Percussion Vests: Are you using one? Is it working for you?
Anyone willing to guess how many “regulars” on this forum use a vest?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Anyone willing to guess how many “regulars” on this forum use a vest?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
F l i b, How ‘bout nebulizing while getting thumped to reduce the size of the chunk?
Where in Texas Sue?
Way south, just west of the city of McAllen
@sueinmn Thank you for the thought. Both the shoemaker and Velcro are good ideas. I'll let you know.
@rits If all else fails you can apply for a job in the circus.
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1 ReactionIn hospital last year, pulmonary therapist had me use vest, then had me try Vibralung. Says they produce equal results. I tried each in hospital over several days. Much prefer VibaLung. I use it after every nebulizing with 7% saline twice day. Most insurance won’t cover it, tho, too new. But awesome.
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1 ReactionI use the Smart Vest and have been using it diligently for about 1 1/2 years. I love it, to tell y'all the truth. I use the time to read and relax. If I secure it too tightly, yes, it can hurt. If that happens, I pause it, loosen the tabs just a bit and then restart it. I'm not familiar with VibaLung. sounds interesting. Do they work in a similar fashion?? Everyone keep safe. Personally, I'm home and don't go out anywhere except to take myself for a drive once in awhile. Just me, myself and I in my car. Blessings to everyone ! Toni
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1 ReactionHi Toni.
How sick did you become before you were prescribed a Smart Vest? Also, what do they cost? I am doing so much better since diagnosed a year ago but just found out that I've grown out pseudomonous again. This is the third time in a year. Last fall had antibiotic via a PICC line for two weeks and nebulizing Tobramycin for a month. today they are wanting to do a month of Tobramycin only. just wondering what I can do to stop this reoccurrence. anyone who wants to chime in--welcome.
Hi, 63. They prescribed the Smart Vest to me right away, as soon as I was diagnosed. I didn't use it for about the first six months, but then started using it. Actually, I really like using it. I know a lot of people do not, but I do. I don't nebulize, tho. My doctors have never talked about using a nebulizer. I am on the Big 3 tho. Every Monday, Wednesday and Friday. Trying to kill off those little booger bacteria. I keep my shower hose and nozzle dry and clean ( actually I use a copper nozzle to kill off bacteria). I also stopped using my waterpik. That may sound stupid, but I figure it's just another aerated water source and it's in my mouth..... maybe not a wise thing to do. So, I don't.
Oh, as for the cost of the Smart Vest, I didn't pay anything.... it was prescribed.....I would ask my doctor about that for yourself. See about the possibility of getting and using one. Being as my lungs harbor a lot of mucous, the Smart Vest is to break it up and help move it out of my lungs. So it's a medical device and was covered by Medicare. Hope this helps! Toni
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1 ReactionHello Toni, I understand your reluctance to use the waterpic but you could make it safe to use by boiling distilled water for at least 10 minutes. Just thinking about your gums! Bill