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


August 28, 2007

The World Turned Upside Down - June 4th 2007

Madelaine had been unwell for several weeks; lethargy, swollen glands in her neck, a high temperature and she was off her food and sleeping all the time. We has visited the GP 3 times within this time. After speaking to many staff at the hospital, it is clear now that Madelaine's symptoms were almost exactly like those of a virus. Apparently, GP's only ever come across leukaemia patient once in their career. I don't hold any grudges. As far as I am concerned, she is still here now, getting treated and we are hopeful that she will be as fit as a fiddle after her treatment has ended.
We were advised that Madelaine had a virus and medication would not work. After almost 4/5 weeks, we took Madelaine to an emergency Doctors as it was a Saturday. He again, advised us that Madelaine had a virus. He wasn't concerned about her temperature being so high (over 39). He even advised us not to give her Calpol to reduce her temperature.....
8 hours later we found ourselves at Leeds General Infirmary. It was about 1 am. Immediately the staff moved us into the Resusitation Room. There were staff all over the place. It felt surreal. Madelaine was laid on the bed limp, hot and looked very ill. We had no idea how ill.
After about 90 minutes, one of the consultants and a nurse approached us. We were told that our Daughter was 'very poorly'. She had a blood disorder. Even at this point I didn't quite know what that meant. Dave asked the dreaded question, 'Are you saying that this could be Leukaemia?' I nearly passed out when he asked that because in my mind, of course it wasn't Leukaemia.

It was.

Our Daughter has Leukaemia.