RareDiseaseDayDublin

28TH FEBRUARY - DUBLIN CITY HALL. RARE DISORDERS WITHOUT BORDERS - AN ALL-IRELAND CONFERENCE TO MARK INTERNATIONAL RARE DISEASE DAY

[RareDiseaseDayDublin @RDWB13]

@realmikefox grateful if you could RT this video message from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

@davidmcw grateful if you could RT this video message from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

@daraobriain grateful if you could RT this video message from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

@piersmorgan grateful if you could RT this video message from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

@nickybyrneoffic grateful if you could RT this video from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

@sportsdes grateful if you could RT this video message from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

@MiriamOCal grateful if you could RT this video message from patients with rare diseases on #rarediseaseday #rdwb13 http://t.co/YE5GuV6rHg

[RareDiseaseDayDublin @RDWB13]

#rdwb13 That's all from us here at Rare Disease Day in Dublin City Hall. It's been a thoroughly worthwhile day. Hope you've all enjoyed it!

[MND Campaigns @mndcampaigns]

Proud to win a poster prize for the @MNDAssoc #MND charter at @RDWB13 There’s still time to sign up so #RDWB13 delegates please pop by!

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Prize also given to the poster for http://t.co/ZmAil8SKTt.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Second prize in the poster competition goes to 'The MND Charter'.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Dr. Paula Byrne takes home first prize in the poster competition for her poster on 'Training Medical Students on Rare Diseases'.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 "Next year we'll have a joint rare disease day in The North", hopeful comments from Christine Collins.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 "This should not be a single day event, this should be the start of a process". Christine Collins.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Big thank you to all of our speakers! Christine Collins of the NI Rare Disease Partnership is up now to bring the day to a close.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Rare Disease Day about to come to a close, thanks to everyone who was involved! It's been a very successful day here at City Hall.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Speakers from Multiple System Atrophy Trust up at the moment. Providing us all with a great insight into issues surrounding MSA.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 There are many complexities associated with cross border care, there is no one-size-fits-all approach.

[RareDiseaseDayDublin @RDWB13]

#rdwb13 Alastair Kent from Rare Disease UK is up now.

[Brenda Drumm - Tobin @BrendaDrumm]

Today is rare disease day and as someone living with a rare form of cancer I am very grateful for all the research and advocacy work #rdwb13