A warm welcome to the South Lancs Branch of the MND Association (MNDA)

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After only a couple of face to face meetings we're back to Zoom again.
 

We just want to let you know that we are having an on-line Zoom meeting next week, which is our usual date of the third Wednesday of the month. It starts at 7.30pm. We will post the link at the beginning of the week.

We are planning to return to face to face meetings next month at the Holiday Inn in Haydock at the usual time, 7:30pm.  

Our March meeting will be our AGM. We will post details nearer the time in March.

We look forward to seeing those of you who can attend next Wednesday.

 

 

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South Lancs Branch Monthly Meetings

 

        Jan 19, 2022 19:30
        Feb 16, 2022 19:30 (Zoom Meeting - Link below)
        Mar 16, 2022 19:30 (AGM)
        Apr 20, 2022 19:30
        May 18, 2022 19:30
        Jun 15,2022 19:30
        Jul 20, 2022 19:30
        Aug 17, 2022 19:30
        Sep 21, 2022 19:30
        Oct 19, 2022 19:30
        Nov 16, 2022 19:30

 



MNDA South Lancs Branch Monthly Meeting
Time: Feb 16, 2022 19:30pm.

Join Zoom Meeting
https://us02web.zoom.us/j/88543360080?pwd=bjhPdEJpcHZ4YlhqSXQ0QWpyUXZ0dz09

Meeting ID: 885 4336 0080
Passcode: 989293

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The South Lancs Branch covers St.Helens and Warrington in the south through Cronton, Whiston, Leigh, Wigan, to Standish Skelmersdale and Burscough in the north. We hold get-togethers every 3rd Wednesday of the month at the Holiday Inn Haydock, Lodge Ln, Haydock, WA12 0JG at 7:30pm. We always welcome new faces to join us for a cuppa and a chat. Our venue is modern, wheelchair friendly and very welcoming. Meetings and Parking are free but please log your car registration with reception.

Contact our chairperson on mndachairsouthlancs@gmail.com or 07908 441 040 for more details.

The branch is run entirely by volunteers and aims to provide the best possible support to local people with MND, their families, carers and those close to them.

 

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What we do:

  • We offer emotional, practical and financial support.

  • Provide a link with other vital services where needed, through our team of trained Association Visitors.

  • Hold regular meetings and other events in the area.

  • Liaise with local health and social care professionals to influence and improve services for people with MND.

  • Campaign to influence and raise awareness of the disease in the wider community.

  • Support and organise fundraising events to contribute to things that improve the quality of life for people living with MND in the South Lancs area, to pay for equipment not provided elsewhere and to help fund MNDA care and national research projects.

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SLB Branch Zoom July 20.PNG

'Embracing technology - Ono of our branch meetings on the Zoom platform'

We had a fantastic time at the 2021 Charity Ball on Saturday the 20th of November 2021.

To book for plce for next year, contact Cris on 07590 266 849 or email mndafundraisingsouthlancs@gmail.com for more details or to book your tickets or sponsorship deal.

 

If you can help here's the link to our just giving page. https://www.justgiving.com/fundraising/mnda-south-lancs-branch

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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2021 South Lancs Charity Ball Flyer.jpg
 

About MND / ALS

What is Motor Neurone Disease (MND)?

 

 

Motor neurone disease (MND) describes a group of diseases that affect the nerves (motor neurones) in the brain and spinal cord that tell your muscles what to do. With MND, messages from these nerves gradually stop reaching the muscles, leading them to weaken, stiffen and waste. Watch the short animation shown above for an overview about the disease, then select from the following to find out more. Our information covers health and social care in England, Wales and Northern Ireland – please contact MND Scotland if you live in Scotland.

 

If you are living with or close to someone with motor neurone disease (MND), the MNDA 'About MND' web hub is designed to help you. It also answers common questions about MND and Kennedy’s disease, including how the disease is diagnosed, and how to manage daily life, access support and find information.

Click here for more information 'About MND'..

  • Facebook Social Icon
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  • Flickr Social Icon
  • YouTube Social  Icon
  • Pinterest Social Icon
  • Instagram Social Icon

Click here for more information about 'What is MND?'..

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South Lancs Branch now has a new Instagram Page.

You'll find links to our each of our Social Media Feeds on each page on our website, look for the Social Bar Icons at the bottom-left of each page and simply click the icon for the feed that you are interested in.

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A huge thank-you to Bill Horton and the team at Salford Community Walking Football Club who have raised £500 for the MND Asociation.

If you can help here's the link to our just giving page. https://www.justgiving.com/fundraising/mnda-south-lancs-branch

 

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South Lancs Branch Dec Quiz Night Flyer_

Big thanks to all who participated in our Xmas virtual quiz night event on the 12th of December 2020. Email fundraisingsouthlancs@gmail.com or scan or click on the QR code for more details of fundraising events.

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Save the Dates.
A Selection of some of our fantastic events for 2021/2022...

We'll be at Warrington Disability Awareness Day ("DAD") at Walton Hall Gardens in Warrington on Sunday the 12th of September 2021. Why not pop in and see what's on offer at the world's largest 'not for profit' voluntary-led disability exhibition, held annually in a huge tented village within the grounds of Walton Hall Gardens in Warrington'.
Entry to the show ground is completely FREE and so is the programme.
Visit https://www.disabilityawarenessday.org.uk/ for more information.


 

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Thank-you all for coming out to support the MNDA and the South Lancs Branch at our Totally Amaze-balls 2018 MNDA Charity Ball. We'll be back with the 2021 Charity Ball on Saturday the 20th of November 2021.
See the flyer at the top of this page for more details..

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The 4th Annual MNDA Awareness Film Evening will be back in June 2022.
This 2020 / 2021 events had been postponed due to CV19
 

MNDA MND Awareness Film Evening

South Lancs Branch Just Giving Page

 

Our branch has a Just Giving page which supports all of the branch fundraising events thoughout the year. Donating through the site is simple, fast and totally secure! We guarantee that the money raised here will go to helping people living with MND and their families in the South Lancs area.  Thanks.

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SLB MNDA QR Code.bmp

Emergency Winter Appeal

The South Lancs Branch of the Motor Neurone Disease (MND) Association has launched an Emergency Appeal for donations to maintain their vital support for people living with MND, a terminal illness.

Local people with MND turn to the South Lancs Branch for advice, face-to-face meetings and importantly can apply for financial grants to help improve their quality of life.

The MND Association expect to lose over £2 million this year due to the cancellation of community and sporting events as a result of the COVID-19 pandemic. But our fight against MND can’t be delayed. Local people affected by the disease need our support now, they need their voices heard today.

But with the COVID-19 restrictions continuing, volunteers at the South Lancs Branch are determined to find other ways to raise money to continue supporting local people facing the devastating illness. 

Our branch is run entirely by volunteers and provides vital support and services support to local people with MND, their families, carers and those close to them.

People with MND are extremely vulnerable and are relying on our help and support now more than ever.

Around 150 people are living with this brutal disease in the South Lancs area, MND is a fatal, rapidly progressing disease which affects the brain and spinal cord. It attacks the nerves that control movement and eventually leaves people unable to move, communicate or breathe. It kills a third of people within a year of diagnosis and half within two years. There is no cure. Thank-you.

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What is the Act to Adapt campaign?

Act to Adapt is a Motor Neurone Disease Association campaign to advocate for accessible homes and a fairer and faster system for delivering housing adaptations for people with motor neurone disease (MND).

 

Currently, many people living with MND face significant challenges when having to adapt their homes or move to accessible housing. These include high costs, a lengthy process and lack of information and support. Without an accessible home, people living with MND may be trapped in one room, unable to reach the bathroom or get out of the front door. In some cases, the COVID-19 pandemic and the need to self-isolate has exacerbated the situation.

 

The Act to Adapt report sets out recommendations for local and national governments to help people living with MND and others in desperate need of accessible housing, based on good practice.

Laura Jaqueline MNDA Spnsored Walk Poste

A huge thank-you to Laura & Jaqueline who raised over £1000 for the MND Asociation by doing a sponsored walk from Wrightington Hospital to Wigan Infirmary honouring their mum on the 18th of July

If you can help here's the link to our just giving page. https://www.justgiving.com/fundraising/mnda-south-lancs-branch

 

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We're back with the 2021 Charity Ball on Saturday the 20th of November 2021.

Tickets and sponsorship are still available. Contact Cris on 07590 266 849 or email mndafundraisingsouthlancs@gmail.com for more details or to book your tickets.

 

If you can help here's the link to our just giving page. https://www.justgiving.com/fundraising/mnda-south-lancs-branch

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