Nethercote Gardens is a cul-de-sac with several specific strengths and challenges. The River Cole on which we sit is a haven for local wildlife and must be protected - our low position also puts us at risk of flooding and our road was disproportionately affected by such flooding earlier this year. Many residents feel that recent housing developments which have been completed in recent years have increased the risk of localised flooding; by increasing concrete and build areas we are rapidly losing valuable soft ground which absorbs water. This creates water run off during times of extreme weather and means homes like ours are more likely to flood. Adding another property to the road will be to the detriment of our local wildlife population which local residents are already fighting to support. The plot on which the development is planned sits immediately opposite 177a Nethercote Gardens which is a shared supported living home for people with assessed care. The residents of this property are extremely vulnerable adults and not able to object to this build, which would impact their daily lives, on their own behalf. Our residents have faced and are facing enough challenges due to our unique position and feel that we have been let down at numerous points by the local authority over the years, by allowing local building work, by not having adequate flood supports in place both during and after such events. Our small community are opposed to this build and will keep campaigning to ensure that it does not go ahead. Please, please sign our petition and add to our collective voice - we need to make some noise about this; small builds that negatively impact residents can sneak under the radar but they all add up to people having lower quality of life and our countryside being affected. Enough is enough. Please, please sign our petition. Thank you. "What we allow will continue."

The sudden announcement that Totton, Hampshire Mobility Aids Center should close on the 12th October 2018 demonstrates a complete disregard for every local resident. The idea of a Mobility Aids Center is to assist those people most in need. I know personally how difficult it is to obtain such resources. Already there are severe limitations to Patient Transport, Community Transport. Being forced to travel to "selected destinations" will instantly be out of reach for local residents affected by the "change. Due to mobility restrictions of residents Fording-bridge and Lymington is impossible and definitely impracticable for the overwhelming majority. Visiting the Mobillity Aid Location in Totton has been my last resort and have been using the service for the past 15 months. Hampshire County Council have a duty of care for her residents. To allow closure is not the answer or a reasonable adjustment. What is certain Geoff Chesire "refuses to acknowledge people in crisis" This can not be ignored. Thank you everyone for your support.

£300m of funding has been ear-marked by the Department for Transport to improve access at railway stations. Stroud station should have funding to be inclusive and allow everyone the choice to use rail transport and enjoy a smooth and comfortable journey. At the moment, the alternative route for wheelchair users or those who cannot manage the steps is a difficult route without dropped kerbs, over rough surfaces and with gradients that would be impossible for those not in a motorised wheelchair.

A lease agreement for our 4 acre woodland (named Ladybird woods by our toddler children) is vital for Ignite Unlocking Potential as a social enterprise to support schools, community & families with educational services including Wales's only Nature Kindergarten, Ladybirds Parent & Toddler group, Adventure camps and activity days for children with physical disabilities & additional learning needs. During the 4 years as a business tenant paying against a draft agreement of 21 years, we have transformed 4 acres of unused land into a centre for excellence in Nature based Pedagogy. To date, this learning & play space has enabled us to make a real difference to the lives of over 8000 children and provides leading edge education and training services to education & health professionals across Wales and the UK. Please read some of our reviews from parents & teachers that we have recently supported. Your signature will provide our children with the hope that we can continue to enrich their lives and provide a place that nurtures and unlocks their potential. "My little one went to the summer camp up the country park he has ADHD and struggles sometimes with friends and groups, to say he had an amazing time is a understatement he loved it the staff where amazing with him , come bk a very different child and much more confident, he can't wait to go again thank u all !!!!" Leanne Evans (Parent). "You don't know what a massive part your team has played this summer for my kids x so thank you all x" Caly Cross (Parent). "Had a wonderful time volunteering with the Ladybirds Parent and Toddler group today- very wet and soggy but a beautiful atmosphere, Thank you" Catrin Doyle (Volunteer). "This week I started my Forest School Leader training with you guys and I've loved every second. So many amazing ideas, people and open-ended resources! Just what I needed to get my mind back on track, can't wait for the next sessions!" Jordan Baxter (Teacher). “The community has nothing but wonderful things to say about the organisation and we’ve been waiting years to be able to attend!” “Ignite embody all of the goals and principals of the Well-being for future generations ACT. The adults love it.The Children love it.The community Need it.They promote health and wellbeing - both physical and mental, through a connection with the outdoors.They need the space!” Eve Harris (Parent).

Fusion won’t allow Charlie Barkers assistance dog George go to the music Festival! PLEASE HELP BY SIGNING & SHARING. From Charlie: ____________________ "I'm 23 and for one day I would just like to be that care free 20 year old who enjoys live music. But it's being taken away from me because Fusion won't let me take my Assistance Dog, George! I have a condition called Ehlers-Danlos Syndrome. EDS affects the body’s connective tissue. Connective tissue lies between other tissues and organs, keeping these separate whilst connecting them, holding everything in place and providing support, like the mortar between bricks. EDS causes my joints to dislocate, mostly my shoulders and hips. My gorgeous George helps me to relocate them. Without George, I will end up in A&E, meaning I could miss most of the concert but more importantly Fusion will have put me through unnecessary pain. George does Deep Pressure Massage for pain relief #myrock" ____________________ Please help show Fusion Charlie needs his assistance dog George and they are discriminating against him! https://www.equalityhumanrights.com/sites/default/files/assistance-dogs-a-guide-for-all-businesses.pdf

With the upcoming ban on flasks, we find this unacceptable for many people. Some people bring soup to a game (something that is not sold at the stadium), some people bring tea or coffee as they cannot afford to buy Hot Drinks at the stadium. (This may be a family or someone on a reduced income). A flask at football is a right of passage and is for refreshment purposes not as a weapon. How many times has a football player been hit with a rogue flask? Is this really for safety or a way of increasing revenue from drink sales?

The Forward Centre was purpose built 35 years ago as a base for adults with physical disabilities to meet others who faced similar problems and encourage each other to try things they had never thought of doing Many of the activities require specially trained staff to assist people with a wide range of disabilities often caused by accidental injuries or long term illness The Social Work Services are having to make cuts of £100,000 to their annual budget and the only way open to them is buildings or staff. If the staffing levels are reduced the service to the members will suffer so they have decided to demolish a perfectly sound building

This is important for us as we pay a license to trade and we have overnight free camping which sometimes our spot gets parked in and we cannot trade, we are paying a license to trade and the council license team seem to think it’s not their problem if I can’t trade! Which then means I can’t provide a service to all my customers who come to Polzeath for my pancakes!! I employ local staff, and my carbon footprint is zero, I live here, all year round. Please sign and share and let the council know why you think this is important to you and your families when you come to visit Cornwall.

I myself am disabled and I now have to walk 20 minutes to the new bus stop, then walk 20 minutes to work. This is without standing around waiting for buses. If I choose to catch the new bus - 27 I will have to wait around for another bus to take me to the city. Also a lot of elderly people live on my housing estate and the change will make it harder for them to go to Harbourne as it does not go down the high street and also when they want to go to birmingham they will have to change buses and wait around for another one, this will be especially hard for them and myself in the winter months.

Hello! My name is Zack, and I'm a prospective animation student. I have multiple psychiatric and physical disabilities that make it very difficult for me to live independently - to counter this, I am owner training my own assistance dog. The university were made aware of this, and accommodation have already agreed - but the course leaders have stated that my dog cannot attend classes. If my dog can't come, then neither can I, that's simply the reality of how my conditions affect me. On top of this, if my dog cannot attend then how will he ever learn to be calm in such an environment? I understand that it is a complex and difficult situation, so this survey is for my fellow Animation students who are starting in September 2018 and will theoretically share the classroom with myself and my puppy. By signing, you're saying that you don't have a problem with my puppy (his name is Mochi by the way) being in the classroom, and understand that it may not be perfect but that without him I can't come. I know it sounds silly, but I have been trying to "get better" enough to attend university for nearly 6 years, and I have finally found a viable solution that gets me away from relying on family and carers and gives me more independence.

Jean is 68 years old and lives in Edinburgh. She was born with arthrogryposis, a condition which affects the joints and muscles and prevents development/growth in the legs. Jean is 4 foot 5 inches and wears heavy callipers and surgical boots weighing 3kgs. Each step is a challenge and for the past 20 years Jean has relied exclusively on her specially adapted Motability car to lead an independent life. Recently due to new guidelines for Personal Independence Payments, she has been told that she is no longer entitled to a car. This is unacceptable. Everything Jean undertakes is adapted, adjusted and limited by her physical handicap. Her balance is poor due to no ankle or knee flexion, she struggles with cobbles, uneven ground, steps, kerbs and slopes. If one of her callipers breaks, she is 100% immobile. Public transport is not an option. Boarding a bus requires the use of both arms, leaving no option for carrying any shopping. The height of the seats leaves her legs dangling unsupported, causing swelling and pain. It is of the utmost importance that Jean is permitted to maintain her independence through the provision of a specially adapted car. Her condition will never improve. Taking her car away will leave Jean housebound and reliant on the help of others. To deprive Jean of her car after 20 years, at the time of her life that she needs it most, is cruel and unnecessary. Under the new PIP guidelines Jean’s mobility was reassessed and she was deemed to walk with a “good gait”. The assessment was conducted by target-driven private contractors employed by the DWP. Given her medical condition and profound disability this assessment is evidently deeply flawed. Edinburgh West MP Christine Jardine said that assessments were often “box ticking exercises with no understanding of peoples’ situations”. This certainly rings true for Jean. There is no doubt that Jean should qualify for the enhanced rate of the mobility component of PIP. Please help us persuade Sarah Newton to support Jean’s case by signing and sharing this petition.

Because currently I have a 4 year old daughter with Down syndrome that now exceeds the limit on a baby changing table, therefore leaving me to either put her in danger by using the changing table, changing her on the floor which is a huge infection control risk and undignified OR change her in a pram (which she will soon outgrow) or my car?! I can’t be the only parent in this predicament.