Cassidy's Journey Through Osteosarcoma

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This is a dedicated blog for updates on Cassidy's fight against Osteosarcoma, and to witness and testify the greatest love of God to all humanity by all the love, prayers and supports the brothers and sisters in Christ are pouring onto little Cassidy and the Sheng's family. . . . . . . . . . . "God is Love" John 4:16

< 直接進入祈禱網<<Go Directly To The Prayer Page!>>直接進入祈禱網 >

By the request and suggestion of some concerned brothers and sisters, due to the reason that some of those who are diligently praying for Cassidy and her family are from all around the world and may not know our circle of friends personally, the regular Blog posting may confused them because Dr. Jesse would sometimes refer to people by the names known to local circle only. Therefore, this new Prayer page is made for those who would like to just see the updated prayer needs of the Sheng Family so they can pray more specific prayers for them. So feel free to pass this site onto more prayer buddies to effect a greater prayer power. Thus the name of this new site http://PowerPray.blogspot.com


Tuesday, August 19, 2014

Cheerful Surprises! Treatment to be Confirmed...

August 18, 2014.

I like the prayer which Michelle had shared on Cass's Facebook. We are so thankful to have so many loving friends together with the brothers and sisters in Christ around who have given Cass lots of care and prayers unceasingly with their every-day-new creative ways. This has been very encouraging and supportive to Cass.

The prayer
Karen EE's calligraphy from Hong Kong
We came home from another MRI this evening. Cass was happy when her two kindergarten friends visited her with the little cute handmade crochet toys. Then, such happiness was followed by a big surprise from Auntie Ada who had come over to see Cass with a gift prepared with a lot of thought. Auntie Ada made her a digital collage of photos with her Grad pictures. It's a huge surprise to her and she was super happy to see it. On top of that, Auntie Ada's little son and daughter made her some little cute stuff, the very pretty rainbow loom bracelets and a little cute card of a unicorn. They really cheered her up. All these little things and support, from friends, have lifted up her spirit to help face her difficulties every day. However, please do not spend money on buying things for Cass as she is worrying everybody is wasting (Cass use this word) their money on her. You may come over with some board or card games or bring her books to read.
Digital Collage
Little Cute Stuffs

We will be back to Sickkids again to meet with the doctors tomorrow to discuss the next treatment plan that Cass will be receiving. The whole treatment plan has been delayed a bit as the doctors want to review all her MRI results and are still considering whether the chemo drugs should be used, or if Cass should have another radiation treatment on the sacrum first since her foot is getting the numbness feeling. Up to this moment, it is very probable that the treatment will start on Wednesday, but this will be confirmed tomorrow.

Posted by Listener at 9:48 AM

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