HDdennomore (@hddennomore) 's Twitter Profile
HDdennomore

@hddennomore

HDdennomore is a global coalition of Huntington's disease (HD) advocates.

Join us on May 18 for Pope Francis' special audience with the HD community.

ID: 834500563484209152

linkhttp://HDdennomore.com calendar_today22-02-2017 20:30:13

1,1K Tweet

377 Followers

349 Following

HuntingtonStudyGroup (@huntingtonsg) 's Twitter Profile Photo

Do you know about our referral program? Refer health care providers to CME4HD online and win a scholarship to #HSG2018 Unlocking HD. Deadline June 30 #HuntingtonsDisease #CME4HD #IamtheDIFFERENCE bit.ly/2xqTaxp

@huntingtonsc (@huntingtonsc) 's Twitter Profile Photo

At Vicki's long term care home in Waterloo, she has been participating in music therapy through song writing with her social worker and music therapist. Vicki has recorded her song and is using it as a fundraising initiative! Visit ow.ly/D3oV30kfI2x for more information.

HuntingtonStudyGroup (@huntingtonsg) 's Twitter Profile Photo

Learn more about clinical trials at huntingtonstudygroup.org/current-clinic… #HuntingtonsDisease #IamtheDIFFERENCE x.com/HDAwareness/st…

NSI Early Career Researchers Network (@youngneuroirl) 's Twitter Profile Photo

Are you an early career Neuroscientist living in Ireland? This is the conference for YOU! Neuroscience Ireland #YoungNSI18 Full details can be found here: neuroscienceireland.com/young-nsi-conf…

Are you an early career Neuroscientist living in Ireland? This is the conference for YOU! <a href="/NeuroscienceIRL/">Neuroscience Ireland</a> #YoungNSI18 Full details can be found here: neuroscienceireland.com/young-nsi-conf…
Huntington's Disease Association of Ireland (@hdai_ie) 's Twitter Profile Photo

President of Ireland Last May, HDdennomore the Pope met with Irish / international Huntingtons disease patients two days before President of Ireland had his meeting.Pope Leo XIV spoke of a commitment, not a slogan to caring for Huntingtons Disease. The first ever Papal mention at the biggest global gathering

Huntington's WA (@huntingtons_wa) 's Twitter Profile Photo

Thank you Thursdays // We'd like to thank Live Nation Australia & New Zealand for their generous donation of two tickets to Def Leppard Friday Nov. 2 for out High Tea for HD fundraiser event!

Thank you Thursdays // We'd like to thank Live Nation Australia &amp; New Zealand for their generous donation of two tickets to Def Leppard Friday Nov. 2 for out High Tea for HD fundraiser event!
Huntington's Disease Association of Ireland (@hdai_ie) 's Twitter Profile Photo

UCC Anat. & Neurosci Still time to win Two Premium Tickets to @officialGAA 🎉🇮🇪🎉🇮🇪Hurling Final could be yours! A 10 euro donation could win you the tix (Value €300!) and help people with Huntingtons Disease! bit.ly/2vMAqoN pls RT entries open until 11am today!

HDdennomore (@hddennomore) 's Twitter Profile Photo

Seeing the #selfie with Pope Leo XIV we are reminded about Dr Lauren Byrne in Rome last year! What a pic! Nothing in this life is perfect, but some moments transcend our usual experience and that creates space for us all to see each other in this one human experience.

Zhaleh Khaleeli (@zhalehk) 's Twitter Profile Photo

Looking for a career in Neurology? Or for confidence in Neurology as part of internal medicine? Now recruiting for CMT Level Clinical Fellow posts at the National Hospital for Neurology to start Feb 2019 (or earlier) Apply now nhs jobs Ref 309-SHB195-PM-RA-M.Neurology Trainees

Huntington's Disease Association of Ireland (@hdai_ie) 's Twitter Profile Photo

Hi midge ure💙 there’s a huge meeting for Huntington’s Disease in #Vienna It means lots to us! As does awareness for Huntington’s Disease. We can’t hear the word without hearing the song m.youtube.com/watch?v=xJeWyS… so we are thinking of our friends there and humming along

Huntington's Disease Association of Ireland (@hdai_ie) 's Twitter Profile Photo

Genetic Counsellor Alanna Ward tells us that every year 2.5% of children born will develop a rare disease #rareisnotrare. We need improved services now!

Genetic Counsellor Alanna Ward tells us that every year 2.5% of children born will develop a rare disease #rareisnotrare. We need improved services now!