A sincere apology for those of you who have been checking on the blog to see if we have any news. Ever since November I have found it impossible to post anything, whether from lack of energy or enthusiasm or just not having the time to sit down and think about what to write next. For two months or so, Allison was rebounding nicely and growing hair, becoming more like herself, and returning to things she loves to do. In March she started to get tired again, from the treatments, and is trying to keep up with school and other routine things. When I read the last post I wrote in November, I realized that she sounds very much like she did then, even though emotionally I think she is stronger and I've seen more of her old personality come through. Physically, though, she is just holding on and a little bit of activity or stimulation makes her pretty tired. We have two more treatments to go, in April and May. Then about six months of recuperation before she will start to feel better. Every three months for the next two years she'll be getting MRI's to see if the cancer cells start back again.
Holding pattern would be the best way to describe us right now. Our first anniversary of her diagnosis is April 4th.
We have some photos to post. We have also learned about two wonderful foundations who support Children's Hospital through donations, but are close to our own situation: The Morgan Adams Foundation and the Gabby Krause Foundation. Links are on the left.
Thanks for all of the love, queries, and support.
Best,
Dianna
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3 comments:
I have been checking but totally understand why you have not updated. I was so pleased to see the update today. Allison is an articulate, talented little girl. Her story of her cancer is so touching and beautifully illistrated as to her feelings. She has a career as an artist as well as expressing her feelings. I think of you all ofter and have you in my prayers. I so understand how much energy it takes to get through the day, keep families on an even keel and just put one foot in front of the other at times. Take care and love to you all, nancy
What a talented, articulate little girl you have. It was so good to see your update and of course, the great pictures.
I hope you will plan to come to the Race for Research in Washington Park on Aug. 24. As you know it also benefits brain cancer research. I will get the information to you.
We are thinking of you often. Know that life is pretty nuts for you right now....and we understand.
Jon and Sondra
Dear Dianna and family -
Thank you for taking the time and energy to post an update...I have been checking and I am very grateful to hear that things are moving along...two more treatments...that's great. It will be a good summer for you and your family. I just want you to know that I think of you often. Wishing you all of the strength in the world. Take care...Love, Sandy Floyd (Gersbach)
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