Metabolic Support @MetabSupport
The leading patient organisation for inherited metabolic disorders supporting thousands of patients worldwide to live well today, tomorrow metabolicsupportuk.org Joined January 2022-
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The DfE’s national SEND conversation is live ahead of the Schools White Paper. Some online sessions are still open to hear what’s working, what isn’t, and what real reform should look like. Join a virtual event and share your views: gov.uk/government/new…
Major milestone for the cystinosis community in Scotland! 🎉 SMC has accepted Procysbi for use within NHSScotland, following years of advocacy by Metabolic Support UK, @CystinosisUK & @Kidney_Research . 👉 Read more: shorturl.at/YlAEr
Today is #WorldMentalHealthDay 📷 In 2021, nearly 1 in every 7 people experienced mental health issues. Living with an IMD can bring with it challenges that can affect our mental health but you are not alone. Access our A-Z of mental health orgs: shorturl.at/Ayy8I
💙 October is HCU Awareness Month and we’re bringing the community together! 💙 Join us for a Virtual Meet Up IN ONE WEEK on Sunday, October 12 at 4 PM CT / 5 PM ET / 3 PM MT. 📲 click here to register: bit.ly/HCUmonthmeetup #HCUAwareness #GoBlueForHCU #HCUCommunity
Throwback to #CC24! 🎉 Just over a month to go until our annual community conference. Tickets are flying, and we’ve even had to move to a bigger room to fit everyone in! 👉 Kick off your weekend right and grab your FREE tickets now: shorturl.at/fmoLj
👉 Check out our Monthly Medicines Roundup for September: metabolicsupportuk.org/news-and-event… 📧 Email me what you'd like to see on our website: [email protected]
Are you impacted by genetic conditions? Join online and share your views on new tests and treatments for genetic conditions during pregnancy. Organised by @GOSHCharity and @UCLchildhealth Find out more at redcap.link/tbl4h8v6
Our fundraisers are incredible! Just look at all of these amazing people raising money to help us supporting people living with IMDs. 🎉 Are you planning a fundraiser? Get in touch, let us help you share your amazing work and celebrate your wins!
How do you prepare for a clinical trial? 🤔 Hear from Professor Paul Gissen and find out more on our Research Ready Hub. Interested? Check it out, here: buff.ly/NlRvS77
At 3, James fell dangerously ill with undiagnosed MCADD and slipped into a coma. He’s since overcome huge challenges, body image, mental health & bullying, and proves MCADD “cannot hold you back.” 👉 Read his inspiring story: buff.ly/0iXozi3
Our CEO, Kirsty, and Information and Advice Officer Ellen are at the IMD Metabolic Study Day hosted by Birmingham Women's and Children's Hospital. Here, they're meeting experts and attending interesting lectures. Keep your eyes peeled for a video from their day!
Only two months to go until #CC25! 🎉 Check out this video from Sarah, our Community Lead, on what to expect, and get your FREE tickets by clicking the following link: shorturl.at/JsTeP 🎟️
💡 Think Ammonia. Test Earlier. Save Lives. Hear from Sophie, mum to Rory who experienced dangerously high ammonia as a result of his IMD, Argininosuccinic Aciduria (ASA). 👉 Read more about the Think Ammonia campaign in our one year report: issuu.com/metabolicsuppo…
@RareRevolutionM Thank you for sharing 👏👏👏
Metabolic Support UK's (@weareMSUK) #ThinkAmmonia year one report is now LIVE! The campaign aims to save lives through earlier and accurate ammonia testing. Read the report at bit.ly/3I21RUe
🔥 @RareBeacon are hosting a one-day business planning workshop for rare disease patient groups & charities! 📅 23 Oct, 10:00–16:30 BST. 📍 Notre Dame London 🎯 Leave with a draft plan + practical advice tailored to your goals. Register now 👇 ow.ly/bpg450WihjZ
The #ThinkAmmonia campaign was inspired by too many stories like Rohan's. Read our one year report which shares the progress made possible through collaboration and sets out the next steps to improve outcomes globally. 👉 Read it, now: issuu.com/metabolicsuppo…
When IMDs can't necessarily be prevented, what does the NHS 10-year plan mean for the IMD community? 👉 Read more in our latest article: tinyurl.com/y72kpu2e
Just one week until the launch of our "Think Ammonia: Year One Report". 🎉 Want it directly to your inbox? Sign up to our mailing list: metabolicsupportuk.org/get-involved/m…
Beacon for Rare Disea... @RareBeacon
12K Followers 10K Following Beacon is a UK-based charity that is building a united rare disease community with patient groups at its heart. Previously known as Findacure.
Kate Learoyd @PKUFamily
1K Followers 1K Following Mum, charity trustee, ask awkward questions, trying to cope with this icky platform: support @NSPKU for better future for #RareDisease #pku, tweeting own views
NSPKU @NSPKU
3K Followers 1K Following The NSPKU exists to help and support people with PKU, their families and carers. It was formed in 1973, see https://t.co/f9QHejwhkW
MedicsforRareDisease @MedicsForRare
5K Followers 2K Following This account is no longer active, please continue to follow our work on Instagram and Bluesky! @medicsforrare
Clair W 🧡 @ClairBear42
644 Followers 816 Following Ginger #PKU Adult & Mumma. She/Her. Blogger.👩💻🍓 Expert on films, ice cream, cats and tea. 🎮🌜#ADHD 🏳️🌈
Cambridge Rare Diseas... @camraredisease
8K Followers 6K Following Improving outcomes for those living with rare conditions. Also find us at: https://t.co/kZWskP9Ojj
RARE Revolution Magaz... @RareRevolutionM
12K Followers 7K Following Digital magazine giving a voice to those affected by rare conditions and the charities that support them. Contact us: [email protected]
Genetic Alliance UK @GeneticAll_UK
15K Followers 2K Following National charity working for everyone affected by genetic, rare and undiagnosed conditions. We run the campaign Rare Disease UK and support network @SWAN_UK.
Caroline Graham @CarolinePKU
406 Followers 643 Following Mum, Designer, Artist, NSPKU volunteer, 3 kids 2 with #PKU all views my own
Rhys Holmes @RhysHolmes
460 Followers 1K Following Brain Tumour survivor, hydrocephalus, previous CSF Leak and now battling the rare neurological disease, superficial siderosis.
dazzle4rare @dazzle4rare
1K Followers 1K Following Est. 2016 | Signal boost RARE with #dazzle4rare every Aug | #Signalise is our #podcast | Our 🔗 https://t.co/bS5LyCTiZ5
David Ross @mensraredisease
713 Followers 831 Following MRDMH supports men’s mental health for those suffering with a rare disease. #raredisease #malementalhealth #mentalhealth #rarementalk #mrdcharity
Pauline O'Connor @poconnor
304 Followers 186 Following Author & Advocate. Subscribe for updates, as not here often. Books #TheRedHatStories #LivingWithPKU #LivingWithMildBrainInjury #RareDisease #BrainInjury #PKU
Bernadette Sheehan Gi... @sheehangilroy
1K Followers 5K Following Lecturer Researcher Advocate #PKU #LowProtein #BrainHealth #RareDisease "Ní neart go cur le chéile" The views and opinions expressed here are solely my own
Rareminds @RaremindsUK
858 Followers 2K Following Specialised mental health and wellbeing services for the rare disease community. https://t.co/eVmeTw0aah…
Patient Worthy @PatientWorthy
8K Followers 7K Following We're a resource for engaging, informative content and rare patient news, well done.
Ataxia and Me CIO 118... @Ataxia_and_Me
4K Followers 3K Following #Ataxia is a #raredisease affecting #Balance #Speech and #Coordination #Patients Helping Patients #MovementDisorder #Health #Medical #pharma
Flutters and Strutter... @FibroFlutters
3K Followers 4K Following Non Profit for chronic (FibroFlutters) & rare illnesses (ZebraStrutters) Patient Advocacy Organisation Reg. No. 14065901
James Fasham @JamesFasham
3K Followers 3K Following 🧬👨⚕️Academic Consultant in Clinical Genetics 💬 Social media chair: @ESHGsociety. 🤖 @DiseaseGenes bot creator #Genetics #Genomics #RareDisease
NCBRS Worldwide Found... @ncbrsfoundation
288 Followers 430 Following Our aim is to help families by providing practical advice, annual conferences, raising awareness of #NCBRS and possibly help to fund any future research studies
Ayomide Lasisi @ayolasisi08
17 Followers 85 Following
Special Needs Parents... @Funwithfood31
4 Followers 36 Following Having fun with life , special needs Parents
Bekir ALDAS @Bekiraldass
2 Followers 45 Following
Graham Butler @Portland_Owl
305 Followers 1K Following Life throws you challenges everyday, step up to each and every challenge and become stronger with every accomplishment.....
Alfie Ford @a4asdawareness
901 Followers 822 Following Autistic and a proud Birmingham City supporter. Multi award-winning fundraiser and campaigner for autism and disability awareness and acceptance. Views my own.
Alex @Alex_Paschim
662 Followers 5K Following Jai Gurkha and QOGLR. Strength & Honour. Destiny Is All. Arise, Riders of Théoden. Advance Britannia. Long Live the Cause of Freedom. God Save The King! 🇬🇧
Philip Medd @Philmedd
11 Followers 207 Following
Panayotis Pachnis @PPachnis
31 Followers 316 Following
@plpp153M @plpp153M
14 Followers 213 Following
Fleur Ayling @FleurMurphy1997
310 Followers 936 Following 26 year old fanatic, probably tweeting about bastille! Love supernatural and the walking dead 🧟♀️
Rareatives @rareatives
114 Followers 494 Following Share Your Rare | Amplifying Rare Disease Voices 🎙️ 📖 Sharing stories from the 1 in 10 🧬 New patient-led publication #RareDisease #PatientVoicesMatter
CheckRare @CheckRare
3K Followers 2K Following Leading publisher and learning platform focused on rare diseases. Rare Diseases Are Our Focus, Expertise, and Passion.
Chen Minhui @Minhui698
45 Followers 1K Following Entrepreneurial | Single | My daily goals are learning, laughing, supporting, and encouraging each other 💪 | Communicate politely and stay positive ✨ |
JAY O'CONNOR @JayAlicemay777
185 Followers 2K Following Female 59, living with Myalgic Encephalomyelitis, POTS and MCAS.
JJGO @JGuirao19
358 Followers 5K Following Pharmacy - Clinical Chemistry at Hospital Universitario Mancha Centro
Susannah H @firebug70
2K Followers 5K Following Mum. Carer for my son. Former English teacher. Researching bacterial and viral infection &symptoms #Lyme #ME #LongCovid #Pandas #Pans #Bartonella #Convalescence
Rebecca Herbert @Re23h
18 Followers 111 Following
Harriet Carroll: Long... @angryhacademic
9K Followers 4K Following #LongCovid Scientific Consultant Hon Research Fellow, Lund Uni PhD Nutrition & Metabolism Tweets: nutrition▪health▪all-things-science▪activism▪#TeamClots
Kevin Deans @DeansKevin
2K Followers 890 Following Chemical Pathologist - Clin Biochem, Obesity, Nutrition, Inherited Metabolic Diseases. Personal profile; all views my own. Tweets are not medical advice.
Tharthear @Tharthearbf1
62 Followers 1K Following
Sek Sokseyha @SokseyhaSe15786
1 Followers 352 Following
CureLGMD2i @CureLGMD2i
13 Followers 102 Following Limb Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9) is a life limiting disease, which causes progressive muscle weakness mainly in the shoulder and hip areas.
Jane Peers @JanePeers89
5 Followers 14 Following
PWSA UK @PWSAUK
1K Followers 214 Following Supporting all those affected by Prader-Willi Syndrome, a rare condition causing a near-permanent state of hunger, learning & physical disabilities.
Charles Marques Loure... @CharlesLourenco
68 Followers 468 Following Clinical Geneticist Neurogenetics and Hereditary Metabolic Disorders Specialist
BHD Foundation @BHD_Foundation
428 Followers 339 Following Your resource for Birt-Hogg-Dubé Syndrome: research and support. Managed by @myrovlytis #RareDisease #Pneumothorax #KidneyCancer #BHDSyndrome
Dr Kerry Montgomery @kmonty83
982 Followers 802 Following Research Fellow at the Centre for Appearance Research Current areas of research: visible difference and genetics- factors that influence family planning.
Soretarfr @SoretarfrcZZVG
56 Followers 2K Following
Dr Cath Lunt @cathl555
327 Followers 827 Following Research & Evaluation Manager @DCPcampaign . Inclusivity l Disability l Complex Needs l Long- Term Conditions l 1stgengrad l All views my own.
Alan Thomas @alanROYGBIV
3K Followers 2K Following Founder of @Ataxia_and_Me to support #Ataxia (Rare Neuro. condition) from the #patient view. PASSIONATE about Inclusion for #disabled citizens - views are mine
Miriam SR @MiriamS14576699
471 Followers 4K Following CEO ADCUM - Inborn errors of metabolism. Chronic Diseases. Human Rights Activist WHO Commissioner and organization at the UN
Kamran @DrKamranIqbal
95 Followers 650 Following
Dr Nima Ghadiri @DrNimaGhadiri
2K Followers 7K Following Medical Ophthalmology Consultant (Ophthalmic Physician) | FRCP | Med Ed | HCA Professor | Uveitis Lead Clinician | Ocular Inflammation | Neuro 👁️⚕️🧠📖
Beau @SShute110633
44 Followers 43 Following
The ED Society @EDSocietyUK
213 Followers 379 Following Our vision is that every individual affected by Ectoderma Dysplasia is equipped with the knowledge needed to manage ED effectively and live life to the full.
Chris Croke @ChrisCroke10
0 Followers 17 Following
Alison Sampson @AlisonMSampson
67 Followers 235 Following Passionate about Hornsea and Hornsea Pottery, fabric printing, all things Japanese, Leeds United, and going out.
Beacon for Rare Disea... @RareBeacon
12K Followers 10K Following Beacon is a UK-based charity that is building a united rare disease community with patient groups at its heart. Previously known as Findacure.
Kate Learoyd @PKUFamily
1K Followers 1K Following Mum, charity trustee, ask awkward questions, trying to cope with this icky platform: support @NSPKU for better future for #RareDisease #pku, tweeting own views
Anita MacDonald @macdonj
2K Followers 634 Following All tweets discuss low protein foods to help children on low protein diets. All views are my own.
NSPKU @NSPKU
3K Followers 1K Following The NSPKU exists to help and support people with PKU, their families and carers. It was formed in 1973, see https://t.co/f9QHejwhkW
Unique @Unique_charity
8K Followers 2K Following Unique supports and informs anyone born w/a rare chromosome or gene disorder, their families and carers. Eurordis Patient Organisation Award winner.
Alvaro Hermida @Info_Rares
2K Followers 1K Following Specialist on Metabolic Diseases and always looking on the bright side of life.
MedicsforRareDisease @MedicsForRare
5K Followers 2K Following This account is no longer active, please continue to follow our work on Instagram and Bluesky! @medicsforrare
Clair W 🧡 @ClairBear42
644 Followers 816 Following Ginger #PKU Adult & Mumma. She/Her. Blogger.👩💻🍓 Expert on films, ice cream, cats and tea. 🎮🌜#ADHD 🏳️🌈
SWAN UK (syndromes wi... @SWAN_UK
8K Followers 4K Following SWAN UK (syndromes without a name) is run by @GeneticAll_UK, offering support and information to families of children with undiagnosed genetic conditions.
Cambridge Rare Diseas... @camraredisease
8K Followers 6K Following Improving outcomes for those living with rare conditions. Also find us at: https://t.co/kZWskP9Ojj
NHS Genomic Medicine ... @NHSgms
7K Followers 784 Following Information for and from the NHS Genomic Medicine Service 🧬 #Genomics. https://t.co/MizyyMpX02…
𝔸𝕝𝕖𝕩𝕚�... @mrs_martin_2012
289 Followers 301 Following Wife, mum to an 16 year old with phenylketonuria (PKU), new dog mum, ELCE in Clacks
RARE Revolution Magaz... @RareRevolutionM
12K Followers 7K Following Digital magazine giving a voice to those affected by rare conditions and the charities that support them. Contact us: [email protected]
Genetic Alliance UK @GeneticAll_UK
15K Followers 2K Following National charity working for everyone affected by genetic, rare and undiagnosed conditions. We run the campaign Rare Disease UK and support network @SWAN_UK.
Caroline Graham @CarolinePKU
406 Followers 643 Following Mum, Designer, Artist, NSPKU volunteer, 3 kids 2 with #PKU all views my own
Effie Parks @OnceUponAGene
7K Followers 4K Following Rare Disease Advocate | Award Winning Podcaster | Speaker | Captain Connection | RareMama to my sweet, Ford, who lives with #CTNNB1 🦓
dazzle4rare @dazzle4rare
1K Followers 1K Following Est. 2016 | Signal boost RARE with #dazzle4rare every Aug | #Signalise is our #podcast | Our 🔗 https://t.co/bS5LyCTiZ5
North Thames Genomic ... @NorthThamesGMS
1K Followers 712 Following Working to provide equitable access to genomic testing and innovation for people across North London, Hertfordshire and Mid and South Essex.
David Ross @mensraredisease
713 Followers 831 Following MRDMH supports men’s mental health for those suffering with a rare disease. #raredisease #malementalhealth #mentalhealth #rarementalk #mrdcharity
Rareminds @RaremindsUK
858 Followers 2K Following Specialised mental health and wellbeing services for the rare disease community. https://t.co/eVmeTw0aah…
Ruth_TV @Ruth_ITV
41K Followers 16K Following I'm Ruth. 💕 Television and radio presenter. Journalist. Advocate for sunshine, and life after #domesticabuse #coercivecontrol 💕
Charles Marques Loure... @CharlesLourenco
68 Followers 468 Following Clinical Geneticist Neurogenetics and Hereditary Metabolic Disorders Specialist
EUPATI @eupatients
7K Followers 2K Following The European Patients' Academy on Therapeutic Innovation is an independent, non-profit organisation committed to patient engagement through patient education.
Spinal Muscular Atrop... @SMA_UK_
3K Followers 820 Following Supporting anyone living in the UK affected by Spinal Muscular Atrophy (SMA). On Twitter to raise awareness of the condition, our activity and related topics
Jeans for Genes UK @jeansforgenes
15K Followers 9K Following Wear your jeans, donate & transform the lives of people living with genetic disorders. Find out more about us and all the ways to get involved!
Rare Diseases Clinica... @rarediseasesnet
9K Followers 490 Following NIH-funded network fostering collaborative research among 21 teams of researchers, patients, and clinicians, each focused on a group of rare diseases.
ISCBH @childrensbones
1K Followers 801 Following We're no longer updating this account, you can still find us on LinkedIn and Facebook
Newcastle Hospitals N... @NewcastleNMAHPs
3K Followers 4K Following Our 7,000 nurses, midwives & AHPs’ shared vision is to achieve excellence and global reach through compassionate, innovative healthcare, education and research.
The Neurological Alli... @NeuroAlliance
7K Followers 891 Following 100+ organisations working together to make sure everyone affected by neurological conditions can access the support they need, when they need it #BackThe1in6
Cure Usher @cureusher
530 Followers 371 Following Raising funds & awareness for Usher syndrome research. Secretariat for All Party Parliamentary Group. Registered charity, 1181293.
Amanda Skinner @AmandaSkinner1
304 Followers 729 Following Genomics Nurse Practitioner SW Peninsular All views expressed are my own.......
Rarity Life @raritylifemag
235 Followers 817 Following A new online publication that offers those affected by rare disease, disability & cancer the opportunity to unify & share our collective experience.
Newcastle Hospitals @NewcastleHosps
18K Followers 4K Following Newcastle Hospitals is one of the UK's largest teaching NHS Trusts including Freeman Hospital, RVI & Great North Children's Hospital. Tweets Mon-Fri: 9am-5pm
The Brain Charity @TheBrainCharity
16K Followers 4K Following We help people with ALL neurological conditions to live longer, healthier, happier lives. 🧠 Practical advice 🧠 Emotional support 🧠 Championing neurodiversity
HCU Network America @HCUAmerica
723 Followers 953 Following The mission of HCU Network America is to help patients with #Homocystinuria and related disorders manage their disease and to find a cure. #HCUNetworkAmerica
CASK Research UK @CASKResearch
150 Followers 324 Following We are a charitable foundation promoting research into CASK gene mutations and associated neurological conditions in hope of finding therapies and treatments
ACTA2 Alliance @Acta2Alliance
105 Followers 691 Following Supporting families living with Multisystemic Smooth Muscle Dysfunction Syndrome #MSMDS #UltraRare #ACTA2 mutation https://t.co/7qW46wFU8x
Joanne Ward @jolou20
186 Followers 279 Following NF2, Rare, deaf patient & mum, NF2 community supporter. Raising awareness and funds for NF2. Chief Operations Officer & Trustee at Cure NF2 Foundation UK
Pressat @pressat
7K Followers 7K Following The UK's leading press release distribution service. Connecting businesses & organisations with journalists and media outlets. Grow your brand with @pressat
iHV @iHealthVisiting
17K Followers 999 Following A UK centre of excellence, supporting the development of universally high-quality health visiting practice.
Ian Rankin @Beathhigh
195K Followers 2K Following The car’s on fire and there’s no driver at the wheel… Contact: [email protected] MD Alternative National Treasure.
Rare Disease Research... @RDRUKHub
237 Followers 177 Following We hope to be able to significantly impact the RD research landscape and improve the lives of those directly or indirectly affected by rare diseases.
CACNA1A Foundation @cacna1a
2K Followers 2K Following Nonprofit dedicated to a brighter future for those with CACNA1A variants. On a mission to fund life changing research while supporting families along the way.
SJSAwareUK @sjsawareuk
87 Followers 36 Following Our mission is to bridge the gap for those affected by SJS/TEN through info & support from the point of diagnosis & through their recovery & adaptation process
Nystagmus Network @NystagmusUK
2K Followers 883 Following Supporting the #NystagmusCommunity https://t.co/47C19PvBWb Registered charity no. 1180450
SUDC*UK @SUDCUK1
1K Followers 407 Following A registered charity dedicated to raising awareness, funding research and supporting families affected by Sudden Unexplained Death in Childhood (SUDC).
FahrBeyond @FahrBeyond
216 Followers 490 Following Official account for Fahr Beyond. We are a charity that supports people with #FahrsDisease & #Fahrs like conditions, to educate & research. #Parkinsons #PFBC
Flutters and Strutter... @FibroFlutters
3K Followers 4K Following Non Profit for chronic (FibroFlutters) & rare illnesses (ZebraStrutters) Patient Advocacy Organisation Reg. No. 14065901
RDLA @RareAdvocates
6K Followers 2K Following A program of the EveryLife Foundation committed to growing the patient advocacy community and working collaboratively, thereby amplifying the patient voice!
ExeterGenomes @ExeterGenomes
2K Followers 440 Following Latest news and updates from the exome and genome sequencing service at the Exeter Genomics Laboratory, Royal Devon University Healthcare NHS Foundation Trust
Cure and Action for T... @Tay_Sachs
781 Followers 838 Following Furthering research and supporting families affected by Tay-Sachs and Sandhoff #taysachs #sandhoff #cure #rarediseases #smallcharity #10YearsofCATS
Verity Cockbain (Hart... @VerityCockbain
352 Followers 696 Following Clinical geneticist, PhD. Interested in rare diseases, congenital heart disease.
South West Genomic La... @SWGLH
1K Followers 532 Following Working hard to provide genetic testing for the South West region and beyond. Promoting equity of access of testing for patients.
ern euro_nmd @euro_nmd
2K Followers 672 Following Building bridges and breaking barriers in rare neuromuscular diseases.
The North West Genomi... @NWGLH
3K Followers 2K Following News and updates from the GLH for the North West led by @MFT_nhs, working together with @nwgmsa @LiverpoolWomens, @NWCGMC and @lplclinlabs.#NHS #Genomics
World Orphan Drug Con... @OrphanConf
5K Followers 860 Following Get regular updates on #WorldOrphanUSA! June 9-11, 2026 | Boston Convention & Exhibition Center
AGNC @theAGNC
1K Followers 440 Following The Association of Genetic Nurses and Counsellors, representing the profession in the UK and Ireland.
Jillian Hastings Ward @HastingsJ123
1K Followers 1K Following 'that mother' - #R4Today🎙Patient advocate, mum and wife. Genomics fan. Write a bit, talk a lot. MBE!
CheckRare @CheckRare
3K Followers 2K Following Leading publisher and learning platform focused on rare diseases. Rare Diseases Are Our Focus, Expertise, and Passion.
Gemma Chandratillake @GemmaChand
1K Followers 700 Following Genetics, genomics, genetic counsel(l)ing, generally waxing helical Work for @east_genomics and @Cambridge_Uni Vice-Chair @BritSocGenMed,Trustee @camraredisease
PKU Association IE @PKU_Ireland
1K Followers 3K Following PKU Association of Ireland #SUPPORTINGPKU #LowProtein PKU Awareness in Ireland Registered Charity Number (RCN) 20202487










