My name is Sue Boman. Yes, that’s me in the picture posted here. I have called this blog White Cane Connections because I am one of the many people who use a white cane. I began this blog because I wanted to write about a project I undertook in 2012. The plan was to complete a series of walks using my white cane. Between March and September, I walked in 82 different locations across Canada. So, the blog begins by telling of my experiences and the many people I met along the way.
While this particular journey has now been completed, I find that I still have much to write about. I am continuing to make new white cane connections, and so for the time being I will continue to add regular posts to this blog. I am hoping that you will be a partner in the journey.
Sue
Friday, 28 April 2023
April 28 - Tunisia
Sunday, 23 April 2023
April 23 - Low Vision Badge
At
home, when I go about my everyday life, I try to avoid drawing
attention to my sight challenges. When we are travelling, the opposite
is true. I use my white cane and I wear a low vision badge. If we are
travelling by plane, ship or tour bus, I register as a legally blind
passenger. I do this all for my own safety and to protect others. I
don’t want to bump into people or things that I can’t see. I don’t want
to trip or fall. Last Thursday, Lyle and I
flew from Calgary to Montreal, connecting on to a flight to Rome. In
spite of preboarding with my white cane, wearing my low vision badge and
being listed as blind on the passenger manifest and boarding card, I
wasn’t given a safety briefing nor did I receive any other attention to
my special needs. The second leg of the trip started in the same
manner. Then about twenty minutes in, and observant flight attendant
noticed by low vision badge. Kimberley crouched beside me to ask if
there was any way she could offer assistance, adding that she would
alert other crew members to my situation. This was helpful when the
lights were dimmed or when the meal was served. I
sometimes wonder if wearing my low vision badge is a bit of overkill -
but obviously not. It was interesting to me that it was the very
smallest thing that was a signal to my sight disability. | ||
Friday, 14 April 2023
April 14 - Vision and Travel
Over the past few days I have been chatting with friends about travelling. If you have been a reader of this blog, you might have guessed that travel is one of my favourite topics of conversation. I truly enjoy going to new places and having experiences that are out of the ordinary. In saying this, I must admit that Lyle and I both realize that we are fortunate to be able to travel as much as we do.
Anyway, as I was speaking with one friend, she explained that she was too nervous to travel any more because of her diminished sight. Now, I know that this friend has an eye condition that might mean even more decreasing sight in the future. I asked her if she wouldn’t want to use what sight she had right now before her ability to see decreased even further.
Seizing the present is definitely my own philosophy. Certainly there are some anxious moments when I am out of my comfort zone but to face the challenge is exhilarating in itself - especially when the experience ends up being a positive one. Even with failure, I can feel a certain satisfaction in knowing that I have tried something new.
Traveling with my white cane has only served to add a new dimension to the travel experience. Perhaps I will write more about this in my next post because by next week we will be on the go again.
Thursday, 6 April 2023
April 6 - Peer Support Groups
Yesterday at our support group meeting, our guest speaker was a retired optometrist. Dr. Perry gave a very interesting presentation about macular degeneration. It was good to get the facts and anything relevant in the terms of latest research. We learned of the difference between dry and wet macular degeneration and what we might expect with each. Dr. Perry stressed the importance of preventative and stabilizing measures. I think that we all learned something from his presentation and it was surely more gripping hearing it all in person rather than reading the same information on a brochure.
After the presentation, of course we had refreshments. In some ways that is the most important part of a support group meeting. The coffee time gives us an opportunity to chat and share with each other.
While vision loss can be explained from a clinical point of view, the impact on the individual is very much emotional. Vision loss, whether it is sudden and dramatic or slow and gradual, can point the way to a different way of life. I believe that peer support groups can be an effective tool with this journey. Even though I lead our local support group, I gain as much from the other members as anyone else in the group.