Bronchiectasis Make A Stand! NO LONGER NEGLECTED by NHS The British Lung Foundation.. sign

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Bronchiectasis Must Go has launched a serious revolutionary campaign this year that we believe will make a major impact in newly diagnosed and old/current patients with the disease,  that will change the way the professionals in the field think and look at Bronchiectasis and how they deal successfully with monitoring treating and stabilizing the disease correctly and efficiently. Bronchiectasis is a very complex and  progressive disease which under correct treatments can slow down the progression of the disease and in doing so gives a better cycle of life for a Bronchiectasis sufferer. At the moment we believe we are not getting taken seriously, we feel like there is a  lack of education in the whole field of the NHS in the UK, from GPS surgeries to even specialist in the department of Bronchiectasis throughout chest clinics in the country. 

PLEASE  SIGN AND SHARE IF YOU AGREE AND WANT  TO SEE CHANGES.

CHANGES:

INTRODUCTION OF CYSTIC FIBROSIS MEDICATION SUCH AS PULMO (MUCUS THINNER) AND OTHER MEDICATION THAT MAYBE BENEFICIAL AS THE TWO CONDITIONS ARE CONNECTED THERE ALMOST LIKE CONJOINED TWINS.

MORE BRONCHIECTASIS CHEST SPECIALIST, LESS CHEST SPECIALIST SECRETARY'S, EASIER ACCESS TO GET IN CONTACT WITH OUTSIDE ROUTINE APPOINTMENTS, GPS WITH TRAINING IN BRONCHIECTASIS CONTRIBUTING TO A BETTER LEVEL OF UNDERSTANDING. 

MORE HOSPITAL ADMISSIONS WHEN BRONCHIECATASIS SUFFER ISN'T RESPONDING TO TREATMENT OR RECUSE PACKS. 

MORE IN THE COMMUNITY, COUNSELLING, MORE NEEDS TO BE DONE.

 PLACES YOU CAN FOLLOW THIS CAMPAIGN HERE:

 https://www.facebook.com/pg/bronchimustgo/about/?ref=page_internal

 



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