The Vest

julie

New member
Yes, we got Marks through tricare about a year ago, maybe a bit longer.

It's 2 boys and 1 girl. I'd share the details but this is someone elses thread. You can go to the website or email me if you like division902@hotmail.com
 

wallflower

New member
I've been using the vest forever - I won't say its my best friend, but I do find it very helpful, and wouldn't get rid of it.

Sometimes it doesn't seem like it does a whole lot when my health is doing well, but when I'm congested, it does wonders. Its important to remember that you have to work the settings to get the different vibrations (or shakes) to reach the different areas of your lung - one setting won't get your whole lung. It's also important to remember that you still need to huff. The machine loosens it up, but its up to you to cough it out!

I recently got the acapella for use at work and traveling, but I don't get it. I have tried all the resistance settings, it doesn't provide a challenge to me at all to breath with it. I just feel a very slight sensation. Does anyone know if there is a special trick to it? Or maybe my lungs are too clear for it to work as well as it is for others?

Anyway, back to topic. I prefer the vest because I can do it anytime by myself. Living on my own, that is a huge benefit. It also takes up a lot less room than a BD table (I HATED having to put that thing up and down twice a day!!!) Mine was covered by insurance, so cost wasn't an issue for me - although I am not able to upgrade to the newest model yet (which is fine, I'm happy with what I have).
 

Faust

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>shoom1</b></i>

I would just like to say that we ahve just managed to buy one off ebay and get it shipped all the way to New Zealand and it has been a god send for our daughter - she is only 15 months and it is the first that we know of in New Zealand. <span class="FTHighlightFont">If any of you have vests that you dont use - how about listing them on ebay and letting someone else have the benefit of the machine.</span ft> In new Zealand there is no insurance available to CF patients so it was completely self funded. The local physio had never seen one before and was very impressed with how they work.</end quote></div>


You should have told me, i've been trying to give my older model one away for a while now. I even posted about it on here. Guess I might look to sell mine on ebay...I'm pretty lazy though.
 
C

Cariann2005Rob

Guest
Julie,
Do you mind me asking what kind he has? is it from Hill-rom too? I have the version 103 i think it is and the new one is much much smaller the 104 version. I would love to have that one!! so i e-mailed my doctor today if there was anyway that i could possibly get a new vest since i have had mine since i was 13 and now im 21!! alright thanx again and congrats!
Cariann 21 w/cf cfrd mrsa
 

julie

New member
Cariann, yes it is from hillrom. I'm honestly not sure what version it is, it's a little over a year old. GOod luck, I hope your doc. puts in for it! Keep us posted.
 

anonymous

New member
Thanks for all your responses. I really think that my daughter's Doc should at least let us give it a try. We do physio for her twice a day before her neb and she does loads of physical activity, running, bouncing, etc. I'll let you know.

Charlotte<img src="i/expressions/face-icon-small-wink.gif" border="0">
 

anonymous

New member
PS the only problem though is that she is only 2 1/2 and she would outgrow them pretty fast, perhaps that's what's putting him off?! I dunno.

Charlotte<img src="i/expressions/face-icon-small-tongue.gif" border="0">
 

NoExcuses

New member
Hill-Rom will replace the Vest when she grows <img src="i/expressions/face-icon-small-smile.gif" border="0">

They're a fantastic company.

I can't imagine how much healthier I would be if I had the Vest at 2.5 years old! It would be really exciting to get her a Vest.

Keep us posted <img src="i/expressions/face-icon-small-smile.gif" border="0">
 

kayleesgrandma

New member
Sorry Charlotte, don't have a computer so use one where I work when I work. Kaylees mom didn't do manual like she should have--is kind of in denial. Thinks K has <i>mild</i> cf. Title 19 is for single parents with children.
 
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