My apologies. This isn't the best way to introduce myself, I know, but ...
My name is Neil Brooks. I'm 52 years old. I was declared permanently disabled due to chemically burned eyes. I've been disabled since 2004.
And I lost everything -- my home, my life's savings, and my health -- simply because I needed, and asked, to be able to sleep in my first-ever, brand new home in Fort Collins, Colorado.
Yes, I am a PWME.
Against medical advice, I flew to Stanford in 9/2016 to be seen in Jose Montoya's clinic where I received my Dx. Despite significant risks, I am currently on LDN, Valtrex, and Doxycycline (along with piles of supplements), but I'm still getting worse.
Like many of you, I've battled with my health for decades. ME/CFS seems like the grand unifying diagnosis I've been chasing after for all these years. But I've always been able to manage it ... at least reasonably well.
Until I moved into that house in Colorado.
This is my story:
http://nbeener.blogspot.com/2014/11/the-destruction-of-medically-disabled.html
OR: Google: The Destruction of a Disabled Man in Colorado
I have to imagine that many/most of you can imagine what would have happened to your health in this situation.
I'm asking for your help.
I'm asking people to do two simple things:
1) Share my story via social media, and
2) Send a short email to the editors of these Colorado media outlets, asking them to cover my story.
Nobody needs to vouch for me. Nobody needs to take a position about what happened. Just ... ask them to cover the story of what really happened to Neil Brooks in Fort Collins.
The email addresses:
KathyJack@coloradoan.com, lgustus@coloradoan.com, JStahla@Reporter-Herald.com, ggriffin@denverpost.com, lcolacioppo@denverpost.com, susan@coloradoindependent.com, greeneindenver@gmail.com, lshapley@denverpost.com, patricia.calhoun@westword.com, JohnFerrugia@rmpbs.org, LoriGliha@rmpbs.org, marybelgonzalez@rmpbs.org
Nearly 1 in 2 Americans lives with chronic illness. That number is rising. The overwhelming majority of these chronic illnesses are 'invisible,' like ours. Being disabled doesn't necessarily mean using a wheelchair.
You all know that.
Apparently, not enough people do. We need to raise awareness in any way we can.
My story is, at its core, the story of bullying of a disabled man. All I did was ask to be able to sleep in my new home. Nothing more. And the neighborhood -- with the help of the city -- went "Lord of the Flies" on me.
I am now stuck living in Fort Collins again. I'm not well enough to move. As you can probably imagine, I'm intensely uncomfortable here, particularly because nobody has ever been held to account for what happened to me in this town.
Please help me get accountability and raise awareness. Please. Help me reduce the odds that what happened to me ever happens to another sick or disabled person.
My humble and sincere thanks,
Neil
My name is Neil Brooks. I'm 52 years old. I was declared permanently disabled due to chemically burned eyes. I've been disabled since 2004.
And I lost everything -- my home, my life's savings, and my health -- simply because I needed, and asked, to be able to sleep in my first-ever, brand new home in Fort Collins, Colorado.
Yes, I am a PWME.
Against medical advice, I flew to Stanford in 9/2016 to be seen in Jose Montoya's clinic where I received my Dx. Despite significant risks, I am currently on LDN, Valtrex, and Doxycycline (along with piles of supplements), but I'm still getting worse.
Like many of you, I've battled with my health for decades. ME/CFS seems like the grand unifying diagnosis I've been chasing after for all these years. But I've always been able to manage it ... at least reasonably well.
Until I moved into that house in Colorado.
This is my story:
http://nbeener.blogspot.com/2014/11/the-destruction-of-medically-disabled.html
OR: Google: The Destruction of a Disabled Man in Colorado
I have to imagine that many/most of you can imagine what would have happened to your health in this situation.
I'm asking for your help.
I'm asking people to do two simple things:
1) Share my story via social media, and
2) Send a short email to the editors of these Colorado media outlets, asking them to cover my story.
Nobody needs to vouch for me. Nobody needs to take a position about what happened. Just ... ask them to cover the story of what really happened to Neil Brooks in Fort Collins.
The email addresses:
KathyJack@coloradoan.com, lgustus@coloradoan.com, JStahla@Reporter-Herald.com, ggriffin@denverpost.com, lcolacioppo@denverpost.com, susan@coloradoindependent.com, greeneindenver@gmail.com, lshapley@denverpost.com, patricia.calhoun@westword.com, JohnFerrugia@rmpbs.org, LoriGliha@rmpbs.org, marybelgonzalez@rmpbs.org
Nearly 1 in 2 Americans lives with chronic illness. That number is rising. The overwhelming majority of these chronic illnesses are 'invisible,' like ours. Being disabled doesn't necessarily mean using a wheelchair.
You all know that.
Apparently, not enough people do. We need to raise awareness in any way we can.
My story is, at its core, the story of bullying of a disabled man. All I did was ask to be able to sleep in my new home. Nothing more. And the neighborhood -- with the help of the city -- went "Lord of the Flies" on me.
I am now stuck living in Fort Collins again. I'm not well enough to move. As you can probably imagine, I'm intensely uncomfortable here, particularly because nobody has ever been held to account for what happened to me in this town.
Please help me get accountability and raise awareness. Please. Help me reduce the odds that what happened to me ever happens to another sick or disabled person.
My humble and sincere thanks,
Neil