those dammed boots
Posted by: Carrie Ann Lucas in Disability Culture, on parenting with a disability, telethonI have friends who watch the telethon, not in support, but to monitor the nefariousness. I do not, in fact, I block the channels that carry the telethon from the channel guide on our cable system so that the kids don’t accidentally stumble upon it. (It’s really not that big of deal, I also block ABC family for fear they will stumble on the 700 club, just like I block the naked people channels.)
What I can’t do is stop the fire department and their dammed boots.
We live in an area served by a small volunteer fire department. The fire station is a block and a half down the street. The fire department has responded to my house several times while I have lived here, mostly for small things, like my aide being trapped in my garage when the garage door springs broke. The only time it has been serious is when my daughter Adrianne went into a status seizure lasting 45 minutes (and they kept her oxygenated the whole time, no easy task).
We are fairly well known to the fire department. I want them to know us, partly so that they don’t devalue our lives if they respond in a life threatening emergency, and partly so that if I am incapacitated, the first call they make is not to social services. Two of my kids have sensory and/or anxiety issues when the fire trucks come past our house, so we’ve gone to visit to alleviate their concerns. We go to the open houses and barbecues at the station. They have keys to my house (so they don’t have to bust my door in during an emergency) and contact information for people who can take my kids in an emergency.
Because we go past the fire department almost every day, we see them with the dammed boots. They set up in the middle of our small arterial street, with sandwich boards encouraging donations and the boots. All traffic stops while people drop money into the boots. Every year I have to explain to my kids why we don’t give money, and every year I try to educate our fire department.
The boots are really an ingenious fund raising technique. I don’t object to that technique. I object to the telethon, and as long as the boots are associated with the telethon, I will object to the boots as well.
For 21 hours each Labor Day, the telethon is synonymous with pity. Millions of television viewers hear time and time again about how people with disabilities are doomed to live sad and tragic lives. They hear that without a cure, life is hopeless.
But we poor cripples have a knight in shining armor ready to save us. We have MDA coming to our rescue. A cure is near. Just give a little bit more money and these poor crippled people will be no more.
That is what I object to. Despite having a label of one of those MDA diseases, I certainly don’t live a sad and tragic life. Even though my disability is progressive, my life is far from hopeless. I know my kids, who have non-MDA labels, also don’t have sad and tragic lives, and their lives are far from hopeless.
(Well, okay, sometimes they think they do — you know I do work them like slaves, making them do things like folding laundry, and helping with dishes, raking leaves, and worst of all, cleaning their own rooms — sad, tragic and hopeless their lives may be, I know it’s definitely not their disabilities that creates the sad, tragic, and hopeless moments in their lives.)
While there are people with and without disabilities who choose to live sad and tragic lives, sad and tragic is not ubiquitous with disability. However the telethon promotes the notion that it is, hence creating a problem for people with all types of disabilities. The telethon is not simply a problem for people with MDA disease labels, but for people with all disabilities. The pity in the telethon does not stop when someone changes the channel, but continues when traffic stops for the boot.
Neil Marcus once said:
Disability is not a ‘brave struggle’ or ‘courage in the face of adversity’… disability is an art. It’s an ingenious way to live.
That is the view of disability I try to instill in my kids. That is how I want them to view me, and how I want them to view themselves. I’m proud to be a disabled person, and I believe my kids are too, or at least they are practicing to be proud. The telethon is completely antithetical to this social model of disability. Just as I won’t let my kids stumble upon Pat Robertson’s hate mongering, I will not let my kids stumble upon the equally oppressive telethon.
The problem is that we can’t avoid the dammed boots.
I have worked hard in the last year to help my kids learn about money, and charity. We don’t give money to panhandlers, but we do engage in charity in a variety of ways. We donate clothes, toys and household goods to the Arc. The kids use part of their allowance to give to the monthly mission project at church. We give food to food pantries. We drop off food at a local TV station a couple of times a year when they have canned food drives. I am proud my kids are generous and want to help. They want to put money in the boot, and in their minds the boots are no different than dropping food off at the TV station, plus it is the fire department. They like the fire fighters. They help people. My kids can’t imagine the fire fighters hurting people.
Last year I got away with having the two younger kids give the firefighters some literature about the problems with the telethon. They had no idea what they were doing. This year that won’t work. We’ve worked so hard at learning about money, and engaging in charity with their money, that they wanted to give money, not paper to the fire fighters.
I don’t want to quell their new found, and appropriate, feelings of charity, nor do I want them to be negative about the fire fighters, but I absolutely will not, can not let them give money. As much as I want my kids to understand the the problems with the telethon and relate them to the boots, they aren’t there yet. My kids are too concrete. In my kids mind, the fire fighters help people — period.
The result is that we are avoiding the fire department, and it pisses me off that the telethon is affecting our lives in this very concrete way. We are going out of our way to not drive past the fire department this year. We are skipping power chair driving practice, and bike riding practice because my kids will see the backed up traffic and flashing lights from the bike path where we practice, and want to investigate. We are shopping at a different grocery store, taking the long way around to Costco and church, and buying gas at the more expensive station that is the opposite way up the street.
All that for those dammed boots.
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September 3rd, 2007 at 5:01 pm
[…] Carrie at Disability Pride writes about what it’s like to be a parent of children with disabilities on the day of the telethon. […]
September 3rd, 2007 at 6:26 pm
I’m wondering if you have any advice on how people could give money to support research into MD without that money also supporting the pity-a-thon (oh, excuse me, TELE-a-thon)?
I ask because I’ve blogged on this too at http://reunifygally.wordpress.com/2007/09/03/why-deaf-people-should-boycott-jerrys-telethon/ and some of the people who left comments are arguing that it’s still worthwhile supporting MD research because some forms of it do limit the life span, and one person says she doesn’t like what Jerry says either but supports what he does … apparently because she doesn’t see any other way to get money into research for MD. I can’t help but wonder if the campaign against Jerry’s pity- er, tele-a-thon might go further if it were coupled with more education for other ways people can give. Any advice on the best way to respond to some of the comments that have been left at my blog?
If you do choose to come look at my telethon post then I hope you’ll also stay and look around at some of the posts I’ve done about the ADA Restoration Act of 2007, which I think is another subject that people with disabilities should be up in arms about. And BLOGGING ABOUT!
September 3rd, 2007 at 7:19 pm
I take the opposite approach. There are so many lies about what MDA actually does. I know I’ve never received a free piece of equipment from MDA. My young family members who have MDA diseases have never been to a free summer camp.
I think the response is not to give money to MDA at all. If someone is really wanting to give money to research, I guess giving it directly to the hospitals that do the research might be better.
Frankly, the money would be much better spent, and would benefit people with all types of disabilities by giving it to advocacy organizations. Give money to your local ILC, ADAPT chapter, and if you are in Colorado, to organizations like the Colorado Cross-Disability Coalition. These are the organizations that really make a difference in the lives of people with disabilities. Giving money for research into neuromuscular diseases does nothing to improve the lives of people living with the diseases. For 40 years we have heard Jerry Lewis claim we are millimeters away from a cure. Yeah, and I have some swampland in Kansas to sell you.
September 3rd, 2007 at 8:05 pm
Hi Carrie,
What a powerful post! I’m not sure if you remember me, but I used to live in Denver. I last saw you in Washington, DC, when I was living there. It was with Not Dead Yet at the Supreme Court, maybe a couple of years ago — my memory is not the best. You had Adrienne with you.
Now, I am in Rochester, NY, where I have been for almost a year. I just wanted to thank you for such a powerful post, and to say hi.
Anita
September 4th, 2007 at 6:16 pm
mda works hard all year long to raise money for the local families that need it. im sorry that you hate those boots but those boots are out there for good reason. everyday i help someone in our community and it makes me feel good. i don’t have pity for anyone i just want to help in any way i can. i spoke on the phone with a woman the other day who just found out that her 8 month old baby has spinal muscular atrophy type II I can’t imagine having a child and finding out 8 months later that something is wrong with it’s health. the woman was scared and i hoped i was helpful to her. im not trying to start anything i would just like you to explain to me why your blog is making me feel like i should not be proud of all of the hard work that i put in everyday to help others. once again im not doing this to brag “i work with the disabled” I have family members who are disabled and blind…I do this because i want to have some purpose in my life by helping others.
Thanks for your time.
MDA employee who loves their job very much.
September 4th, 2007 at 6:28 pm
also, Carrie Ann Lucas
if your family members have not had any thing given to them that is not provided by your insurance from MDA… be it leg braces, wheel chairs, repairs to equipment, rides to and from doctor’s visits and an opportunity to go to summer camp then your local MDA isn’t doing their job and you should contact the national office in Arizona and let them know. I work with our healthcare service coordinator and i have set up PO’s for all of the above and paid invoice’s for all of the above… put your foot down and say something… are your family members registered with us because we cant help if we don’t know who you are…
September 4th, 2007 at 8:30 pm
As a friend to countless friends who have and have passed on from Duchenes MD, I am sorry mda employee, but no amount of money you raise by portraying people with neuromuscular disease as pathetic could ever justify the negative effects of the telethon. The last tie i watched the telethon was to see mattie stepanek, before that it was in 1993. The last conversation I had with my best friend he was upset because mda was refusing to pay for camp after age 21. mda employee, will you grant my website an interview? maybe you can tell me why i should watch a sexist homophobic and ableist washed up comedian whose ex-pr guy tried to sue me? and it is Very paternalistic to consider that Miss Lucas “doesn’t know” how to access MDA’s services. She probably has more education than you, actually, come to thi nk of it, i probably do as well.
September 4th, 2007 at 8:47 pm
It’s a bit like beauty pageants constantly protesting, “But we’re a scholarship competition! We give so much money for young women to go to college!” Okaaaaaaay, but if they really cared about young women, they could do all that without the bikinis, the heels, the evening gowns….
If the MDA really cared about the lives of people with neuromuscular disease, they would surely end the pitython, dump JL, apologize for forty-two years of inflicting pain, and get on with doing whatever good they can do, led by the individuals and families affected.