EMPHYSEMA & ASTHMA COPD FRIENDSHIPS FOR SUFFERERS AND CARERS
MESSAGE TO ALL WHO VISIT THIS WEBSITE
Dear Friends,
Sadly and suddenly, John Kirtley who created and ran these Breathless websites, died peacefully in his sleep on the 10th of June. He was buried and received a private woodland funeral nearby. As his wife, I have become the owner of the various sites he created. We are advised that they are valuable to patients and a great international memorial to a very brave man. Together with my daughter Camilla, we have decided to ask John's close friends David and Terry if they will continue to run them. (Details below) Please accept our apologies for the delay in posting this announcement, but it has taken us much longer than expected to gain access and arrange for its insertion.
To all of you who have used the sites or have corresponded with John, please accept my sincere thanks. The letters you have written and questions you have asked were the things that kept him going long after the medics had predicted. They were a lifeline for him and maybe also in return, for some of you. Although it will be hard to match John's wide experience, David and Terry are both very knowledgeable COPD patients. When you get to know them you will realise that they have the same motivation to help fellow sufferers as did John. They await your wisdom and your questions.
Yours in friendship, Joan Kirtley
Messages from David and Terry
Dear Friends of John and all who use his Websites,
Please note that we are entirely free from any commercial interests.
I am David Boswell and live in Dorset. I am a retired microelectronics engineer and now a free-lance journalist. As a lifelong asthmatic my COPD is rated as severe. I will be attempting to look after the management and administration of the site itself and dealing with most of the general issues other than emphysema, i.e., I will cover all asthma, bronchitis and related pulmonary subjects. John has already published articles by me in the website so some of you may already know my darkest secrets. I hope, over the coming months, to get to know as many of you as possible. For the time being I ask that all correspondence relating to any of the websites should be e-mailed to me at Boscon@metronet.co.uk. Also for the time being I will forward Terry's mail to him within 24 hours of receipt and organise the posting on site of your various points, letters and advice. We will both reply direct to you where appropriate. The wording of contact data in the sites had needed to be changed. This has been done.
Personal letters to Joan may still be sent to John's existing e-mail address, but please appreciate that she is not in a position to deal with any matters connected with the websites. We will attempt to answer any e-mails addressed to John at his own address during June and up to 30th July.
My name is Terry Mackay I am 67 years old, a retired police officer and I live with my wife in Hatfield, Hertfordshire. I have chronic emphysema. I am currently on 2lt. of oxygen per minute for between 12 and 20 hrs per day. I will be more than happy to hear from anyone and I will do my best to answer an questions or help with any problems. We had a saying in the police force, "If I don't know the answer, then I will find someone who does". I am about to go into hospital to have a cataract removed (not one of my 'must do' things before I die) but it will be one more thing I will be able to answer any questions about! My general role will be to deal with matters related to emphysema, oxygen issues, and I have a good working knowledge regarding claiming Disabled Living Allowance.
Best wishes to you all, David and Terry
THIS IS A COMPANION SITE TO OTHER SITES
WWW.EMPHYSEMA-COPD.CO.UK and WWW.COPDPATIENTDIARY.CO.UK
THIS SITE IS FOR COPD SUFFERERS AND CARERS WHO WOULD LIKE TO CONTACT EACH OTHER FOR SUPPORT, FRIENDSHIP OR EXCHANGE INFORMATION.
HAVE YOU EVER FELT CUT OFF FROM SOCIETY OR WISHING TO COMMUNICATE WITH OTHER SUFFERERS WHO UNDERSTAND YOUR PROBLEMS AND MAY EVEN SUPPLY SOLUTIONS, OR EVEN CARERS?
ARE YOU A CARER WHO WOULD LOVE TO STRIKE UP AN INTERNET FRIENDSHIP WITH ANOTHER CARER OR EVEN A SUFFERER?
IF YOU ANSWERED YES TO ONE OF THOSE THEN THIS SITE MAY JUST BE FOR YOU.
PLEASE NOTE THAT CARERS SOMETIMES WOULD LIKE TO SPEAK TO COPD SUFFERERS. THEY SAY THAT, IF THEY DO.

JOHN & JOAN - EVERYBODY NEEDS A FRIEND.
HOW DO I GO ABOUT IT?
Well you just have to provide us with a SHORT PROFILE of yourself and your first name or assumed name.
IT WOULD BE EXTREMELY HELPFUL IF YOU COULD ALSO SUPPLY AN E-MAIL ADDRESS THAT DOES NOT INCLUDE YOUR SURNAME SO WE CAN PUBLISH THAT AS WELL AND FRIENDS CAN WRITE DIRECT TO YOU. IF YOU CANNOT DO THAT, ITS STILL OK AND THE REPLIES WILL GO THROUGH US. OBVIOUSLY SINCE WE SUFFER FROM SEVERE COPD OURSELVES AND HAVE TO RUN THE OTHER TWO SITES WE DO NOT WANT TOO MUCH WORK ACTING AS POSTMEN!,
HOWEVER IN ORDER TO MAINTAIN A "HEALTHY" SITE WE SHOULD LIKE YOU TO TELL US YOUR MAIN ADDRESS.
MANY PEOPLE HAVE WANTED A FORUM IN THE TRUE SENSE OF THE WORD, BUT IT WOULD COST AN EXTRA £10 A MONTH. SORRY.
WHILE STOCKS LAST, UK SUFFERERS AND CARERS WHO CONTRIBUTE TO THIS PAGE CAN, IF DESIRED, RECEIVE A FREE DVD ON EXERCISE, BUT WE REGRET THAT WE CANNOT SUPPLY ELSEWHERE IN THE WORLD.