This path is now open in the evening due to a new school having been built in the park. The path is heavily used by parents, children and local people going between Acton Central Station and buses on Uxbridge Road. It is very dark in winter. The Churchfield Community Association has asked Ealing Council to install lights (solar if suitable) to come on only in winter and for limited hours, e.g. 6-8.30am and 4-8pm. The Council have asked us to show support for this proposal.

**REFUSE TO DRINK IN STARKIE ARMS TILL SAM IS REINSTATED AS MANAGER** Sam has brought our local pub back to life before Sam starkie arms was not the place to be she is funny friendly and the most caring person we have ever met she always puts us first. Sam has been given 26 days to leave Starkie Arms for not reaching a certain target. Bravo inns really need to listen to the people of padiham

There is an increasing focus on the recycling of many different materials. Whilst this is obviously vital for environmental sustainability, we should also encourage the use of recycled and reclaimed resources, to ‘close the loop’ and increase the demand for these materials.

This is the link between New Cumnock and the main town, Cumnock. The path was constructed after a man was fatally injured on this stretch. As it is quite a level section it would help able bodied, disable, sight impaired people to both exercise and commute in safety. Many cannot afford to commute by bus for groceries etc.

It is needed by the community and is a key part of our local infrastructure - lots of people use it and it has easy access for the disabled and elderly. A lot of businesses in the town rely on the branch to do their banking and have business accounts there.

As a disabled resident I often walk my dog at Busby Glen. I use a mobility scooter so I’m unable to access the top part of the park as the only access is stairs. There is access if you are able to walk up the grass verges but on a mobility scooter, it’s impossible. I would like the council to address this issue.

Over the past couple of years, we've become aware that climate crisis is approaching even faster than we expected. We've seen record-breaking temperatures around the globe, and that's given rise to some apocalyptic scenes. Bats and birds dropping out of the sky during heatwaves in Australia. Wildfires in Greece and whole towns destroyed by wildfire in America. The Intergovernmental Panel on Climate Change has warned us that swift action must be taken in the next eleven years to avoid the worst consequences of climate change. 40% of the UK's emissions come from households. Every year, the average household emits 2.7 tonnes of CO2 just from heating. That's more than a person should emit every year from ALL sources - travel, food, shopping - if we're going to avoid climate chaos. Before the Zero Carbon Homes policy was scrapped in 2015, we were on track to reduce this 2.7 tonnes to zero in new homes. That wouldn't just have helped the planet - it would have helped people to keep their energy bills down, too. The abolition of the Zero Carbon Homes policy was called "short-sighted, unnecessary, retrograde and damaging." Ed Davey, former secretary of state for energy and climate change suggested the then PM, David Cameron “may as well hug a coal power station”. But we're in a new era now. Politicians across the political spectrum are being forced to admit just how important it is to cut out the carbon. Bringing back the Zero Carbon Homes standard would be a massive step forward, showing the public and the world that the UK Parliament's declaration of a Climate Emergency isn't just empty words.

We don't typically name conditions/diseases/illnesses based on their symptoms. Recently Bile Acid Malabsorption was renamed to Bile Acid Diarrhoea. We shouldn't label this condition by its already stigmatised and extremely horrid symptom. From the age of 12 I have suffered from debilitating and soul destroying unpredictable diarrhoea. For 20 years I was told that I was 'probably just an anxious person' and 'must have a lot of intolerances' by medical professionals. It was so bad that I couldn't eat out, or really go on holiday, and some days, it made it hard to leave the house. I've had accidents when out with friends, family and at work. Honestly, it is absolutely soul destroying. I would later find out that because I could actually leave the house sometimes, I had it better than some... In 2017 I finally got answers as to why I constantly had diarrhoea; my digestive system had an overload of bile - I was constantly producing it (our bodies only usually discharged when we eat then reabsorb and produce if needed) so overall it was too much for my body to handle. It wasn't caused by anxiety/nerves, but it certainly caused a lot! When I was diagnosed by an amazing consultant in 2017, the condition was known as Bile Acid Malabsorption. It was first discovered in 2008. It has three main types: Type 1 BAD affects people who have BAD as a result of either inflammation of the small bowel due to Crohn's disease or surgical removal of the small bowel. Type 2 BAD (previously referred to as idiopathic/primary bile acid malabsorption). Type 3 BAD affects people with various gastrointestinal diseases such as removal of the gallbladder (Cholecystectomy), small intestinal bacterial overgrowth (SIBO), post radiation treatment for cancer, coeliac disease and chronic pancreatitis. Research studies suggest that 1:3 people who have Irritable Bowel Syndrome with diarrhoea (IBS-d) as a prominent feature could have primary BAD. (Source: https://bad-uk.org). Type 2 is the most prevalent, and is no other disorder affecting the small bowel. It's believed those with Type 2 BAD have a hormone defect - our bodies don't produce enough of the 'off' hormone to tell the liver to stop producing the bile. This is the biggest proportion of sufferers of the condition. Estimates say that around 17% of the UK population suffer from IBS. (Source: https://www.bjmp.org/content/irritable-bowel-syndrome-primary-care-physicians) So, a nasty condition, that causes debilitating diarrhoea, and all the pain, low energy and serious mental health issues that go along with that. Top that with 1:3 of those diagnosed with IBS potentially having it, (that's 5.6% of the UK population, or roughly the same amount of the population who are diagnosed with depression*!), and you see it's a major concern to those who have it, and those who may have it. Rightly, in 2017/2018, the NHS teams working on and with Bile Acid Malabsorption decided that the name didn't really fit with the latest findings - only one of the three causes was to do with malabsorption. They decided to call it Bile Acid Diarrhoea, because diarrhoea is the one thing all three causes had in common. Unfortunately for those suffering with the lifelong condition, this meant that we now have to explain to medical professionals, friends, employers, and anyone else who may need to know, that we suffer from bile acid diarrhoea, but the reality is that most people will just hear the "diarrhoea". As a sufferer, I want to be in some control over who knows what symptoms my condition comes with. Though we completely agree that there should be no stigma around diarrhoea, or any other 'embarrassing' bodily conditions, the truth is that the new name of our condition is making it even harder to live with. Imagine if you had to explain an illness/disease/condition primarily by one of its symptoms - it's horrid, isn't it. I therefore would LOVE to see the lovely and incredible medical professionals within our wonderful NHS and across the world rename our condition to something that doesn't include it's biggest and most embarrassing symptom, or even better perhaps after one of those who discovered it. This petition is by no means meant to offend those who worked/work so tirelessly in discovering the condition and how to treat it, and the wonderful charities that support it - they have changed all of our lives for the better. We just want to be able to talk about our condition openly, and not worrying how non medically trained people might perceive it. We might not be able to cure the condition, but we can make it a little easier to talk to people about it. *Source: 3.8 million in the UK suffer from depression according to https://digital.nhs.uk/data-and-information/publications/statistical/quality-and-outcomes-framework-achievement-prevalence-and-exceptions-data/quality-and-outcomes-framework-qof-2015-16, and 5.7% of the UK population is 3,591,000.

Mr Cummings was incharge of the worst case of misleading the people of Uk ever, he was the major campigner and director of the leave campaign. This has been shown to have broken electral law and the missused data against GDPR rules. He refused to answer to the commons committee on his actions during the campaign and is in contempt of parliament. He has no respect for either our laws or our parliament and is it i therefore of utmost impotance that he face the parliamentary committee to answer questions re his conduct in the leave campaign

Bristol has one of the highest rates or bike usage in the UK, in fact 57,000 walk or cycle to work, the highest in England & Wales. Over a quarter of Bristolians ride a bike at least once a week, let's get those numbers up by improving safety and consideration on the roads. We must ensure there is less traffic wars between cars and bikes by, when it is possible, providing dedicated bike lanes. 80% of Bristolians feel traffic congestion is a major problem, an increased use of bikes would have an immediate effect on car usage, just removing 10% of cars at peak time has a huge effect on traffic flow. In order to meet the Net Zero target for 2030 we should really be pushing to encurage bike uptake. Bicycles are safe, clean, green, convenient and fun, not to mention all the health and social economic benefits, so let's build a city than Bristolians want and so rightly deserve. Thank you, Bristol Citizens

48% of people with epilepsy in the uk have refractory epilepsy (not controlled). This places them at increased risk of death and injury. In the uk deaths from epilepsy have increased 70%. Many people would benefit from a change of licence for epidiolex which has been shown to help in these cases but are been denied it due to current licensing guidelines. Sadly families and individuals are suffering currently due to the current situation.

I was shopping with my son the other day and we saw that Heinz soups and beans are available as single cans or multi-packs. The multi-packs are wrapped in plastic yet sell for less per individual item. We feel that it is morally wrong that individuals have to make a choice between buying affordable food with a higher plastic footprint or spend more on a product with less packaging. We are asking Heinz to cut stop this wasteful practice now.