A constant refrain from the two-headed Drumm-Harney HSE beast is that vast sums of money are being invested in our health service, which is therefore improving all the time. It takes little information and thought to realise how imaginative a story this is. In relation to a specific area, that of cystic fibrosis, The Socialist has done a little research.
Ireland has the highest rate of cystic fibrosis in the world – one in 1,600 births. This being the case, it would be reasonable to expect Ireland to be a world leader in the treatment of the condition. The truth, however, is sadly but predictably different. Death rates of cystic fibrosis sufferers in Ireland are far higher than in Britain or Northern Ireland. A comprehensive report by Dr. Ronnie Pollock in 2005 revealed serious shortcomings in the service. In summary, he observed "current staffing… is seriously inadequate…very unbalanced, and is too thinly distributed over too many, too small, units." In response to this, the HSE commissioned a working body to examine the same issues (could this be an example of bureaucratic waste?).
So three years later, how do things stand? The Socialist spoke to Pamela O’Connor, a cystic fibrosis patient in Cork. Pamela told us that there had indeed been some changes in staffing levels in Cork – a physiotherapist and a dietician have been employed full-time. Compared to the recommendations of Dr. Pollock, however, this is wholly inadequate – he called for a minimum of 1.2 dieticians and six physiotherapists. Pamela also informed us that there is a full-time cystic fibrosis nurse employed in Cork – which compares unfavourably with Dr. Pollock’s recommendation of four such nurses. Throughout our conversation, Pamela was at pains to emphasise that the staff are extremely dedicated and do excellent work, but that they are starved of the necessary resources.
Shockingly, Pamela also informed us that these new staff are not funded by the HSE, but are in fact funded by the Cystic Fibrosis Association! As if this were not sufficient to underline the neglect of cystic fibrosis patients by the HSE, there are no isolated rooms for cystic fibrosis patients in Cork, which means that when these patients are ill and vulnerable to infection they are not protected from cross-infection from other patients in the hospital.
Any society can only truly be judged by how it treats its most vulnerable citizens. Cystic fibrosis is a chronic, incurable condition which requires a great deal of care. A government whose primary health policy is to make healthcare profitable for private enterprise is never going to provide the resources necessary to care for cystic fibrosis patients, or indeed for patients generally. The only way in which appropriate care can be provided for all is through a publicly-funded health service which is free from the point of entry, and which assesses people on the basis of medical need rather than bank balance.