My latest project is raising money to buy a Community Public Access Defibrillator (cPAD) for Tottington.
I went to a Police and Communities Together (PACT) meeting organised by our PCSOs in May. They had been on a Heart Start course, run by the ambulance service Community First Responders. This gave up to date life saving training. However, they said what would really make a difference was a community defibrillator. These are kept in an easily accessible public area and can be used 24/7/365. They are housed in robust cases that are usually locked with a key pad. When 999 is called following a person having a sudden cardiac arrest, the emergency service operator will tell the caller where their nearest cPAD is and give them the access code. The catch? Well they cost £1750 per unit, plus installation costs of £150 and upkeep costs. The idea was only mentioned in passing, but hey, this is Tottington, and we can do anything we put our minds to!
I went home and did a bit of research. When a person suffers sudden cardiac arrest (SCA) action is needed quickly. While waiting for an ambulance cardiopulmonary resuscitation (CPR) must be given. Statistics suggest that survival changes after a SCA with just CPR is around 5%. By using a defibrillator quickly survival chances can increase to around 50%. The defibrillators that are used are extremely easy to use. As soon as the defib is opened it 'speaks' instructions, so it can be used with no training. There are schemes to increase awareness, and good first aid training can be arranged, so that local communities can be confident if the defib needed to be used.
Tottington village is quite busy. We have 3 pubs in the centre, 2 restaurants, a take away, a cafe bar, 3 churches and various shops and hairdressers etc. There are also lots of shops etc in the District of Tottington, which covers quite an area. SCA can happen in people of all ages at any time. I decided a cPAD was just what was needed and let Twitter know.
Within a few minutes I'd had a response from a business owner in the village who was sure other businesses would support the idea. Within a few hours we had decided the idea was do able, and we could have a fund raising activity at Tottington's Music in the Park to launch the appeal. I had it in my mind that this was in September, and when I found out it was actually on 1 July I nearly needed a cPAD myself. Another business owner was 'recruited' to be involved and she hasn't stopped since either.
I hand delivered letters to all businesses in the area asking for support in the way of raffle prizes. Response was great, with people donating prizes and vouchers, all to be used locally. We also received some donations from businesses who couldn't really give a prize. We had one business have a Dress Down Friday and donated the proceeds. It was an incredibly busy time, and in between I was in regular contact with a charity set up to promote the provision of life saving defibrillation equipment, to find make sure we were 'doing things right'. A local graphic designer designed us some flyers to promote the appeal, and the local newspaper, The Bury Times, also gave us some great publicity.
To create an eyecatching launch the charity said I could borrow one of their steel cabinets, a defibrillator, some display stands and lots of leaflets. The only problem was that they were based in Nottingham. I arranged to meet their Secretary at Meadowhall Shopping Centre in Sheffield, and set off on the Friday before Sunday 1 July with a neighbour for moral support. The man we met was fabulous and knew everything we wanted to know. We came back with a car load of goodies ready to make Tottington sit up and think.
Sunday 1 July 2012 was one of the rainiest days of the year. Setting up stalls in the morning was horrendous and we were all soaked ages before the event started. We had a great display though, and it really helped having an actual defibrillator and storage box to show people exactly what we wanted to buy. We had some people that couldn't believe they could use the equipment, but we also had a training defib to demonstrate how easy it was to use. Tottington's Music in the Park usually attracts thousands of people but due to the weather it was a lot quieter than usual. The stall was kept busy with people coming to have a look though, and by the end of the day we had over £400 raised for our appeal. Only another £1350 to go....
Next, we put collection boxes in local shops. The local Knit and Natter group said they would make a weekly donation, and villagers were very supportive. Our MP, who lives in Tottington, has given his support. We got together a committee and arranged to meet to discuss future fundraising. However, the initial publicity had done us great favours.
The Freemasons approached us. They have a community fund for schemes where the whole community can benefit. I had to put together all the background information and cost information and application for a grant was submitted. It was a very formal nailbiting few weeks, but on 11 September 2012 we went along to the lodge to collect a cheque for £3120!
Unfortunately one of our collection boxes was stolen during a break in at our local Coop. Luckily, we had emptied it very soon before so there can't have been too much in. We were still chunnering from this when we received an email from a company in the UK that manufacture the type of defibrillators used in the community. They offered to give us one of their defibs! Arrangements were made for someone from HeartSine,the company, to fly in from Belfast and come to Tottington on Friday 14 September to make the presentation. This was a top of the piece of equipment that was quite pricey. When John McMurty from HeartSine found out about the appeal he also said he would donate a training defibrillator. This is a 'dummy' unit and it arrived this week. It shows people exactly what the equipment does and how to use it. It should hopefully assure people that they are easy to use.
We were approached by Peel Lions who said they would like to hold one of their Race Nights to raise money for our appeal. That event was on Saturday 22 September and was held at St Anne's Parish Hall. This isn't just any church hall. It has been recently refurbished, and there was a bar (well, we couldn't have a race night without one!). It was a great family fun event and it raised a whopping £1067.
We have had to change our goal somewhat. We should be able to install 3 defibrillators in Tottington in a fairly short time. There is a still a lot of red tape to get through and permissions to obtain, and when I thought the fundraising would be the hard part it seems I was mistaken. We need to make sure we have the money to run the equipment for a few years, but you never know, we may end up with four (wishful thinking) in the area, to cover Tottington, Walshaw and maybe Greenmount.
There has been some negativity about the scheme, and I have been surprised at some of the people who have been less that enthusiastic. However, this is a fairly new idea and I'm sure that before too long there will be lots of other defibrillators appearing in the area. They are all over in France in different areas, so there is no reason they shouldn't catch on here too. They do need maintaining, and I know I'll have to do weekly or fortnightly checks, but this can be done when I'm passing them.
I will be so pleased when the first one is officially up and running, and the people of Tottington have mainly had a great 'can do' attitude. Thank you for supporting the appeal!
Blog of someone trying to fit as much as possible into life. Lover of the Camino de Santiago. I live in Tottington and try to improve it where possible. I'm married to Paul and have two children. Follow me on X @LoveTottington and Instagram @tottingtonjude and @journeysbyjude
Thursday, 27 September 2012
Saturday, 12 May 2012
How can you say you're lonely?
So how can you tell me you're lonely, and say for you that the sun don't shine? Let me take you by the hand and lead you through the streets of any town or city in the UK, and I'll show you something to make you change your mind.
This morning I managed to stay in bed until 6.50am, the longest lie in I have had all week. My frozen shoulder has been really troublesome and is affecting the length of time I can sleep. Work have benefitted greatly, as I've been at my comfy desk chair by 6am most mornings, but I've been a bit down the last couple of days. This morning was the most painful it has been, so I was feeling very sorry for myself. Feeling down already I started to think about everyone who must have far worse pain than this on a daily basis, with no propsect of it getting any better.
The sun was out though, and it was time to put on a brave face. I found my iPod the other day so I could listen to feelgood music while getting on with some paperwork. I managed a first listen to Annie Lennox's 'A Christmas Cornucopia'. This was just what was needed. A loud cheery sing-a-long to Christmas carols with a twist while looking at the sunny May morning outside the window. After that I took pot luck and put the iPod on Shuffle. The first song on was Ralph McTell's 'Streets of London', and suddenly, although I was at risk of running out of tissues, I realised how good things really were for me.
Have you seen the old man
In the closed-down market
Kicking up the paper,
with his worn out shoes?
In his eyes you see no pride
Hand held loosely at his side
Yesterday's paper telling yesterday's news.
I have a wardrobe full of shoes that I hardly ever wear. I wear the same 2-3 pairs day in day out, and it takes years to wear them out because I spend as much time as possible being comfortable in my slippers at home. Just over two years ago I spent the most I'd ever spent on a pair of shoes. (They were about £80. Not a lot for a lot of people but for me it was a fortune). For about 8 months of each of the following two years I wore these shoes practically every day, whether I was climbing up hills or going to a wedding. This year I got them out again and apart from looking a bit battered the soles had started to wear through. I decided that based on a 'cost per wear' calculation they had probably been good value, but when I tentatively went to enquire about the cost of a new pair I found they had been discontinued. I was disappointed, but what a thing to be disappointed about! I'm lucky, I have plenty more pairs to choose from.
The "In his eyes you see no pride" was thought provoking. How long do people have to be down for to completely lose pride in themselves? You can visit any town and find someone passing time in this way, on their own and with nothing rewarding to do. I wonder if there has been a gradual change, or has there been a specific life event that has 'helped' them along to this stage in their lives? Do they have something they can look forward to? Is tomorrow going to be just the same as today? Vulnerable people that are on their own without support can expect less and less help due to the ongoing government cuts. Day centres and support groups are closing around us, and if these people didn't have mental health problems to start with I suspect they they would soon start to experience problems. Eighteen months ago I would have argued that keeping the support groups going would be the cheaper option for the government, to prevent people deteriorating and needing more assistance from the NHS or the benefits system. I must have been very naive. Recent cuts to the NHS and benefits system have shown that whatever help a lot of people need, they just aren't going to get it. I have often seen people sat with a polystyrene cup at their feet asking for money, and I have been reluctant to help, thinking it could be used for their next fix. More and more times now I see people and see their desperation for a hot meal.
Have you seen the old girl
Who walks the streets of London
Dirt in her hair and her clothes in rags?
She's no time for talking,
She just keeps right on walking
Carrying her home in two carrier bags.
I could fill two carrier bags with the possessions I have scattered on my bedroom floor at the moment. This 'old girl' must have at least as many aches and pains as I do, and I'd struggle walking up to the village shops with a couple of heavy bags just now. Where I lived as a child we had a village 'tramp'. I don't know how the system had failed him, or how much of it was a lifestyle choice (I know a strange one but in those days there were hostels open that people could get a bed at). Nowadays you hear stories of people who have had a job and a house, been married and had children, and their lives have changed beyond recognition, with them ending up sleeping on the streets. I haven't got the answers (although I'm confident a change in government wouldn't be a bad thing) but how can these people get themselves out of their situations, or how can we give them the support to be able to do this? In my 45 years I have only slept rough on one occasion. It was by choice - we either slept rough or missed the end of the Farewell GLC Jobs for a Change Concert in London in 1985 in order to catch the train home. We chose the night in Battersea Park, and although it was a glorious day in July it was incredibly cold, and everytime I found a decent bench to lie down on I couldn't sleep as I was convinced the rats would come and eat me. People have to cope with this every night, whatever the weather. Again, certainly in Bury, not too long ago there was no need for anyone to sleep rough. There were enough beds in short term hostel accommodation for anyone who needed one. I very much doubt that is the case now.
In the all night cafe
At a quarter past eleven,
Same old man is sitting there on his own
Looking at the world
Over the rim of his tea-cup,
Each tea last an hour
Then he wanders home alone.
I've passed time sitting with a cup of tea in a coffee shop on many occasion. As I'm trying to cut back a bit, and it never fails to amaze me how much places can charge for a value teabag and some boiling water, I do think twice. However, these places have their uses when I'm killing time and want to sit down somewhere warm and dry. This man may have had no electricity to be able to make his own cuppa. I haven't had an electricity meter but my daughter tells me you can't just put a small amount of money on them. When living on benefits, especially the benefits that have recently been reduced so much, at the end of the week choices need to be made. Heating or food? And that is if there is money left for either of those. A cup of tea late at night in a cafe could provide a much needed hot drink somewhere warm, with some sort of company even if it is only the interaction when ordering a drink, before going back to a cold bleak bedsit.
And have you seen the old man
Outside the seaman's mission
Memory fading with
The medal ribbons that he wears.
In our winter city,
The rain cries a little pity
For one more forgotten hero
And a world that doesn't care.
It isn't just our heros that this government is trying to forget; it is whole groups of our society. These are groups that need and deserve help, and you can take away their rights, their benefits, their healthcare and their self-respect but they are still going to be there. What are those with the power to make the required changes going to do about them? I recently thought I was helping someone living in supported housing that was being encouraged to 'bid' for a council flat. They really didn't want to live in the areas where flats for single people were available as they didn't know anyone and would have to travel to be near and have the support of their friends and family.They would also have to travel if they were lucky enough to find work. They needed one bedroomed accommodation for Housing Benefit to even contemplate covering the cost. I managed to find a tiny one bedded house in the right area, and the cost worked out at less than Housing Benefit would have paid for the council flat. I was fortunate enough to be able to help with the deposit and the rent in advance, and the letting agency agreed they would rent the house to a tenant out of work.
The next stop was to get a definitive answer about Housing Benefit. I found that in 2008 a Local Housing Allowance was brought in for tenants who privately rented their accommodation. This was sold as being beneficial to people, giving them the flexibility to choose what was right for them. In 2011 rates were vastly reduced, and from January 2012 in Bury a single person could only receive an allowance to live in one roomed shared accommodation, currently £46.15 a week in my area. All our hopes were dashed as there was no way this property could now be rented. We looked elsewhere, and the cheapest single room we found in Bury, in a house with a shared bathroom and kitchen was £65 a week. I'm thinking of block booking a room next time there is a Travelodge sale. For not much more than this, this person would get a double room with a bathroom, all heating an electricity, a TV and have tea and coffee provided. How can this be right, and how are they going to be able to better themselves?
I am well aware that some people don't help themselves, but I cannot believe that the majority have chosen to be in the situation they have found themselves in, and the way things are I can't think how they can escape. I work hard and I work full time, but like everyone else my bills are rising, I have had no pay rise for two years, my pay is frozen, and I have just had a big increase to the contributions I make to my pension. However, I am lucky that there are cuts I can make. If necessary I can cancel my gym membership, I don't need an iPhone contract, and I can stop drinking altogether, instead of my cut back to Asda 3 for £10 wine. Others aren't so lucky.
My GP has advised me to see an NHS physiotherapist and assured me the wait won't be long. If it was though I could make some cuts and see a private practitioner. If I'm in pain I can go to the pharmacist and buy a strong painkiller.
When I get down I can pick up the phone and speak to friends and family who I know are there for me. So many people haven't anyone they can call even if they had the phone. I can go out for a walk and will always have someone I can stop and speak to. That wouldn't be so easy if I hadn't been able to shower for weeks and was wearing all the clothes I owned. When I've done that I can come home, snuggle on the sofa and watch a feelgood DVD. That is such a little thing that we take for granted, but so many people would love to do that, and can't.
I can't do much for people, and my voluntary work tends to be with youngsters who are actually really privileged, getting them to appreciate the outdoors instead of getting too attached to their games consoles. A few minutes listening to my iPod this morning though has certainly given me food for thought. The fact that you are reading this now indicates that you have privileges that many don't.
Next time you see someone like those described in the song, spare a thought for how they may have found themselves in that situation, and how lucky you are. Have a think if there is any small way you can help. Just a few words of kindness can help, it doesn't have to cost anything.
I can't say I'm lonely, and the sun has been shining on me all my life which I am hugely grateful for and do not take for granted. I am very lucky.
Finally, one way to help is to have a say in how the country and your local Council is run. You can't have this if you don't vote. In Bury just one third of people had their say and voted last week. People need to lose this apathy, and if we can find a way of getting normal people to show their dissatisfaction in the ways things are going for this country, in 2015 we may get the chance to start the long process of putting things right again.
So how can you tell me you're lonely,
And say for you that the sun don't shine?
Let me take you by the hand and lead you through the streets of London
I'll show you something to make you change your mind .
Link to Streets of London
This morning I managed to stay in bed until 6.50am, the longest lie in I have had all week. My frozen shoulder has been really troublesome and is affecting the length of time I can sleep. Work have benefitted greatly, as I've been at my comfy desk chair by 6am most mornings, but I've been a bit down the last couple of days. This morning was the most painful it has been, so I was feeling very sorry for myself. Feeling down already I started to think about everyone who must have far worse pain than this on a daily basis, with no propsect of it getting any better.
The sun was out though, and it was time to put on a brave face. I found my iPod the other day so I could listen to feelgood music while getting on with some paperwork. I managed a first listen to Annie Lennox's 'A Christmas Cornucopia'. This was just what was needed. A loud cheery sing-a-long to Christmas carols with a twist while looking at the sunny May morning outside the window. After that I took pot luck and put the iPod on Shuffle. The first song on was Ralph McTell's 'Streets of London', and suddenly, although I was at risk of running out of tissues, I realised how good things really were for me.
Have you seen the old man
In the closed-down market
Kicking up the paper,
with his worn out shoes?
In his eyes you see no pride
Hand held loosely at his side
Yesterday's paper telling yesterday's news.
I have a wardrobe full of shoes that I hardly ever wear. I wear the same 2-3 pairs day in day out, and it takes years to wear them out because I spend as much time as possible being comfortable in my slippers at home. Just over two years ago I spent the most I'd ever spent on a pair of shoes. (They were about £80. Not a lot for a lot of people but for me it was a fortune). For about 8 months of each of the following two years I wore these shoes practically every day, whether I was climbing up hills or going to a wedding. This year I got them out again and apart from looking a bit battered the soles had started to wear through. I decided that based on a 'cost per wear' calculation they had probably been good value, but when I tentatively went to enquire about the cost of a new pair I found they had been discontinued. I was disappointed, but what a thing to be disappointed about! I'm lucky, I have plenty more pairs to choose from.
The "In his eyes you see no pride" was thought provoking. How long do people have to be down for to completely lose pride in themselves? You can visit any town and find someone passing time in this way, on their own and with nothing rewarding to do. I wonder if there has been a gradual change, or has there been a specific life event that has 'helped' them along to this stage in their lives? Do they have something they can look forward to? Is tomorrow going to be just the same as today? Vulnerable people that are on their own without support can expect less and less help due to the ongoing government cuts. Day centres and support groups are closing around us, and if these people didn't have mental health problems to start with I suspect they they would soon start to experience problems. Eighteen months ago I would have argued that keeping the support groups going would be the cheaper option for the government, to prevent people deteriorating and needing more assistance from the NHS or the benefits system. I must have been very naive. Recent cuts to the NHS and benefits system have shown that whatever help a lot of people need, they just aren't going to get it. I have often seen people sat with a polystyrene cup at their feet asking for money, and I have been reluctant to help, thinking it could be used for their next fix. More and more times now I see people and see their desperation for a hot meal.
Have you seen the old girl
Who walks the streets of London
Dirt in her hair and her clothes in rags?
She's no time for talking,
She just keeps right on walking
Carrying her home in two carrier bags.
I could fill two carrier bags with the possessions I have scattered on my bedroom floor at the moment. This 'old girl' must have at least as many aches and pains as I do, and I'd struggle walking up to the village shops with a couple of heavy bags just now. Where I lived as a child we had a village 'tramp'. I don't know how the system had failed him, or how much of it was a lifestyle choice (I know a strange one but in those days there were hostels open that people could get a bed at). Nowadays you hear stories of people who have had a job and a house, been married and had children, and their lives have changed beyond recognition, with them ending up sleeping on the streets. I haven't got the answers (although I'm confident a change in government wouldn't be a bad thing) but how can these people get themselves out of their situations, or how can we give them the support to be able to do this? In my 45 years I have only slept rough on one occasion. It was by choice - we either slept rough or missed the end of the Farewell GLC Jobs for a Change Concert in London in 1985 in order to catch the train home. We chose the night in Battersea Park, and although it was a glorious day in July it was incredibly cold, and everytime I found a decent bench to lie down on I couldn't sleep as I was convinced the rats would come and eat me. People have to cope with this every night, whatever the weather. Again, certainly in Bury, not too long ago there was no need for anyone to sleep rough. There were enough beds in short term hostel accommodation for anyone who needed one. I very much doubt that is the case now.
Ken Livingstone, 1985 |
In the all night cafe
At a quarter past eleven,
Same old man is sitting there on his own
Looking at the world
Over the rim of his tea-cup,
Each tea last an hour
Then he wanders home alone.
I've passed time sitting with a cup of tea in a coffee shop on many occasion. As I'm trying to cut back a bit, and it never fails to amaze me how much places can charge for a value teabag and some boiling water, I do think twice. However, these places have their uses when I'm killing time and want to sit down somewhere warm and dry. This man may have had no electricity to be able to make his own cuppa. I haven't had an electricity meter but my daughter tells me you can't just put a small amount of money on them. When living on benefits, especially the benefits that have recently been reduced so much, at the end of the week choices need to be made. Heating or food? And that is if there is money left for either of those. A cup of tea late at night in a cafe could provide a much needed hot drink somewhere warm, with some sort of company even if it is only the interaction when ordering a drink, before going back to a cold bleak bedsit.
And have you seen the old man
Outside the seaman's mission
Memory fading with
The medal ribbons that he wears.
In our winter city,
The rain cries a little pity
For one more forgotten hero
And a world that doesn't care.
It isn't just our heros that this government is trying to forget; it is whole groups of our society. These are groups that need and deserve help, and you can take away their rights, their benefits, their healthcare and their self-respect but they are still going to be there. What are those with the power to make the required changes going to do about them? I recently thought I was helping someone living in supported housing that was being encouraged to 'bid' for a council flat. They really didn't want to live in the areas where flats for single people were available as they didn't know anyone and would have to travel to be near and have the support of their friends and family.They would also have to travel if they were lucky enough to find work. They needed one bedroomed accommodation for Housing Benefit to even contemplate covering the cost. I managed to find a tiny one bedded house in the right area, and the cost worked out at less than Housing Benefit would have paid for the council flat. I was fortunate enough to be able to help with the deposit and the rent in advance, and the letting agency agreed they would rent the house to a tenant out of work.
The next stop was to get a definitive answer about Housing Benefit. I found that in 2008 a Local Housing Allowance was brought in for tenants who privately rented their accommodation. This was sold as being beneficial to people, giving them the flexibility to choose what was right for them. In 2011 rates were vastly reduced, and from January 2012 in Bury a single person could only receive an allowance to live in one roomed shared accommodation, currently £46.15 a week in my area. All our hopes were dashed as there was no way this property could now be rented. We looked elsewhere, and the cheapest single room we found in Bury, in a house with a shared bathroom and kitchen was £65 a week. I'm thinking of block booking a room next time there is a Travelodge sale. For not much more than this, this person would get a double room with a bathroom, all heating an electricity, a TV and have tea and coffee provided. How can this be right, and how are they going to be able to better themselves?
I am well aware that some people don't help themselves, but I cannot believe that the majority have chosen to be in the situation they have found themselves in, and the way things are I can't think how they can escape. I work hard and I work full time, but like everyone else my bills are rising, I have had no pay rise for two years, my pay is frozen, and I have just had a big increase to the contributions I make to my pension. However, I am lucky that there are cuts I can make. If necessary I can cancel my gym membership, I don't need an iPhone contract, and I can stop drinking altogether, instead of my cut back to Asda 3 for £10 wine. Others aren't so lucky.
My GP has advised me to see an NHS physiotherapist and assured me the wait won't be long. If it was though I could make some cuts and see a private practitioner. If I'm in pain I can go to the pharmacist and buy a strong painkiller.
When I get down I can pick up the phone and speak to friends and family who I know are there for me. So many people haven't anyone they can call even if they had the phone. I can go out for a walk and will always have someone I can stop and speak to. That wouldn't be so easy if I hadn't been able to shower for weeks and was wearing all the clothes I owned. When I've done that I can come home, snuggle on the sofa and watch a feelgood DVD. That is such a little thing that we take for granted, but so many people would love to do that, and can't.
I can't do much for people, and my voluntary work tends to be with youngsters who are actually really privileged, getting them to appreciate the outdoors instead of getting too attached to their games consoles. A few minutes listening to my iPod this morning though has certainly given me food for thought. The fact that you are reading this now indicates that you have privileges that many don't.
Next time you see someone like those described in the song, spare a thought for how they may have found themselves in that situation, and how lucky you are. Have a think if there is any small way you can help. Just a few words of kindness can help, it doesn't have to cost anything.
I can't say I'm lonely, and the sun has been shining on me all my life which I am hugely grateful for and do not take for granted. I am very lucky.
Finally, one way to help is to have a say in how the country and your local Council is run. You can't have this if you don't vote. In Bury just one third of people had their say and voted last week. People need to lose this apathy, and if we can find a way of getting normal people to show their dissatisfaction in the ways things are going for this country, in 2015 we may get the chance to start the long process of putting things right again.
So how can you tell me you're lonely,
And say for you that the sun don't shine?
Let me take you by the hand and lead you through the streets of London
I'll show you something to make you change your mind .
Link to Streets of London
Monday, 7 May 2012
Opening of the new Woolfold Viaduct
We have just got back from an 'historic event' in the Tottington area.
The Bury to Holcombe Brook Branch Railway was in use from 1882 to 1963. In 1972 the then Tottington Council considered changing the track of the railway into an off road path. Today, 40 years later, that path finally opened. It is now possible to walk or cycle from Greenmount, through Tottington, Woolfold and Brandlesholme, to Bury without having to negotiate roads.
In December 1974 the old Woolfold viaduct was demolished. The rest of the path could be opened fairly easily, but having no viaduct at Woolfold would mean a lot more planning, and more importantly money, would be required. However, in December 2007 Sustrans' Connect2 programme was awarded £50M of lottery fund money following a TV vote. Sustrans Homepage. This meant that the project could begin.
There was a lot of planning, design and land acquisition to be done, but work started in February 2011.
Sustrans also has a Portrait Bench project, which is for public art. A Portrait Bench is a simple bench with three life sized figures close by. These figures are chosen by the community for their contribution to local life, culture or history (NB it is now my ambition to be next to a portrait bench....or be a mayor). The figures are cut from sheet steel. Next to the Woolfold viaduct we have David Swithenbank, Reginald Harris and Ralph Rooney.
Ralph Rooney (1862 to 1949) was well known in the Tottington area as a councillor, long distance walker and naturalist. After working for 44 years in a mill he became under gardener at Croich Hey.
Reg Harris OBE (1920 to 1992) grew up in Bury. He won two silver medals in the 1948 Olympic Games as well as several other professional titles. He was awarded an OBE (another of my ambitions) in 1958 and was named Sportsman of the Year by the BBC Sporting Record in 1949.
David Swithenbank is a lifelong resident of Holcombe. He is a walker and an artist, currently being the president of Bury Art Society. He campaigned for public rights of access on Holcombe Moor, and it was partly due to his campaigns that it was sold to the National Trust by the Ministry of Defence.
It is David Swithenbank who officially opened the viaduct today, piecing together the off road path. The whole event came together with planning from several organisations, in particular Greenmount Village Community. www.greenmountvillage.org.uk. Bury Ranger Service were there along with Sustrans, and South Lancs Bat Group came to give a talk on the bats around the Kirklees Trail (they bought a bat with them too). I was there representing Tottington Wildlife Watch Group (TWIGs), the children's branch of The Wildlife Trust. Our group is for 8 to 13 year olds, although we aren't strict about the ages. We meet every month and do 'something' outdoors. This can be pond dipping, vegetable planting, willow weaving, a bat walk and many other activities. Today, we ran the family quiz that people could complete as they walked along the trail.
After the official opening people were invited to walk the approximately two miles along the trail to Greenmount Old School where there were displays and exhibitions about the area, as well as pasties and peas for people to replenish their energy with. I was 'livetweeting' along the way, and I was amazed how many people turned up. It was fabulous seeing so many people walking and cycling along the Kirklees Trail and then joining us at the school afterwards. It was a real sense of community, and when I got home, over six hours after I had left this morning, I really felt like some good had been done.
The sun stayed out until most people were safely at the school having a cuppa, which was brilliant as the forecast had been awful. I think this will encourage people to get out in the open more as it is so safe for children to be on their bikes. It is now a lovely walk to the town centre for those feeling energetic, and there are so many entrances along the way that people from all the way from Bury to Greenmount can find somewhere to join it.
We are so lucky living here, and today everyone pulled together to make this event a huge success. Well done everyone.
Train going over the old Woolfold viaduct |
In December 1974 the old Woolfold viaduct was demolished. The rest of the path could be opened fairly easily, but having no viaduct at Woolfold would mean a lot more planning, and more importantly money, would be required. However, in December 2007 Sustrans' Connect2 programme was awarded £50M of lottery fund money following a TV vote. Sustrans Homepage. This meant that the project could begin.
The new viaduct, officially opened 7.5.12 |
Sustrans also has a Portrait Bench project, which is for public art. A Portrait Bench is a simple bench with three life sized figures close by. These figures are chosen by the community for their contribution to local life, culture or history (NB it is now my ambition to be next to a portrait bench....or be a mayor). The figures are cut from sheet steel. Next to the Woolfold viaduct we have David Swithenbank, Reginald Harris and Ralph Rooney.
Ralph Rooney, taken before the opening. |
Reg Harris, taken before the opening. |
David Swithenbank is a lifelong resident of Holcombe. He is a walker and an artist, currently being the president of Bury Art Society. He campaigned for public rights of access on Holcombe Moor, and it was partly due to his campaigns that it was sold to the National Trust by the Ministry of Defence.
David Swithenbank today, 7.5.12 |
The start of the walk. |
Nearing the end of the walk. |
The sun stayed out until most people were safely at the school having a cuppa, which was brilliant as the forecast had been awful. I think this will encourage people to get out in the open more as it is so safe for children to be on their bikes. It is now a lovely walk to the town centre for those feeling energetic, and there are so many entrances along the way that people from all the way from Bury to Greenmount can find somewhere to join it.
We are so lucky living here, and today everyone pulled together to make this event a huge success. Well done everyone.
Saturday, 21 April 2012
Spring Shows and Festivals
The line-up for the 2012 Ramsbottom Festival (the North West's newest boutique festival no less) was announced this week. I got an early bird weekend family ticket for 'Im Indoors for Christmas (OK I suppose it was for me) which was a brilliant saving. Glastonbury is no good for me. I don't want to camp in a field of mud and have to queue for hours for horrible flooded toilets. Ramsbottom is great. We can all go if we want to, and it is so close we can just phone a taxi if we miss the last bus home. I can't wait. I like to see live music, and on the Friday night I'll be there jumping about to The Inspiral Carpets. My 10 year old can have his first 'festival' experience too. http://www.skiddle.com/festivals/ramsbottom/lineup.html
I've been busy baking today. I 'don't do' baking, but my excuse is that my oven is so poor that it doesn't heat up to what I tell it to, is different temperatures in different places, and you can't predict how it will behave. This time next year will be a different story, when I have my new kitchen, but for now, I'm stuck with it. I decorated my 'Jubilee cake' for the Tottington Horticultural Society Spring Show last night. Harrison had suggested I did a street party and it sounded like a good idea. I must think a bit more before agreeing to these things in the future. I spent hours making miniature bunting then had to decide how to stick it up. I decided on cocktail sticks and my dad, @halegc, gave me some superglue. I don't think he'll do that again. Within minutes of starting glue was everywhere, and I was stuck fast to a cocktail stick. I had a job to complete though, so after setting @halegc the task of finding out a 'cure' I cut the stick so it was short and battled through. The 'cure' turned out to be nail varnish remover (I had none) or a quick trip to A&E as they keep something there for these occasions. Obviously I couldn't seek medical advice and would rather have walked round with a stick on my finger for weeks than tell a doctor in Bury what I'd done. Luckily, later on, after being soaked, it fell off.
I also have some home make sloe gin and rhubarb vodka. The vodka was particularly awful and takes the coating off your mouth, but I was persuaded to enter it (I think for comical value and to make other entrants feel good). I thought the sloe gin would be ready but when I went to decant some last night disaster struck. It had 'gone missing' a while ago, but I found it in a corner under the stairs. I had kept it hidden from before my holidays in February and was to finish it off when I returned. Unfortunately I forgot and the sloes were still in the jar. It was a lovely colour, but not a great taste! That's been entered too. I also made shortbread. Harrison is very impressed, 'Im Indoors isn't! The cherry and cheese (not together) scones were more of a disaster but one I'm blaming wholly on the oven. The middle didn't seem to cook, and one cherry scone is burnt on one side. They have all gone off for judging though. I couldn't enter a non burnt one as you have to show 3 of each, and I only made 3 plus a tiny one to taste! Finally I entered the photography competition that had to be on the theme of 'celebrations'. I don't think I'll need help carrying trophies home this time, but I won't give up.
A while ago my shoulder started hurting. I thought it was the arthritis that was diagnosed 6-7 years ago and then mysteriously disappeared making a comeback. It got worse and worse, and getting dressed each morning was a terrible struggle. Swimming in the middle of the day was also a trauma as it would take me twice as long to get changed then dressed again than it did to have the swim! I gave in this week and went to the doctors. I don't like doctors, hospitals etc so I had put it off as long as I could. A frozen shoulder was diagnosed, which I wasn't happy about. I (wrongly) thought that the cure for this was a big injection into my shoulder bone, which was one reason I was avoiding the doctors. I was prescribed some anti-inflammatory tablets to try before a decision is made about physiotherapy etc.
The tablets I have are enormous (and so they should be, the price I paid for the prescription!). I like to know everything about what I'm taking before I have them, so I trawled though the information leaflet and the British National Formulary. I wasn't too happy about the list of possible side effects and even unhappier that I didn't see the usual 'side effects are very rare but we just need to mention them in case' bit. By the time I'd read everything I was convinced that within days I would have (among other things):
A swollen neck and face (how could I tell?);
Blisters on my hands and feet;
Pus filled spots;
Alopecia;
Jaundice;
Hepatitis;
Death of part of my kidneys;
Heart failure
Insomnia;
Tinnitus;
Visual Disturbances; and my favourite bit of the leaflet
"If you think you may be having a stroke contact your doctor immediately".
I have only had 3 days worth and I can see no benefit just yet, but I still have a full head of hair, am not yellow, and my heart seems OK. Unfortunately I have a rash and am spotty. That should help clear the swimming pool when I go later though. Every cloud etc...
It must be awful to have something like this for years. I couldn't even fasten my pinny this morning! If I'm not around for a while, it could be the side effects.
I've been busy baking today. I 'don't do' baking, but my excuse is that my oven is so poor that it doesn't heat up to what I tell it to, is different temperatures in different places, and you can't predict how it will behave. This time next year will be a different story, when I have my new kitchen, but for now, I'm stuck with it. I decorated my 'Jubilee cake' for the Tottington Horticultural Society Spring Show last night. Harrison had suggested I did a street party and it sounded like a good idea. I must think a bit more before agreeing to these things in the future. I spent hours making miniature bunting then had to decide how to stick it up. I decided on cocktail sticks and my dad, @halegc, gave me some superglue. I don't think he'll do that again. Within minutes of starting glue was everywhere, and I was stuck fast to a cocktail stick. I had a job to complete though, so after setting @halegc the task of finding out a 'cure' I cut the stick so it was short and battled through. The 'cure' turned out to be nail varnish remover (I had none) or a quick trip to A&E as they keep something there for these occasions. Obviously I couldn't seek medical advice and would rather have walked round with a stick on my finger for weeks than tell a doctor in Bury what I'd done. Luckily, later on, after being soaked, it fell off.
A while ago my shoulder started hurting. I thought it was the arthritis that was diagnosed 6-7 years ago and then mysteriously disappeared making a comeback. It got worse and worse, and getting dressed each morning was a terrible struggle. Swimming in the middle of the day was also a trauma as it would take me twice as long to get changed then dressed again than it did to have the swim! I gave in this week and went to the doctors. I don't like doctors, hospitals etc so I had put it off as long as I could. A frozen shoulder was diagnosed, which I wasn't happy about. I (wrongly) thought that the cure for this was a big injection into my shoulder bone, which was one reason I was avoiding the doctors. I was prescribed some anti-inflammatory tablets to try before a decision is made about physiotherapy etc.
The tablets I have are enormous (and so they should be, the price I paid for the prescription!). I like to know everything about what I'm taking before I have them, so I trawled though the information leaflet and the British National Formulary. I wasn't too happy about the list of possible side effects and even unhappier that I didn't see the usual 'side effects are very rare but we just need to mention them in case' bit. By the time I'd read everything I was convinced that within days I would have (among other things):
A swollen neck and face (how could I tell?);
Blisters on my hands and feet;
Pus filled spots;
Alopecia;
Jaundice;
Hepatitis;
Death of part of my kidneys;
Heart failure
Insomnia;
Tinnitus;
Visual Disturbances; and my favourite bit of the leaflet
"If you think you may be having a stroke contact your doctor immediately".
I have only had 3 days worth and I can see no benefit just yet, but I still have a full head of hair, am not yellow, and my heart seems OK. Unfortunately I have a rash and am spotty. That should help clear the swimming pool when I go later though. Every cloud etc...
It must be awful to have something like this for years. I couldn't even fasten my pinny this morning! If I'm not around for a while, it could be the side effects.
Saturday, 14 April 2012
Dear Mr Cameron
I've been very quiet on here as there is so much going on elsewhere. I have other things I need to finish off before I get back into blogging again but hopefully it won't be too long off.
However, this week I had sight of a letter written by a 12 year old girl to David Cameron. This had been written without any prompting and help, and she presented her parents with copies to send off to anyone they could think of. This 12 year old had heard her parents worrying and decided to join in the fight. I'm hoping this gets emailed to anyone they can think of to make some kind of an impact. Read on (I did seek their permission first and took the name out).
However, this week I had sight of a letter written by a 12 year old girl to David Cameron. This had been written without any prompting and help, and she presented her parents with copies to send off to anyone they could think of. This 12 year old had heard her parents worrying and decided to join in the fight. I'm hoping this gets emailed to anyone they can think of to make some kind of an impact. Read on (I did seek their permission first and took the name out).
Dear Mr Cameron,
I am writing this letter on behalf of my father who has a
disability. He was put into the Work Related Activity Group of the Employment
Support Allowance instead of the support group which he should have been put in
in the first place. Because of this he is losing £400 a month! Because my
father has multiple sclerosis he is unable to work, which means he isn’t
earning a wage. Now, the government are stopping any money coming into my
father’s account by 30th April 2012, however, if my father had been
put in the right group (the support group) he would still be getting the money
which we rely on every month.
I understand that I am only 12 years old, but I understand
what is happening to this country and I believe that I should have a say in the
matter. I also understand that you only receive a certain amount of money over
the year and that you have to spend it on things that matter, but there is one
thing I do not understand. Lots of money has been spent on new things for the
country like new community centres etc. but why isn’t the money being spent so
you can help people in need like my father. Some families cannot work because
they are too ill, but if you stop their money coming in to their bank accounts
every month then they will not have any money to rely on when they need it.
I do respect you and the government Mr Cameron, and I respect
what you are doing, but some families like mine are not happy with your choices
and as you are the prime minister, I think you should respect them and help
them like you would help any other person that matters to you. If this country
did not care about the money we earn or about the buildings we have in this
country and we just cared about each other and help everyone who does not have
a great amount of money, then I am sure you would not be receiving any letters
off people asking for money and benefits because you would already be helping
everyone who is in need.
I do hope that you read this letter and that it changes your
mind about stopping money coming into my father’s account. Once again, I do
respect you and I hope that I do not sound like I am being disrespectful to
you.
Yours sincerely,
Personally I think this 12 year old must have been brought up very well to be so polite, and after a few weeks of being without this money she might have lost her respect for Mr Cameron and the government. Good luck to them and Mr Cameron, shame on you.
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