Madelaine's Journey With Leukaemia

Welcome to 'Madelaine's Journey with Leukaemia'.

This is a site about my Daughter, Madelaine.

Madelaine was diagnosed with Acute Lymphoblastic Leukaemia when she was 14 months old.

The purpose of this site has many facets. Firstly, we (Mummy and Daddy aka Lisa Howe and David Armistead) find it therapeutic to look back on her journey through her illness. We believe she will get better with every breath in our bodies and we want her to read this in her adulthood and wonder what all the fuss was about!
It is for our families and close friends in the hope that they too may have a deeper understanding of her illness and also the issues surrounding it. Also, other parents that find themselves with seriously ill children may find some comfort knowing that they are not on their own. We are are all on this journey together.

Mostly, this is for Madelaine.
One day she will read this and realise her parents have gone mad.........
And she will know how much she is loved..

Dave and I would like to also thank everyone who has supported us throughout Madelaine's illness.

Many people have asked what they can do to help us. Well, we have created a fundraising page on behalf of Madelaine and ourselves with proceeds going to the Candlelighters Trust. The Trust help children with cancer and their families. They have helped us. Unfortunately, there will always be children with cancer and there will always be a need for Candlelighters. So if you want to help, please donate and click on http://www.justgiving.com/madelaineeve

Also, Madelaine and children like her rely on the availability of blood. Madelaine has had many blood transfusions. So if you don't already, please give blood if you can.

And please continue to say your prayers.

Thank you. x


January 16, 2008

Intensive Block Number 2....almost....

Intensive block (number 2) was supposed to start today. However, Madelaine's neutrophils were too low. At first I felt relieved but it soon turned to concern. She has had a week off mercaptorpurine (the chemotherapy that we administer orally at home). We hoped that her neutrophils would have recreated themselves and increased, ready for the block. I wish I had asked the doctor more questions now. I will next time. (Note to self - ASK MORE!). I worry when I don't know the answers. So I worry most of the time!
Apart from this hiccup, Madelaine is learning so much. She has much more confidence with her walking and she can now talk the hind legs off a donkey. Her appetite is huge and has a penchant for Happy Meals ('Burger and chips, please, Mummy. Soon.')
I want this intensive to start and be gone. The sooner it starts, the sooner it finishes.

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