Tag Archives: disability

If you don’t like challenges, you’ll never thrive.

Life is full of challenges, but when a disability strikes there are even more. Then it can be challenging to like challenges.

If you don’t like challenges what are you to do?

You can crawl in your cave and hide, but cave dwelling went out of style a long time ago. I wonder why? Could it have been that caves are sort of cold, dark and damp?

Then maybe you could crawl out of the cave and enjoy the sun. There are so Many things you can enjoy when you take on the challenge of getting out of your cave.

This is how you start enjoying a challenge. Pick a simple challenge to start with, one that might even bring you some joy. Remember though, you need to realize that you took on a challenge and prevailed. Then remember how many days you couldn’t even do it?

Next you can set a bigger challenge like gathering some firewood while you’re out. That way you can warm your cave. Doing this will also light your cave and cook your food.

Next time you go out you might even see if you can get some food to cook on the fire.

After having the first hot meal in a while you can sit back and enjoy how it feels. You set some goals and now you are enjoying the benefits of taking them on.

Taking on too big a challenge can lead to failure and frustration. So set a simple challenge to begin. One that will reward you when it is done. It also needs to be measurable. So be sure to measure things like how long you are out of your cave, the amount of firewood harvested and the amount of food collected. I doubt that you will get fat and sluggish anytime soon.

While you are out of your cave you might also see other people and invite them to join you. That could be fun and might get you invited back to their caves.

But don’t focus on the fact that some days it might be cold and rainy when you leave your cave. As you collect firewood you will have to go farther and farther from the mouth of your cave. That means you will have accomplished more just to make the same fire each day. Celebrate that you are growing stronger and more capable by venturing out of your cave.

While you are out look around and see what else you might do. Can you set a goal for next week or month?

If you can do this you will learn to like challenges.

You will have:

  • taken on a real and achievable challenge
  • measured the challenge
  • enjoyed the feeling of success
  • gradually increased the difficulty of the challenge
  • shared the success of the challenges with others
  • set harder and harder challenges
  • Then you’ll learn to like challenges.

So why are you still in your cave?

What challenge did you meet today?

What challenge will you set for tomorrow?

As all Ways, Seek Joy,

How to deal with a Disability in a Marriage with Ana Loiselle

Relationship coach Ana Loiselle talks about how an illness or disability affects a marriage and how to cope. We explore what sorts of situations arise in a marriage when a chronic illness or disability occurs. This can be with a parent of an adult child or a marriage partner.

We also explore how the brain can be retrained to learn new habits. She uses a method called Habit Coaching.

She offers an 8 week onlne course to strighten relationships.For more information r to sign up for her 8 week course click here.

David Shadbolt the benefits of overcoming addiction and depression

To overcome his alcohol addiction he had to address the emotional and spiritual wounds of his adolescence. This led him to deeper spirituality. He talks about the cost of a relapse. When he asked God to take his addiction he became free of it. He now benefits from 30 years of sobriety.

Once sober, he found he also suffered from depression. Since about age 10, he lived with a low level of depression. He lived with a glass half full. He drank to laugh. To overcome this, he used professional help.

He and his team now help midlife and older adults achieve peak fitness. Not just physical but mental and spiritual fitness as well. The team includes a nutritionist and hypnotherapist. Much of it is online, check them out at http://www.peaksymmetry.com

Can the Disabled “You” Thrive?

It may seem like an oxymoron to say a Disabled person thrives, but is it? Disabled may mean not “able”, but it does not mean dead. “Thrive” refers to how we are living. Can’t we live a full and abundant life with fewer abilities than most?

Can a person with a disability have the same traits as other Thrivers?

Let’s go thru the 8 traits of Thrivers and see.

  1. Thrivers are aware of their situation. Often we get so caught up in our inabilities we forget what is happening around us. Is this good for us? Pause for a moment and think about what is going on with you. Close your eyes and tell yourself what is happening to you. Then notice how the people around you feel? What do they need. If you can answer these questions you can be aware of what is happening around you.

How did you feel as you created this image? If you are like me your aches and pains subsided if not ceased. So, not only can you do this, it is more pleasant to adopt this trait of thriving.

  1. Being optimistic or just oriented to the future: when we struggle to get thru the day it is hard to contemplate the future. Yet, as you pause to look back, can you see that things have been worse? I certainly can. The things I struggled to do a year ago are now easy. I have made progress. In the last day I have found a resource to do something I struggled to do several times over the last month. What difficulty have you resolved in the last month? Is it safe to expect that you will overcome some of the things you now struggle with? You, too, can see a better future. You can be optimistic.
  2. Enjoy a challenge: That thing you struggled with and overcame in the last month might not have given you joy while you were struggling with it. Can you find joy in the fact that you overcame it? I certainly can. Let’s learn to see obstacles as chances to thrive.
  3. Friendly: what does it take to be a friend? Is it not about taking a moment to focus upon those around you and see what they are doing and what they need and then trying to meet those needs. A simple smile can go a long way toward being friendly. You don’t need to have deep heart to heart conversations with everyone. If you tried it might wear you out very quickly.
  4. Willingness to try new things: this can be hard when you struggle to do just the simple things. Could we change this to, “being willing” to try doing things differently?”

Doing things differently is a must when we can’t do things the way we were used to doing them. Willing or not we must do things differently. Sometimes simply not doing things at all is different from trying and failing.

  1. Willingness to share our creativity: Creativity is the trait we use to survive. There is no one around us telling us how to do it. Yes there are resources but we must seek them out and find a way to use them. Are you like me; willing to share your ways to be creative with others?
  2. Can find a purpose in life; this is challenging when we often wish to escape the pain we find ourselves in each moment. For example, the way Brandt Morgan found the purpose in his life was by reaching out to others. By doing this he found that he was overcoming the pain of the moment. See hiss podcast episode in disability Freedom.
  3. Are connected to more than just the physical reality: this means we are spiritual. When the physical reality in which we live fails us, where else are we to turn. When I turned to the non-physical I found such warmth that I longed for more. Since then I have glimpsed it in several moments. I have learned to just pause and let God connect with me. How have you experienced the spiritual dimension of life?

In what ways do you know to Thrive?

When do you feel you are Thriving?

As All Ways, Seek Joy,

Coach Dr. Dave

PS, this is the first in a new blog series, learning to Thrive with disability

We all have different abilities, so why are some of us, “disabled” and others not?

We all have different abilities, so why do some have the “disabled” label and others not? Maybe we should start by defining a disability. Going to the internet we get the following definition of a disability: “a physical or mental condition that limits a person’s movements, senses, or activities.”

According to this definition many of us are disabled. We all have limitations. Can you throw a ball as well as a pitcher? Can you run a four minute mile or a marathon?

Yes, I am comparing us to the best here. It might be better to say a disability is a physical or mental condition that prevents a person from performing in life as well as most others.

If we look at conditions individually we are hard pressed to find any single condition that uniformly disables people.

Take blindness for example. There are many who see nothing at all and function well in society. There are musicians, speakers, and even a Governor who cannot see.

Then maybe we should ask why those with a condition that disables most people doesn’t disable them? . This is the question I am exploring by interviewing such people in Disability Freedom.

Some of the things I have found are:

  • An attitude of being “able.”: This is apparent in how some who were born blind just went ahead and did what they wanted. I remember the story of a three-year old blind girl getting stuck in a tree. She got up in the tree by herself, but like many three-year olds she could not figure out how to get back down.
  • Parental support: Children who overcome significant limitations can usually point to one or more parent who was there to insure that opportunities were found for the child to do things. They would see to it that the child was taught the necessary adaptive skills to do school work.
  • Options to do things: Lewis Braille had to invent the writing code that bears his name. He didn’t invent it so he could take notes. He invented it so Napoleon could send messages at night. However, Lewis was blind and lived with other blind children. His braille writing system soon caught on and the rest is history.
  • Community support: Lewis Braille had been sent to a school for blind boys. This school had been set up and run by adults. He (like many other blind boys) learned to play the organ. That was a common occupation for blind persons in his day.
  • Social supports: having people around when we need help is universally important. Parents ensure that their children have the opportunity to play with other children. Schools and clubs provide these contacts.

All this is find for children, but how do adults who develop a condition that might disable them in some way continue to function?

The biggest disabling factor is attitude. The Rep. John Boehner who says he has both a bad back and anxiety clearly does not want to stop being in the public eye. He has the idea that he is not “disabled.” He is able to compensate. What sort of abilities does it take to get elected and stay elected? Clearly, he is able to read people and influence them. Many others tried to get nominated and elected but he is the one in office. He could be a politician working from a wheelchair the same way FDR did.

How many of us have exceptional abilities that allow us to function in spite of a disabling condition?

The resource of a parent is lost once we become adults. Some of us replace our parents with mentors. That role has to be sought out and agreed upon by both people. Mentors are a new concept in our society. I would have done things differently if I had a mentor earlier in my medical career. My failing eyesight might not have been so much of a problem. I would have been doing a lot of administrative things that I avoided early in my career. The lack of those experiences prevented me from getting interviews for medical administrative roles.

Options to do things differently: We live in a time when each day brings new options. A Few months ago I added an app to my smart phone that allows me to take a printed page or a sign and have my phone read it to me. Soon my phone will also be able to read US money to me. I know about these because I have been able to gain membership in a supportive blind community.

The third way a child overcomes a disability: Community support systems are available to those of us who are adults. There are vocational rehabilitation services in all states. They are limited in that they are funded primarily to put people into jobs. For many people that is the least of their problems when a disability hits. There whole social support system crumbles.

For those no longer seeking to work there are limited funds available for their rehabilitation. Rehab. Services can help people learn to get around or use adaptive software on a computer.

There is no formal way to recreate a social support system. Your family will always exist. However, how many of your family members know anything about living with a disability, especially the one you have?

Where did we get our support system originally? I met my wife at a summer job while I was in school. Most of us met our life partners either at school or work. Now there are on-line dating services. Do they help to find those who will support someone with a disability? This weekend I met three people who found someone to marry that way. Two of them are blind.

There are organizations of persons with almost any kind of disability. They are both in the community and on-line. Facebook has many such groups and a review of the posts shows that Facebookers are supportive of each other.

So a Disability is a condition you blame for not being able to function. Not being able to function results from so much more than one condition.

As you can see learning to live with a disability is complicated. That is why I focus my life coaching upon those with disabilities.

As All Ways, Seek Joy,

  1. Comments and sharing my blogs are welcome. Who do you know who is struggling with their decreased abilities?

How to succeed with a challenge when disabled

When we have a disability in our lives we often feel just living is enough of a challenge. However, taking on additional challenges can make the “challenge” of disability seem minor. That’s right! Trying to do more, not less, can make it easier to do the normal things.

Why you should take on a challenge in spite of a disability.

When we live with a disability we often find ourselves stuck in a sort of purgatory. Because we know that we have limitations we don’t try new things. That leaves us stuck without the thrills of achievement.

If we accept the label of “disabled” we will have disabled our lives. When we were children we couldn’t’ do many things, yet we still tried. We would ride a bike even if we fell off the last time. So why don’t we keep trying after a disability. Yes there were many times we fell off the bike, yet we were usually able to go farther each time once we got back on. Each incremental improvement kept us trying to ride, so why is it that as adults we accept failure when the first attempt doesn’t go well?

There are several reasons why we might not try a second time, but none are valid. You should expect to do better with second and subsequent attempts. You should be able to gain both skill and knowledge with each failure. The fact that you keep trying defeats that self-image of a failure.

Now that you feel like trying, what should you try?

Here are guidelines for what challenges to undertake:

  • Choose a challenge that excites you. Bike riding is exciting. That was one of the reasons we kept trying.
    • The challenge needs to make you focus. You did not worry what you would watch on TV after you rode your bike.
    • The challenge needs to keep offering you room to improve. Once you could ride the bike downhill, you then had to learn how to turn around and ride it back up the hill.
    • The challenge needs to offer you milestones. Bike riding had those, ride down, turn, and ride up the hill.
    • Each step along the way needs to make you feel you accomplished something.
    • You get to share your achievements. Initially your parents were there to cheer on your bike riding. True they also picked you up and tended to the scraped knees.
  • You need to be able to focus upon the process. You looked forward to each attempt to ride the bike. Then riding the bike became a joy in itself.
  • To really get your life going as an adult you now need to set challenges for yourself each day, week and month in the various areas of your life, physical, emotional, social, and work. Yes, you need to pay attention to all these areas. Would your life be fuller if you lost weight, found more reasons for joy, made more friends, and did a better job at work?
    • Don’t expect to conquer your challenges alone, you did not learn to ride that bike by yourself, so why should you go it alone now?

So, ask yourself:

  • What will be the next bold challenge I undertake?
  • What challenge did I avoid because I feared how others would react?
  • What will be the challenges I will choose each month for the rest of the year?

Now make your plans and get your team together. I have assembled a team to help me with this blog, the podcast, “Disability Freedom” and to find ways to reach more with these two mediums.

As all ways, Seek Joy

Ps this is the eleventh in the series on making a disability your biggest Gift. They are based on Brendon burhcard’s book, The Charge

 

How to succeed with a challenge when disabled

When we have a disability in our lives we often feel just living is enough of a challenge. However, taking on additional challenges can make the “challenge” of disability seem minor. That’s right! Trying to do more, not less, can make it easier to do the normal things.

Why you should take on a challenge in spite of a disability.

When we live with a disability we often find ourselves stuck in a sort of purgatory. Because we know that we have limitations we don’t try new things. That leaves us stuck without the thrills of achievement.

If we accept the label of “disabled” we will have disabled our lives. When we were children we couldn’t’ do many things, yet we still tried. We would ride a bike even if we fell off the last time. So why don’t we keep trying after a disability. Yes there were many times we fell off the bike, yet we were usually able to go farther each time once we got back on. Each incremental improvement kept us trying to ride, so why is it that as adults we accept failure when the first attempt doesn’t go well?

There are several reasons why we might not try a second time, but none are valid. You should expect to do better with second and subsequent attempts. You should be able to gain both skill and knowledge with each failure. The fact that you keep trying defeats that self-image of a failure.

Now that you feel like trying, what should you try?

Here are guidelines for what challenges to undertake:

  • Choose a challenge that excites you. Bike riding is exciting. That was one of the reasons we kept trying.
    • The challenge needs to make you focus. You did not worry what you would watch on TV after you rode your bike.
    • The challenge needs to keep offering you room to improve. Once you could ride the bike downhill, you then had to learn how to turn around and ride it back up the hill.
    • The challenge needs to offer you milestones. Bike riding had those, ride down, turn, and ride up the hill.
    • Each step along the way needs to make you feel you accomplished something.
    • You get to share your achievements. Initially your parents were there to cheer on your bike riding. True they also picked you up and tended to the scraped knees.
  • You need to be able to focus upon the process. You looked forward to each attempt to ride the bike. Then riding the bike became a joy in itself.
  • To really get your life going as an adult you now need to set challenges for yourself each day, week and month in the various areas of your life, physical, emotional, social, and work. Yes, you need to pay attention to all these areas. Would your life be fuller if you lost weight, found more reasons for joy, made more friends, and did a better job at work?
    • Don’t expect to conquer your challenges alone, you did not learn to ride that bike by yourself, so why should you go it alone now?

So, ask yourself:

  • What will be the next bold challenge I undertake?
  • What challenge did I avoid because I feared how others would react?
  • What will be the challenges I will choose each month for the rest of the year?

Now make your plans and get your team together. I have assembled a team to help me with this blog, the podcast, “Disability Freedom” and to find ways to reach more with these two mediums.

As all ways, Seek Joy

Ps this is the eleventh in the series on making a disability your biggest Gift. They are based on Brendon burhcard’s book, The Charge

How you can be competent with a disability

One of the key things we lose with a disability is our competence. There are so many things we can no longer do. Tasks we mastered years ago are now impossible. How can you ever expect to do the things you used to do? Or even do some of the simple things that would help you get through the day?

I used to feel that way, too. I felt incompetent. Then I looked around and found many people doing many things that I did not think were possible. Yes, blind people don’t drive cars, but there are so many other things they can do. Recently I found a blind internist (that was the role I performed as a physician). If I sought him out I am sure I could learn his tricks and regain my clinical competence. There are ways to get your competence back!

What is competence?

Brendon Burchard defines Competence as, “our ability to understand, successfully preform in, and master our world.” As adults facing a disability most of us still understand our world. Yes, we discover that there are many things we had overlooked. How others respond to my disability has been eye-opening. I feared that others would take advantage of me. Instead I discovered that most people wanted to help.

What disability takes from most of us is our ability to perform many tasks. We don’t lose all of our abilities, but many key ones. The loss of abilities can cause us to feel that we lost our identity. I used to see myself as a runner. Now when I have trouble seeing obstacles and responding to them in a timely manner when walking, I am afraid to run.

Want to regain your competence?

What parts of your identity have been stolen by your disability? Pause and make a list. Include in that list the areas of personal care needs, job talents, and professional/social skills.

Why is competence important?

This may seem like a silly question. As you began the review of your list of lost skills you probably felt a loss of confidence, too. When we find we can’t do something we are afraid to do other things. When I couldn’t run I was afraid to ride a bike. In fact I did ride a bike and managed to crash it and hurt myself.

The loss of competence leads to a loss of confidence. This loss of confidence can also lead to many other things as well. When I couldn’t do one thing I hesitated to try other familiar tasks. There is a light switch that needs replacing. I have yet to try this familiar chore.

I have done many fix up chores around the house. To spend time among others I went on a Habitat “Build” project. There I was teamed up with another man to cut and install the floor molding. He had never done this before. I found myself trying to tell him how to cut the molding. Cutting molding is complicated because you have to visualize how the peace will fit with the others and then figure out how to cut it. Often you have to place the board upside down or backwards to the way it will ultimately fit. After a while I found myself just cutting the boards. Yes I feared I would cut a finger. but all ten fingers are still intact.

This experience gave me some of my confidence back. I found I still possessed a competence that was valuable. I started the day seeing myself as a helper and finding myself as the leader.

With the feeling of confidence we are apt to try new things, or try old things we were afraid to do. I discovered new ways to hammer a nail when I couldn’t see how to hit the nail on the head.

Competence also determines how quickly we bounce back from setbacks. When I watch football, I see this all the time. When a team makes a first down, it is apt to keep making progress. After that, there is usually some event that stops the drive. It is not the fault of the offense, but a sack, penalty or interception. Success breeds success.

Want to regain your Competence?

Make a list of things you know you can still do. Which ones can you do masterfully?

Acknowledge yourself for what you can do. Doesn’t that feel good?

Now let’s build our competencies up even >

A few weeks ago I talked about our dreams. What are your dreams? Now let’s start to make them come true. Make a list of the things you would need to do to achieve your dreams. Which ones are on the list of competencies you just made? Which ones do you need to develop?

Now make a plan to develop those competencies. Here is how to do that.

  1. Make a relearning schedule: Pick small tasks that you feel unsure about being able to do.
  2. Write them down in as specific a form as you can. How can others observe your progress? When will they be completed?
  3. Get a coach to help you. This can be a friend or a professional coach, (those focused upon life, career or health will have the most expertise in helping you).
  4. List those reasons that come to mind that make you feel you will not be able to achieve them. Now, with the help of your coach address each of these excuses.
  5. As you make progress, celebrate. This is very important because we need to see that what we thought was impossible we are getting done.
  6. Keep all this in a journal. That way when you feel stuck you can review and see your progress, reflect on the strategies learned and create new ones to overcome any new obstacles.

Now you are on your way to regaining your competence!

As All Ways, Seek Joy,

  1. Share this with anyone you know who might feel incompetent. Let them know that this is part of my series on how to thrive after a disability. You can find the other blogs by clicking on the category link to the right. If you have not signed up for my Newsletter do that too, and be sure not to miss any of the Upcoming blogs and other helpful materials.

 

How to reestablish control in your life after a Disability

When a disability enters your life you will lose control. There will be things you are no longer able to do. That is what a disability is. However control is essential for thriving in life.

Why reestablish control in your life after a Disability?

Control is one of the drives that are essential for one to thrive in life. Brendon Burchard in his book, The Charge, calls this being “Charged.” He lists 10 drives that are essential. This is the first blog about these drives.

We have sought to control our lives since infancy. When we learned to say “No” we used it constantly. It drove our parents crazy, but gave us control. We could stop what was going on. As soon as our parents realized how we would respond they asked questions so our response would be aligned with their wishes. Then they, too, had control again.

As we grew we sought to control more of our lives. This lead too many confrontation’s with our parents. We would refuse to go to bed even though we were just about to fall asleep where we were.

When we lose control we try to control what we can. When I rotated through Pediatrics the children suffering from cancer would choose who would draw their blood and do other things to them. This was one way they could control part of their lives. They would still feel the pain of a needle, but they would have someone of their choosing using the needle.

As my eyesight failed, I knew I would have to stop driving. For years I would fail the eye test and get my eye doctor to fill in the form. I realized that this would only work for a while. I decided that I did not want to hurt someone else due to my poor eyesight. Thus, after a very close call, I prayed on the issue. The answer came almost immediately with another near miss.

By choosing to stop driving I still maintained some control. I found resources that I did not know existed. A neighbor offered me rides to a civic group we were in. Others also offer me rides.

How to assess your level of control?

You can ask yourself three questions to assess your level of control (rate them on a scale of 1 to 10):

  1. How in control of your life do you feel?
  2. How in control of your emotions are you?
  3. How in control of the immediate world around you are you?

True, control is never absolutely all or nothing. There are times when no one can see – the lights went out. Even in the dark we can visualize what we feel and hear.

Since control is relative we need to establish references. But these references can either serve to trap us or let us thrive. If we choose references that trap us, we will be limited by them. When we choose references that let us thrive, they give us energy.

I could choose to define my eye sight as not as good as an athlete, or as it used to be. Or, I could say it is adequate to get around. And I can find the tools I need to supplement my poor eye sight. The latter lets me feel in control.

It is this feeling of being in control that is important. That is why the second question. Choose a reference that will let you score a 10. Don’t choose to compare your mobility to jelly fish.

Controlling the immediate world is what the kids on the pediatric ward were doing. By making choices and having them honored they were able to undergo things that could have left them in a tantrum and tears.

So, how do you get control of your life after a disability?

  • Look at your attitude: as the old phrase goes, “Shit happens.” What is shit anyway? Is it the bodies waste or fertilizer?
  • Do something new! As children we were always trying new things. Doing new and different things is “the spice of life.” Always doing the same thing is boring. So change your routine; eat something different, use a different route to get to the store, meet someone new.
  • Control what you can. It might be simple as choosing who does the procedure, but find a way to control.
  • List the things you can do.
  • List the things you just did.
  • Schedule some simple tasks before the hard ones.
  • Challenge yourself to come up with new and novel ways to do things.
  • Add to this list.

 

As all Ways, Seek Joy,

 

PS, when you are in control you are ABLE!

How to Envision your Dreams after a Disability

As we fight to recover from a Disability we need to envision ourselves again. Before the disability struck we all had a vision of who we were. When the disability struck, that vision ended up shattered. The self-vision served us. Now we need to create a new self vision.

Why is a self-vision important?

Self visions are important because they serve as a reference when we need guidance. How did you see yourself before your disability struck? You were probably capable and self-sufficient. You might have been a leader or a caretaker. If you saw yourself in those roles, you would feel comfortable doing those things.

As someone who was self-sufficient you did not ask for help. You would step forward and do what you needed to do.

As a caretaker, you would step forward and help others. You would take opportunities to learn how to care for others. Did you take first aid classes? Would you step forward and offer that first aid to those in need? If your help was rejected, would you take it personally? I did.

Now that you are disabled can you still help others? Is it hard to accept the help of others? These feelings come about because you can no longer live up to your self-image.

Your self-image gave you permission to do and act in certain ways. When you acted in those ways you felt good about yourself. When you failed to live up to your self-image you felt bad about yourself. That is one reason you feel bad when you are disabled – you can’t live up to your self-image.

How to create a new self-vision

Our self visions come about from the messages we receive from others. I was the oldest child, and thus told to look out for my sister and brother. When my sister started school, I was responsible to walk with her and be sure she got to and from school safely. Now, that our parents have passed on, I am even more aware of how they are doing. I still think of myself as the big brother, and now also as the Patriarch.

I now am disabled and not in contact with my sister and brother very often. They live in other states and care for themselves and their spouses. They would probably say they worry as much about me as I do them. Both ways, that worry does not take up much of our time or effort.

Day to day we need a clearer self-image. How I interact with my wife and those people I meet each day is the real result of my self-image.

Some questions I had to ask myself as I accepted my disability are:

  • Would I admit to be disabled?
  • How would I react to others help?
  • Would I fear others taking advantage of me?
  • Would I still seek ways to help others?
  • Would I still accept responsibilities and serve in organizations?
  • What would I do at home?
  • How would I do these things?

As I pondered these questions, I allowed myself to act in various ways. I resisted carrying a white cane. Then I realized that I could not walk about and feel safe without it. Carrying it told others that I was different (it is surprising that not everyone knows what a white cane is or means).

We fear that others will take advantage of us because we admit to being blind. I was asking for help, when I was used to being the helper. I am pleasantly surprised how comforting it is to have others looking out for me. Yes, I feel guilty about accepting a seat on a bus, when I can stand just as well as others. Also there are places on the bus where it is easier to hear the driver announce the stops than in the front. They have PA systems. I also like to sit facing forward. The sideways seats strain my back.

To find out whom you are after a disability you need to try out the various roles. You need to evaluate how well you feel you do in those roles. Are their skills you need to master? Should you just let those roles lapse? How do you feel about those options?

How do you see yourself now? Do you want to be happy and self-confident? Or are you willing to be a crippled shell of who you were? Now that you have some idea of whom you will become,

How will you use your new self-image?

Self-images have many forms. There is the mental and emotional image I have been talking about. However, these images show up in many places. Every time we post on Facebook and elsewhere on the web our photo appears. This might be called a logo or avatar. It shows others how we want to be seen.

How often do people replace their headshot with a photo of family or friends? Some even replace the photo with another image. That is the way they show up each time they post on Facebook. It is their avatar.

While we don’t use animals or other images on Facebook, they are convenient ways for us to see ourselves. What animal were you? Take a moment to put a name and recall that animal.

Now what animal are you? Is that the animal you want to become? If not what animal do you want to become? How does that animal act? How do you feel when you think about being that animal?

Once you have decided upon what animal you want to be, what attracts you to that animal. How would that animal act? Do you need to change anything about your present self to become that animal?

This envisioning is what Life coaches help people do. If you want help with the process set up a consultation and see if I would be a good Life coach to help you with this. There is a sign up box in the right sidebar.

As All Ways, Seek Joy,