Just thought I would share this...Blowing up a balloon
No blowing up a balloon is not a big deal to most people. To me it is a very big deal, I am a laryngectomee, a neck breather and have no vocal cords and can't breathe through my nose or hold my breath. I do have a TEP which is a prosthsis in my neck [just under 6mm] that lets me divert air to my throat so I can talk. Because of the TEP I can now whistle, blow out candles on a cake and blow up a balloon. All of those things I'm not suposed to be able to do. It took two months to learn how whistle and had to practice every day. So everyone needs to know they can do this and fight as hard as you can, you too can beat the beast and the "New Normal" can be just as good as you let it be.
11 months cancer free..........
Here is the link blowing up the balloon, the whistle isn't much as everyone was asleep when I did this.
Highlight with mouse then Right click on mouse, select GoTo Https. and I hope you enjoy it. It's just a rough draft so far.
https://www.dropbox.com/s/f0bm54smj801psc/Video 3.wmv?dl=0  
Have a wonderful day
Bill 10/2013
Comments
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2014-09-04 I think I will
2014-09-04 I think I will hire you for my next party ha ha
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You are great! My hero!
You are great! My hero!
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LOL...Way to go!
I'm truly impressed with both the whiste and the balloon! My mom was a lary, and I don't think she ever knew any of these things could even be possible.
p
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bill, you are definitely my
bill, you are definitely my hero. i've tried and tried and CANNOT do any of those things. you rock.
dj
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Thank you all..........
It is because of the TEP that it can be done. You can also blow your nose as well. I thought there has been many "new Members" and all seem vary scared, [which is normal] and thought this just might help in some small way let them know you can beat this and never stop trying.
Thanks
Bill
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FantasticCivilMatt said:humbled
Bill,
I just watched your video upon returning from speech therapy. Thanks for the incentive to try a little harder.
Keep whistling,
Matt
That is great, shows what the human spirit really is. There is a guy named Tony Talmich, drummer with the Jersey Boys, look up his name on youtube, you and he are truly inspiring.
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Thanks Denistddenistd said:Fantastic
That is great, shows what the human spirit really is. There is a guy named Tony Talmich, drummer with the Jersey Boys, look up his name on youtube, you and he are truly inspiring.
Thanks for the complament. Yes I have seen Tony's video's on YouTube. He really can get the most out of the EL.
Bill
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wow
Thanks for posting the video. I learn something everyday here. So the TEP passes air flow but with no vocal cords how does one speak? Is there something in the TEP that acts like the vocal cords? Seems like a huge advantage to have the TEP so air can flow up to the mouth and sinus. You mention not being able to smell, if you can move air through the nose shouldn't your smell work? Thanks don
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Thanks Dondonfoo said:wow
Thanks for posting the video. I learn something everyday here. So the TEP passes air flow but with no vocal cords how does one speak? Is there something in the TEP that acts like the vocal cords? Seems like a huge advantage to have the TEP so air can flow up to the mouth and sinus. You mention not being able to smell, if you can move air through the nose shouldn't your smell work? Thanks don
If you go to my expression you will see a photo [drawing]showing a laryngectomee with a TEP.
I am a neck breather, all my air comes and goes out my neck. My treach has been seperated from my throat. The Tep is a oneway valve so when I inhale it goes to my lungs, now I block my stoma so the exhale is forced through a hole that is 5.6mm round and then out my throat. The mucus folds in my throat now vibrate and that gives me sound. The words are formed by my mouth. The TEP justs keeps food and liquid from entering my lungs with the oneway valve. If I use an electric larnyx to talk [ that is the tool you put to your throat and it vibrates] all I have to do is move my mouth to form the words, no air. You get a robot sound but it will give you a voice for those who can't use the TEP.
Because it is a oneway valve you can't get air in, only out. I have made a tube that will fit in my stoma and the other end goes in my mouth. Now when I inhale it will go in my nose then out my mouth and in my throat. That is how I can smell. I do not go outside with that. It is only used to help unplug my nose.
Try this test: Close your eyes and remember seeing a peach. Next try to remember the sound of a bell. You can do both of those. Now try to remember how a peach smells....... I can't, or a rose.
Bill
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Thank you and your niece KritterKritter said:WOW
Watched your video and that is just awesome. It really did inspire me, I have showed that video to my family, and my niece said.. Whoa! he rocks!.. LOL..
Kritter
I was asked to put one on YouTube by my SLP and Dr. just have not done a good one yet. I put this up with the hope it would give people hope and understanding that you can overcome many things, you just have to try and if you want it don't give up. For me after the surgery I wake up with no voice and not allowed to swallow anything, not even saliva for six days. You write everything down. If you have an emergency you pull the cord to the nurse call box out of the wall. You will learn to swallow, then eat, and talk all over again because everything was cut. Now the best part is you can relearn. You also get your life back you almost lost. You also get some great stories to tell.
Have a great day
Bill
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Goyca......YESGoyca said:Thanks for posting the video
Thanks for posting the video Bill
I guess we should keep going no matter what :):)
You give it 110% and you will be amazed what you can do. From what I have been told I am the only one my SLP has ever seen do that. She is one of the SLP who certifies others from all over the US. She had me go to a seminar and show about 20 of them and they did not know it could be done. So YES you keep going. You are doing so good and getting closer to the end of the RAD. You go girl..........
Bill
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Hi Sir,wmc said:Goyca......YES
You give it 110% and you will be amazed what you can do. From what I have been told I am the only one my SLP has ever seen do that. She is one of the SLP who certifies others from all over the US. She had me go to a seminar and show about 20 of them and they did not know it could be done. So YES you keep going. You are doing so good and getting closer to the end of the RAD. You go girl..........
Bill
I am so happy toHi Sir,
I am so happy to hear this.Congratulations and carry on with your journey.
Thanks
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Thank you Hopehope3210 said:Hi Sir,
I am so happy toHi Sir,
I am so happy to hear this.Congratulations and carry on with your journey.
Thanks
Thank you and your father will come through this fine. Keep giving him support and remind him to take one day at a time. Only today matters. The road is bumpy but it does get better, slowly, but it will. Never give up and you can do amazing things. When you do get to the point that you accept the "New Normal" it just gets better for you. Be proud of who you are, you fought the beast and are a suvivor.
Bill
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Hi Bill
Great post, I too have problems blowing as the soft palate is so damaged when I blow all the air comes out the noise. No problem I just pinch my noise close and keep blowing, Ha ha then the air comes out my ears, all we can do it to keep trying.
Tim Hondo
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