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Disaboom » Health » Fibromyalgia » Living

Living

Last post Tue, May 06 2008 8:19 PM by living. 5 replies.


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  • living living
    Posts: 9
    • permalink Living

    • Posted: Wed, Apr 30 2008 9:55 PM

    • Hello everyone. We are a new television show, called, “Living,” built to raise awareness for various diseases. Each show is accompanied by the appropriate medical foundation. We are looking for people that would like to be featured on our program to give us a day in the life of a certain, disease, illness, or disorder. This would require us to interview you, your loved ones, and possibly your doctor; or at least a doctor in said field. This would also require us to show your home life and possibly your life at work and how your condition effects your everyday functions. If you are interested in sharing your story please email us at livingpilot@gmail.com. Our intension is to put a human face on illnesses and to spread the awareness of what people must go through to live every day life. Thank you for you time, and we wish the best to all of you.

    • Filed under: hard, show, pain, living, anyone, tv, illness, I
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  • DSB DSB
    Posts: 319
    • permalink Re: Living

    • Posted: Thu, May 01 2008 1:01 AM

    •  Minor question why do you not have a pr5ofile and well no image here? Like this sounds like anything I'd ever have a thing to do with/


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  • KaraSwims KaraSwims
    Posts: 1,848
    • permalink Re: Living

    • Posted: Tue, May 06 2008 12:32 AM

    • Hello Living,

      Welcome to Disaboom. Have any of the pilot shows been filmed yet? If any are available on YouTube, maybe members could check out the flavor of what you're looking for. Sounds like a good opportunity to educate the public on LIFE with a disability but we're all a little way about the way these stories are told...would love to hear more.

       


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  • living living
    Posts: 9
    • permalink Re: Living

    • Posted: Tue, May 06 2008 11:04 AM

    • Hi there, At this moment, we do not have any pilots made yet. We are still working on gathering people's stories. WE need to have about ten stories that we can have ready to be filmed before we can even shot the first one. That's just how they work in television. They need to know that they can repeat the process of the show every week before they start putting money into it. So, right now, it is just me and a couple producers from another medical show that are working on it With me doing most of the leg work and them working on production company and network negotiations. As far as the flavor of the show, It is more about the people than most medical shows. What we really want to do is show an active life style and show how the disease effects them. As far as extreme cases where people are confined to there bed, we will show this as well as a different segment of the show. Most of the show will be a documentary of people's everyday life, how they have to cope. Another portion of the show is scientific explaining what the disease is from a the disease, or doctor's point of view. And lastly all show's will direct the audience to the foundations that are associated with that disease. There is a lot more to it, of course, but as far as the basic lay out, this would be it. We are looking for people that would be part of the show. Even still, we are looking for people that don't want to be part of the show, but are still willing to tell us their story. The more that we can get on paper, the better it will be for the show. So even if you don't want camera's in your house, simply by telling us your story, you would be helping a lot. I have worked on three other medical shows. And still, I am learning so much and I realize even more how most people don't really have a clue about most diseases. And we should because we are all human and capable of acquiring most of them. If not us, then someone we love. My fiancee could possibly have MS, so that wears on us from time to time. What makes it hard is that doctors can't really tell us a yes or a no, at this point. So she currently does part time work at the MS foundation. But like most people, it wasn't until she got a scare that she started doing that. Because she probably never really thought about it. I hadn't either. Truth is, I'm not sure why I started this show, started out as just an Idea, but when people started responding in a positive way, it really seemed to spiral into something that could do a a lot of good. And it feels good to be a part of that. And now I'm using up all my spare time, day and night to do it because I almost feel like a show like this is a necessity.

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  • MaggieRay MaggieRay
    Posts: 390
    • permalink Re: Living

    • Posted: Tue, May 06 2008 5:05 PM

    • Hello!

       

      This show sounds like a great idea to me and one whose time is long overdue.  I am so happy to hear that someone is finally going to show what living with this, Fibromyalgia, and other diseases is really about on a daily basis.  I have written to Oprah and Dr. Phil twice now requesting that they do a show on Fibromyalgia, but never got any response.  It is only through this kind of information and education that we will finally help to dispel the myths surrounding so many illnesses, but especially the "hidden" diseases like Fibromyalgia. 

       

      I watched a show a few weeks ago on the Documentary Channel called "Morphine on Trial" and it was an eye-opener for me.  I am in Canada, Ontario specifically, and was trying to deal with the rage and anger one feels at hopelessly dealing with doctors who will not prescribe pain medication for this, nor will they even listen to us describe our pain or talk about it at any length.  This program educated me on what doctors are up against with the law on the "war on drugs".  The doctor who was portrayed on the program, got arrested and thrown in jail for prescribing pain medication to his chronic pain patients, who were all doing well for the first time in many years thanks to his insight into the need for pain relief for these poor suffering people.  As a result of the legal harassment this dr had to go through, he finally closed up his practice here in Ontario and moved back to Texas.  After hearing the story, I couldn't say I blamed him.  I also understood a lot better why doctors won't even discuss pain medication as an option here in Ontario and it has helped me dissipate the anger I felt towards them directly.  I am still very upset with the police and legal system that is preventing this course of treatment for so many people who so desperately need it.  It is such a shame that the "powers that be" have to be so damned narrow-minded!  People who are in chronic pain are not addicts and should not be treated as such, but in this province they definitely are.  It is so wrong, I can't even begin to describe how "criminal" this whole way of thinking is.  In my mind, as a chronic pain sufferer, they are the criminals, for denying people who are suffering a way of being able to get their lives back again to some degree and not suffer needlessly. 

       

      I would never normally wish this illness and the constant pain on anyone, but I think these people who control our doctors and the medical system from doing their jobs would only learn what they are really affecting if they had to live just one day in this kind of constant pain.  I am sure they would find a way, legal or not, to get what they needed!  Not to mention that denying patients what they need for relief is doing nothing towards the "war on drugs" as these people are not "drug-seeking" or abusing their medications.  It is absolutely ridiculous and defies all logic to me, but nevertheless, it is the way it is. 

       

      I hope your show will be aired with the full honesty of what people go through trying to get the medical help they need, as it is quite an educating journey to have to spend years working through the medical B.S. of our system, here in Canada and the States, just to get the help we so desperately need, or even to get a doctor to listen.  I thank you for bringing these issues to the forefront of our consciousness where it can hopefully affect some positive change, or at least if nothing else, educate the average person on what it is like to try and live with our limitations.  People don't really know or understand, and they need to.  We have buried our heads in the sand over this issue long enough!  God Bless You!

       

      Gentle Hugs,
      Maggie


    • We are each of us angels with only one wing, and we can only fly by embracing one another.
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  • living living
    Posts: 9
    • permalink Re: Living

    • Posted: Tue, May 06 2008 8:19 PM

    • Thanks MaggieRay, This is exactly the sort of stuff that I need to know from people like you that live with this and other illnesses. I can learn what Firbromyalgia is through some research, but really know the pain the people go thru is what it is about. Adding that doctors don't yet know how to fix it and then the legal matters that are involved with the doctors that want to prescribe meds to you for relief is a whole other take. Of course we cannot build a show on hear-say, when such things like legal matters are concerned. And I don't know if the laws in Canada are different than the laws in the US. I do know that the whole health care system is different, and that may have something to do with it; maybe not. But it gives us something to research and come up with an answer to. Actually showing someone being denied for pain meds is an angle that we would want to go for here. Because we want to show the people how these illnesses effect YOU, from every angle, inside and out. I want to thank you for your input. I would also like to again pass along the email address for the show incase people would like to email me directly. Thanks a bunch. Jason livingpilot@gmail.com

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