Broadened Horizons
Pneumatischer Kissenschalteraktivator
SwP0639.p
€66,95 Ausverkauft
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Entworfen von den Behinderten
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100% Zufriedenheit
Garantie -
Niedrigste Kostenversand
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Beschreibung
Verwenden Sie es im Kissenbezug, unter der Hand, neben dem Kopf, den Füßen (11,4 cm Durchmesser). Zur Verwendung mit allenPuff-SchalterAusgewählte Variante
0.8 lbFAQ
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Let customers speak for us
I’ll write something later, I’m still learning to work it efficiently.
Excellent
Excellent
This is at least the second of this model. My daughter has a power chair and uses it to get more time to use her iPad.
Excellent
Excellent
My son was paralyzed in an atv accident Aug 2020. He is 6'3" and 250. His injury is c6-c7. He feels so free and relaxed in the water but nobody had anything but regular life jackets so we would have to add a pool noodle to support his head and neck and a square flat float to hug in front. We also had a problem because he isn't a small man. Nothing that would allow his arms free so he could get some exercise. This life jacket has helped a lot. There are a few tweaks with the neck and crotch straps. If they weren't tight enough in the crotch area then his head could slip lower even though we had the neck piece as secured as we could. But the crotch straps when tightened too much they would be a little irritating and cause Autonomic Dysreflexia. I think I will try adding a pad of some sort around the straps. That was the only issue other than the cost, but we would pay anything to see that smile on his face! Now we just need to buy a pool for our own backyard so we don't have to go on vacation to swim. Thank You! I would highly recommend this life jacket. From a very happy mom that cried with happiness to see her son in a pool and able to move around.
I use it today for the first time. My son love it!
My husband who had been diagnosed with Bulbar ALS disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from naturalherbscentre. com after undergoing their ALS/MND natural protocol, he no longer requires a feeding tube. God Bless all Lou Gehrig’s disease Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.
I used a comfort carrier @ Disney and lost the case
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