FightingBackForJack
@fightingbk4jack
Family fundraising group for Muscular Dystrophy UK. Our Muscles Matter
ID: 2473545610
10-04-2014 09:01:24
106 Tweet
780 Followers
552 Following
Muscular Dystrophy UK
@mduk_news
We connect a community of over 110,000 people living with muscle wasting and weakening conditions. Together we are stronger. Join us. Our #MusclesMatter.
BTS
@btis
Science, muscle regeneration (muscular dystrophy), music, chess, big data, ...
Sheonad Laidlaw
@h0pefulmummy
Constantly juggling life unfamiliar. Mum to 2 girls, 1 with SMA. Palliative Care SAS Dr: special interest in young adults, transition & neuromuscular disease
Kerry Spink
@kerryspink
Trusts Fundraising Manager/SEN parent/ FSH muscular dystrophy advocate/ dog walks, great books & a brew. All views are my own
CureDuchenne
@cureduchenne
We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community.
Muscular Dystrophy Canada
@md_canada
MDC's mission is to help people with neuromuscular disorders live life on their own terms. #WalkRollMDC #MuscularDystrophy FR: @Action_Musclee
Lesley - FPL ⚽️
@weggster
Managed to offend Fess Hole. My laugh triggers fire alarm systems. Music junkie. Gig addict. Incompetent Fantasy Football Manager. Potty mouth. #FPL
🌻🩷 Linzie P 🩷🌻
@linziep17
Owner at @PhotographyLMP1 📸 Part-time admin, Events & Social Media Assistant @LoveBrumUK ❤️ #VisuallyImpaired👩🏼🦯 Chapter 42👣 #KRO 💙#keratoconusAwareness
Jodie Whitham
@lalajodielala
Regional Development Manager at MDUK, love fundraising, gigs & animals :) All opinions my own Support my Trek to Petra for: bit.ly/3vT3DxE
Muscles Matter Martin
@musclesmartin
#MusclesMatter #LUFC Always fighting 4 @MDUK_News The views expressed here are my own and don’t necessarily reflect those of my employer
Keegan Woolley
@keegan_woolley
Faith, Family, Football
Holy Family School
@holyfamilyscho1
We live, love and learn together in the light of God.🧡🧡
Blues Collective
@bluescollective
BCFC and Bluenoses that are raising for good causes....
Duchenne UK
@duchenneuk
Duchenne UK has one clear aim – to end Duchenne, a devastating muscle-wasting disease. We are the leading Duchenne muscular dystrophy charity in the UK.
Terri Ellsworth
@terriellsworth
Duchenne Advocate/Rare Disease Activist Mom, Designing Mom-Creating awareness & advocating for approval of safe & effective drugs. Words are always my own.
Join Our Boys Trust
@joinourboys
Now 2 boys in need of life saving treatment. Let's get to 77k for 7/7 in memory of Archie.🧡 Please Follow us & Donate ⬇️
Susanne Driffield
@s_driffield
Regional Development Manager at Muscular Dystrophy UK. Proud Trustee of Disability Action Yorkshire. Mum to my DMD superhero Joe. All views are my own.
futeri
@blueprinces17
nothing
Joaquim Brites
@joaquimbrites
Electrotécnico - Gestor Presidente da Direção da APN -Associação Port. de Neuromusculares Conselheiro no Conselho Nacional de Saúde, Patient Advocate, EURO NMD
Ryan Sipple
@ryansipple
National Development Officer at @The_WFA | #PowerchairFootball
❤️citizen Macca
@p15pm
No turning back, no giving in . originally from Acton west London former station assistant with London Underground now a care giver gofund.me/30f57932
RupjaniB
@rupjanib
Passionate about harnessing the power of new technologies and turn health data into trusted intelligence for better health outcomes
Emily
@emilyrjohnson5
Follower of Birmingham City Men and Women’s teams. Also follow England Lionesses. 💙⚽️
somreena jabeen
@zainabmusa66
KRO_BCFC_1875
@kro_bcfc_1875
UTFB 🌍🏐
Help4harry
@help4harrynow
Raising funds and awareness for Duchenne Musculary Dystrophy
Laura McLinn
@lauramclinn
Founding President, Best Day Ever Foundation. Passion for helping patients access treatments. Duchenne mama bear.
Patient Worthy
@patientworthy
We're a resource for engaging, informative content and rare patient news, well done.
Dr Ali Kay 🧬📚🌳
@alimakeshay
Interested in people, genetics, genomics and health. Researcher @RDMOxford & Research Fellow @CPMoxford + Rare disease parent & volunteer for MDUK
Kihto Healthcare
@kihtohealthcare
KIHTO Healthcare hire a range of specialist beds & cots manufactured by Centrobed. For short or long term hire, contact our team on 01233 635353/[email protected].
Holy Family Year 2 🌺 🧡
@holyfamilyyear2
Welcome to your Holy Family Yr 2 twitter platform. We will use it to guide your daily learning
Carmela Chillery-Watson BCyA
@cure4carmela
Age 10 disability #influencer #ambassador with a muscle-wasting condition, a heart condition, diabetes type 1 and Lipodystrophy, giving hope to others.
World Duchenne Organization
@worldduchenne
Global organization to find a cure and viable treatment for those lives affected by dystrophinopathies: Duchenne and Becker Muscular Dystrophy. RT ≠ endorsement
Avidity Biosciences, Inc.
@aviditybio
Avidity Biosciences is pioneering a new class of oligonucleotide-based therapies to address the unmet needs of the rare disease community.
Grace Brown
@gracebrown74340
Valentina Williams
@valentinaw64732
Holy Family Year 4
@year_family
Welcome to the Year 4 Holy Family twitter platform. Follow us to keep updated on our daily learning and exciting activities we do in school 📚✏️
Larlie Hoyer
@hoyerlarli32699
Francisco Ureta
@franciscoureta4
Wucof
@wucof9031
Matt Rife
@rifematt32
private account of Matt Rife
Revio Therapeutics
@reviotx
أبومحمد عبدالله
@benaicha_rabah2
مسلم أبا عن جد ورثت إسلاما مشوها فلما تركت المشوه للصحيح صرت غريبا عند قومي ، وكذلك ستراني غريبا .
Matt Gilbert
@mattgillyg14
Craig
@cra1gbluenose
Hannah McCulloch
@hannahmac66
help.waleed
@helpwaleed
Support Waleed Fight Against Duchenne Help Waleed,a child battling a rare muscular disorderget the care he needs.Your support brings hope and transform his life
Oliver
@olliescrowdfund
My name is Oliver, I'm 35 years old and I have Duchenne Muscular Dystrophy. My mum and I are trying to raise the funds to replace my 15 year old Wheelchair.
MS
@mudassirzfamily
Erron Pierce
@erronpierc
Çiğdem 🇹🇷𐱅𐰼𐰇𐰰
@cigdem_dalli
Dmd li annesi (duchenne muskuler distrofi) memento mori...
Marry Rose
@marryrose233591
محمد الزهراني َ
@mmdlzhrnya60029
Louise
@louise684553
Snfrurr
@snfrurr4vpom
kirubakaranpalaniyappan
@kirubakaranpal1
Rare Disease Research Network (RDRN)
@the_rdrn
A new, inclusive, online hub facilitating patient-initiated #raredisease research. #NIHR funded, co-created by the rare disease community, #CamRARE & #PLRH.
ILaura H Parhusip
@ilaurahannap
Dr Imada Laura H P is a medical doctor with 25 years work experiences with mostly muscular dystrophy social work. My Virtual Hospital via telp 62217271766.tx
The You
@thanky1230
Mohamed Kamal
@drmkms81kamal
Leety
@leetymyqebg2
PerrinPower
@enddmd
Advocacy and Fundraising for Parent Project Muscular Dystrophy
The only lady on earth with my quality
@austinscot61938
Love is when you look into someone's eyes and see everyting you need.
Patrick robert
@patougg5
God fearing en educated loves sports music en leisure
Andrew Olsen
@andrewolsengame
RxDataWatch
@rxdatawatch
LupeCatozzi
@catozzilup21544
Luna
@celiapa270631