Tag: MND Awareness

  • Building bridges…

    Building bridges…

    HiRes

    Someone recently called me a “patient” entrepreneur. Yes, I am an ALS patient, but no, I am definitely not patient! 🙂

    The things I undertake to battle my disease can be described as entrepreneurial. However, it’s just who and what I am. Do I have a choice? I certainly do, although I can’t help being me. Don’t put me in a wheelchair and ask me to just stare out the window. It would probably break me… Don’t sit me in front of a TV. I’d probably just switch that crap off! Don’t give me face time with politicians unless you want me to tell them what their doing wrong. I’ll lecture businesses on what to do and how to spend their money, and scientists on what they should try to discover. Now, surround me with my fellow patients and I immediately feel a compassion that fuels my drive to find a cure. Facing my family fills me with love—something that everyone needs in their life!

    On my journey, I encounter stigmas towards patients, rigid social dogmas and oftentimes, outdated scientific paradigms. I am surprised at how our society has embedded fear into the roots of the very stakeholders that should be striving to make a difference, instead choosing compliance and governance over innovation and revolution. What has happened to the revolutionary mind of mankind that brought us to where we are today? How can we call ourselves innovators, when in reality, we’re just maintaining the status quo?

    Cultural and national differences are amongst the challenges I face in my endeavours, but our disease is global. It has no borders and certainly needs a more cosmopolitan approach. One of the lessons I try to share with others is that despite the adversity being faced, cultural norms dictate that people are always approaching it from different angles. We must be compassionate, but not blind. In my opinion, this is the only way to fill the pre-judged gaps in our opinions.

    As human beings, we are the only species that can feel both love and compassion. We have evolved beyond the confines of natural selection where the weak are left to themselves and the strong survive. When we combine compassion with our will to survive, we can overcome many issues and hell yes, even make the weak stronger!

    Right is not always right, and wrong is not always wrong. Hence, why I keep building bridges…

  • Freedom of Thought

    Freedom of Thought

    When I was 11 years old, I decided to take a stand, not just for myself, but for others as well. I jumped up on a crowded lunchroom table at boarding school, declaring that we hated the food we were being served and demanded better. Even though I had a right to an opinion at that age, unfortunately I didn’t feel like I was taken very seriously. However, a few years later the school did adjust some of their policies and even more importantly…the menu! I guess I’ve always had a bit of a problem with authority. 😉

    The reason I attended boarding school was because my parents and I lived on an inland barge that they also owned and operated. There were simply no other education options available. The years I spent at boarding school helped form who I am today and how I think about the world. Not that I am a socialist by any means, but I do believe in freedom of speech, freedom of choice, and most importantly in the freedom of thought. I also believe that despite one ‘s talent, not everyone can grow up to become a world-famous CEO.

    I have taken care of myself my entire life. Everything I do, I do with passion, focus, and a drive for success. Looking back, I have ticked many of the boxes on my bucket list, which I have of course extended over time. I am grateful for the life I’ve lived and happy with the choices I’ve made. That being said, I despise injustice, selfishness, and jealousy. In my heart, I want to improve the world around me and have a strong opinion about how to go about it.

    Having been confronted with a terminal disease, I have noticed that people bolster me with their love, and admire me for my strength and positive attitude in coping with my condition. However, I also sometimes feel a sort of skepticism, as if they have given up on me, thinking, “It’s too late for you mate, sorry…”

    Then my child’s feelings come back to mind and I get angry and more motivated to fight, but also disappointed that today’s society has individualized people to such an extreme. We have become more egocentric, not necessarily selfish, but in a way, we’ve forgotten what life is all about. We let our thoughts and fears be dictated by the media and have buried our inner philosophers. 2,400 years ago, Plato said, “There are two things a person should never be angry at, what they can help, and what they cannot.”

    I strongly believe in freedom of choice. This is what distinguishes us from all other living species. If a person wants to voluntary end his life, because he does not want to suffer from his disease any longer, that is his justified, individual choice. If others want to fight as long as they can, the same rule applies. Plato also said, “Death is not the worst that can happen to men.”

    People living with ALS/MND eventually lose the ability to speak, and in essence a bit of their freedom. However there is one thing we will never lose for as long as we live and is not affected by our disease. Therefore I now say that “silence is the fuel for our freedom of thought.”

    One Man

  • Knocking on doors…

    Knocking on doors…

    Social Media and Rare Diseases

    Like I said in my blog post entitled “Extraordinary Measures“, it’s all about BIG data. How can you make it easier to be discovered online? Especially when you want to connect with fellow patients, raise awareness for your cause, and raise more money for your disease?

    Here’s a short overview of what’s out there and some ideas to get started…

    Facebook

    In the world of social media, Facebook seems like a logical place to start; you already have a network of friends (and their friends) that can help you get more “Likes.” From a practical perspective, you have a built-in targeted audience who likes your page and is interested in you. What more could you want?

    There are over 150 Facebook pages devoted to ALS/MND. I probably haven’t found them all, but the point is that most of them are not connected to each other. The reach is limited to separate, local communities instead of a larger global one. To complicate matters, you also have to be very specific with regards to the content on your profile page and bio, otherwise your page won’t be found. It is a terrific medium for interaction and providing information, but you unfortunately still miss people that are not using the social network.

    Facebook also seems to be the wrong platform for fundraising. Maybe this will change when the platform introduces a payment system in 2014. Unfortunately, many Facebook users are only “viewers” and not “participators.” Judging from my own experience with my community of contacts, only about one third of my friends are active, with the rest (a dormant majority) only watching passively and occasionally interacting.

    Twitter

    The infamous 140 character message board of Twitter is not only useful for sharing news and pushing opinions to your followers, but also even handier for interacting with fellow patients and other advocates. However, it is crucial that you make yourself known to tweeters by using useful hashtags in your messages, having an informative bio, and keeping an up-to-date description of yourself on your profile. Otherwise you might remain hidden anonymously amongst the other 300 million users, sending roughly half a billion messages every day. I use programs like HootSuite and SocialBro to optimise my hashtags, to find fellow patients, advocates and associations, and to effectively target tweeters interested in other rare diseases and chronic illnesses.

    I can see that many users are not used to these tools, but rest assured that the amount of tweeters on rare diseases correlates with the real world prevalence of our conditions. This means that becoming a trending topic is hard work.  On www.symplur.com you can find the healthcare hashtags that are most used on twitter. It’s a very good start for you to have a look at how you can improve your chances of being found online.

    As a fundraising platform Twitter is useful to grab attention, but due to the structure of the tool, you always have to refer tweeters to an external site.

    Blogging

    There are many blogging sites, but the three I would like to mention here are Blogger, Tumblr and WordPress. Honestly, I only started blogging a couple of weeks ago. Why? Well, I guess before now, I wasn’t ready for it…and after doing some research, I ended up with choosing WordPress. The simple user interface and layout attracted me, but it is all very personal. You have to find the one which suits your needs. With blogging you can write your story and share your opinions in more than 140 characters…

    Video

    If you want to raise awareness, video is the way to do it! If a picture is worth a thousand words, a video is worth even more. You can show the world how relentless and cruel your disease is, that it needs everyone’s attention, and that a cure must be found…but hey, remember again, it’s all about the BIG data!

    Everyone wants to make a viral video like “Gangnam Style” and “Charlie Bit My Finger.” Or maybe not? Think twice about who your target audience is and who you really want to reach. If you want to reach the entire world, take another look at my blog “Extraordinary Measures.”

    Email 

    Most people think that email is over, but I would argue from my own experience that for fundraising purposes, this is absolutely not true. Out of a targeted email campaign sent to 1,300 addresses, I got over 50% to open, 14% to click and 3% to actually donate to my charity. Whether or not you possess  a large database of email addresses, email is still the best way to get people into action and donate for your cause. If you think it’s too difficult, just try MailChimp for free and you will see that it’s dead simple.

    World Wide Web

    A website is still the best way to inform the public, but the landscape of design and setup of websites is rapidly changing, pressed by the growing prevalence of tablets. Today’s websites should be very simple, with fewer buttons and preferably, a scrollable one-page design.

    Many of you won’t need a website as you can easily refer to the homepage of your local associations, but for fundraising purposes, there are many online platforms, such as Fundly, GoFundMe and JustGiving, where you can initiate your fundraising action for your cause and connect it directly to your charity. Keep in mind that you still need to promote this via Twitter, Facebook, etc.

    I hope I’ve helped to guide you through the various options you have to advocate for your illness via social media. Let’s all work hard to improve the attention for our causes!

    For various reasons, like small communities, only news or photo sharing, etc., I have left some options out of my review. Here are some of the others: Google+, Scoop.it, Instagram, Pinterest, and Flickr.

    And if this digital forest of possibilities still seems a bridge too far, well get your hat, go out and start knocking on doors to tell your story…

    One Man.

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