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| Pediatric Tracheostomies For parents and caregivers of children with tracheostomies. Please limit discussion to seeking and sharing of information pertaining to tracheostomy care, medical issues, special needs, disabilities, networking and moral support. |

09-22-2011, 08:30 AM
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Administrator
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Join Date: Feb 2002
Location: Grafton, MA
Posts: 4,176
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Parent volunteers needed for on-line survey
Dear Parents,
Rachel Joseph, a doctoral student at Duquesne University is inviting you to participate in a research study. If you care for your child with a tracheostomy and your child is less than three years of age, you are invited to participate in a study on 'Quality of Life of Parental caregivers of Children with a Tracheostomy' by clicking the link provided.
https://www.surveymonkey.com/s/W7ZQH3Z
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Cindy - Mom to Aaron (age 19), trached for 4 years, subglottic stenosis, ADHD, learning disability, former 26 week preemie and identical twin to Eric (age 19), spastic quad CP, moderate MR, seizure disorder; Anthony (age 19), spastic quad CP, g-tube, seizure disorder, cortical vision impairment, profound MR; and Natasha (age 6) CP, cortical blindness, seizure disorder, profound MR, shunt, g-tube.
Home Page: http://www.bissells.com
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09-23-2011, 08:59 AM
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Member
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Join Date: May 2011
Location: West palm beach
Posts: 580
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Just took the survey. Only took 5 minutes  Glad to help in any way!
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 SUSAN-mom to Harrison, born full-term(11/1/10) with an undiagnosed congenital diaphragmatic hernia (CDH), hypoplastic right lung (caused by hernia), trached at 4 months, g-tube and fundo at 6 weeks. Home in March 2011. Weaned completely off of the vent in July  Wearing PMV 24/7, 02 at night, failed decannulation in October. Hoping for better results next time!
www.caringbridge.org/visit/harrisonsnow
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09-23-2011, 10:50 AM
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Administrator
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Join Date: Feb 2002
Location: Grafton, MA
Posts: 4,176
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Quote:
Originally Posted by Sweet Harrison's mommy
Just took the survey. Only took 5 minutes  Glad to help in any way!
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Thanks Susan, Yes, I think it is important to note that the survey does not take very long for most people, maybe an average of 15 minutes. I'm guessing they estimated the time on slow readers and that Susan is a speed reader 
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Cindy - Mom to Aaron (age 19), trached for 4 years, subglottic stenosis, ADHD, learning disability, former 26 week preemie and identical twin to Eric (age 19), spastic quad CP, moderate MR, seizure disorder; Anthony (age 19), spastic quad CP, g-tube, seizure disorder, cortical vision impairment, profound MR; and Natasha (age 6) CP, cortical blindness, seizure disorder, profound MR, shunt, g-tube.
Home Page: http://www.bissells.com
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09-23-2011, 10:19 PM
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Member
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Join Date: Apr 2011
Location: Lawrence, KS
Posts: 262
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Took me a little longer, but no more than 15-20 minutes. 
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Alex, mom to Samantha born 38 weeks on March 7th, 2011 with Congenital Nasal Pyriform Aperture Stenosis, trached 3.30.11. Grade I Congenital SGS, diagnosed 11/30/11. Also mom to big brother Luke (3).
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