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
March 20, 2013
May 10, 2011
May 5, 2011

December 4, 2009
From your big sister Beth
From her big sis Beth :) x
August 28, 2009
THIS IS IT!!
She had her very last treatment! She had a Lumbar Puncture and some Bone Marrow taken.
After the op, as soon as she opened her eyes she gave me the the biggest , cheesiest smile ever.
It was wonderful.
For 2 years and 3 months, we have not been able to think about the future, or to think about the end of her treatment for fear of what may happen. It has felt like an eternity since her diagnosis.
Thank you to all our friends and family who have supported us and loved us though throughout this time.
Thank you to all the wonderful people at St James' who are amazing. We cannot express exactly how we feel; you have given her back to us.
Specifically to Dr Geoff Shenton who has been with us since Madelaines diagnosis.
Thank you, Geoff. 'Thank you' doesn't quite seem enough....
I am reminded how lucky I am.
Lisa
x
August 17, 2009
Can you believe it.....!!!!
In the beginning I couldn't even imagine it. Nearly 2 years and 3 months Madelaine has been in treatment. That is two-thirds of her entire life.....
At the moment, Madelaine is a little bit out of sorts as she is on a course of Steroids and they play havoc with her sometimes. However.......this is the last course of steroids she will have!!!!
She is still coming on so so well.
We are all counting down to the the 27th August, 2009....its gonna be a great day.......
So proud of you Madelaine, my darling xxxxx
June 19, 2009
10 weeks of treatment to go!!!
Her blood count is good and the doctors are pleased with her.
Sometimes the vinc. does have adverse effects apon her. Last night she said she didn't feel very well. We took her temperature and she seemed fine. So she slept in bed with us last night for extra cuddles and comfort. After sleeping all through the night she awoke as bright as a button!
We have noticed that the steroids also have their own effects; Madelaine's mood swings change and are very interchangeable and she also has an appetite of a adult! She eats non-stop on this treatment. Its good to see too.
Here's hoping for a troublefree remaining 10 weeks of treatment for Madelaine.
xx



