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Posts Tagged ‘Helen Keller’


I have been working for months and probably longer informally to learn new music. Music has and always will be a very important part of my life. Many Deaf people can’t understand that, but some do. I love how it makes me feel physically, emotionally, and mentally. Problem was that I couldn’t learn new music, so I sought to change that. The results I wrote in an article that went live today on Home and School Mosaics. I am putting myself out there for the world to see, not just on Home and School Mosiacs, but YouTube, too. That is a little scary because people could think I am seeking attention, but that is totally false. I hadn’t thought of sharing until so many people (without hearing me) insisted that I should to show what disable/handicapped people can do. I do share that now for that reason only and for the glory of my Lord and Savior. Don’t expect an amazing performance because my voice is just normal. Do expect to be shown that DeafBlind people can do and learn many things. Singing is just one of them. It really doesn’t matter if they learn to sing or not. It is only important to know that everyone can get something from music including the DeafBlind.

Please enjoy it for the purposes it was intended. ASL version is also provided.

http://homeschoolmosaics.com/music-for-deafblind-ears/

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I saw a blog post today from a friend that reviewed a book about Helen Keller. Because of my friend’s wonderfully worded description of the pictures I can tell you that the book is a great resource for understanding DeafBlindness. You might just start to “Get it” that DeafBlindness isn’t just adding deaf and blind. It is exponentially multiplied. So, I am going to give a little link love to my friend. Please check it out. There is no way, being DeafBlind, that I could have written a review with the descriptions of the illustrations and intent of this book so well. So, this post is to my friend at Mom’s Musings, http://hexwit.blogspot.com/2013/07/concept-building-and-coolest-book-on.html

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Laura Dewey Bridgeman

This week is DeafBlind Awareness Week! Helen Keller’s birthday was June 27th. She and her predecessor, Laura Bridgman, made advancements for all DeafBlind people. Both worked hard to overcome their disabilities to become educated. They both wrote and spoke about the needs of the disabled.
Today, there are approximately 100,000 DeafBlind children and adults. We all work hard to overcome the obstacles in our life. We all want to be as independent as possible. We all want to contribute to society and make the world a better place. We are capable of learning and doing many things. We prove that every day.
Sometimes, though, we need help. Education, training, assessable technology, support service providers, etc. are all expensive. There is also a lot of medical research going on to help improve our lives and even one day to provide cures for the causes of DeafBlindness. There are a few organizations that help the DeafBlind. Your support would be appreciated.
Helen Keller National Center for DeafBlind Youth and Adults in Sands Point, NY is the largest by far. They provide intensive training in all areas of a DeafBlind adult’s life. You can learn more about them at http://www.hknc.org.
The American Association for The DeafBlind is another. It is an organization run by the DeafBlind to help educate the public, government, etc. about the needs of the DeafBlind. They also work to provide support to the DeafBlind. You can learn more about them at http://www.aadb.org.
Another organization that helps to provide training and accessible technology to DeafBlind children and adults is DeafBlind Hope. DeafBlind Hope is a small non-profit, but over 99% of the donations go straight to the DeafBlind clients of DeafBlind Hope. We assist parents in learning how to teach their DeafBlind children and raise funds to provide training for adults. We provide technology to children and adults that is suitable for the individual needs. We also work to teach the public that the DeafBlind can do if given the tools they need to become independent. DeafBlind Hope is another organization operated by the DeafBlind for the DeafBlind. The CEO is Renée K. Walker who is DeafBlind and writes this blog. Yes, I am talking about me. I sincerely work every day to make the lives of the DeafBlind easier and more productive. We all just want to become as independent as possible and do our part in making the world a better place. You can find out more about us at http://deafblindhope.org
Please learn more about deafblindness and how it affects these children and adults. Consider helping one of these organizations. You will be bringing Hope to the DeafBlind!

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Well, today is the day I have a new post on Homeschool Mosaics! Please check it out. I think it is pretty interesting and informative. I enjoyed writing it, anyway. LOL http://homeschoolmosaics.com/mama-look-its-helen-keller/

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Well, the weather has been frightful, but I have seen more snow than I have ever seen before. Joey has never seen snow before. We had a ball playing in it. Joey running and sliding and I throwing snow over him. He likes to try and catch it.

Joey in the snow making shadows.

"Joey in the snow making shadows."

Snow in the HKNC yard

"Snow in the HKNC yard"


Training has been more practice of all that I have learned so far. I talk in sign everywhere pretty much. Tactual is still my best mode. In most classes, we are doing the final goals and filling out requistions for my state to authorize payment. I don’t know if my state will pay for everything I need or not, but I hope and pray they do.

Jesus has been at work this week through me. I just hope I rose to the occasion as He wanted me to do. One of my instructors actually came to me after hours and asked me to tell her about Jesus. I was ecstatic. How lovely it was to share my love and experiences with her. In case you are wondering, this is not the same person that I have spoken of before. That person is saved and I can tell the person has faith. Jesus has something for that person to do and needs to prepare. The instructor that came to me this week is not from a religious family. She doesn’t know Christ and isn’t even sure there is a God. I hope that I answered her questions, but I hope even more that Jesus was able to work through my answers. I am praying mightily for her to feel Jesus. I can tell that the Holy Spirit is calling her. I just pray that she will accept that call.

We also had a holiday party that was actually a Deaf party. It was fun, but loud. I turned everything off and I left Joey at the center with my friend, Ginger. Basically, they have these very large speakers and some are turned down on the floor so that you feel the vibrations through the floor, tables, everything. I could feel the vibrations all through my body. The Deaf use the vibrations to dance by. It was very interesting.

A friend, Peter, in his Christmas tux and his SSP, Carol.

"A friend, Peter, in his Christmas tux and his SSP, Carol."

Saturday, we had another party at a Sportsman’s Lodge near the Long Island Marina. We at HKNC were invited, but it was mostly for the many special needs children from the area. I loved watching the children and adults of various ages with various forms of mental retardation playing and laughing. They all loved Santa and were so appreciative of the hand-knitted afghans we all got. I was too. Mine was a gorgeous lavender, purple, and pink coloration. I really couldn’t see the colors, but the staff described it to me very well. I like those colors. Many of the children wanted to pet Joey. Some were afraid of him, but as usual Joey was perfect with each and every one. He always seems to know how to act. With those who were afraid, he laid down next to them and let them reach to him. With others, he reached up and gave a big “Joey kiss” which is very special, you know. The children’s faces shined as Joey poured out his love for all of them. The others danced for a while. I enjoyed seeing everyone loving moving their bodies to the music in any way they could. I, of course, can always measure my fun level on a scale of 1 to full blown asthma attack. The party made it to full blown asthma attack. Lovely… Actually, what happened was I didn’t know that the lodge allows smoking in the building where they have a bar in the back. There was no smoking at the time, but I can’t be around it at all, so after a couple of hours I couldn’t breathe. We did a nebulizer treatment in the van on the way back to the center. I did a couple upon my return. I eventually got better without going to the hospital. I was very thankful. I have had enough of hospitals for a long while.

Here is the HKNC Christmas tree in the lobby. Next to it is the large paining done by a former totally deaf and blind student. The picture depicts the scene where Helen Keller and Anne Sullivan are at the well with water running over Helen’s hand as “Teacher” as Helen called Anne, fingerspelled “W-A-T-E-R” into Helen’s other hand. Helen’s says this is the moment that her world became alive with the true understanding of language.

HKNC's Christmas tree in the Lobby along with the painting by a DeafBlind student of "Helen's Well.

"HKNC's Christmas tree in the Lobby along with the painting by a DeafBlind student of Helen at the well.

This is a close-up view of that painting of Helen Keller at the well learning "W-A-T-E-R".

"This is a close-up view of that painting of Helen Keller at the well learning "W-A-T-E-R".

It began to snow late Saturday night and continued all day Sunday. I got to go to church with my friend and HKNC interpreter, Jessica. Jessica is 24 years old, but very spiritually wise. Her parents and Jesus have done a wonderful job with her. Jessica is Pentecostal, so her church service was a little bit louder than the ones at my Baptist Church. I loved it though. I couldn’t hear the music, so it was hard for me to worship like I normally do. Jessica though tactually signed everything for almost 3 hours so that I could experience things. That may not sound like a big deal to you guys, but interpreting is very tiring mentally and physically. Tactual sign is even more demanding. The interpreters have very strict regulations for when they are working. At HKNC, they do interpreter switches about every 30 mins or so, because it is so demanding of them. Jessica interpreted for me almost continually for about 3 hours. I asked her about half way through if she wanted a break, but she said she was fine. Jessica never complained. That was very special to me.

Well, the good news is that I am beginning my last week here. I don’t know when my flight is yet, but I hope it is Friday, 21st or Saturday morning at the latest. I will update here as soon as I know. That will probably be my last blog, too, since I will have to pack and ship everything before I leave out. The experience has been wonderful, and I have learned so very much. I have friends that I can call lifelong friends, as well. However, I am ready to get home. I have family, friends, and students to get home to. Things will be different, though. Signing has become my main mode of communication, so I hope a few of my close friends are willing to learn some. I am going to need an SSP or Support Services Provider, too. Hopefully, we can find someone to fill that role. Anyway, more on that after Christmas. I just want to get home now. Little Joey wants to play with his sister and brothers and give Daddy a big wet kiss. I do, too.

Take care, everyone!

Renee’ and Little Joey

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I have been unable to post for a while now. I became sicker and sicker with my asthma. I had a migraine for the week after Thanksgiving working on a speech I had been asked to do as keynote speaker for a technology seminar. I never got to give it, unfortunately. Saturday afternoon, I was found on my bed semi-conscious. I had evidently gotten up and tried to ask for help earlier, but I don’t remember it. Little Joe kept trying to push me up and licking my face. His urgency is what got me moving at all I am sure. I spent Saturday thru Wednesday in the hospital with pneumonia and exacerbation of asthma. I had IV antibiotics and IV steroids. I was back at HKNC for 5 hours when they had to return me to the hospital. I came back the next day. I am still confined to my bed and unable to speak because I don’t have enough air, but it is getting better slowly. I am still on steroids. I will say that my signing is getting much better because I have no choice, but to sign everything. I also was unable to hear anything since being profoundly deaf, I have to concentrate to understand. I was totally unable to do that. The hospital had to bring in a tactual sign language interpreter for me. I was able to do it fortunately. God does provide in all things. Pray for me as my chest still hurts and I am still wheezing.

Thank you Jesus for Little Joey.

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Retro Look:

This week has been really great. I received a care package from my Sunday School class at Mabel White Baptist Church, and my son, Brian, flew up here to spend Thanksgiving with me. The care package had several items that I have needed such as lip balm and warm slipper socks plus some fun things including sugar free candy and a red University of Georgia cap. The cap was a nice touch. I really appreciated the package. I have a pic where Joey somehow managed to get the hat on his head when I had laid it on the bed next to him. He was so cute. Joey knows how to make me smile just like my friends at church.

Brian flying in was a nice touch, too. He went to classes with me on Tuesday and Wednesday. He asked my instructors questions, and they taught him some signs. The instructors explained to him all about my training and what we could expect as my vision and hearing decrease. Brian was very attentive, and all the staff here said he was a nice young man. They were amazed at how polite he was and that he said, “yes, sir and no, ma’am” to everyone. I was extremely proud of him, of course.

Thursday, my case manager-Molly- took Brian, Martin (another student), and I to have Thanksgiving dinner at the Miller Ridge Inn. It is a replica of an old inn that stood on the property and the history goes back to 1632. They have a replica town of shops that you can walk through as well. We took pictures at the stocks and listened to the band playing guitars and banjos. The food was very good, even the stuffing was good despite not being Southern cornbread dressing. Molly is very special. She really went out of her way to be with us on her holiday off, and I greatly appreciate it. I could tell that Martin, though quiet, really enjoyed it as well. I don’t think he ever gets visitors. I seldom see him talk or smile except when he is talking about sports. Martin is deaf-blind. He hears nothing, but sees a little better than me. He signs for communication; therefore, Molly signed everything we all said during the meal. Molly made sure he was included in everything. That takes a lot of time and patience, but she does it so well. God is truly using her for special work.

Brian, Joey, and I standing behind photo props making us look dressed in long dress and tux.

"Brian, Joey, and I looking dressed to kill."

Molly and Martin in the stocks like prisoners.

"Molly and Martin in the stocks."

Brian, Joey, and I in the stocks.

"Brian, Joey, and I in the stocks."

That evening Brian and I took dinner up to our room where we had an e-Thanksgiving over the internet on X Box Live with Scott and Brendan at home on their X Box 360. Their food was much better than ours, but the company was great. We spent several hours eating and talking after praying and thanking God for our many blessings. Despite being here and away from friends and family, I actually enjoyed Thanksgiving. You never know what the journey God has you on will bring, but it will always be enlightening and memorable.

I am standing next to the image of Albert Einstein.

It's just Albert and I.

I have only been to the city one other time. This past Sunday, we went to Madame Toussaud’s off 42nd Street. We toured the wax museum and could feel the faces and costumes. I have some pics of Joey and me checking things out. The statues seem pretty real.

HKNC Students standing next to Helen Keller wax figure which is sitting holding a book that has braille dots on it.

"HKNC students with Helen Keller. The book she is holding has real braille dots on it"

This is Steffy. She feels the statues with her hands to “see.”

Steffy is feeling Robin Williams' wax figure in order to see him.

"Steffy is feeling Robin Williams' wax figure in order to see him."

Yes, some blind really do this despite the TV jokes you might hear. DB tend to do it a little more, but I would say it is only for people we really care about wanting to know exactly what they look like.
Friday, Brian and I left very early by cab to the Long Island Railroad. We took the LIRR to Penn Station in Manhattan.
Penn Station

"Penn Station"


Then took the red line down to South Ferry and Battery Park.
Battery Park

"Battery Park"

There we took pictures of the Statue of Liberty in the New York Bay.

Statue of Liberty

"Statue of Liberty"

This is my son, Brian, with the water behind him.

"This is my son, Brian."

 It was about 35 degrees plus very windy. We had wanted to take the boat past the Statue of Liberty and onto Ellis Island, but there was over an hour wait in the cold wind to get tickets. I knew my asthma could not stand that, and Brian said that it was even too cold for him who stays outside in tents 24/7. We took the pictures and headed back to the subway.
This was a weird sight on the way back. The city has overtaken some things.

There is this older, very small building right next to a skyscraper. It looks so out of place.

"This building just doesn't look like it belongs there.

We rode the subway north to Central Park and toured the Museum of Natural History during the very cold morning.

Natural History Museum

"Natural History Museum"

Afterwards, we ate at the City Grill, which was very good and reasonably priced. I had an Apple Walnut Grilled Chicken Salad similar, but much better than they serve at Applebee’s. My friend, Ruthann, would have loved it. I couldn’t help but to think of her as I savored its flavor. This break gave us all, including Joey, the energy we needed to walk through Central Park. I was really shocked at how beautiful it was, and it was very strange that it was in the middle of one of the world’s largest cities. There are several large reservoirs that they allow boating on. There are pathways galore all mingling around greenways for picnicking and play. There are huge rock outcroppings where children scrambled. It was absolutely gorgeous. We saw many places that we recognized from episodes of CSI: NY, including one that was in this week’s episode that I didn’t get to see until we got back that night and watched it streamed over the internet. The area was a couple of brick terraces overlooking the lake with the lower terrace having a huge fountain next to and overlooking the water.

Manhattan Cafe where we ate.

"Manhattan Cafe where we ate."

We exited the park onto 5th Avenue, which is lined with multimillion-dollar apartments along the Central Park border where rich financial executives and many celebrities live.

5th Ave apartments in Manhattan

"5th Ave apartments in Manhattan."

Strolling south of the park, you find the famous stores and their storefront windows filled with the most expensive and outlandish fashions that I have ever seen in my life. I assure you that I was not the least bit envious. I love my simple life and fashion. If no one else does, that is tough. I have better things to spend my money on like my children, husband, and beautiful students such as ShaynePatrick. They are what make life worth living. We ended the day after dark shooting videos of Times Square

and then walking down 34th Street to Macy’s. Brian grew up loving “The Miracle on 34th Street.” I think he found that some things are better just left for memories. After riding the LIRR back to Port Washington, we ate delicious NY pizza at a local pizzeria before taking the cab back to HKNC. We were all exhausted. Little Joe ate his supper and crashed on the bed with me beside him. I managed to give him a well-deserved massage before calling it a night.

I awoke early at 6:00 am to see Brian off to the airport. He had to be back at work at the wilderness rehab camp in Ga. by 5:00 pm that afternoon. I really loved the fact that he was willing to come up, and we had such a great time. I was reminded of those days after my divorce from his biological father when it was just the two of us. We were so close back then. I hope he felt some of that closeness this week. I know I did.

After he was gone, Joey and I curled up on the bed and slept until noon. I missed breakfast completely. Of course, I merely got up, took a shower, ate lunch, and came back to the room where I slept until dinner at 4:30 pm. I don’t remember ever sleeping that much. It was worth every minute of it, though.

I wasn’t able to make my usual calls to my mom, sister, and Aunt Pat. I really missed that. So, Mom, Traci, and Aunt Pat: I love you, and I hope you had a great Thanksgiving. I also hope my in-laws, Marsha and Aubrey, had a nice Thanksgiving. I love you, guys, too. There was absolutely no cell phone signal the last few days here. We haven’t even had internet service the last couple of days. We have to wait until Technology staff comes back Monday to get it fixed, so this post will be late.

As you can see, there was a lot to be thankful for this Thanksgiving. God is truly good to me. Some may say how can you say that when you are going deaf and blind, but I tell you that I see and hear God now more than I ever have before. Life is filled with heartache and disappointment, but with Jesus living through us, it is also filled with great joy and accomplishment. I love my Jesus with all my heart. I don’t ever want to live again without Him guiding me. He is the reason I bother to wake up every morning. He is the reason I am living. I can do all things through Christ who strengthens me. So can you! Take care this week. I am working hard to come home by Christmas, so keep praying for me. I really need the strength. There is still a lot to learn and overcome.

God bless you,

Renée and Little Joe

P. S. That special person I told you about last week who needed to find their way back to Jesus. Well, they made it to a church this past Sunday. This person almost changed their mind, but prayer helped to get them there. Keep praying for this person. God really has a plan.

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