![\"\"](\"\/\/www.aselpijama.com\/app\/uploads\/2020\/06\/iain-armstrong-left-and-john-harrington-right-following-their-31lb-combined-weight-loss-1024x693.jpg\")
<\/figure><\/div>the challenge was inspired by the uk-wide 26.2 initiative, designed to support charities losing money due to the pandemic. their fundraising total of \u00a31736 will benefit the beplay.asp
<\/a> (pha uk), a national charity based in chapeltown.<\/p> pulmonary hypertension (ph) affects just 7000 people in the uk and is caused by the thickening and stiffening of the blood vessels supplying the lungs. the life-limiting condition has no cure but can be managed with specialist care.<\/p> the pulmonary vascular disease unit at the royal hallamshire hospital is one of just six specialist ph treatment centres in england. <\/p> iain, who lives in stocksbridge, is a nurse consultant within the unit and chair of the pha uk. he said: \u201cpeople living with ph are classed as clinically extremely vulnerable and have had their lives turned upside down by the coronavirus pandemic. john and i wanted to do something to raise money for the charity which supports them, take control of our own health during a very stressful time, and reinforce that we really are all in this together.\u201d<\/p> father-of-two john is the unit\u2019s ward manager. he said: \u201clike so many charities, the pha uk has suffered from a downturn in fundraising activity due to the pandemic, so i wanted to do my bit to help. trying to diet whilst running a hospital ward during the covid-19 crisis hasn\u2019t always been easy, but i\u2019m delighted with how much we have raised. thank you to everyone who has supported our endeavours \u2013 we promise to try and keep the weight off now!\u201d<\/p> you can still sponsor iain and john at justgiving.com\/fundraising\/iainandjohn<\/a>.<\/p> the main symptom of pulmonary hypertension is breathlessness. other symptoms may include dizziness, feeling faint, swelling of the feet or ankles, and chest pain (particularly during exercise).<\/p> people can be born with pulmonary hypertension or develop it at any time, and it can affect anyone, regardless of age or ethnic background. it affects more women than men.<\/p> thanks to a range of highly advanced treatments developed over the last 15 years, people with the condition have seen quality of life improve and life expectancy increase to around six to seven years on average. many live longer, but there is no cure. <\/p> notes to editors<\/p> image shows iain armstrong (left) and john harrington (right) following their weight loss.<\/p> media contact: mary ferguson on 07496 872142 or at mary@capitalbmedia.co.uk<\/a><\/p> about the pha uk<\/strong><\/p> iain founded the pha uk in 1999 after recognising the need for a charity to support people diagnosed with pulmonary hypertension (ph), which affects just 7,000 people in the uk.<\/p> the organisation now has 4,500 members and as well as providing information, support and advice, it funds medical research and health education initiatives to promote better awareness, diagnosis and treatment of ph.<\/p> the pha uk is based in chapeltown, sheffield. it is a registered charity no: 1120756.<\/p> about pulmonary hypertension (ph)<\/strong><\/p> pulmonary hypertension (ph) is a rare, serious condition caused by the thickening and stiffening of the blood vessels supplying the lungs (pulmonary arteries). <\/p> the reduced blood flow makes it harder for the right side of the heart to pump blood through the arteries, which can result in heart failure.<\/p> the seven adult specialist ph centres in the uk are within the freeman hospital in newcastle; golden jubilee national hospital in glasgow; royal hallamshire hospital in sheffield; papworth hospital nhs trust in cambridgeshire; and hammersmith hospital, royal brompton hospital and royal free hospital in london.<\/p> for further information about pulmonary hypertension visit www.aselpijama.com<\/a>, call the pha uk office on 01709 761450 or e-mail office@phauk.org.<\/a> \u00a0<\/p>","protected":false},"excerpt":{"rendered":" press release: a pair of sheffield nurses have raised over \u00a31700 for a rare disease charity after taking on a sponsored slim during the coronavirus crisis.<\/p>\n","protected":false},"author":4,"featured_media":5315,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-5314","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorised"],"acf":[],"_links":{"self":[{"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/posts\/5314"}],"collection":[{"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/comments?post=5314"}],"version-history":[{"count":7,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/posts\/5314\/revisions"}],"predecessor-version":[{"id":8888,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/posts\/5314\/revisions\/8888"}],"wp:featuredmedia":[{"embeddable":true,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/media\/5315"}],"wp:attachment":[{"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/media?parent=5314"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/categories?post=5314"},{"taxonomy":"post_tag","embeddable":true,"href":"\/\/www.aselpijama.com\/wp-json\/wp\/v2\/tags?post=5314"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}