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
October 22, 2007
Back in.....
She has lots of sores in her mouth. Mark, who is the Charge Nurse has said that its expected that she is experiencing this at this point in the intensive block of treatment. Its still quite soul destroying though. She isn't eating much or drinking. I know she is so uncomfortable and it must be painful for her. She still can manage a cheeky little giggle though, when she is drawing in her cot. Raina and Beth came to see her today and Madelaine's face just beamed when she saw them. It was just lovely.
All the staff at the ward are again being really great. Madelaine is in Bed 15 this time. In the bay we have Olivia and Miles. LilyMai was in until today but she has had her last chemo now and has gone home for good and she looks really well. How wonderful. I am itching for that.
That day will come...
Dave and I are taking turns again at the hospital. It really helps to have a decent sleep when you are home as you don't really sleep in the hospital at all. There are some parents who don't have each other to lean on, so I think Dave and I are very lucky in that respect.
She is due more Chemotherapy on Thursday but it will depend on her neutrophil count. They may delay it yet.
Watch this space.....

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