Ymgyrch Byw’n Annibynnol

Mae polisiau cenedlaethol ar Fyw’n Annibynnol wedi cael eu cyflwyno yn Lloegr a’r Alban, ond nid yng Nghymru.  Cafodd trafodaeth yn y Cynulliad ar 12 o Fai 2010, gefnogaeth unfrydol yr holl bleidiau o egwyddorion ymgyrch Anabledd Cymru, Byw RWAN!, a oedd yn galw am Strategaeth Cenedlaethol ar Fyw’n Annibynnol.  Cafodd  deiseb gan Anabledd Cymru yn dangos cefnogaeth o Strategaeth Cenedlaethol ar Fyw’n Annibynnol ei arwyddo gan 719 o bobl ar draws Cymru.  Mae’r ddeiseb yn cael ei chysidro gan Bwyllgor Deisebau y Cynulliad.

“Mae Byw’n Annibynnol yn ein caniatau ni, fel pobl anabl, i gyflawni’n bwriadau ac i fyw ein bywydau yn y ffordd rydym yn dewis i ni’n hunain.” (Anabledd Cymru 2010)

Mae Byw’n Annibynnol yn cael ei ddisgrifio gan y Swyddfa ar gyfer Materion Anabledd fel a ganlyn:

“Mae Byw’n Annibynnol yn golygu fod pobl anabl yn cael yr un lefel o ddewis, rheolaeth a rhyddid yn eu bywydau bob dydd ag unrhyw un arall.”

Mynychodd Anabledd Cymru Dai’r Cyffredin ar 24ain o Fai i roi tystiolaeth ar lafar i Ymchwiliad y Cyd-Bwyllgor Hawliau Dynol ar weithredu’r hawl i Fyw’n Annibynnol.

Darllennwch Maniffesto Anabledd Cymru ar Fyw’n Annibynnol

 

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NYTH/NEST – help am pobl mewn tlodi tanwydd

Nyth yw rhaglen newydd Llywodraeth Cynulliad Cymru a gynlluniwyd i helpu pobl sy’n ffeindio hi’n anodd i dalu eu biliau ynni. Mae’r cynllun yn cynnig ystod o welliannau gartref i deiliaid tai i’w helpu i wresogi eu cartrefi’n fwy effeithlon a chadw’n gynnes heb wynebu biliau ynni mawr.

 

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Adroddiad ESA a Chyflyrau Ansefydlog yn Cael ei Gyhoeddi

Mae adroddiad wedi cael ei gyhoeddi, sy’n gwneud argymhellion ar gyfer gwelliannau i’r Asesiad Gallu i Weithio (WCA, Work Capability Assessment) i bobl hefo cyflyrau ansefydlog. Bu i Forward-ME (cynghrair o elusennau ME ym Mhrydain) a phump elusen sy’n cynrychioli ystod o gyflyrau meddygol, gynnal archwiliad oherwydd bod nifer fawr o bobl ar draws Prydain gyda chyflwr iechyd ansefydlog wedi cael eu pennu’n ffit i weithio, er nad oedd hyn yn gywir, ar ol cael yr Asesiad Gallu i Weithio (WCA) ar gyfer y Lwfans Cyfflogaeth a Chymorth (ESA Employment & Support Allowance)

Mae’r 12 o argymhellion yn cynnwys:

  • gofyn mwy o gwestiynau mewn asesiadau er mwyn deall yn well sut mae cyflwr ansefydlog yn effeithio, mewn gwirionedd, ar allu rhywun i weithio
  • newid y ffordd mae’r prawf wedi’i eirio er mwyn gofyn os gall pobl gwblhau gweithgareddau’n ‘ddibynadwy, dro ar ol tro ac yn ddiogel’ ac, fel bo’n gymwys, ‘o fewn cyfnod o amser rhesymol’ a ‘heb anesmwythyd arwyddocaol, anadl yn fyr neu lesgedd’
  • gwella’r prawf i gydnabod y rhwystr rhag gweithio a gyflwynir gan boen, llesgedd neu broblemau gwybyddol

Caiff yr adroddiad ei archwilio nawr gan grwp annibynnol o wybodusion a chaiff yr elusennau gyfle i roi mewnbwn i’r argymhellion cyn iddynt gael eu gyrru yn yr hydref i’r DWP ac i Weinidogion drwy’r Athro Harrington, sy’n gwneud archwiliad annibynnol o’r Asesiad Gallu i Weithio (WCA).

Trafodwyd yr adroddiad ar raglen radio ‘Radio 4’, ‘You and Yours‘, ddydd Mercher, 11eg o Fai, 2011

 

 

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WAMES’ campaign launched during ME Awareness week

WAMES’ campaign launched during ME Awareness week

ME & CFS information for all

10 years of campaigning for better services and talking to people with ME, carers and professionals has shown us that accurate information about ME is not reaching those who need it. During ME Awareness week WAMES is launching a campaign to provide better information in Welsh and English for all who need it, beginning with our new website. We are using research results, clinicians’ experience and patient and carer stories to produce information sheets on a wide range of topics. By including the results of biomedical research we hope we can change many of the misconceptions about the illness that exist within the health service and general public, thus improving dialogue between professionals and those affected by ME, leading to an improvement in their quality of life.

 

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UK Disease register for ME/CFS possible

The National ME/CFS Observatory has successfully completed a pilot study which has found a way to identify people with ME/CFS so they can be included on a register. This will be a pool of possible participants in research trials and sampling studies.

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Wear blue for ME during ME Awareness week

Wear blue for ME during ME Awareness week

WAMES invites people with ME, their friends and family to raise awareness of ME by wearing blue ribbons or items of blue clothing during ME Awareness week.

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Sharon Price invites you to join her in raising funds for WAMES

Sharon Price invites you to join her in raising funds for WAMES

Please help me raise funds for WAMES

On 29th April 2011, I will have had ME for 20 years. (Yep, a Bank Holiday has been declared in my honour!) I want to do something positive to mark the occasion. I am volunteering with the Welsh Association of ME & CFS Support (WAMES) and am supporting their campaign for ME Awareness week 2011 to wear something blue on May 12th, which is International ME Awareness day. Please join me in:

  • Wearing an item of blue clothing such as a tie, cravat, scarf, blouse, skirt or other item of clothing to help raise awareness of ME.
  • wear a Blue Ribbon (contact BRAME, Sharon or Jan if you don’t have one)
  • ask family members, friends and colleagues to join you wearing blue ribbons
  • Tell people why you are wearing blue and what the blue ribbons represent

Please would you be kind enough to not only wear blue on May 12th, but also to pay for the privilege and make a donation to WAMES? WAMES is a voluntary organisation which gives a national voice to people with ME & CFS in Wales, campaigning and raising awareness on our behalf.

If you would like to contribute, please send a cheque payable to:

Sharon Price 10, Hill Crest, Langland, Swansea, SA3 4PW

Or to the WAMES treasurer.

When I have received all your donations, I will send one (hopefully big) cheque to WAMES with the total donated. I am aiming to raise ÂŁ400. (ÂŁ20 for each year I’ve had ME). Apologies for fundraising again, but I haven’t done so since 2009!

Hopefully in 20 years’ time, the world for people with ME will be a very different place and people will no longer have to go through the intolerable pain and suffering I have.

THANK YOU so very much in anticipation of your help and support.

Love Sharon. xx

 

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WAMES’ patron Lord Barry Jones sends message of support

WAMES’ patron Lord Barry Jones sends message of support

Lord Barry Jones has been WAMES’ patron since our inception 10 years ago. During his 40+ years as a politician he has been moved by many encounters with people who have ME and their families. Now in the House of Lords he continues to live in his native Deeside and sends a message of support to WAMES on our 10th birthday.

 

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WAMES is 10 years old!

WAMES is 10 years old!

WAMES was set up by local support groups in April 2001 to improve services for people with ME and CFS in Wales. Progress has been slow but 10 years on people with ME and their carers haven’t given up hope and have a vision for a better life in Wales for all affected by ME.

 

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Welsh care pathway for CFS/ME published but Map of Medicine dropped

Welsh care pathway for CFS/ME published but Map of Medicine dropped

Plans to make the new Welsh care pathway for CFS/ME available to health professionals through the Map of Medicine database has been scrapped by the Health Minister Edwina Hart. Budgetary cuts have led to the subscription for the MoM being dropped but all care pathways will be available to the NHS through the HOWIS e-library. WAMES responded to the consultation as the patients’ representative but cannot recommend the final care pathway. It fails to give sufficient information to help doctors identify neurological ME and does not highlight the limited usefulness and possible dangers of CBT and GET as treatments fort all patients.

 

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