About us 2017-06-24T19:27:47+00:00
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Our story

The bronchiectasis Foundation is a new charity formed on the 6th of April 2016 by bronchiectasis patients. Together our trustees share similar stories of the daily difficulty in battling this chronic lung condition.

By bringing the support, expertise and passion of our trustees together, we believe we have a strong new organisation that is focused on supporting other bronchiectasis sufferers.

Our journey to this point has not been easy, however a strong charity fighting for those effected with bronchiectasis is very much needed. Our drive and determination comes from the fact we have similar stories of being diagnosed with bronchiectasis far to late having all been given a diagnosis with having Asthma from childhood. This is sadly all to common and needs to change.

The foundation

We recognised the need for a National Bronchiectasis Charity.

We are here to improve awareness and understanding of this condition, to support those affected, and ultimately, to find better treatments for an improved quality of life for people living with Bronchiectasis.

Improving the lives of people with Bronchiectasis is central to everything we do.
We are driven to make real progress towards more effective treatments a better quality of life and ultimately a cure.

We also aim to make our voices heard with decision-makers within the NHS, pushing Bronchiectasis further up the health and social care agenda. The lack of awareness, late diagnosis and often years of wrong diagnosis ”Asthma in the case of many” is simply not acceptable in the year 2016.

Our Goals

To ensure new and better treatments in years, rather than decades.
Invest in specific medical research and trials
Provide better treatment protocol
Continue to build relationships with relevant medical organizations
Be an active member of the community and maintain a respectable and untarnished reputation in the community




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