{"id":11763,"date":"2025-03-11T16:26:17","date_gmt":"2025-03-11T16:26:17","guid":{"rendered":"https:\/\/genomicspartnership.wales\/?p=11763"},"modified":"2025-03-11T16:24:19","modified_gmt":"2025-03-11T16:24:19","slug":"safbwynt-y-bwrdd-seinio-dyma-georgina","status":"publish","type":"post","link":"https:\/\/genomicspartnership.wales\/cy\/newyddion\/safbwynt-y-bwrdd-seinio-dyma-georgina\/","title":{"rendered":"Safbwynt y Bwrdd Seinio: Dyma Georgina"},"content":{"rendered":"\t\t
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Safbwynt y Bwrdd Seinio: Dyma Georgina <\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Ymunodd Georgina \u00e2 Bwrdd Seinio\u2019r Cleifion a\u2019r Cyhoedd Partneriaeth Genomeg Cymru yn 2024 a hi yw\u2019r Cynrychiolydd Cleifion a\u2019r Cyhoedd mwyaf newydd ar Fwrdd y Rhaglen, sy\u2019n dod \u00e2 rhanddeiliaid allweddol mewn genomeg ynghyd i drafod ystod o weithgareddau strategol.\u00a0<\/span>\u00a0<\/span><\/p>

Buom yn siarad \u00e2 Georgina i ddysgu mwy am pam ymunodd \u00e2\u2019r Bwrdd Seinio a\u2019i r\u00f4l newydd fel aelod o Fwrdd y Rhaglen.\u00a0<\/span>\u00a0<\/span><\/p>

A allwch chi ddweud wrthym pam y gwnaethoch ymuno \u00e2 Bwrdd Seinio GPW?\u202f<\/span><\/i><\/b>\u00a0<\/span><\/p>

Mae gen i 26 diagnosis meddygol, gan gynnwys Syndrom Ehlers Danlos hypersymudol (hEDS) a chlefyd Crohn, felly rydw i wedi cael cryn dipyn o brofiad gofal iechyd. Mae hEDS a Crohn’s yn enetig, fe wnaethom lwyddo i olrhain fy hEDS o fy mam-gu, i lawr at fy mam ac yna i mi a’m brodyr a chwiorydd. Hyd yn hyn, nid ydynt wedi dod o hyd i’r union fwtaniad genynnol sy’n achosi hEDS, ond maent wedi gwneud ar gyfer mathau eraill o EDS. Oherwydd hynny, rydw i wastad wedi bod \u00e2 diddordeb mewn geneteg a sut maen gweithio.\u202f<\/span>\u00a0<\/span><\/p>

Dechreuais weithio yn y maes cynnwys cleifion a’r cyhoedd mewn ymchwil chwe blynedd yn \u00f4l, ac ers hynny, rwyf wedi cynnig safbwynt claf ar dros 40 o brosiectau a chynigion. Rwy’n anabl ac yn weithgar iawn o fewn y gymuned pobl anabl, felly rwy’n dod \u00e2 phersbectif gwahanol i faterion hygyrchedd mewn astudiaethau, efallai na fyddai pobl abl yn meddwl amdano. Pan glywais am y cyfle i ddylanwadu ar y byd genomeg drwy Fwrdd Seinio GPW, achubais ar y cyfle.<\/span>\u00a0<\/span><\/p>

Ers ymuno, sut brofiad a gawsoch?<\/span><\/i><\/b>\u00a0<\/span><\/p>

Ers ymuno, rydw i wedi dysgu cymaint am y byd genomeg. Mae gennym ni ddiwrnod hyfforddi chwe awr, i helpu i gwmpasu hanfodion yr hyn y mae angen i ni ei wybod, ac rwy’n meddwl fy mod yn dysgu mwy ym mhob cyfarfod Bwrdd Seinio am wahanol feysydd o genomeg! Mae fy mhrofiad wedi bod yn gwbl gadarnhaol, a dweud y gwir, ni allaf ddod o hyd i un peth negyddol i\u2019w ddweud am y Bwrdd Seinio. Rwy’n edrych ymlaen yn fawr at bob cyfarfod, oherwydd gwn y bydd yn wahanol i’r olaf a byddaf bob amser yn gadael yn gwybod hyd yn oed yn fwy am eneteg. Gellid gofyn inni edrych ar gynllun profi genetig a rhoi ein barn ar ba ganlyniadau y byddem yn gwerthfawrogi eu cael, neu roi sylwadau ar Strategaeth Ymchwil Genomeg Cymru, er enghraifft.<\/span>\u00a0<\/span><\/p>

Rwyf hefyd wedi mwynhau\u2019n fawr y cyfleoedd y mae\u2019r Bwrdd Seinio wedi\u2019u rhoi i mi i gymryd rhan mewn mwy o brosiectau sy\u2019n seiliedig ar eneteg, fel siarad yng Nghaffi Genomeg y Nadolig ar gyfer Parc Geneteg Cymru a\u2019u helpu i greu rhestrau termau genomeg ar gyfer gwahanol lefelau gallu.<\/span>\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Beth oedd eich hoff beth am fod yn aelod o’r Bwrdd Seinio?<\/span><\/i><\/b>\u00a0<\/span><\/p>

Fy hoff beth am y Bwrdd Seinio yw cael gweld sut mae ein safbwyntiau a’n barn yn siapio genomeg. Daw ymchwilwyr a grwpiau partner yn \u00f4l atom gydag adborth ynghylch sut yn union y mae ein safbwyntiau wedi cael eu hintegreiddio ac mae gweld ein gwaith yn gwneud gwahaniaeth gwirioneddol yn rhoi boddhad mawr.<\/span>\u00a0<\/span><\/p>

Beth wnaeth i chi fod eisiau gwneud cais i ddod yn rhan o fwrdd Rhaglen GPW?\u202f<\/span><\/i><\/b>\u00a0<\/span><\/p>

Ym mhob cyfarfod o\u2019r Bwrdd Seinio, rydym wedi cael adborth gan Guy a Sarah fel rhan o\u2019u r\u00f4l fel Cynrychiolwyr Cleifion ar Fwrdd y Rhaglen. Bob tro roedden nhw\u2019n rhoi adborth, roedden nhw bob amser yn siarad yn gadarnhaol am y cyfarfodydd a\u2019r gwaith roedden nhw\u2019n ei wneud, roedden nhw\u2019n dweud bod pobl yn gwrando arnom ni ac y gallem roi barn y claf i Fwrdd y Rhaglen yn dda. Roedd y ffyrdd roedden nhw\u2019n bwydo\u2019n \u00f4l bob amser yn ddiddorol ac yn ddifyr hefyd, er enghraifft, fe wnaethon ni ysgrifennu ein gobeithion, ein hofnau a\u2019n cymhellion ar gyfer ymwneud \u00e2 genomeg, yna fe wnaethon nhw greu PowerPoint o\u2019r holl atebion i roi adborth i Fwrdd y Rhaglen.<\/span>\u00a0<\/span><\/p>

Bob cyfarfod Bwrdd Seinio, rydym yn rhannu i ystafelloedd trafod mewn gr\u0175p ac mae un person yn gwirfoddoli i roi adborth i’r gr\u0175p cyfan, y rhan fwyaf o’r amser rwy’n cynnig gwneud oherwydd rwy’n ei fwynhau’n fawr. Rwy’n meddwl bod bod yn gynrychiolydd Bwrdd y Rhaglen yr un peth, dim ond ar raddfa fwy!<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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What are your hopes for the future of genomics?\u00a0<\/span><\/i><\/b>\u00a0<\/span><\/p>

One of my hopes for genomics is to reduce the fear and misconceptions that are still very prevalent. I really want to help spread the word about genetics and genomics and put people\u2019s worries at bay. I think the world of genomics needs to prioritise allaying fears people have on things like genetic engineering and \u201cdesigner babies\u201d, that\u2019s not what we do at all. I think once you know that the fear goes away and people can see the incredible benefits, like in early intervention for genetic conditions. I think being on the Programme Board will enable me to present these fears and hopefully work with the board to find a way to reduce them, this will allow us to show the positive impacts that genomics has and the potential to improve everyone\u2019s lives.<\/span>\u00a0<\/span><\/p>

One of the areas I find most exciting in genetics is pharmacogenomics, for example using testing to see if someone is more likely to get side effects from a medication, or which drug will be most effective for them. I\u2019ve spent my life being put on and taken off different medications, while the doctors try to work out what medication is most effective and how to minimise the side effects I get. I\u2019m currently prescribed 26 pills a day, some of them are needed just to counteract the effect of other medications. Pharmacogenomics could have potentially prevented me from having reactions and side effects to certain medications that made me very unwell or put me in hospital. I\u2019m always on the lookout to see what breakthroughs have been made and how they\u2019re going to be used to help people.<\/span>\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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What are you looking forward to as a member of the Programme Board?\u202f<\/span><\/i><\/b>\u00a0<\/span><\/p>

My first meeting is soon, I\u2019m looking forward to meeting everyone on the Board and hoping that I\u2019ll be able to do the Sounding Board proud and represent everyone well. I met with Sarah, the other Sounding Board representative, and she told me in more detail what sort of things we\u2019ll be doing together. I\u2019m excited to work with her and hopefully feedback to the Sounding Board in the same fun ways her and Guy have become so well known for. I\u2019m hoping that I\u2019ll be able to further influence the world of genetics through the Programme Board by putting forward the patient\u2019s and public\u2019s viewpoints well.<\/span>\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Safbwynt y Bwrdd Seinio: Dyma Georgina Ymunodd Georgina \u00e2 Bwrdd Seinio\u2019r Cleifion a\u2019r Cyhoedd Partneriaeth Genomeg Cymru yn 2024 a hi yw\u2019r Cynrychiolydd Cleifion a\u2019r Cyhoedd mwyaf newydd ar Fwrdd y Rhaglen, sy\u2019n dod \u00e2 rhanddeiliaid allweddol mewn genomeg ynghyd i drafod ystod o weithgareddau strategol. Buom yn siarad \u00e2 Georgina i ddysgu mwy am […]<\/p>\n","protected":false},"author":143891588,"featured_media":11754,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"advanced_seo_description":"","jetpack_seo_html_title":"","jetpack_seo_noindex":false,"jetpack_seo_schema_type":"","_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_wpcom_ai_launchpad_first_post":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"{title}\n\n{excerpt}\n\n{url}","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"_wpas_customize_per_network":false,"jetpack_post_was_ever_published":false},"categories":[1396],"tags":[],"class_list":["post-11763","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-newyddion"],"jetpack_publicize_connections":[],"jetpack_shortlink":"https:\/\/wp.me\/pb2bmH-33J","jetpack_sharing_enabled":true,"amp_enabled":true,"jetpack_featured_media_url":"https:\/\/genomicspartnership.wales\/wp-content\/uploads\/2025\/03\/Nat-Rose-Rare-DIsease-Day-case-study-.png","_links":{"self":[{"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/posts\/11763","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/users\/143891588"}],"replies":[{"embeddable":true,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/comments?post=11763"}],"version-history":[{"count":9,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/posts\/11763\/revisions"}],"predecessor-version":[{"id":11795,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/posts\/11763\/revisions\/11795"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/media\/11754"}],"wp:attachment":[{"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/media?parent=11763"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/categories?post=11763"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/genomicspartnership.wales\/cy\/wp-json\/wp\/v2\/tags?post=11763"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}