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Ursula Bick

County Representative 

My name is Ursula Bick, my husband is John.  We live in Tamworth, Staffordshire.  We had three children, our daughter Catherine, is the eldest and two sons, Vincent and David.  David was the youngest. 

 

Christmas 1995 was a joyous occasion.  David, John and I went to London to spend Christmas with Vincent and his family; I didn’t realise at the time that it would be the last time we would spend Christmas together.  On Christmas morning David and I went for a walk whilst John and Vincent prepared the meal.  It was a lovely morning, cold, brisk but the sun was shining and the air was clear.  We walked for miles, talking and laughing, with a special closeness between us.  We discussed a forthcoming holiday that John and I intended taking on 4th January, we were going on a Round the World tour to celebrate John’s retirement.  That Christmas morning walk will remain as one of my most precious memories.  There was no warning of the tragedy that would occur in a few weeks time. 

David died on 23rd January 1996.  He was 33 years of age.  John and I were in South Island, New Zealand, when Vincent telephoned to say that David had died.  We couldn’t believe that our beautiful, super-fit, athletic son had died so suddenly.  On the previous day he had gone to work as usual, he returned home at 23.00 hours, made himself a drink and went to bed.  He died at 03.20 hours, his battery clock, which was on the bedside table had been knocked onto the floor and stopped at that time.  David’s girl friend Laura, who lived next door, realised that his curtains were closed and found him twelve hours later.  David died of Obstructive Hypertrophic Cardiomyopathy (HCM) which is the most common cause of sudden cardiac death.  It is hard to accept that our lovely, caring son has gone from our lives forever.  His death devastated our family and his many friends. 

David’s death left us completely shocked; bewildered and with feelings of guilt.  I kept asking myself why I hadn’t noticed that there was something wrong.  Were there signs and symptoms that I had overlooked?  He had been such a healthy child, strong and robust, always the tallest in his class and very keen on sports and athletics.  He loved rugby and captained the school rugby team.  He played for Tamworth Colts and was selected to play for Staffordshire Schoolboys.  He enjoyed swimming, tennis and squash; was a motorcycle enthusiast, and would think nothing of cycling 40 miles after a hard day’s work.  He also had a wonderful personality, loved animals and all humanity, he would fight for the under-dog and hated injustice.  He was popular with all who knew him. 

Two years after David’s death a friend sent me a newspaper cutting out of the Birmingham Mail.  It showed a picture of Roy Ball and gave information regarding his involvement with CRY.  I was impressed with what I read and contacted Roy immediately.  Here was an organisation that not only supported research into Sudden Death Syndrome, but offered help and counselling to families who had suffered from a young sudden cardiac death.  I recalled  how bereft we felt when we lost our son, friends and neighbours rallied round and offered a shoulder to cry on; but what we desperately needed was support from another family who had lost a child in similar circumstances. 

John and I made contact with Alison and offered our support to CRY in any capacity whatsoever.  We are not fundraisers but felt that we might have other talents that could be utilised.  Before retirement John worked as a Maintenance Engineer, I was a Practice Nurse and did voluntary work as a Bereavement Counsellor.  We became involved in CRY’s early ECG Screening Programme and have watched it dramatically develop over the years.  When we first became involved with CRY we said: ‘If we can help save one life it will make it worthwhile.’  We did not realise that one life was going to be our own grandson.  One Sunday afternoon Catherine was visiting with her children.  John was doing maintenance work on one of the ECG machines.  Usually, I used John as a guinea pig to test the machine, but Cathie suggested that Stephen, her 15-year-old son might be a better proposition.  I read the tracing which showed an abnormal electrical pathway that implied Wolfe Parkinson White Syndrome.  Stephen was duly treated at St George’s Hospital, London and is now a fit and healthy 20 year old. 

Five years ago I was offered a place on the CRY Counselling Skills Course and have recently completed the Theory.  The counselling programme offered by CRY can be extremely valuable.  There is no magic formula to ease grief but sometimes talking to an empathetic listener can help us to move forward. 

We feel that our involvement with CRY has helped to ease the burden of our loss.  We know that we are not alone in our grief and it is our fervent hope that one day our Government will introduce mandatory screening for school children as part of their School Medical Programme.  Only through early screening and research will tragedies such as ours be prevented.  If we, through CRY, Alison and the CRY team can help to bring this about then we will know that our beloved son did  not die in vain. 

 

If you would like to contact one of our Representatives or a Bereavement Supporter please call the CRY office at 01737 363222 or e-mail cry@c-r-y.org.uk and we will put you in touch with someone who may be able to help you.

 

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