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Thread: CHERUBS in the hospital

  1. #1

    CHERUBS in the hospital

    I was just sitting here in the hospital and thinking how I could help parents with CDH babies. I started to think, what if I could be an on-call parent here at our hospital, Sacred Heart. I went over to the NICU last night just to say hi, and asked them if they think I could start something here at the hospital, like a support group for CDH parents and families. They told me that it was a great idea. I also talked to the charge nurse, and I asked about how many CDH babies they have had since Ayda, and she told me that they have seen 30! I had no idea so many where here in Spokane. I new that Ayda was the first for a while, but it has really gone up. So, I just wanted to see how I would start something here at the hospital. I don’t have to call it CHERUBS, but I could have it just like “ CDH support” or something. It would kinda be like Child Life. This is what I thought I could do

    Whenever the NICU gets a CDH baby, they could ask the parents if they want to talk to a CDH parent or On Call CDH parent, and if they say yes, I can come and talk to them. I downloaded a whole bunch of material, and I will make packets and give it to them along with my intro letter. Then if they decide they want more communication with me and so on.


    So, how does that sound
    Shanell Browand- CHERUBS Idaho State Representative, mommy to Ayda Rose Browand, our one and only (LCDH- 4 CDH surgeries, 2 surgeries to remove fluid from around her heart, has severe hearing loss, asthma, febrile seizures, weak immune system)

  2. #2
    That sounds great Shanell!!
    Am I able to do the same thing for our hospital here in Townsville, Australia? Or is this what the Surviving/Greiving Support is for? It's a great idea Shanell
    Mummy to Savanna Saige - born 27/07/2008 with LCDH- Repair at 6 hours old with mesh patch- nitric oxide for 4 days- ventilation for 6 days- oxygen for 14 days- released home with mummy & daddy after 26 days in NICU & Special Care Unit!!

  3. #3
    Rebecca, Danielle can tell you all about what the Aussie group does for hospitals and I'm sure they will take any help you want to volunteer for!
    Mom of Shane (1/28/93-9/11/99) LCDH x6 and multiple complications and birth defects.

    Founder and President of CDH International.

    Executive Director of:

    CDH International USA
    CDH International UK
    CDH International Canada
    CDH International Switzerland
    CDH International Netherlands
    CDH International Singapore
    CDH International Hong Kong

    Messages may be answered by CDHi Team.

  4. #4
    It's all pretty much at the hospital's discretion. Before they could start giving my info out everything had to be read by the directors and in the NICU listings they had to make sure I wasn't representing myself as an "employee" of the hospital. Maybe it won't be so stringent at other hospitals, it seems it feast or famine with CDH babies
    Ohio Co-Rep/Indiana Rep Mother to Jeremiah Isaac Deskins 9/21/2007-1/12/2008 Left Sided Agenesis Type CDH. NICU 3 months- Home 22 days. 1 repair- nissen- gtube- wound vac & graft- enlarged liver- kidney reflux due to malformation of kidney valves-narrowed aorta- malformation of right pulmonary vessels and of course- the ever present hypoplastic left lung. http://www.jeremiah-deskins.virtual-memorials.com http://heavenly-angels.org/graphics/...ingmyangel.gif http://lilypie.com/pic/2009/10/29/V8wd.jpghttp://lagf.lilypie.com/tQNem4.png http://lbdm.lilypie.com/ucO7m4.png

  5. #5
    Shanell I really think that it is a great idea. I just found out a couple of weeks ago and I was going crazy because there was not a lot of information at that time. I really think that talking to somebody that knows and lived thru CDH would have help me a lot during those hard days; and the days to come. I am myself think of doing something like that here in my city, there has been a couple of cases a year but we still do not have the ECMO machine available. So I am thinking of reaching the Cherubs representative of the state to find out what I can do. I am still on hte process but still want to start soing something for the future cherubs in Texas.
    Best wishes, keep us posted.
    http://i618.photobucket.com/albums/t...bonsmall-1.jpg http://i369.photobucket.com/albums/o...las/img253.jpg JM having a bath- favorite time of the day !!! Marilu- mom to Gael 10 years old, Derick 4 years old and my cherub Juan in a Million diagnosed in utero @ 18 weeks with LCDH. Born at 38 weeks- repair day 12- 2/3 of diaphram missing (in two sections) part of the bowels and liver in chest cavity. Oscillator 8 days- vent 14 days- extubated day 22- 1st full bottle day 28- chest tube for 21 days- Home day 42!!!! NOW 6 YEARS OLD And still doing miracles, Loves karate classes. -*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-

  6. #6
    Marilu-
    Melissa Kelly is Texas State Rep.
    Her e-mail address is mkelly@cherubs-cdh.org.
    Stephanie (Shelby's Mom LCDH 7-10-06)- ECMO 7 days- 2 DH repairs- hital hernia repair- Cliff Lip repair- Nissen and Mickey button. Shelby is eating and drinking by mouth now!!! THIS IS FANTASTIC!!!!! Mom to Lexi 8- Morgan 6 and Taylor 5. Blessed to have our little butterfly and our beautiful girls. [url]www.youtube.com/cdhsupport[/url] - Shelby's Journey [img]http://i258.photobucket.com/albums/hh257/gracebutterfly/CDHAwarenessRibbonShelbysmall.jpg[/img]

  7. #7
    I don't think there's a Rep/CDH contact in Alabama. Dawn, how would I go about becoming an Alabama Rep?
    From older Silver Linings, I noticed there was a rep from ALabama, but when I tried to call her phone number, it had been disconnected.
    Grayton Karleigh Creekbaum diagnosed at birth on 5/09/08 with RCDH and she went to heaven on 6/22/08. She also had Pulmenary Hypertension- problems with blood clotting factors- and she went through 5 EMCO machines which got her the title of "Queen of the ECMO" by the head nurse - hence the boa and crown! bowel- liver- small intestines up with gortex repair had her repair while on ECMO on ECMO for 44 days (her entire life) Nitrate for 30- vent for 34 days- oscilator for 10 days Our Blog: www.thecreekbaums.blogspot.com

  8. #8
    Hi Leigh - email Stephanie and let her know that you are interested in being Alabama's state rep. I think you would be great! Stephanie is the State Rep. coordinator. Her email address is: solivarez@cherubs-cdh.org
    Tracy - mom to Ian, LCDH diagnosed at birth, 4/3/04. Ian was born at 36 weeks, spent 53 1/2 days in NICU, 7 days on ECMO, surgery was on day 5, 29 days on a vent, 23 days was an oscillating vent, 546 days on oxygen. Inguinal right and left hernias and undescended left testicle surgeries were done on day 48. Currently has heart related medical issues and exercise induced asthma, but is one happy, happy boy!! Also mom to Cole - 13, Shane - 9, and Toby - 4. CHERUBS Parent Advisory Board Member and Co-Chair, Volunteer Co-Coordinator, and Wyoming State Representative.
    email: tmeats@cherubs-cdh.org

  9. #9
    Thank you Stephanie, I wrote it down, I am still in and out of doctors so as soon as I get a chance I will contact her.
    http://i618.photobucket.com/albums/t...bonsmall-1.jpg http://i369.photobucket.com/albums/o...las/img253.jpg JM having a bath- favorite time of the day !!! Marilu- mom to Gael 10 years old, Derick 4 years old and my cherub Juan in a Million diagnosed in utero @ 18 weeks with LCDH. Born at 38 weeks- repair day 12- 2/3 of diaphram missing (in two sections) part of the bowels and liver in chest cavity. Oscillator 8 days- vent 14 days- extubated day 22- 1st full bottle day 28- chest tube for 21 days- Home day 42!!!! NOW 6 YEARS OLD And still doing miracles, Loves karate classes. -*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-

  10. #10
    Rebecca

    Jo is the Aussie volunteer co-ordinator, she lives in Brisbane. You can contact her at volunteer@cdh.org.au and she can speak with you re Townsville!
    Maryanne (mum to Rebecca born 11/11/02 with LCDH)

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