Random acts of Kindness is a web site my friend is setting up before this occurs there have been a few this week i want to share with you
John- Friend visiting and bring a beautiful bunch of roses havent seen him in about 8 months.
Julie- Lady i have never met delieved a box full of chocolate to me to get my appetite back.
A lady came to visit to colect some leaflets and posters to put in her shop to advertise transplants
My sisters in law and friends cleaned and ironed and made dinner.
and finally :
A donor gave Diane the gift of life
What will your random act of kindness be ?

Louise receives the call
Diana Sanders
Four years ao Diana couldnt not walk to the end of her garden . She faced a choice:die young or go through a life -threateneing surgery followed by an uncertain recovery and a fuure full of medication. Diane wrote a book to share her experieneces wih us called 'Will it still be me'
Diane has kindly offered to sell the book to any of our readers you can order her book through www.dianasanders.net or send an order to Day books,Orchard Piece,Crawbrough,Charlbury,Oxfordsire, OX7 3XT.
For any one who really wants to know whats its like living with this dilema its well worth a read. I laughed and cried .
Todwick woman's 'agonising' wait for donor
A TODWICK woman who is waiting for a crucial lung transplant has admitted her time is running out – after an agonising TEN false alarms.
Dianne Wakefield, of Staniforth Crescent, remains positive that a life-saving donor will be forthcoming, but says the wait is 'absolute torture'.
The 52-year-old, who suffers from auto-immune disease polymyositis, has been as far as the waiting room at Freemans Hospital in Newcastle before finding out a donation is unsuitable.
"You can't describe the emotional and mental torment that you go through," said Dianne, who has pleaded for more people to sign up to the organ donor register.
"It's absolute agony. But I now go up there with every intention of coming back. It minimises the stress that you put on yourself."
Husband John, 64, was a credit manager for a steel company before giving up his job to become a full-time carer for Dianne.
"We are really just on death row, just hoping that somewhere along the line we are going to get a reprieve," he said. "And it could be any time, day or night."
"Dianne disappears after they call, and I know that, if she gets the lung, our lives will start a new regime when she arrives home."
"I'm basically a nurse for her, 24 hours a day and seven days a week. I do the housework, cooking and washing. I do everything basically, and Dianne can't go out anywhere without me."
"We're really just surviving day by day. It's a time thing, and Dianne's is now running out very, very quickly. We have to guard against any infection, we are on tenterhooks all the time."
And when he officially retires next week, John will lose his £50-a-week carer's allowance.
"If you're not claiming any benefits then you have to do it all by yourself," he said. "We just feel so isolated sometimes and there are no support groups as such."
"We need to change people's perceptions. If people could see how Dianne is and not just stick their heads in the sand and do nothing about it, we can do that."
Dianne's problems began in 1997, when she was diagnosed as having a rheumatoid lung.
"I had some aggressive treatment back then, which helped," she said. "But it started to come back quite badly in 2002, and the same aggressive treatment didn't work that time. The lung disease just took on a life of its own after that."
"I have what they call an interstitial lung disease, which causes pulmonary fibrosis. It basically means all the little sacks start to die off, and so my lungs just get smaller and smaller and smaller."
"In 2005 I asked for a second opinion at the Royal Brompton Hospital in London, one of the best chest hospitals in the country. They told me that it was actually polymyositis, which is very similar."
She originally applied to be put on the list in January last year, but wasn't given the go ahead for a further four months.
"At first they said I wasn't suitable enough to go on the list," said Dianne, who had to give up her career at a big insurance company.
"I had to undergo a really strict exercise programme because at that time my upper body wasn't strong enough. We went back in May and they put me on the list."
Since then, 10 trips to Tyneside have seen eight end in unsuitable lungs, while the other two turned out to be double lung transplants, and so were given to someone needing two.
"I've been as far as wearing the operating gown in the waiting room," said Dianne. "About three months ago I had three illnesses virtually at the same time, and since then I've deteriorated quite a lot."
"So now I'm a top priority, which is ironic, because I've not had anymore calls since then. My time is running out. In July they were saying I would have about six months before I become too ill for the operation."
"I would plead with people to just contact UK Transplant and register as a donor. The donors are treated with as much respect as the transplantees."
"A lot of people say they want to be a donor, but then just don't sign up. It's so much easier if they have. Because, God forbid, if anything were to happen, checking the register makes it so much easier to approach the families. I definitely agree with the opt-out idea."
She added: "It will be so worth it when it happens. We are both still positive: it is going to happen."
You can find out more about joining the NHS Organ Donor Register by telephoning 0845 60 60 400 or visiting www.uktransplant.org.uk.
John- Friend visiting and bring a beautiful bunch of roses havent seen him in about 8 months.
Julie- Lady i have never met delieved a box full of chocolate to me to get my appetite back.
A lady came to visit to colect some leaflets and posters to put in her shop to advertise transplants
My sisters in law and friends cleaned and ironed and made dinner.
and finally :
A donor gave Diane the gift of life
What will your random act of kindness be ?
Louise receives the call
| 21st October Heard that Louise is still in Intensive care but is slowly recovering . Dianne Wakefields husband is keeping me up to date whilst looking after Dianne in ICU and then relaying messages to me . Yesterday 19/08/08 Louise received the call we have all been hoping for. The transplant was carried out last night and we all hope and pray that Louise continues to fight and gain the courage and strength to get better and live life to the full. My hopes and prayers are with you and your family Louise . Love Helen . 26th September 2008 Received a text last night at 11.00 pm from Louise she was in ICU for 5 weeks and was having a blood transfusion as she txt me ( naughty naughty!!!!!! ) But thank god she is ok and is getting stronger every day. |
Diana SandersFour years ao Diana couldnt not walk to the end of her garden . She faced a choice:die young or go through a life -threateneing surgery followed by an uncertain recovery and a fuure full of medication. Diane wrote a book to share her experieneces wih us called 'Will it still be me'
Diane has kindly offered to sell the book to any of our readers you can order her book through www.dianasanders.net or send an order to Day books,Orchard Piece,Crawbrough,Charlbury,Oxfordsire, OX7 3XT.
For any one who really wants to know whats its like living with this dilema its well worth a read. I laughed and cried .
Todwick woman's 'agonising' wait for donor
Published Date:
25 September 2008
25 September 2008
A TODWICK woman who is waiting for a crucial lung transplant has admitted her time is running out – after an agonising TEN false alarms.
Dianne Wakefield, of Staniforth Crescent, remains positive that a life-saving donor will be forthcoming, but says the wait is 'absolute torture'.
The 52-year-old, who suffers from auto-immune disease polymyositis, has been as far as the waiting room at Freemans Hospital in Newcastle before finding out a donation is unsuitable.
"You can't describe the emotional and mental torment that you go through," said Dianne, who has pleaded for more people to sign up to the organ donor register.
"It's absolute agony. But I now go up there with every intention of coming back. It minimises the stress that you put on yourself."
Husband John, 64, was a credit manager for a steel company before giving up his job to become a full-time carer for Dianne.
"We are really just on death row, just hoping that somewhere along the line we are going to get a reprieve," he said. "And it could be any time, day or night."
"Dianne disappears after they call, and I know that, if she gets the lung, our lives will start a new regime when she arrives home."
"I'm basically a nurse for her, 24 hours a day and seven days a week. I do the housework, cooking and washing. I do everything basically, and Dianne can't go out anywhere without me."
"We're really just surviving day by day. It's a time thing, and Dianne's is now running out very, very quickly. We have to guard against any infection, we are on tenterhooks all the time."
And when he officially retires next week, John will lose his £50-a-week carer's allowance.
"If you're not claiming any benefits then you have to do it all by yourself," he said. "We just feel so isolated sometimes and there are no support groups as such."
"We need to change people's perceptions. If people could see how Dianne is and not just stick their heads in the sand and do nothing about it, we can do that."
Dianne's problems began in 1997, when she was diagnosed as having a rheumatoid lung.
"I had some aggressive treatment back then, which helped," she said. "But it started to come back quite badly in 2002, and the same aggressive treatment didn't work that time. The lung disease just took on a life of its own after that."
"I have what they call an interstitial lung disease, which causes pulmonary fibrosis. It basically means all the little sacks start to die off, and so my lungs just get smaller and smaller and smaller."
"In 2005 I asked for a second opinion at the Royal Brompton Hospital in London, one of the best chest hospitals in the country. They told me that it was actually polymyositis, which is very similar."
She originally applied to be put on the list in January last year, but wasn't given the go ahead for a further four months.
"At first they said I wasn't suitable enough to go on the list," said Dianne, who had to give up her career at a big insurance company.
"I had to undergo a really strict exercise programme because at that time my upper body wasn't strong enough. We went back in May and they put me on the list."
Since then, 10 trips to Tyneside have seen eight end in unsuitable lungs, while the other two turned out to be double lung transplants, and so were given to someone needing two.
"I've been as far as wearing the operating gown in the waiting room," said Dianne. "About three months ago I had three illnesses virtually at the same time, and since then I've deteriorated quite a lot."
"So now I'm a top priority, which is ironic, because I've not had anymore calls since then. My time is running out. In July they were saying I would have about six months before I become too ill for the operation."
"I would plead with people to just contact UK Transplant and register as a donor. The donors are treated with as much respect as the transplantees."
"A lot of people say they want to be a donor, but then just don't sign up. It's so much easier if they have. Because, God forbid, if anything were to happen, checking the register makes it so much easier to approach the families. I definitely agree with the opt-out idea."
She added: "It will be so worth it when it happens. We are both still positive: it is going to happen."
You can find out more about joining the NHS Organ Donor Register by telephoning 0845 60 60 400 or visiting www.uktransplant.org.uk.
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