Skip to main content



2. Introductions

Jenny welcomed everyone to the meeting and asked how we were all feeling.

Generally people were feeling ok but were finding the amount of Zoom meetings tiring.

Andrew, Olcay, Joanne, Kieran, Chris and Eve attended The Clarity Project -

Supporting Decision-Making

second session about

1

Session 3 is about Lasting Power of Attorney and

Deputyship - 13.01.2021 7:30pm 9:30pm
People who attended fed back to the rest of the group.

Olcay spoke about her feelings about the use of the term ‘burden’ when speaking about people with learning difficulties.

We then spoke about terminology such as, burden, challenging behaviourand vulnerable.

Petitions about the vaccine were mentioned and the article in Disability News Service.
Petition update · Covid-19 Vaccine Plans Must Prioritize People With Learning Disabilities · Change.org

Andrew provided comments for the Disability News Service article on 3rd December about the vaccine priorities. https://www.disabilitynewsservice.com/vaccine-priority- decision-is-campaigning-victory-but-concerns-remain/

3. Topic: How we communicate about our group

Everyone agreed it would be good to write a bit more about the group and who we are.

This is in addition to the leaflet and will say a bit more about what we have done.

2

Andrew asked everyone to say a couple of words on how they would describe the group to others.

Heres a summary of what was said:

  •   The title of the group is self-explanatory its supportive and campaigning

  •   Campaigning and challenging

  •   Very information Ive picked up a lot

  •   Comradeship and companionship

  •   Meeting with others who have common aims and

    goals

  •   Friendship and meeting new people have fun

    while doing work

  •   Proud of the group and what weve done and

    achieved

  •   Learn from each other

  •   We listen, we learn and we challenge

  •   Jolly and insightful

  •   Its a helpful and interesting group

  •   Members have helped me understand more about

    the virus and other things in plain English

  •   Helped me learn to use Zoom and meet new

    people

  •   Able to share important feelings and concerns

  •   Important way to keep in touch

  •   Its provided an emotional support structure

  •   All though far apart, strong friendships have

    developed

3

  •   Informative and supportive

  •   Its important to me, its a lifeline

  •   It has built my confidence

  •   Its been a political voice and a supportive voice

    when the world wasnt watching or listening to us

  •   Its been a bright light during a dark time

5. Information exchange

Bringing Us Together project

Meetings will start in January 2021. Eight members of this group will be working with 8 family carers

  •   To learn from one another and learn from each other

  •   To develop trust and relationships

  •   To share a common goal and common language

  •   Agree ways of working, our priorities and put

    together our plan of action

  •   Agree on ways of holding bodies accountable

  •   To understand and use the legislation effectively

    and appropriately

    Dates:

    Monday 4th and 11th January 2021 10.00am to 12.00pm
    Monday 8
    th and 15th February 2021 10.00am to 12.00pm

    Monday 8th March and 15th March 2021 10.00am to 12.00pm

4

Andrew asked who would be interested in attending the sessions.

Eve, Kieran and Christopher expressed interest in attending the sessions.

Skills for Care Workforce Expert Advisory Group

The next meeting is 14th December 2020
A pre-meeting will be organised for the new members.

The Clarity Project - Free legal sessions

https://www.eventbrite.co.uk/e/clarity-session-2- supporting-decision-making-tickets-128153186631

Christopher’s artwork for the session

The second session (Tuesday 8th December 2020 at

7.30pm-9.30pm) will cover Supporting Decision-

Making

5


Comments

Popular posts from this blog

SURVIVOR HISTORY NEWSLETTER

>From Andrew Roberts Secretary Survivors History Group http://studymore.org.uk/ studymore@studymore.org.uk telephone: 020 8 986 5251 home address: 177 Glenarm Road, London, E5 ONB Survivor History Group Summer 2012 Newsletter The July London meeting of the Survivors History Group will be held on Wednesday 25.7.2012 from 1pm to 5pm at Together, 12 Old Street, London. Everybody is welcome and refreshments will be provided. The September meeting has had to be moved from a Wednesday to Thursday 27.9.2012 (subject to approval by this Wednesday's meeting) because of the availability of a room at Together.   -------------------------------------------------------------------- The agenda for the July meeting will be drawn up at the beginning of the meeting, but it will include Peter Campbell's regular report back on the research he is leading on the history of Survivors Speak Out and discussion of material received from other people about Survivors Speak Out.  Rick Hennelly has se...

The DLA and Workfare Scandals.

This ConDem Coalition is exploiting the apparent helplessness of disabled people by taking essential money away from them and forcing vulnerable people, for example, people with mental health difficulties. I remember, when I was a practising social worker, the horror experienced by service users when they received a letter summoning them to undergo a medical examination (25 miles away in Norwich). Some became absolutely terrified at the prospect and the stress of having to get to and face the appointment led to one or two relapses and hospital admissions. Against local authority policy, I always took them to the appointment, went in with them and supported them through the interview acting as advocate. The doctors at these reviews were employed by the Benefits Agency and usually retired from practice. They were also usually empathic with the service user and mostly helped to reduce the terror of the interview. The new 'Workfare' reviews which every DLA claimant will have to und...

inappropriate!!!

I tried to respond to a Patient Citizen Exchange blog by Laura Greene today. I said: Hello Laura. Welcome - and my admiration? for you "single-handedly representing the entire health voluntary sector and 1000+ PCX membership..." My first question has to be: what is the composition of the Strategic Advisory Board? And my second question: what proportion of service users to professionals is there on that Board? There are indeed millions of impatient citizens out there. They are called Service Users (primarily because 'Patient" carries the labels 'One that has things done to her/him'; 'One that is subservient to the "We know what is best for you" approach'; 'One that is at the wrong end of an imbalance of power.' etc). The Americans prefer the term 'consumers', but whatever, we should avoid the term with the negative connotations. I was listening to the 5 Live debate this morning on the Strictly Come Dancing row about whether...