Sue packs a lot into each day, sometimes more than she should. When that happens, it’s like her body hits the…
Author: Linda Moore
Sue’s New Pages 2/17/2017
More about what goes into reading speed.
Reading Speed is NOT Speed Reading
Sue’s been waiting for over a year for notification that the stem cell trial she’s hoping to be part of is actually going to happen. Turns out it is delayed…again. But there is a second stem cell study and she’s hoping that it’s…
Sue’s New Pages 2/16/2017
In the year since we started the website, we have heard all kinds of inaccurate & misleading information that comes from a person’s eye doctor, especially from those who are not retina specialists.
Sue’s been reading about reading, specifically the factors that go into reading speed such as visual span (how far you ‘look’), eye movement and peripheral viewing.
Sue’s New Pages 2/13/2017
Thanks to questions from our followers & Facebook group members, Sue & I continue to learn about AMD. Thanks to a one of them, we found out about the variation in visual distortions and how they impact things like reading from the screen or printed text. Sue also shares that when her vision worsened about this time last year, she took time off from work to regroup.
We’ve talked about the results from the Vita Risk test. Now we review the additional information that most patients (those with early, intermediate or advanced AMD in only one eye) get when they have the Macula Risk test.
Sue’s New Pages 2/11/2017
Sue’s dad was an important part of her life. He was a GREAT man and gave her many positive traits and lessons. He did NOT give her AMD.
My turn, my genes!
Sue’s New Pages 2/8/2017
In yesterday’s page, Sue didn’t think she’d have a problem testifying in court. Today we find out what happened.
Sue continues trying to figure out what’s up with her genes.
Sue’s New Posts 2/6/2017
Sue talks more about her trip to Iceland. What will she remember about the trip?
The day that Sue got the results from her genetic test was NOT a good one, to say the very least.
Genetic Rant & Roll – The Miniseries: Part 2
Sue’s New Page 2/4/2017
Sue admits that she’s a ‘vision snob’. What does that mean? You’ll find out as she talks about how she decided that this was the year that she would SEE Iceland!
Sue’s New Page 2/3/2017
This page is from last September right before Sue & her husband took off for their vacation in Iceland. She’s done her homework about what anyone who is visually impaired will encounter in an airport.
What YOU Can Do for Low Vision/Macular Degeneration Month 2017
Sue & I thought we’d do something special for Low Vision/Macular Degeneration month so she’s written a letter that we are sending to our local print & online newspapers, bulletin boards, special interest publications. You are welcome to copy this letter and send it to YOUR local publications. If you do, let us know if you were published!
February is low vision awareness month. It is also Age-Related Macular Degeneration Month.
Age-Related Macular Degeneration, or AMD, is the leading cause of blindness in the developed world. It is found in ‘mature’ adults although there are similar degenerative, retinal disorders found in younger populations.
There are 2 million individuals in the United States who have AMD. This number can be expected to grow significantly as the population ages. The current estimate is 5 million AMD patients will be living in the United States by 2050. This is more than a two-fold increase in incidence. The need to care for these individuals can be expected to be a significant burden on families and community and government resources.
Wet AMD can be treated but there is no cure. Dry AMD, the more common form of the disorder, has no treatment and no cure. However, there are a number of encouraging clinical trials being undertaken around the world. A breakthrough is hoped for very soon.
In addition to the cutting-edge research being done in AMD, there are other reasons to be hopeful. Assistive technology has advanced greatly in recent years. There are many private and public agencies able to provide education, support, and, in some cases, materials to make the lives of the visually impaired much easier.
If you or someone you know has been diagnosed with a visual impairment, please contact your state or local visual services agency for help. You may also wish to contact a national organization such as the National Federation for the Blind.
Early detection is important. The National Eye Institute recommends that starting at age 60, everyone should have an eye exam through dilated eyes once a year. If you have symptoms of eye trouble, call your doctor right away.
There is help. There is hope.
