagonist. I’ve had Young Onset most likely since my late teens early twenties as the Non Motor symptoms showed up early. Didn’t have the “Pinky Twitch” until about 35, then after that the shakiness, balance and overall health of my “Vagus Nerve” went downhill. I’ve spent since 1997 studying this disease as well as the other relevant movement disorders so with that and having a Father in the last stages of it I was able to tell without a Doctor that Parkinson’s was my future. Still have many atypical Doctors with large Ego’s that doubt how someone without a Doctorate in Neurology could figure out themselves it’s Parkinson’s and not Essential Tremor, Wilson’s or Huntington’s diseases! I’m here to discipline those bad doctors with large inflated egos and will have my RU-vid Channel up soon so everyone can watch the “Who’s Who of Americas most embarrassing doctors still in practice”.. if an M.D. is willing to waste the patients time with Ego then that Doctor shall be famous in shameful and embarrassing way….
