jojobaudin.blogspot.com
Joseph and His Family: Life with SMA: April 2011
http://jojobaudin.blogspot.com/2011_04_01_archive.html
Joseph and His Family: Life with SMA. Thursday, April 28, 2011. A Trip To ER. At this time last night, we were preparing ourselves for a long wait in the ER. Earlier in the night, Brady was brushing Joseph's teeth when. Of his teeth came loose and made its way to who-knows where. We spent more. An hour at home poking in his mouth, and looking for the tooth and in the process. Loosening the other tooth that we were expecting to fall out first. That tooth Brady. In quickly, but they did. What he tells us,.
lifeaccordingtoliz123.blogspot.com
Life According to Liz: What Mitochondrial Disease Means to Me
http://lifeaccordingtoliz123.blogspot.com/2011/10/what-mitochondrial-disease-means-to-me.html
Life According to Liz. My life living in Boston as a recent college grad looking for a job while working towards my goal of becoming a Child Life Specialist. Nothing to Sneeze At. Wednesday, October 12, 2011. What Mitochondrial Disease Means to Me. Because of Mito, I have three mito sisters. Chelsea, myself, Sarah and Stefani after sledding in February(? I know for a fact that if I did not have Mitochondrial Disease I never would have met my mito sisters. I knew Stefani. The day after my G-tube surgery.
lifeaccordingtoliz123.blogspot.com
Life According to Liz: Child Life Certification Process
http://lifeaccordingtoliz123.blogspot.com/2012/05/child-life-certification-process.html
Life According to Liz. My life living in Boston as a recent college grad looking for a job while working towards my goal of becoming a Child Life Specialist. Nothing to Sneeze At. Tuesday, May 8, 2012. Child Life Certification Process. Child Life Council Logo. Many weeks ago (sorry! I conducted a survey about Child Life. The question was, What do you know about Child Life and if you know what it is, what do you want to learn? My Alma Matter, Simmons College. The next step is 10 college-level courses in C...
threelittlesaints.blogspot.com
Three Little Saints: September 2010
http://threelittlesaints.blogspot.com/2010_09_01_archive.html
Promote Your Page Too. Visits from my friends. Grab Kyle's button to add to your blog*. Seventeen. . . Capturing the Miracles in Everyday Life. No choice but to laugh! Wednesday, September 29, 2010. It made me go back to that dark place where I find so much anger at God. We did a chest x ray.I could tell when the team came in something was up. His lungs looked ok. And that we need to get to Columbus. And figure some things out. We have our dates for Columbus. And we will be meeting with surgery, gi.
jojobaudin.blogspot.com
Joseph and His Family: Life with SMA: January 2013
http://jojobaudin.blogspot.com/2013_01_01_archive.html
Joseph and His Family: Life with SMA. Sunday, January 13, 2013. Just a quick update. Joseph has a book report due on Tuesday. It was not a very specific assignment; just any book. He and I chose the first book, I think, in the Goosebumps series:. Welcome to the Dead House". I just wanted to post it here, being that this was the first book that. Joseph ever read by himself with no stopping. Except for a couple of bathroom breaks. I think it took him just over three hours. YouTube videos that he watches.
shesnotcontagious.blogspot.com
She's not contagious...really: First day...
http://shesnotcontagious.blogspot.com/2014/04/first-day.html
Sunday, April 6, 2014. After a absolutely overwhelming day of travel we are here. Alana did an amazing job getting here, she really did. We lucked out with security and the Delta crews we had. Anyway, we are here and alive. Tomorrow at 7 am we have to be at the hospital.then the real fun begins. Alana has been complaining of a stomachache most of the day and has really not felt like eating besides some cereal for breakfast. I didn't. Subscribe to: Post Comments (Atom). AP for Eosinophilic Disorders.
shesnotcontagious.blogspot.com
She's not contagious...really: March 2010
http://shesnotcontagious.blogspot.com/2010_03_01_archive.html
Wednesday, March 17, 2010. So lets just copy and paste the beginning of the last post onto here. I was so tired yesterday that no, I didn't get a chance to post how the day went. Anyway- we go to do the HRCT which we hope is going to show us something and yep, it cannot be done b/c Alana cannot breath how they want her too so therefore it has yet again been rescheduled. AGHHHHH! I know when we get home and all the information from her HRCT, sleep study, scopes, etc. come back we may have some answers...
shesnotcontagious.blogspot.com
She's not contagious...really: Hotel
http://shesnotcontagious.blogspot.com/2014/04/hotel.html
Thursday, April 17, 2014. We are at the hotel now. I'll do a more detailed description of the day tomorrow but basically I called it and canceled the sleep study for tonight. I'll explain more tomorrow but it boiled down to her physical and mental state. Subscribe to: Post Comments (Atom). AP for Eosinophilic Disorders. Childrens Interstitial Lung Disease (chILD). From the Banks of Jordan. Life with the ferrells. My crazy normal life. Rare Lung Disease Consortium. Tales from a NEHI momma. Coming to an end.
SOCIAL ENGAGEMENT