Hello, World!

I guess a good way to start is to tell the story behind the blog name.  My husband Zach is legally blind, and I love him.

Zach has a genetic degenerative eye disease called retinitis pigmentosa (RP).  Usually, RP causes vision loss in a person’s periphery, resulting in tunnel vision.  Zach’s case, however, is a little different.  He has islands of sight all over his field of vision.  His brain fills in the leftover blind areas, so he perceives a full picture, but can’t really trust if what he sees is accurate.

The progression of RP is highly unpredictable, but vision loss usually occurs over time, sometimes culminating in complete blindness.  In Zach’s case, he lost a lot of vision around age 14, but has been pretty stable over the past several years.  We hope he won’t go completely blind, but we will just take it one day at a time and make adjustments to our lives as needed.  And even if he does lose his remaining vision, it wouldn’t be the end of the world – with the right training, blind people can do pretty much everything sighted people can do!

Depending on how you look at it, Zach’s vision is either no big deal or a huge deal.  It’s no big deal in that the things that make people happy are not really dependent on vision.  Our relationship is great because of love, respect, communication, commitment, shared values, humor, and, most importantly, our faith and redemption in Christ.  None of those things necessitates vision.  Zach is able to work and pursue his interests with no problems.  There are little ways we have adapted our life to deal with his deteriorating vision, but they are really not that hard.  Zach can’t drive, so I drive us places, and we live close to public transportation so he’s not completely dependent on me.  We have a special way of walking together (an adapted version of the sighted guide technique), and I try to verbalize when we approach steps or other obstacles.  At mood-lit restaurants I read the menu aloud.  Sometimes drinking glasses are accidentally knocked over and broken, but we just sweep it up.  Easy adjustments to make.  No big deal.

In another sense, though, Zach’s vision is a huge deal.  The adjustments I’ve talked about are easy enough, yes, but they also indicate that blindness affects nearly every aspect of everyday life, and constantly dealing with that reality can be exhausting.  It can also be difficult for outsiders to understand.  Zach wants to be known for who he is (which is an amazing, smart, funny, interesting, handsome, godly man!), not for his blindness, so right now he chooses to walk without a white cane (the international symbol of blindness).  It’s not that he’s ashamed of being blind, or even that he doesn’t want people to know, but he’s afraid that with the cane, people will treat him differently.  And there’s a reason for that fear: people do treat him differently.  Eventually, he might have to carry the cane, which would be fine, but for now since he can get around without it, he chooses not to use it.

I think the biggest obstacle for Zach is the social effects of blindness.  He does not have access to the social cues we sighted people take for granted.  Facial expressions are completely lost.  When most sighted people try to imagine being blind, they often think about how difficult it would be to walk around without running into things, but those skills can be learned easily and are not the true onus of the blind person.  Imagine sitting in a circle with your friends (so there’s no risk of running into anything or anyone) and trying to relate to them with your eyes closed.  That would be hard!  Now, imagine sitting in a big circle with a bunch of strangers and trying to make friends with your eyes closed…for me, a born-and-bred introvert, that sounds like torture!  It also sounds incredibly exhausting.

Zach has had most of his life to process and accept his vision loss, but all of this was introduced to my life fairly recently, when we met in 2011.  So I feel like I’m still learning and processing what his vision means for me, for our relationship, and for our future.  This blog is designed to document my process and experiences in being married to Zach, my legally blind love.

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5 thoughts on “Hello, World!

  1. Hi, Miriam! I just came across your blog via FB and was struck by the similarity of our recent histories. I am married to the most amazing, godly man, and he is blind. He has congenital glaucoma (born with glaucoma) and has extremely limited vision. I would love to talk with you more about your experiences if you’re interested. I really appreciate what you’re doing by communicating and correcting common misconceptions, etc. with your blog. Take care and many blessings, Tiffany (Swann) Schmidt

    • Hi Tiffany! Thanks so much for your comment! Yes, I would love to talk with you more – please email me! There seems to be a lot of online support for the blind and parents of the blind, but less support for us spouses. I’m excited about the blog as a place for me to go with my thoughts and feelings on the issue, especially since I seem to go through a cycle, most of the time feeling fine, but sometimes feeling sad. I really look forward to talking with you more!!

  2. I’m so excited you have a blog!!

  3. Pingback: legallyblindlove | Born Blind vs. Becoming Blind

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