We'll let the service users explain in their own words... 'Someone got in touch with me regarding the cuts to Newmarket's Children's Centre. People are way more switched on than the Tories take them for. They see through the double speak. I've taken out the name. If this brave individual wants to come forward I'm leaving it up to her. 'With regards to Foley House being part time and how it will affect people locally , the childrens centre is a life line for new isolated mums! It is chance to meet new people in the same boat as you when you are all of a sudden stuck at home with a newborn. I have used their groups the past 2.5 years with my daughter all of their groups and classes seem popular such as wiggle and jiggle and infant massage. If anything they should be offering more groups and classes for people to attend. The help and support is there all week, they welcome new mums to breastfeed, bottle feed and change their babies at foley house if they are in town. This ican be quite important for new breastfeeding mums as it can be quite a daunting prospect feeding in public early on. Also their groups are all free, there are other baby toddler groups in town but not all mums on maternity pay and low income families can afford the going rate of £5 per group (without paying for siblings!) 3, 4 or 5 days a week. Im not sure what the 'revamp' means but i can only presume part time means a cut in support for mums, families and their children and a cut in what foley house has to offer as a whole! Fair enough there are other childrens centres in red lodge and mildenhall but not everybody drives or can attend centres further afield.' ''When I was pregnant with my first child I didn't know anyone in Newmarket and I really wanted to meet other mums and learn more about babies and parenting. I went with my husband to Foley House to sign up and that's how it all started. I have attended so many different groups, classes over the years..from baby sensory to potty training sessions, toddlers groups, weaning, breastfeeding, almost anything that was offered. I have met many mums that some of them are now my best friends. In a short time I went from not knowing much about pregnancy, babies and not knowing anyone here to then having so much support and many great friends. It felt great, I was doing groups every day, seeing people every day. Sometimes people on maternity leave say they feel lonely and don't know who to ask for help and staying home with small babies can sometimes be very isolating - that's why having a place like Foley house is so, so important! This is definitely not the area where the money should be cut and rather where it should be invested even more. Parents who have more support are I believe happier and will be able to raise their children in a calmer and more educated way. This is investing in our future. I do hope that the cuts won't affect the Foley house as they are really providing a great support for local families.'

Suffolk County Council have declared a Climate Emergency and an intention to make Suffolk the 'Greenest County'. Yet they have joined Ipswich Borough Council in a plan to build a dual carriageway through some of Suffolk's most beautiful countryside, including the lovely Fynn Valley, where critically endangered Turtle Doves can still be heard. They plan to pay for this road by building 20,000 new homes, concreting over yet more countryside. There is not work for anything like that many people in the area. This will result in tens of thousands more car journeys as people commute long distances to work and result in an environmental catastrophe for the county and the country as a whole. Please stop this madness.

This is important because it is ruining the biggest and the best sport in the world. It is ruining it because fans don’t even know when to celebrate. For example, Manchester City vs Tottenham. In the UCL, where tensions are the highest, no one realised that the player was offside which is the referees fault for not realising and the players fault for not calling it. I know it makes the game more fair but it also slows the game down tremendously which is unfair for people who buy the ticket just to go watch referees decide whether that was a penalty or not. Also, it takes away the atmosphere factor in the game as it slows the game down so much. For example, there were more penalties in the 2018 World Cup than any other World Cup, which resulted it in being more boring as it took too much time out of the game looking at VAR. Right now, football is trying to counter that by not listening to every VAR call which is very unfair. For example, Tottenham VS Manchester City, the referee didn’t review the city player being fouled in the box but reviewed the slight handball later on. If You want football to return the way it was sign this petition. If you have PASSION and If you have LOVE for the game then you would sign this petition to remove VAR or make it better. Thank you for reading through this

The 13 hospice beds at the In Patient Palliative Care Unit, St Charles Hospital, Ladbroke Grove are used by people with a life limiting illness for respite, symptom control and care in the last days of life. They’ve been closed “temporarily” because of staff shortages but now policy makers are claiming they are unnecessary and that beds can be found elsewhere. However alternative hospices are under pressure themselves and difficult for many to access. At the end of their lives people and their loved ones need care that’s familiar and easily reached.The Pembridge is well regarded and well used – its beds should be saved.

Students from all over Europe can benefit by studying abroad for a year through the Erasmus Programme. For UK students this hugely beneficial programme will end in 2020 as a result of the UK leaving the European Union. The benefits of Erasmus are many, but one of the great achievements of the programme is to have brought Europeans closer together, exchanging ideas and lifestyles. British students will lose out to their European counterparts after the funding for this programme ends next year. If ever there was an action that showed how Britain is raising the drawbridge and keeping out our European neighbours this symbol of unity among people being unceremoniously dropped is a symbol of our isolation. We must let future generations benefit from this great programme and help UK students share in this fabulous programme.

The Hay Lane crossing is used by school children, including young children attending Tregoze Primary School which is around the corner from the crossing. Residents regularly hear cars screeching down the road and there have been multiple near misses. Ultimately the road is a death trap and action needs to be taken now not after another collision takes place. Over two years ago my son was hit by a car while he was crossing Hay Lane and suffered severe injuries. Since then I have been promised on multiple occasions that the council would make the road safer but nothing has happened.

Indian army has been oppressing Kashmiri people since last 70 years. In the light of recent events, where India has started to extend its illegal occupation of Kashmir, human rights of people there are at stake. Kashmiri people are under siege with no freedom. India’s extremist regime is similar to Nazi regime, and minorities are facing serious risks to lives in India. There are mobs of Neo Nazi extremists, lynching innocent people on streets. Sanctions on India will force India to step back and solve the issue of Kashmir as per the will of Kashmiri people. it is our collective responsibility to protect rights of Kashmiri people and minorities in India.

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

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

This clause contradicts the commitments made by the Assembly in their declaration of a "climate emergency". It was used by the oil and gas giant, Eni, to justify their application for a license in Cardigan Bay this May. It will be set in stone for twenty years, according to Environment Minister Lesley Griffiths, this month, when the WNMP is approved.