I have been really snowed under this week and haven't blogged at all, but just wanted to say to all you lovely people who read my blog, thanks for dropping by this year. I wish you all a very merry Christmas and hope Santa puts many good things in your stockings!
And for all the many people who've gone out and bought Last Christmas (and there really appear to have been an awful lot of you!) I'd like to say thank you very much. At a particularly difficult time in my personal life, it has been very welcome to have a little bit of fairy dust in the shape of a book which I loved writing doing so well. To blow my own trumpet a little bit, thanks to all you nice people, I've been in the Heatseekers chart for six weeks ( I dropped down to no 3 this week), and made it into the top 20 pb bestseller lists for two weeks. I reached the dizzy heights of 15 last week, but have now gone back to 22, which is still fabulous. It has been very exciting and a lovely and unexpected treat. So thank very much for buying it! Fans of Hope Christmas might be pleased to know that going to see our local nativity last night, I came up with a GREAT idea for another Hope Christmas story. Well I think it was great. A fair bit of red wine has passed by me since then...
Anyway, must go and check on the turkey (current plans for the day include transporting a turkey and trimmings up the road to mil's in the wheelchair we borrowed to get her down here. It's going to be an unusual Christmas(-:), and see whether the children have started fighting yet.
A very happy Christmas to one and all!
Friday, December 25, 2009
Friday, December 18, 2009
On second thoughts
Earlier today I posted a bit of a rant about our current family situation. I was feeling angry and upset and letting off steam. On second thoughts, I've decided it was a bit too personal and so I've now deleted it. I'd really like to say thanks for the support I got though. The blogosphere rocks!
Monday, December 14, 2009
RNA Awards
Normally at this time of year, the Romantic Novelist's Association of which I am HUGELY proud to be a member (in my book the RNA is the best friendliest and supportive writer's organisation going) asks its members to publicise the longlist for their annual award, which has just been announced here. I'm always delighted to do so because the RNA has supported me from my very first feeble attempts at writing and more often then not there are one or two of my pals on the list. However, for the first time this year, I'm on it too. I wouldn't brag about something like this normally, but I do feel it is such a huge honour to be on this list, which includes many many more worthy names then mine, I wanted to say thank you to the RNA for my nomination, and also all the readers who voted for me. Am utterly gobsmacked to say the least!
I'd also like to congratulate my fellow RNA nominees: Sarah Duncan, Katie Flynn, Jean Fullerton, Veronica Henry, Erica James, Judith Lennox, Mary Nicholls and Nicholas Sparks, and my fellow Avon writer, Miranda Dickinson whose Fairytale of New York is quite rightly speeding up the charts.
I am under no illusions about making the short list, the competition is far too hot! However I am delighted to have been privileged to be nominated at all - a completely unexpected pleasure. Having just updated my website: http://www.juliawilliamsauthor.com/ I'd better go and update it some more...
I'd also like to congratulate my fellow RNA nominees: Sarah Duncan, Katie Flynn, Jean Fullerton, Veronica Henry, Erica James, Judith Lennox, Mary Nicholls and Nicholas Sparks, and my fellow Avon writer, Miranda Dickinson whose Fairytale of New York is quite rightly speeding up the charts.
I am under no illusions about making the short list, the competition is far too hot! However I am delighted to have been privileged to be nominated at all - a completely unexpected pleasure. Having just updated my website: http://www.juliawilliamsauthor.com/ I'd better go and update it some more...
Friday, December 11, 2009
Hullo I must be going...
Busy busy busy here so not blogging too much.
However, if you should find yourself in the vicinity of Burway Books in Church Stretton tomorrow, I shall be there from 2pm signing copies of Last Christmas.
In the meantime am frantically doing rewrites on The Bridesmaid's Pact. (It's like getting blood out of a stone, since you ask). In order to help me with some much needed inspiration I've been listening to Razorlight's Wire to Wire. A truly fabulous song that sends chills up my spine and is the theme tune of one of my characters. So being a generous sort I thought I'd share it with you...
However, if you should find yourself in the vicinity of Burway Books in Church Stretton tomorrow, I shall be there from 2pm signing copies of Last Christmas.
In the meantime am frantically doing rewrites on The Bridesmaid's Pact. (It's like getting blood out of a stone, since you ask). In order to help me with some much needed inspiration I've been listening to Razorlight's Wire to Wire. A truly fabulous song that sends chills up my spine and is the theme tune of one of my characters. So being a generous sort I thought I'd share it with you...
Wednesday, December 02, 2009
Is there a doctor in the house?
I am a big fan of the NHS. My mother was in the first post NHS nursing set at the London Hospital in 1948. Two of my sisters have worked as nurses, a bil works in NHS management and my husband is an NHS employee.
As a family this year we have had huge cause to be grateful to the NHS. Not only did I have my little A&E encounter in the summer, but I've also had checkups both for heart disease and breast cancer (both thankfully ok). On top of that no 4 has had several hospital visits, including an ultrasound, an MRI and a bone scan to check out a strange lump on her foot (nothing serious either, phew). And if that weren't enough we've had mil in casualty after her fall two months ago, and then back again a month ago when she couldn't get up one day.
From the fall it was established that mil has a blood disorder common in the elderly which means she isn't producing enough red blood cells. Our GP got her into hospital and suggested she needed a blood transfusion. It transpired that she didn't, but she has remained in hospital ever since because her mobility is variable and her blood count is still low.
The first week she was there, she was very poorly, and we feared the worst. She spent two days being assessed in a Clinical Assessment Unit, where no one seemed to know anything, and despite bil and sil's best efforts, we had only fleeting contact with doctors. Then she was moved to a surgical ward because there was no room on the medical one. There, the flow of nurses was constant, there seemed to be no consistency of care, and we all felt we were banging our heads against a brick wall, when we repeated constantly that she suffers from a benign essential tremor and her medication had been altered, that she probably had an infection because she was confused, that it was likely she would just nod and say she was fine when she wasn't. And still we found ourselves unable to get any sense out of a doctor as to what was actually wrong with her.
Eventually she moved into the medical ward, which was much better, as it had just been done up. But there you feel a slight despair about the money that gets wasted in the NHS. As she arrived on the ward, there were engineers putting the finishing touches to a new state of the art, TV/Radio and phone system - so state of the art it's being trialled first in our hospital. The room mil was on was full of the elderly and infirm. Not a single one of whom was going to get any use or show any interest in this new system. I'd rather the money was spent on better communication with the medical profession frankly.
The only person I spoke to who seemed to have a clear understanding of mil's problems, and who also took on board our concerns that her level of confusion had worsened since her stay in hospital, and was different from the confusion caused by her infections, was a wonderful young OT girl. She wrote everything down I said, but whether anyone else took notice I don't know, because it seemed everytime we spoke to a nurse they had to consult the notes, or didn't know anything about mil.
On two occasions bil was told that the consultant would be in in the morning, only for him to turn up and no consultant would arrive. Eventually, after three weeks, though we did manage to see him. He was very nice. He was very informed. He knew what the problem was, but hadn't a clue that she was confused or that had got worse. But why, did it take us so long to get hold of him? The system caters always to the patient, asking the patient what their needs are, which is obviously a good thing. But anyone who's ever spent time in hospital will know, that even if you are relatively young and compos mentis, you will be hard pressed to remember what a doctor has said to you. For an elderly confused individual it must be impossible, and it's abysmal that no one thinks to consult the relatives more. What frustrated me the most is that, having spent the best part of this year being fully conversant with mil's problems, I know what medication she is on, I can give an accurate case history of what has happened to her, and I know (as we all do) that her condition is worse then when she came into hospital. There should be a better way of using people like me as a resource.
The care mil received was perfectly fine, but the ward she's been on was a busy one and not suitable for an elderly lady who needs a lot of help to get back on her feet. So fortunately last week, she was transferred to a local community hospital, where the pace is slower, the nurses ensure she is up and dressed every morning, she's getting physio every day, and she is much calmer and more content. And praise be the lord, the first day she arrived, the sister in charge of the ward actually asked me what had happened to her, and then said the magic words, what outcome do you as a family want? Better late then never, I suppose, but it shouldn't have taken three weeks.
As always in these situations, I can't help thinking about those poor sods who don't have irritating rels like me to fight on their behalf, or the elderly and infirm who don't know how to stand up for themselves. There must be so many of those kind of people who get lost in the system. I saw an elderly man discharged from CAU, who had had a fall. He could barely walk and was clearly in a lot of pain. It didn't seem right that he was being sent home. Neither did it seem correct that another lady who I assume was suffering from cancer, and who also was clearly in great pain, was being sent home to her daughter with whom she lived. The daughter said to me in despair, do you think she looks well enough to go home? It was quite clear she wasn't.
We have a lot to be grateful for in the NHS. It is there for us in emergencies. It is free and the majority of those working in it are dedicated and caring professionals. But there is too often a huge waste of resources, and communication could be hugely improved. I know people are busy and they have a job to do, but it is all too easy to lose sight of the person, and focus on tasks that need doing, particularly when dealing with the elderly. We are lucky that mil has ended up somewhere where she can be properly looked after, particularly as swingeing cuts mean that the number of beds available in community hospitals are being severely reduced, but it shouldn't have been so hard to get her there or fight for information. The patient is entitled to be told the truth about their condition, but when they are not in a state to make informed choices, families need to know to. Because after all, we can help.
As a family this year we have had huge cause to be grateful to the NHS. Not only did I have my little A&E encounter in the summer, but I've also had checkups both for heart disease and breast cancer (both thankfully ok). On top of that no 4 has had several hospital visits, including an ultrasound, an MRI and a bone scan to check out a strange lump on her foot (nothing serious either, phew). And if that weren't enough we've had mil in casualty after her fall two months ago, and then back again a month ago when she couldn't get up one day.
From the fall it was established that mil has a blood disorder common in the elderly which means she isn't producing enough red blood cells. Our GP got her into hospital and suggested she needed a blood transfusion. It transpired that she didn't, but she has remained in hospital ever since because her mobility is variable and her blood count is still low.
The first week she was there, she was very poorly, and we feared the worst. She spent two days being assessed in a Clinical Assessment Unit, where no one seemed to know anything, and despite bil and sil's best efforts, we had only fleeting contact with doctors. Then she was moved to a surgical ward because there was no room on the medical one. There, the flow of nurses was constant, there seemed to be no consistency of care, and we all felt we were banging our heads against a brick wall, when we repeated constantly that she suffers from a benign essential tremor and her medication had been altered, that she probably had an infection because she was confused, that it was likely she would just nod and say she was fine when she wasn't. And still we found ourselves unable to get any sense out of a doctor as to what was actually wrong with her.
Eventually she moved into the medical ward, which was much better, as it had just been done up. But there you feel a slight despair about the money that gets wasted in the NHS. As she arrived on the ward, there were engineers putting the finishing touches to a new state of the art, TV/Radio and phone system - so state of the art it's being trialled first in our hospital. The room mil was on was full of the elderly and infirm. Not a single one of whom was going to get any use or show any interest in this new system. I'd rather the money was spent on better communication with the medical profession frankly.
The only person I spoke to who seemed to have a clear understanding of mil's problems, and who also took on board our concerns that her level of confusion had worsened since her stay in hospital, and was different from the confusion caused by her infections, was a wonderful young OT girl. She wrote everything down I said, but whether anyone else took notice I don't know, because it seemed everytime we spoke to a nurse they had to consult the notes, or didn't know anything about mil.
On two occasions bil was told that the consultant would be in in the morning, only for him to turn up and no consultant would arrive. Eventually, after three weeks, though we did manage to see him. He was very nice. He was very informed. He knew what the problem was, but hadn't a clue that she was confused or that had got worse. But why, did it take us so long to get hold of him? The system caters always to the patient, asking the patient what their needs are, which is obviously a good thing. But anyone who's ever spent time in hospital will know, that even if you are relatively young and compos mentis, you will be hard pressed to remember what a doctor has said to you. For an elderly confused individual it must be impossible, and it's abysmal that no one thinks to consult the relatives more. What frustrated me the most is that, having spent the best part of this year being fully conversant with mil's problems, I know what medication she is on, I can give an accurate case history of what has happened to her, and I know (as we all do) that her condition is worse then when she came into hospital. There should be a better way of using people like me as a resource.
The care mil received was perfectly fine, but the ward she's been on was a busy one and not suitable for an elderly lady who needs a lot of help to get back on her feet. So fortunately last week, she was transferred to a local community hospital, where the pace is slower, the nurses ensure she is up and dressed every morning, she's getting physio every day, and she is much calmer and more content. And praise be the lord, the first day she arrived, the sister in charge of the ward actually asked me what had happened to her, and then said the magic words, what outcome do you as a family want? Better late then never, I suppose, but it shouldn't have taken three weeks.
As always in these situations, I can't help thinking about those poor sods who don't have irritating rels like me to fight on their behalf, or the elderly and infirm who don't know how to stand up for themselves. There must be so many of those kind of people who get lost in the system. I saw an elderly man discharged from CAU, who had had a fall. He could barely walk and was clearly in a lot of pain. It didn't seem right that he was being sent home. Neither did it seem correct that another lady who I assume was suffering from cancer, and who also was clearly in great pain, was being sent home to her daughter with whom she lived. The daughter said to me in despair, do you think she looks well enough to go home? It was quite clear she wasn't.
We have a lot to be grateful for in the NHS. It is there for us in emergencies. It is free and the majority of those working in it are dedicated and caring professionals. But there is too often a huge waste of resources, and communication could be hugely improved. I know people are busy and they have a job to do, but it is all too easy to lose sight of the person, and focus on tasks that need doing, particularly when dealing with the elderly. We are lucky that mil has ended up somewhere where she can be properly looked after, particularly as swingeing cuts mean that the number of beds available in community hospitals are being severely reduced, but it shouldn't have been so hard to get her there or fight for information. The patient is entitled to be told the truth about their condition, but when they are not in a state to make informed choices, families need to know to. Because after all, we can help.
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