March 2016
Support Group meeting
Come along to our Support Group meeting. Meet others living with Vasculitis and learn about what is happening in the Vasculitis world over a cup of tea/coffee. There will be a short talk on meaningful patient involvement in research and development/how we can make a difference followed by discussion. We will also discuss and plan future meetings. Anyone affected by any of the Vasculitis diseases or other auto immune disorders are welcome to attend, patients and/or carers. hope to see you there.
Find out more »April 2016
Lunch, coffee and chat
Come along if you are free and join Julie and Nikki for lunch and chat at the Petit Cafe, very informal social meeting with others affected by Vasculitis. Let Julie know if you are intending coming along so we have an idea of numbers.
Find out more »Coffee and Chat
Come along and join Andrew and Emma for a coffee and chat at Dobbies cafe. Anyone affected by Vasculitis is welcome. Please let Emma know so we have an idea of numbers.
Find out more »November 2016
2016 All Ireland Vasculitis Conferenece
This will be our fifth All Ireland Conference.Come along and join us for our fifth All Ireland Vasculitis conference, where you will have an opportunity to meet others living with similar symptoms and day to day issues. This year we plan to have talks and feedback from those affected by Vasculitis, Specialist Vasculitis Consultants involved in treatment and Research, Information on managing our medications and symptoms and the long term effects of living with chronic illness. The cost of the conference are being subsidised with fundraising by members throughout the year and the generous donation by Eirball run. Lunch and refreshments are included. Come along and learn more about living well with the Vasculitis diseases from others in a similar situation and the specialists. Anyone affected with similar auto immune diseases and interested healthcare professionals welcome.We look forward to seeing you there.B&B available at the Royal Marine at a special rate for attendees €140 double/twin, €130 single, but needs to be booked by September 23rd 2016.
Find out more »February 2017
Nutrition
Nutrition talk being given by Nutrition therapist Sarah Trimble, learn about diet to help our immune system, manage inflammation and reduce risk of depression
Find out more »Galway Coffee and Chat
We are trying to set up a west of Ireland branch and are kicking off with our first meeting on 28th February. These meetings will be suitable for anyone affected by any of the vasculitis diseases, friends and family members are very welcome. Come along and meet others living with these rare diseases and help us provide support by telling us what you want and help us raise awareness of these rare diseases. For further details, please contact the organiser Patricia Ryan.
Find out more »March 2017
Vasculitis UK Symposium and Gala Charity Ball
A day of education and networking with Vasculitis patients and clinicians.
Find out more »Let’s Talk About Welfare Reform
Recently two of our members attended a CAB workshop on welfare reform and how it would affect people living with Vasculitis. We want to feed back some of the information and guidance to our members and hope you can attend. The event will will be held in the community room of Tesco Newtownbreda, Belfast between 12 noon and 2pm on Saturday 25 March 2017. Please let let us know if you plan on attending, by emailing Julie at julie@vasculitis-ia.org Tesco Extra 170 Newtownbreda Rd, Belfast BT8 6PZ 0345 026 9540
Find out more »April 2017
Polymyalgia Rheumatica/Giant Cell Arteritis, NI support group meeting
Contact Caroline Stewart at pmrgca.ireland@gmail.com if you are interested in going along to this support group coffee and chat, especially for those with Polymyalgia Rheumatica/ Giant Cell Arteritis.
Find out more »Munster Coffee and Chat
We are trying to set up a Munster branch and will have a meeting in Dungarvan on Easter Saturday, 15th April 2017, at Meades cafe. These meetings will be suitable for anyone affected by any of the vasculitis diseases, friends and family members are very welcome. Come along and meet others living with these rare diseases and help us provide support by telling us what you want and help us raise awareness of these rare diseases. For further details, please contact Julie at julie@vasculitis-ia.org.
Find out more »