Showing posts with label epetition. Show all posts
Showing posts with label epetition. Show all posts

Monday, 4 February 2013

Birds, Spring and Doing Different Things

It is exactly one year since I logged into Blogger and learned how to set up a blog up and started writing my blog. I had kept a diary of all that happened to me in that first eighteen months of being diagnosed with PH and going on the Transplant List and wasn't quite sure what I would do with it, if anything, but I had by this time a notebook of hurriedly scrawled pencilled notes bursting at the seams just begging me to do something with it.  I ended up transferring it all into this blog and I am now on my 66th post!

delicious pud at Hambleton Hall
It's that time of year as we come into February that if you look really carefully you might just get a hint that Spring is around the corner, even though we are expecting some more snow this week! When I woke up this morning I could hear some birdsong and an odd tweet or two of the feathered kind and I've got bulbs pushing through in the garden, even bluebell shoots! The days seem just a little bit longer and there are daffodils and tulips in the shops, all just giving a promise of a brighter and warmer time to look forward to and some anticipation of warm sunshine - well I can live in hope of that too! I bought some daffodils for the house this weekend - yellow always looks so fresh and bright in February to cheer up the dreariness of winter- automatically it makes you feel uplifted.

Rob and I had a lovely few days away earlier last week, which was very relaxing and a real tonic to get out and about in another environment. We went to Rutland, which is only an hours drive away from us and is a small county sandwiched in between Leicestershire, Lincolnshire and Northamptonshire. It is only tiny, being only 17 miles east to west at its broadest and 18 miles north to south at its longest, but it is relatively unspoiled and you could even describe it as the Cotswolds in miniature or a bite size piece of the Lake District.

We had planned to stay here in November to enjoy a few Autumn walks - well walks of a fashion with me in tow - and to do a bit of Xmas shopping in Oakham, but had to cancel at the last minute because I lost my dad. We managed to re-arrange it for last week and hoped it would give us a lift after all the snow and dreariness of January. A large part of Rutland is covered by Rutland Water, an Anglian Water's drinking water reservoir with several large nature reserves and a visitor centre. It has a 25 mile circular track for walking and cycling and one day I have promised myself a proper long walk or better still a bike ride, which is impossible for me at the moment.

Rob and I visited the bird reserve on the Hambleton peninsular run by the Leicestershire and Rutland Wildlife Trust. We were wrapped up warm with scarves, wellies and the lot. It is a paradise for bird watching and after speaking to the warden we reckoned I could manage the walk to the nearest bird hide, which was about 350m away, just around what I manage to do around when I do my six minute walk tests! This time I would be able to amble more slowly to keep my breath. It was a mild January day and there was seating in the bird hide, so I could rest while we watched the birds before I had to attempt the return walk. I always have to check how far I have walked so I can weigh up whether I'm capable of and have the stamina for the walk back!

Warming stew at the Lord Nelson 
At first we couldn't see many birds then we started to see several cormorants ducking and darting around the water, there plenty of ducks and gulls and some flocks of geese and we were rewarded for our patience with a big flock of lapwings flying above the water then landing near to where we sat watching. While we wandered back we saw thrushes, goldfinches, tree sparrows, wrens, pheasants, robins and blue tits and great tits. So nature rewarded us for our efforts and it gave my spirits a great lift to be outdoors and enjoying the quiet of the reserve.

After that we needed to warm up again and we went off to Oakham, an interesting market town with a small castle, a museum, some bespoke shops and its own market place with stocks. We found a lovely pub and enjoyed a warming lamb stew with crusty bread. It was a quirky place to eat if you love old buildings, beams, fires and antiques. All in all the whole trip was well worth the wait, a real pick me up and really helped me to get thinking of springtime and that it wouldn't be long before we get warmer, milder and longer days. A lot to look forward to while I wait.

For information on Rutland: things to do, Accommodation, where to eat: www.discover-rutland.co.uk/  
And a couple of tried and tested places: www.hambletonhall.com/; www.finchsarms.co.uk/; www.thelordnelsonoakham.com; www.barnsdalegardens.co.uk; www.rutlandwater.org.uk/


View from Hambleton
On and off during our trip and during the rest of the week I thoroughly enjoyed reading 'Life of Pi'. Most of you will know that this is now a major film and Rob has been badgering me to go and watch it at the cinema, but I refused to go until I had read the book. Rob recommended me to read it a few years ago, so I thought I better read it so we can go to the film while it's still on at the cinema. Anyway I was transported from Rutland Water to the Pacific Ocean with a young shipwrecked boy and a tiger! It was well worth the read and I can't wait to see the film soon. After our busy start to the week in Rutland I paid the price for overdoing it later in the week. This is a usual thing to happen with PH, try to act like you are a normal person for a day or two and then you will be exhausted and hardly able to walk for the next day or two if you don't try and rest up. You constantly have to try and juggle how much you can cope with and how much you can manage. It is at those times when I know and can acknowledge deep down that I cannot go on like this for evermore and I do definitely need to get my transplant.

Oakham
I am publishing my blog a little early this week as Wednesday is possibly going to be an exciting day in our household and I might have more things to write about and tell you all by the end of the week. I will give you a clue and lots of you will probably get it - Valentine's week and From the Heart - so keep watching and if all goes to plan I might possibly have some interesting news and pictures of something going on in my home that I have just agreed to do, but we will have to see if it does really happen first!

We have just had another lovely weekend with friends to stay and enjoyed catching up on all our news and I was pleased and moved to hear that they had both signed up to be organ donors and they are spreading the word amongst their own family and friends. So if you haven't already:

sign up to the Organ Donor Register: www.nhsbt.nhs.uk/

sign the epetition for the 'opt-out' organ donor scheme: http://epetitions.direct.gov.uk/petitions/38220

Finally, don't forget to tell your family your wishes!
    


Being fed!


Wanting to be fed! Sorry can't take you with us to the pub!







Friday, 1 February 2013

A Dedication to 1500 Families and Many More ...

7500 plus people waiting for an organ across the UK


Today just happens to be my 500th day of waiting for my heart and lung transplant.

Now I think good luck and good fortune have both been on my side this last 500 days. I have managed to stay stable and reasonably well and I have managed to adjust to my life somehow living with Pulmonary Hypertension and being on the Transplant List. There have been ups and downs along the way, but I'm still lucky enough to be on the transplant list and still hoping and waiting.

1000 people on average die every year waiting for a transplant - that's 3 people a day! 


Not so for many people though, during these 500 days, not so have some stayed well enough to withstand transplant while they endure the long wait, not so have they managed to maintain their health, not so has the medication and treatment kept working wonders for them. During this 500 days many people will have lost that chance of hope that sparkles and twinkles like a star, possibly just a few moments away, enticingly in front of them, keeping them motivated that something can be done to bring them back from illness and back into a normal life again.

While I've been waiting full of hope for 500 days, 1500 will have died while waiting for their transplant, because of the chronic shortage of organ donors. They would have had to face the cruel fact that they will lose their battle against whatever illness they are enduring, they will have to suffer not only being unwell, but knowing they are going to leave their family and friends behind and all the richness that life offers.  

During these 500 days many more will also have been informed that the waiting time has run out and they are no longer fit for the transplant process, yet they will have to continue the battle with their illness, this time without any future hope before them.

96% believe donating organs is the right thing to do!


Imagine those 1500 patients and more have families and friends that will be left devastated and having to cope too, and the tragedy and rippling effect of this shortage of organ donors can be multiplied hundred fold.

I think if 1500 people had lost their lives in a tragic disaster, then there would be a national outpouring and demands and enquiries to know how such a tragedy could be averted, but we are losing all these people quietly and it is slipping by unnoticed, the tragedy is only unfolding within each family, so little gets done about it.

Only Around 30% - The amount of registered organ donors!

 
So why don't people sign the Organ Donor Register? Why is it all so complicated to get people to sign up?

70% -Haven't joined the organ donor register!


Well I only have to look at my own story to see some answers there. Three years ago I was happily getting on with my life, happily enjoying my family, happily enjoying my teaching and happily enjoying and making most of what life has to offer. Dare I say it? I was rather ignorant to the world of transplants because my life had never been affected personally by it. Of course I've been profoundly touched by illness and death, that is part of everyone's life, and not just through family and friends, but through various media too. That said, however, I had never met anyone with a very rare illness or anyone who had had a transplant. All the illnesses I have encountered through friends and family have been various cancers and more common heart and lung disorders and much of what is presented in the media concerns these diseases. That speaks for itself really, of course we need to know as much as possible and be fully aware about these diseases, it is more than likely at sometime in our lives we will be affected by them or someone we know will be and we want to be best informed how to cope or recognise the symptoms. I suppose it is just less common to be affected by transplant in your life.

Around 90% of families are supportive if the potential donor was on the NHS Organ Donor Register 
            Around 40% plus of families fail give consent  


So never having been personally affected and busy getting on with living, I didn't really give much thought to organ donation. I knew that Rob, my husband, carried a donor card and wished to donate his organs if he were to be a victim of tragic circumstances and knowing this don't think I would hesitate to give my consent to his organs being used to save lives.  I suppose, also, knowing this I thought if anything happened to me, then he would decide to do the same for me. I didn't ever really stop and consider how hard this might be for my family in tragic circumstances and I suppose I just pushed it to one side and thought well it's probably not going to happen to me anyway; these things happen to other people! I never in my wildest dreams stopped to consider that I might need a transplant, let alone three organs. I suppose no-one really likes to think too deeply about whether they may be in a tragic accident or not or that they may need a new organ, because they are incurably ill.

96% - The amount who would take an organ if they needed one!


So I guess just from my own experience that it is just complacency and a reluctance to confront the fact that you may be ill or die tragically and this being an unlikely event that means most people don't bother to sign the organ donor register. Let's face it, it isn't really a natural daily occurrence to be thinking about organ donation and transplant unless you are being affected by it somehow. Sometimes when we talk of transplant, it may imply that we are wishing someone to die, so that their organs can be used, but it really isn't like that at all. It's just hope that if there were to be an unavoidable tragic death, which does happen and often, then out of that tragedy some good will come and someone may be given a new life, because that is what the donor has wished for in the event of something tragic happening to them.    
         
So to save all these tragic deaths continuing, we have a culture that needs to change now and we need to make organ donation a natural process and thing to do, for those people who are willing to donate.

It was pleasing to find out this week from Papworth Hospital, that ITV/ITN are running a project to raise awareness of organ donation. They are planning to dedicate a day in February to a campaign to increase the awareness of the need for organ donors, under the title 'Have a Heart'. They plan special programmes to highlight the desperate need for more organ donors. Look out for 'Daybreak', possibly on the 13th when my very special and inspirational friend Stacie will be appearing to tell everyone about her life with Pulmonary Hypertension and what it is like living on the Transplant List. ITN are also hoping to film a real transplant operation taking place at Papworth Hospital, if one so happens to occur during the next week or so and I know several of us have consented to filming in the hope of raising awareness should we be lucky enough to get the call. It is the real stories, from patients themselves that can make a difference.  I'm really hoping that their programmes will get the momentum going and get people thinking and talking about transplant; it is fantastic that a big media organisation is going to do this promotion on our behalf.    

By registering to be an organ donor, you could save or enhance as a many as 9 lives!


Most people will never be in the predicament of either being an organ donor or an organ recipient, but a few of us do find ourselves in unusual positions. Of course my life changed profoundly two and a half years ago when I was diagnosed with a rare, incurable and eventually terminal disease and suddenly found myself needing not only one organ, but three. I was suddenly woken up to a whole new world of transplant, well not just woken up, but brutally kicked out of bed and shoved right into the middle of transplant's midst! Suddenly I was prepared to not just take one organ, but three and in turn prepared to give my organs to others should anything happen to me, also I've agreed to give my diseased organs to research to help others just for good measure.

So my attitude was changed in a very dramatic way, but luckily and hopefully for you, you won't to need to go through any of this drama to start making that small change; all you need to do to help this change happen is simply to stay on your computer for five more minutes and if you haven't done so already:

sign up to the Organ Donor Register: www.nhsbt.nhs.uk/

sign the epetition for the 'opt- out' organ donor scheme: http://epetitions.direct.gov.uk/petitions/38220

 
Finally, don't forget to tell your family your wishes!


Friday, 25 January 2013

January Blues and Robert Burns

'Up in the morning early'

Cauld blaws the wind frae east to west,
The drift is driving sairly; 
Sae loud and shill's I hear the blast-
I'm sure it's winter fairly.

Up in the mornings no for me,
Up in the morning early;
When a' the hills are covered wi snow
I'm sure it's winter fairly.' 

    by Robert Burns

This Monday was what is now becoming traditionally known as 'Blue Monday', when everyone is supposed to be well and truly fed up with winter and summer feels a long way off still, plus all the New Year resolutions have probably been broken. For me, well it's feeling a bit dreary with the weather and it's a struggle to get up in the morning, but then again I've always struggled to get out of bed for as long as I can remember, so that's nothing new!

It seems a long time now since Christmas and as we move away from the New Year, I'm feeing really well again at the moment, therefore I've no cause to complain about January. I'm still managing to keep to my New Year's resolutions, which is to keep myself fit and strong enough for my transplant and trying to balance taking it easy and keeping busy at the same time and of course I want to keep on raising awareness of Organ Donation and Pulmonary Hypertension.  


This Monday it was also the day for my three monthly review with the Transplant Clinic, although on Sunday it looked as though we wouldn't be getting further than our own front door as the snow fell heavily all day long. Surprisingly though on Monday morning, although deserted, the roads had been cleared and we were able to make it up to Papworth.  The clinic was fairly quiet because of the snow and after all the usual tests all was fine and I don't have to go back to the Transplant Clinic again until April, unless I get the all important call that is! They are arranging a bone density scan for me, as they need to check for any signs of osteoporosis as the steroids I will be on post transplant can cause deterioration of this condition and can make me susceptible to developing it. So I expect to get another hospital appointment soon.


I am trying really hard to be as active as I can each day, so I can build up my strength and keep my muscles working well in readiness for my transplant, hopefully this may give me a better chance for an easier recovery. The physiotherapist at Papworth advised me that walking, within my limits and at a pace I can manage is the best form of exercise for me at the moment. So on Tuesday we decided to go out for lunch, then go for a walk in the woods with our cameras. Very cold weather can make me struggle to breathe if it's windy, but this day was a calm day. We went to the Red Lion pub, near Welwyn village - www.theredlionwelwyn.co.uk/, which faces a beautiful woodland called Sherrardspark, which is on the edge of Welwyn Garden City www.sherrardsparkwood.com/

The Selkirk Grace 

'Some hae meat and canna eat,
And some wad eat that want it,
But we hae meat and we can eat,
And sae the lord be thankit'

by Robert Burns

So we had a lovely and relaxed lunch and then wrapped up warm and went for a walk in the woods, which looked beautiful with snow underfoot and snow laden trees. We then drove back through the Ayot villages, which looked very pretty in the snow.  As I write this, if you are wondering what all the poetry is about, it is Burn's night tonight, 25th January, birthday of Robert Burns the 18th century poet from Scotland. Rob, although born in England is of Scottish descent and we will be celebrating tonight with a dinner of haggis, neeps and tatties, the traditional Burn's dinner, washed down with a wee dram of whisky! Unfortunately we haven't got any pipers hiding in the cupboard to pipe the haggis in, a tradition for Burns night, so just the dinner will have to do!

'A Winter Night'

Blow , blow ye winds with heavier gust!
And freeze, thou bitter-biting frost!
Descend ye chill smothering snows!
Not all your rage, as now united, shows

by Robert Burns




In the eighteenth century when Burns was alive the concept of transplant, modern medicine and the NHS were not thought of, but back to modern day and the latest statistics from the NHSBT show that there are only eighteen people in the UK waiting for a heart and double lung transplant. That is not very many of us, but put in the context that only two of these operations have been done in the last year due to the shortage of organ donors, then you will understand that I will be one very lucky lady if I get that all important phone call. It looks very likely that I have one extremely long wait still ahead of me, during which time I need to keep well enough for transplant.

I've been waiting for my transplant for 492 days now, so that means that 1476 people will now have died while waiting for their transplant during this time too. In Burn's day, you would have had to go on horseback riding through the glens and mountains to get help and computers were unheard of, but if you wish to help, if you haven't done already, then just a simple click on the links below is all that's needed, no need to go out in the cold looking for your horse!

          -sign up to the organ donor register on: www.organdonation.nhs.uk/ 

- sign the epetition for the 'opt-out' organ donor scheme: http://epetitions.direct.gov.uk/petitions/38220