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Deana Kenward's Story

By:  Deana Kenward  June 2002

Read Deana's account of  being diagnosed with Addison's disease and subsequently setting-up the ADSHG, as published in a new medical book on endocrinology by Professors G Michael Besser and Michael O. Thorner.

 

Re-printed from Comprehensive Clinical Endocrinology pages 701-702, (Chapter author, Michael Besser) ISBN 0723431175 Copyright June 2002 by permission of the publisher Mosby

© The copyright remain the property of Mosby and you may not printout or otherwise reproduce copies of the material without prior written permission of the copyright holder.

In May 1983 I had 6 minor operation. I recovered quickly and carried on with my life. After 5 or 6 weeks I suffered bouts of nausea and often could not face my food. I went to the doctor, who gave me the same medicine I gave my youngest son for his travel sickness, and It did help a little.

During that summer I had lots of things wrong with me, including lethargy, tiredness, muscle weakness, and cramp, none of which were bad enough to bother the doctor with, as they were quite vague to start with.

I went to the doctor when these symptoms worsened but as we have a group practice I never saw the same doctor twice and was told a couple of times that there was nothing wrong and that it was probably the pressure of working and looking after my family. I never did see my own GP during these early stages. Being of Greek origin my skin had always been fairly dark and I tanned easily in the sunshine but by the end of September I was so dark it was untrue. I'd noticed that my toenails, gums and lips had black marks on them.

By mid-October I was really beginning to feel weak as I had lost about a stone and a half {18 pounds} in weight and had no appetite and I was so cold all of the time, but I looked so well because of the weight loss and my tan, and the doctors still had no explanation for my ailments.

I carried on the best I could, now sleeping downstairs because I could not climb the stairs, and if I rested all morning I had the strength to collect my children from school and cook an evening meal. When I look back I do not know how I ever got through those dark months. I was convinced I was slowly dying but somehow I managed to fool my family I was a lot better than I really was.

November came and I nearly went to meet my maker. I collapsed at my son's playgroup, which was just minutes away from my house. I was brought home and from then on things are a bit blurry.

I remember my own GP coming out and taking blood samples and later I recollect being in an ambulance and the barrage of tests they did in the hospital. I know I cried because I could not keep my legs still and I was so scared of what was happening to me.

Finally, sometime during the night I was told that I had Addison's disease and that it was incurable but treatable with steroids and that I would make a full recovery. I spent 2 days in intensive care and 10 days on a ward before I was allowed home, just in time for Christmas.

At that time I felt only relief because during the months prior to my diagnoses I had been told that there was nothing wrong. It was later that fear and worry took over as I had never heard of Addison's disease before and I did not want to be dependent on medication for the rest of my life.

I later found out that by the time I got to the hospital I was very close to renal failure and death was just hours away, I thank God for those doctors, especially a wonderful Irish doctor whom I am not allowed to name.

It was at least 3 months before I felt really well and had regained most of the weight I had lost, and then I wanted answers to my questions-what will it be like living with Addison's disease? How will it affect my life? Will my children develop it? Many more questions and worries filled my mind constantly.



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