I have to begin our story with the fact that I am a retired principal from a very progressive school. My wife is a Special Education teacher. Together, we have spent the past 30 years helping students with a variety of abilities to learn, encouraging them, helping them to grow, developing parent understanding and creating a positive environment for them to experience failure and to succeed. We have raised two sons that are on their way to successful lives.
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Two years ago, I was only the third parent to post a blog on the NVLD Project website. It is so wonderful to see how many people have found it and now know that they are not alone.
I would like to share with you the many ways Anna has progressed because so many of the people who have contributed seem to be discouraged.
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One of the most perplexing things for me about having NLD is trying to navigate the subtleties of making friends. The question of whether someone is being friendly versus trying to be my friend is something I’ve struggled with my whole life and it’s only gotten harder as the world develops a more casual, laid-back attitude toward each other, so I thought I’d write about it in order put it into words, (which is something us NLDers need), in order to help myself work through it and find some similarities between my already established friendships.
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My name is Robin.
I finally got diagnosed with NVLD when I was 39 years old.
The only reason that happened is because my son was diagnosed with PDD Autism and I asked his doctor who did the neuropsych: Do you know a doctor who does these tests for adults?
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Have tried as best I can with and translate my story from Norwegian to English.
I hope to be able to give others an understanding of NLD, a Functions derogatory who can provide a lot of invisible, despite the difficulties that I have problems with writing, with to get it to look good, and to put it function into a context. I have e therefore decided to write a little about my experience with the NLD.
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Michaela, a Project Social Ambassador, spoke at The NVLD Project’s Benefit Cocktail Party about her experience with NVLD and what the work we are doing means to her. She shared this poem at the end of her speech and we wanted to share it here as well.
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I wasn’t diagnosed with NVLD until the last semester of my senior year of highschool. I’d been seeing a counselor for years but she had retired and I had started seeing a new one who immediately asked if I knew about NVLD, I didn’t. I’d always struggled with my handwriting, coordination, and interacting with others but just thought it was because I was just odd but as I learned about NVLD I realized that the descriptions I was hearing sounded familiar.
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People have always been surprised by my memory, both what I do remember and also what I don’t. I can’t remember where I parked my car, but I can remember when your birthday is. I can’t remember how we set up the room for that event, but I can remember that story you told me about how your parents said they were getting a divorce at Thanksgiving and now it’s completely ruined for you forever. I can’t remember how much rent is going to be for this month, but I can remember how people used to make fun of for your stutter, even as you were just trying to make friends and fit in. Read More
In the 2nd grade or 3rd grade the private school I attended administered the CTP (Comprehensive Testing Program), or as my peers and I nicknamed it the Child Torture Program. I always seemed to score very poorly on these tests year after year but the teachers were unsure why since I was a bright child who seemed to be succeeding in school otherwise. I was always very talkative in class, often times I would get so excited that I would interrupt the teacher or my peers even though it was unintentional. And on unit tests in various subjects I seemed to do well, although I always had to work harder at math.
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Having an NVLD can be very complicated as it is a learning disability that also presents challenges outside the classroom. You may have difficulty reading a map, managing crowds, and not being able to drive. For these reasons, for someone with NVLD, living near a city can be extremely helpful and yes, still challenging.
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