Posts tagged: attitude

The Gift

Marge, Bosco and Foxy

Last week my wife brought home a very special gift. It was a gift of unconditional love for everyone one who lives in our home.  The gift was a 3 month old Bassett Hound from the SPCA.  His name is Bosco. We have always had a dog and very often more than one. However, since my “accident” we have only had one, a lovable mutt named Foxy. We got Foxy about eight years ago after finding out service dogs could cost anywhere between $15,000 and $18,000. I believed it would be possible to train her to pick things up for me, but Foxy had different ideas about what she was going to do. Picking things up was no problem for her, but then she wanted to play her favorite game tug-of-war for which I was no match. She went to, but flunked out of, obedience school. Foxy is a free spirit and we did not wish to destroy that characteristic, so we discontinued with the training. Foxy owns us and she knows it; and so our life went until about a year ago.

Marge decided Foxy was lonely and needed a playmate. The debate went on for over a year, Marge trying to come up with rational reasons and me trying to put the folly of the whole thing into perspective. Given the extra demands placed on Marge by my quadriplegia, I thought it totally wrong to bring into the family another member who would require even more of my wife’s attention. Two weeks ago the scales were tipped in favor of getting another dog. Our neighbor’s brought home a second dog, a cute puppy which looked like a St. Bernard. Foxy when to the edge of her range and barked and whined. The decision was made.   

Saturday morning Bosco arrived. We were anticipating an adjustment period of days, if not weeks, but to our surprise it was hours. Foxy’s playful nature and maternal instincts quickly got the best of any reservation she might have had. I guess I could say the same thing for Marge. I must digress for a minute here. For several weeks prior I had been locked in a battle with Medicare and our secondary insurance company over a repair issue with my wheelchair. After a week or two I was totally frustrated. It was affecting me physically and mentally, and I was strung pretty tight.

Foxy quickly decided Bosco was going to make a great playmate and proceeded to test the theory for several hours.

Bosco & Me

Finally, both dogs tired of the frolic and began to settle down. Marge picked up Bosco and put him on my lap. The impact was immediate. I could almost feel the tension leaving my body. The puppy grunts and his smell soothed my psyche. Talk about pet therapy! It was instantaneous! Bosco sat with me in my wheelchair for over a half an hour. Several times I drove around the house and he was as contented as could be. After I pet him for awhile my fingers began to relax and return to a more normal position. Check out the picture. Bosco accepts me as I am and neither expects nor desires any more. He tries to climb up my leg in an effort to get on my lap. When he is on my lap it is almost like being in a meditative state. One of the great things about love is the more you give the more you have to give.

This Is For Linda ( but you can read it too)

I have a
good friend who is struggling with some very challenging issues in her life
right now. At times, she feels overwhelmed and depressed. If you have never
gone through times like these, most likely you will. In the Austin Powers movie,
The Spy Who Shagged Me, Dr. Evil had Fat Bastard steal Austin Power’s
mojo. The rest of the movie was about Austin’s effort to recover it.

 

In real life
no one can take your mojo, self-esteem, dignity or whatever you want to call it,
unless you let them.  Each and every one
of us already has the inner strength to handle any challenge or crisis that may
confront us.  This becomes very obvious
when we look at people who have dealt with or are dealing with a major crisis in
their lives: Helen Keller, John McCain, Lance Armstrong, Christopher and Dana
Reeve, Kevin Everett of the Buffalo Bills, Bob Woodruff of ABC News, Elizabeth
Edwards who recently lost her heroic battle with breast cancer, and more
recently Congresswoman Gabrielle Giffords. While these people may be famous
they are really no different than you or me. I am sure you know not so famous
individuals who have demonstrated the same inner strength. Did these people get
something at birth that we didn’t receive, of course not. These individuals may
have approached their challenges in different ways but they all found the inner
strength to deal with them. For final proof positive, I’ll turn to Rock And
Roll which I believe holds the answers to all of life’s mysteries. The group
America in their song Tin Man sings:

                       “Oz never did give
nothing to the Tin Man

                         That he didn’t, didn’t
already have…”

 

Think about
the verse above. If you have ever watched the Wizard of Oz, it makes perfect
sense. The basic truths in the movie are why to this day it remains a classic
for children and adults alike.

 

The question
now becomes how do we marshal our inner strengths? I believe we must face life
experiences head on, with a positive attitude looking at circumstances as a
challenge to be dealt with rather than a problem to be solved. Realize some
struggles will be long and that at times situations can become very
discouraging, but that is normal. Colin Powell said “There are no secrets to
success. It is the result of preparation, hard work, learning from failure.”

 

We should
never allow others to define who we are. As with a bully teasing a child on the
school playground, the child should never say, “What’s the matter with me but rather
what’s the matter with that bully.”  So
remember no one can take your mojo unless you let them!  Oh, if you’re reading this and you’re not
Linda, don’t worry; she’s going to be fine.

If I Need Help I’ll Ask

In the 1980s, during the summer, I was an instructor for State University of New York College at Cortland for their 2 week Outdoor Practicum a course required for all Recreation and Leisure Studies majors. The students stayed at Camp Huntington on Raquette Lake in the Adirondacks which is owned by the College. During the first week students were taught outdoor skills they would use the following week. When the instruction was finished students were placed into groups of 8 to 10, assigned a staff member and then taken on a 6 day wilderness experience where they used the skills they had learned. Travel was almost always by canoe, portaging between lakes.

One summer I had a young woman assigned to my group who was legally blind. Prior to our trip she and I met privately to discuss what her expectations were for the experience. I had noticed while we were in camp she could be very defensive and abrasive at times when others tried to assist her. I felt she failed to grasp that they were only trying to help. She was very upfront with me about being allowed to do things herself. We agreed that I would not step in to help unless she asked for assistance. In return, she promised to do whatever I asked of her immediately and without hesitation. There were some potentially dangerous pitfalls on the route where immediate compliance might be necessary for safety.

 The trip we devised would incorporate an opportunity for her to use as many of her senses as possible. We climbed down to Raquette Falls so she could feel the spray from the rapids on her face and listen to the roar of the water. We climbed a mountain called Ampersand near Middle Saranac Lake. The climb is very demanding and lasted several hours even for able-bodied individuals. The trip proved to be a great success and I remember to this day her telling me on the summit of Ampersand, “Now I know I can anything if I put my mind to it.”

The group on the top of Ampersand

How ironic that I now find myself in the same situation with people often offering to help me do whatever it is I’m trying to do. It’s been my observation almost everyone’s gestures are well intended. Most want to convey their empathy, but sometimes I have to remind myself of that. They don’t realize their effort could be misinterpreted as, “I don’t think you can do things for yourself”; for example, when a waitress asks my wife what I would like to order, implying I am totally incapacitated by my disability.

When I talk to a group I always drop a piece of paper on the floor. Ninety-nine percent of the time someone moves to pick it up for me. My wife usually intercedes to stop them. When I’m ready, I pick it up using my paper-pick-up tool. I drop a bottle of soda, a piece of a jigsaw puzzle, a book and one by one pick them up; in public schools the audience usually applauds. I tell them these are not tricks but rather ways that I have developed to function independently. I like to say disability does not mean inability. People need to understand that members of the disabled community are not totally helpless. And members of the disabled community need to remember people offering to help only have the best of intentions. So remember to tell people, “If I need help I’ll ask.”

Emergency Information Sheet

For any of us who have serious medical issues it is probably a good idea to carry a form that would be available to anyone providing emergency care to us any time.  I have a single 8 x 10 sheet of paper that has information on both sides. I have a copy on both of my wheelchairs, there is one in our van, one in my wife’s car, another in her purse and my nurses each have one. It’s folded in way so the words EMERGENCY INFORMATION are clearly visible. A copy also sits conspicuously in

Emergency information on the refrigerator

 an envelope on our refrigerator. Obviously, the information would vary from individual to individual but also some of the data would be the same.  One side of mine has information concerning Autonomic Dysreflexia which is a life-threatening condition that can develop very quickly when an individual has quadriplegia. The information includes warning signs of the condition and the protocol for immediate treatment. I’ve been to hospital emergency rooms where neither the doctors nor nurses had any idea what Autonomic Dysreflexia was or the potential it has. At the bottom of this section I have the website for the Paralyzed Veterans of America and their phone number where information is readily available on this condition.

Underneath that section I have PERSONAL INFORMATION which lists all the medicine I am allergic to and all the medicine and over-the- counter drugs I am taking morning and evening including dosage amounts. It also lists the drugs taken as needed for pain or other temporary conditions. I update this information every time there’s a change in my medications and I include the date of the last update. The paper can also be given to a doctor’s receptionist instead of filling out forms. Also included are my doctors and their phone numbers, the local ambulance number and my nurses including their home numbers, cell phone and work numbers. My wife’s cell phone number is there since she is my health care proxy, has Power of Attorney and knows where my Living Will is kept.

The opposite side contains more medical information including my address, phone number, date of birth, height, weight, blood type and other unique medical conditions I have. Below that I have a list of previous surgeries including dates and the hospitals where they were perform. The bottom half of this page includes a copy of my Medicare card my secondary insurance card (front and back) and finally a copy of my enhance New York State non-driver license which can also serve as picture identification.

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