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Letters from OI Families & Friends who support CUMF


Dear Chunli,

How are you?
How time flies! I am so happy to know that you are beginning to feel better now. I learned from the newspaper of your strong will to fight this disease. It has impressed me and moved me so much. At the same time, the kindness of foreign friends who offered to help you has made me feel so touched...
Best wishes always!

6 Mar. 2002


To Chris, my American friend,

...It is you who found a hospital for Chunli in the United States which can give OI children free treatment. It is you that extended her life. Such a noble humanitarian spirit! If everyone in the world could love, care and help others like you, life would become much better and the world would be more cheerful...
A Chinese friend who supports your work

Ms Lu
17 Apr. 2002


Dear Mr. Barclay,

When the news that you were going to financially assist Linru's treatment came to us, we were extremely happy! She is saved! You are the one who has given her a second chance at life...

Linru's father
14 Mar. 2003



Dear Miss Yu,

How are you?
Thank you for your concern for Shali. Neither my husband nor I have a constant income. Presently we are both temporary workers and our monthly income is only several hundred rmb. It cost us a lot in curing the fractures that Shali has every year. Therefore, we are really in a bad economic situation, and hope so much that you could help us. ...

Shali's mother
Oct. 2004


Dear Uncles and Aunts,

My name is Shali. When I was four months old I was diagnosed as an OI child. Every physical lesson, I could only watch my classmates playing games and chasing each other cheerfully on the play ground from the window instead of going out with them. How lonely I felt!
Uncles, I believe you can help me get rid of this pain and loneliness.

Shali
21 Aug. 2005


Dear Mr. Barclay,

How do you do!
...Please allow us to express the highest respect to you, along with all the children and their parents you have helped with. Thank you so much indeed!
If possible, we are eager to do something for the disabled children like what you are doing. Their pain and hopes for a normal life tear our hearts as parents...

Yuxin's Parents
15 Jul. 2005