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Who Let the Dogs Out?

Today I want to highlight a really incredible organization, and I can't do that without waxing poetic on my favorite subject: my dog. But don't worry, it's completely relevant because Jonas is a service dog who was trained by Freedom Service Dogs. He is considered a Skilled Companion, which means that he helps me out at home doing things like picking stuff up that I can't reach, carrying my phone around, and fetching my crutch when I've left it in another room. Freedom Service Dogs is a non-profit organization here in Denver that trains dogs and places them with clients who have various disabilities. Their dogs can help with any number of things from bracing and balancing to pushing hard to reach buttons. Unlike a lot of service dog organizations, FSD rescues their dogs from local shelters. Trainers visit the shelters regularly, testing strays for the intelligence and temperament they need for such a rigorous job. It costs FSD $25-30,000 to send one dog all the way from the rescue shelter, through the training, and finally pair them up with a deserving client. While they are very conscientious about who their dogs go to, making sure clients are well equipped to handle the animals, Jonas and I are kind of a special case. When I went to FSD, I wasn't looking for a service dog. I was looking for a pet.

Josh and I had joked about getting a service dog, but I'd never felt right about it. I'm very good about doing things for myself, and I have a big, brawny husband to manage the things I can't. Like running me up several hundred temple steps in Indonesia. Or cleaning out the shower drain. (Stand back, girls, he's mine.) So I didn't want to snatch a service dog from someone who might need one more than me. I just wanted a pet. But with my balance and strength limitations, I needed a well-behaved pet. Our first dog, Hero, was great, but I was terrified to walk her since she had a tendency to take off after squirrels, rabbits, and small children. I'm sure it was hilarious to see me dragged along behind her, but I wasn't impressed with the Marmaduke impersonation.

Several FSD volunteers and staff members Jonas and I during trainingattend our church, and from them, I learned that they adopt out the dogs that don't make it through the program. This sounded like a dream come true to me. These dogs already have basic obedience training, with either temperament or health issues that make them less than ideal for service work. When I got on FSD's website, I saw Jonas. [Cue dramatic light from the sky and heavenly choir music.] Jonas was fully trained and placed with a client as a full public-access Service Dog. But due to unforeseen anxiety issues, he was not doing well. He was back at FSD and up for adoption when I found him.

Josh and I went to meet him and everything clicked. Jonas was perfect for me, being very mellow and already trained to walk nicely next to a person with a disability. And I was perfect for him. I don't need him to come with me to scary places like the grocery store or (heaven forbid) Walmart. But with me, he still has a job, a purpose, and more importantly, someone who cuddles with him on the couch. He's my service dog, and I'm his service person. Since our needs matched up so perfectly, FSD “placed” him with me as my Skilled Companion. That means that we didn't have to pay for him (normally they ask for a $300-500 donation for adopted dogs), and we have the support of his trainer for the rest of his life.

Also, I got to go through my own training, learning the secret words that make Jonas do awesome things. I made friends with Bug, Pan, Doppler, Mansfield, Triton and Stryker and the men and women that go with them. Bug, Mansfield and Stryker belonged to Iraq and Afghanistan war veterans. FSD has an amazing program called Operation Freedom to help pair veterans with service dogs.

Jonas still has some anxiety issues, but he does come with me to church where he gets lots of love and affection, which is his favorite thing in the world... besides squeaky toys. But mostly his job is to stay at home and pick stuff up off the floor and get hair all over my carpet.

Jonas and I at graduationSo if you're looking for a dog to adopt, or an organization to donate to, or maybe you could use a service dog yourself, check out Freedom Service Dogs. These amazing people have made a big difference in my life.

When's Your Baby Due?

I encourage questions about my disability, not just from children, but from adults, too. Anyone who's curious can ask “What happened to you?” without fear of reprisal. I won't be insulted. I'd rather answer the question openly and honestly than have people stare and wonder. But in the five years since my injury I've noticed similar questions that spark a response in me that is not nearly so positive. Sometimes I get a really sympathetic look and they'll say “Did you hurt yourself?” or “When will you get better?” or “How long do you have to use crutches?”. There is a fine line between “What happened to you?” and “Did you hurt yourself?”. They sound like they're asking the same thing but there is a critical difference. The second set of questions assumes that my condition is temporary. This is like asking a stranger “When's your baby due?”. These are assumptions that should never ever be made. Implying that I should be getting better is painful. It hurts. It's a reminder of what I can't do. No matter how long it's been since my injury, no matter how well I've moved on, this strikes an emotional nerve. Zing. Like that spot in your elbow that manages to catch the edge of the table every single time. I think I'm justified in resenting the idea that I'm sick or that there's something wrong with me. I know that some parts of me don't work like they do for everyone else, but that doesn't mean that I'm less of a person.

Now, I want to be perfectly clear. I realize that it's not their intention to hurt me. I know that their questions come from a place of deep sympathy and human caring. Also, the concept of permanent disability is not a comfortable subject. No one wants to believe that it can happen to someone they know, or even themselves. And I'm young. I think this more than anything shocks people: the fact that I wasn't born this way and yet I will live most of my life having to use assistive devices to get around. I'm aware of all this, but I want to make sure people understand where I'm coming from. Word choice and phrasing can be subtly offensive and everyone should be aware of the nuances of their speech.

I don't want anyone to be scared or uncomfortable talking to people with disabilities. We're not unapproachable. That's why I'm doing this. Like most people, I just want to be understood.