Ellas Corner
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Tuesday, July 17, 2012. Now I can finally post photos! Our beautiful daughter Qian Yin. Here are some photos of our first moments together on July 6 at the healing home she had been living in. Here are some things we have learned about Qian Yin so far. Favorite English words are mommy and no. Loves to laugh and make us laugh. Likes to act and talk like a baby around us. Selective with whom she will interact.
Just hours ago my students left. They are on their way to summer fun, family-time, and friends. Just as quickly as they walked into my life they walked out; yet they will always be a part of my life. As much as kids need to be accepted in their classroom each one achieves that acceptance in their own way.
The last post on this blog was on August 13, 2011. com Hope to see you there! Saturday, August 13, 2011. The diagnosis was confirmed on August 12, 2011. Her motor neurons are dying and will continue to die. What do we do now? Our minds are filled with what we are to do. And those things will happen.
Our families journey with a life threatening neuro-muscular disease, from searching for a diagnosis to end of life challenges to the grief roller-coaster. PCH1A, a altercation of the VRK1 gene.
Our life since our perfect little Noah was diagnosed with SMA type 2. Tuesday, March 25, 2014. I remember every detail of the day he was born. How it felt to hold him in my arms for the first time. The first time he smiled. The first time he rolled over. Unforgettable and overwhelming blessings that I am so deeply thankful for. These are the challenges that I dread and fear that if I handle them incorrectly, I may damage him. I said the exact thing.
No hands! August 10, 2015. No hands! Aug 7, 2015. More sweetness from little and middle.
Thursday, September 6, 2012. Tuesday, July 24, 2012. The zoo was incredible! Tuesday, July 17, 2012. I love this one of Brayden! This time .
Welcome to my blog! Here you can read all about my crazy life! Wednesday, June 10, 2015. OK, so I apparently am not going to get these posts up in a timely manner. but I left off in March, now I shall continue on in my year long. Things continued to be rather slow in April, with the exception of fracturing my elbow in the middle there were no new injuries. Lex and I at the convention. Being silly at breakfast! We had an absolute bl.
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Following our quot;Squishyquot; as she lives with Spinal Muscular Atrophy SMA, Type 2CONTENT
This web page ellas-corner.blogspot.com states the following, "Thursday, January 4, 2018." We saw that the webpage said " A corner has been turned and Ellas on the straight path to recovery." It also said " Her posture looks incredible as she sits in her wheelchair. Before this post goes any further its important to us to send out a thank you to all of you who prayed for, thought of, and supported Ella throughout the past month. She loved the presents she got and always kept the real meaning of Christmas close to her heart."SEEK SIMILAR DOMAINS
Τρίτη, 16 Φεβρουαρίου 2010. Δευτέρα, 15 Φεβρουαρίου 2010. Και απου χει στην ψυχη φτερα. Οταν τον ταφο του αλλουνουμε αδικο τον σκαψεις θα ερθει καποτε η στιγμη πολυ πικρα να κλαψεις. Σταλαγματια σταλαγματια το δακρι μου σκορπιζω τα ονειρα θαφτηκανε και τιποτα δεν ελπιζω. Δεν ημπορεί να ζήσει,. Όπως το δέντρο δεν μπορεί.
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Good morning, Blogger buddies! I know. Layer it Up closes tomorrow.
Κυριακή, 30 Ιανουαρίου 2011. Αυτήν την σημαία που την πίρε το κύμα,. Αυτή η σημαία, είναι η ψυχή του ουρανού πάνω στην γη. Στο ένα το άγιο το τρειλαμπές το πνεύμα! Μέσα στην αδελφοσύνη και την αγάπη της ολύμπιας ειρήνης ,. Μα σήμερα σκορπισμένα πτώματα περπατάνε επάνω στις ταφόπλακες τους οι ψυχές και δεν το βλέπουνε,. Πως αιώνια τους έχουν να πεθαίνουν,. Απάνθρωποι αποστάτες της αγάπης οι αντίχριστοι.
Παρασκευή, 15 Ιανουαρίου 2010. Οι Αλβανοί και οι Πακιστανοί στο Δημόσιο. Οι Πακιστανοί και οι Αλβανοί που θα πολιτογραφήσει ο Τζέφρης, θα μπορούν να προσληφθούν σε ένα χρόνο στο Δημόσιο. Πέμπτη, 14 Ιανουαρίου 2010. Έλα Πακιστανέ στον τόπο σου! .