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You can join the webinar live from the comfort of your own home or access a recording after the event. <\/p>\n","link_url":"https:\/\/lungfoundation.com.au\/patients-carers\/get-support\/education-seminars\/"},{"image":{"ID":1433,"id":1433,"title":"iStock-881635092","filename":"iStock-881635092.jpg","filesize":901082,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","link":"https:\/\/lungfoundation.com.au\/patients-carers\/living-with-a-lung-disease\/pf\/overview\/istock-881635092\/","alt":"","author":"1","description":"","caption":"","name":"istock-881635092","status":"inherit","uploaded_to":1264,"date":"2018-09-18 00:32:00","modified":"2018-09-18 00:32:00","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":1920,"height":1281,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-300x200.jpg","medium-width":300,"medium-height":200,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-768x512.jpg","medium_large-width":768,"medium_large-height":512,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-1024x683.jpg","large-width":1024,"large-height":683,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","1536x1536-width":1536,"1536x1536-height":1025,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","2048x2048-width":1920,"2048x2048-height":1281,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-1920x1281.jpg","xxlarge-width":1920,"xxlarge-height":1281,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","xlarge-width":1280,"xlarge-height":854,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-480x1080.jpg","header-navigation-width":480,"header-navigation-height":1080,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":200,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":267,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/iStock-881635092.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":400}},"title":"Resources","description":"<p>Accessing information about PAH will help you to better understand your condition and take the important steps to help you live well. We have a range of resources available to support you. <\/p>\n","link_url":"https:\/\/lungfoundation.com.au\/resources\/?condition=21&amp;user_category=31"},{"image":{"ID":1414,"id":1414,"title":"Support-Groups","filename":"Support-Groups.jpg","filesize":778213,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","link":"https:\/\/lungfoundation.com.au\/patients-carers\/conditions\/bronchiectasis\/overview\/support-groups\/","alt":"","author":"1","description":"","caption":"","name":"support-groups","status":"inherit","uploaded_to":1331,"date":"2018-09-18 00:15:26","modified":"2018-09-18 01:07:13","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":1920,"height":1280,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-300x200.jpg","medium-width":300,"medium-height":200,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-768x512.jpg","medium_large-width":768,"medium_large-height":512,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-1024x683.jpg","large-width":1024,"large-height":683,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","1536x1536-width":1536,"1536x1536-height":1024,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","2048x2048-width":1920,"2048x2048-height":1280,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-1920x1280.jpg","xxlarge-width":1920,"xxlarge-height":1280,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","xlarge-width":1280,"xlarge-height":853,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-480x1080.jpg","header-navigation-width":480,"header-navigation-height":1080,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":200,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":267,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Support-Groups.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":400}},"title":"Support groups","description":"<p>Support groups provide people in similar situations the opportunity to come together to support each other, share practical tips and to help break down the sense of isolation that can often be experienced. Lung Foundation Australia can help connect to you a support group near you. <\/p>\n","link_url":"https:\/\/lungfoundation.com.au\/patients-carers\/get-support\/support-groups\/"},{"image":{"ID":1409,"id":1409,"title":"PR","filename":"PR.jpg","filesize":825927,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","link":"https:\/\/lungfoundation.com.au\/patients-carers\/conditions\/bronchiectasis\/support\/pr\/","alt":"","author":"1","description":"","caption":"","name":"pr","status":"inherit","uploaded_to":1480,"date":"2018-09-18 00:14:39","modified":"2018-09-18 01:39:35","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":1920,"height":1282,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-300x200.jpg","medium-width":300,"medium-height":200,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-768x513.jpg","medium_large-width":768,"medium_large-height":513,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-1024x684.jpg","large-width":1024,"large-height":684,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","1536x1536-width":1536,"1536x1536-height":1026,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","2048x2048-width":1920,"2048x2048-height":1282,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-1920x1282.jpg","xxlarge-width":1920,"xxlarge-height":1282,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","xlarge-width":1280,"xlarge-height":855,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-480x1080.jpg","header-navigation-width":480,"header-navigation-height":1080,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":200,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":267,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/PR.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":401}},"title":"Pulmonary Rehabilitation","description":"<p>Research has shown that one of the best things you can do for yourself is regularly exercise to help maintain your fitness, improve your wellbeing and reduce symptoms such as breathlessness. Lung Foundation Australia.<\/p>\n","link_url":"https:\/\/lungfoundation.com.au\/patients-carers\/get-support\/lung-disease-and-exercise\/pulmonary-rehabilitation\/"},{"image":{"ID":1405,"id":1405,"title":"LIA","filename":"LIA.jpg","filesize":896682,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","link":"https:\/\/lungfoundation.com.au\/patients-carers\/conditions\/bronchiectasis\/treatment\/lia\/","alt":"","author":"1","description":"","caption":"","name":"lia","status":"inherit","uploaded_to":1442,"date":"2018-09-18 00:13:45","modified":"2018-09-18 01:22:59","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":1920,"height":1375,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-300x215.jpg","medium-width":300,"medium-height":215,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-768x550.jpg","medium_large-width":768,"medium_large-height":550,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-1024x733.jpg","large-width":1024,"large-height":733,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","1536x1536-width":1536,"1536x1536-height":1100,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","2048x2048-width":1920,"2048x2048-height":1375,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-1920x1375.jpg","xxlarge-width":1920,"xxlarge-height":1375,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","xlarge-width":1280,"xlarge-height":917,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-480x1080.jpg","header-navigation-width":480,"header-navigation-height":1080,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":215,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":286,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/LIA.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":430}},"title":"Lungs in Action Exercise Groups ","description":"<p>Lungs in Action is a safe and enjoyable community-based exercise program empowering people with a lung disease to improve their quality of life through exercise. Classes are offered throughout Australia and are run by instructors who have been specially trained by Lung Foundation Australia.<\/p>\n","link_url":"https:\/\/lungfoundation.com.au\/patients-carers\/get-support\/lung-disease-and-exercise\/lungs-in-action\/"},{"image":{"ID":1407,"id":1407,"title":"Palliative care","filename":"Palliative-care.jpg","filesize":578663,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","link":"https:\/\/lungfoundation.com.au\/patients-carers\/living-with-a-lung-disease\/pf\/treatment\/palliative-care\/","alt":"","author":"1","description":"","caption":"","name":"palliative-care","status":"inherit","uploaded_to":1272,"date":"2018-09-18 00:14:08","modified":"2018-09-18 00:19:07","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":1920,"height":1426,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-300x223.jpg","medium-width":300,"medium-height":223,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-768x570.jpg","medium_large-width":768,"medium_large-height":570,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-1024x761.jpg","large-width":1024,"large-height":761,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","1536x1536-width":1536,"1536x1536-height":1141,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","2048x2048-width":1920,"2048x2048-height":1426,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-1920x1426.jpg","xxlarge-width":1920,"xxlarge-height":1426,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","xlarge-width":1280,"xlarge-height":951,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-480x1080.jpg","header-navigation-width":480,"header-navigation-height":1080,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":223,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":297,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Palliative-care.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":446}},"title":"Support and palliative care ","description":"<p>Palliative care professionals can support you and your family to improve your quality of life so you can live as well as you can for as long as you can.  Palliative care complements your active treatments - such as clinical trials - whilst also addressing your symptoms.<\/p>\n","link_url":"https:\/\/lungfoundation.com.au\/patients-carers\/support-services\/support-and-palliative-care\/"}]},{"acf_fc_layout":"featured_posts_static","heading":"Real Stories","view_more_link":"","posts":[{"ID":379,"post_author":"3","post_date":"2018-09-05 16:18:39","post_date_gmt":"2018-09-05 06:18:39","post_content":"<b><span data-contrast=\"auto\">Despite living with four lung conditions, including Pulmonary Arterial Hypertension (PAH), Bridget is a bubbly and positive young woman who tries to always look on the bright side of life. It\u2019s<\/span><\/b><b><span data-contrast=\"auto\">\u00a0the<\/span><\/b><b><span data-contrast=\"auto\">\u00a0<\/span><\/b><b><span data-contrast=\"auto\">life-long\u00a0<\/span><\/b><b><span data-contrast=\"auto\">friendships<\/span><\/b><b><span data-contrast=\"auto\">\u00a0made<\/span><\/b><b><span data-contrast=\"auto\">\u00a0with others living with PAH, the love and support of her family and the motivation of her role models that encourage and inspire Bridget<\/span><\/b><b><span data-contrast=\"auto\">\u00a0to live her best life.<\/span><\/b><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<b><span data-contrast=\"auto\">This is her story.<\/span><\/b><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">My name is Bridget, I am 2<\/span><span data-contrast=\"auto\">5<\/span><span data-contrast=\"auto\">\u00a0years old and I live in\u00a0<\/span><span data-contrast=\"auto\">Narangba<\/span><span data-contrast=\"auto\">, Queensland with\u00a0<\/span><span data-contrast=\"auto\">a friend. We both recently<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">moved into Specialised Disability Accommodation. My Assistance Dog Lily also moved with me.\u00a0<\/span><span data-contrast=\"auto\">I have\u00a0<\/span><span data-contrast=\"auto\">four<\/span><span data-contrast=\"auto\">\u00a0lung conditions<\/span><span data-contrast=\"auto\">:<\/span><span data-contrast=\"auto\">\u00a0Kartagener Syndrome<\/span><span data-contrast=\"auto\">, Bronchiectasis, Reactive Small Airways Disease and Pulmonary<\/span><span data-contrast=\"auto\">\u00a0Arterial Hypertension (PAH).<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">I was diagnosed with Kartagener Syndrome at 3 months old. It is a genetic disorder which I ha<\/span><span data-contrast=\"auto\">d to<\/span><span data-contrast=\"auto\">\u00a0deal with a lot growing up<\/span><span data-contrast=\"auto\">,<\/span><span data-contrast=\"auto\">\u00a0as I got bullied in school for having a runny nose.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">The journey to my diagnosis of PAH\u202fwas six months after I first started getting<\/span><span data-contrast=\"auto\">\u00a0severe<\/span><span data-contrast=\"auto\">\u00a0symptoms but because of Kartagener Syndrome the doctors thought it was that<\/span><span data-contrast=\"auto\">\u00a0causing the breathlessness,<\/span><span data-contrast=\"auto\">\u00a0or I was a bit unfit.\u00a0<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">I was<\/span><span data-contrast=\"auto\">\u00a0eventually<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">diagnosed<\/span><span data-contrast=\"auto\">\u00a0at 16<\/span><span data-contrast=\"auto\">\u00a0with PAH.<\/span><span data-contrast=\"auto\">\u00a0I\u00a0<\/span><span data-contrast=\"auto\">did not<\/span><span data-contrast=\"auto\">\u00a0understand the diagnosis and what it meant for me. I just thought\u00a0<\/span><span data-contrast=\"auto\">I would have to deal with\u00a0<\/span><span data-contrast=\"auto\">another\u00a0<\/span><span data-contrast=\"auto\">medical\u00a0<\/span><span data-contrast=\"auto\">condition. I was so angry at one stage I pushed a chair against a wall.<\/span><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"auto\">I was scared because I\u00a0<\/span><span data-contrast=\"auto\">did not<\/span><span data-contrast=\"auto\">\u00a0know what was happening. When I was diagnosed mum wanted to find out more information and she was\u00a0<\/span><span data-contrast=\"auto\">very\u00a0<\/span><span data-contrast=\"auto\">sad because she told me I\u00a0<\/span><span data-contrast=\"auto\">could not<\/span><span data-contrast=\"auto\">\u00a0have kids and<\/span><span data-contrast=\"auto\">\u00a0that made<\/span><span data-contrast=\"auto\">\u00a0cr<\/span><span data-contrast=\"auto\">y<\/span><span data-contrast=\"auto\">.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">My treatment has changed a little bit throughout my\u00a0<\/span><span data-contrast=\"auto\">eight<\/span><span data-contrast=\"auto\">-year fight. When my treatment\u00a0<\/span><span data-contrast=\"auto\">started,<\/span><span data-contrast=\"auto\">\u00a0I was on a smaller dose of three different medications, this has since increased to larger dosages and more medication. Along with a long list of daily medication, I also deal with pain and daily symptoms. Some of the side effects of the medications are weight gain, nausea and vomiting, pain and feeling and looking flushed. Treatment and medication has had an impact on my life because I need to think of where am I going and do I need to take my medication with me because I<\/span><span data-contrast=\"auto\">\u00a0will be\u00a0<\/span><span data-contrast=\"auto\">out\u00a0<\/span><span data-contrast=\"auto\">when medication is due.\u00a0 I need to know if places have toilets because of the effect of diuretics<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">I also\u00a0<\/span><span data-contrast=\"auto\">must<\/span><span data-contrast=\"auto\">\u00a0do physio twice daily to get the mucus out of my lungs because it doesn\u2019t move otherwise. I cannot walk long distances on the flat and I cannot walk upstairs or inclines because I become very short of breath and become cyanotic. I am unable to work because of the impact of the symptoms of Pulmonary Hypertension.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">There are positives. M<\/span><span data-contrast=\"auto\">y condition is being managed with the medication, if not my prognosis would have been two years. My parents and I are closer. I have met some life-long friends with<\/span><span data-contrast=\"auto\">\u00a0PAH<\/span><span data-contrast=\"auto\">. My advice to someone who is newly diagnosed with\u00a0<\/span><span data-contrast=\"auto\">PAH\u00a0<\/span><span data-contrast=\"auto\">is to take it one day at a time. Manage symptoms with medications. Everyone with\u00a0<\/span><span data-contrast=\"auto\">PAH\u00a0<\/span><span data-contrast=\"auto\">is different so\u00a0<\/span><span data-contrast=\"auto\">do not<\/span><span data-contrast=\"auto\">\u00a0compare yourself to someone else.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">My motto is Keep\u00a0<\/span><span data-contrast=\"auto\">Phighting<\/span><span data-contrast=\"auto\">, every day is a\u00a0<\/span><span data-contrast=\"auto\">n<\/span><span data-contrast=\"auto\">ew day.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>\n\n<span data-contrast=\"auto\">I have been inspired by\u00a0<\/span><span data-contrast=\"auto\">Turia<\/span><span data-contrast=\"auto\">\u00a0Pitt because she keeps going in the face of adversity and never gives up. Kylie Corkery because she keeps going raises two<\/span><span data-contrast=\"auto\">\u00a0children<\/span><span data-contrast=\"auto\">\u00a0even though she has Pulmonary Hypertension. My mum because she does everything to help me. Tries to do everything herself.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559738&quot;:200,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">\u00a0<\/span>","post_title":"Bridget's story","post_excerpt":"","post_status":"publish","comment_status":"open","ping_status":"closed","post_password":"","post_name":"bridgets-story","to_ping":"","pinged":"","post_modified":"2020-11-01 09:50:52","post_modified_gmt":"2020-10-31 23:50:52","post_content_filtered":"","post_parent":0,"guid":"https:\/\/lungfoundation.com.au\/?post_type=story&#038;p=379","menu_order":0,"post_type":"story","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":440,"post_author":"3","post_date":"2018-09-06 13:18:38","post_date_gmt":"2018-09-06 03:18:38","post_content":"My name is Patricia Giles, I love my job and I love spending time with my family and my dog, Bella. I don\u2019t have any children, just a step son as I cannot have kids. I\u2019ve been married to my husband, David for 18 years in 2018.\r\n\r\nIn 1986 I was diagnosed with lupus and up until 2013, I was doing fine. It was in March 2013, at age 43, I went for an ultrasound on my stomach due to the flu and they went a bit too high and found the deterioration of my lungs.\u00a0 I was sent back to the x-ray place 20 minutes later to have a MRI where they diagnosed me with Interstitial Lung Disease (ILD).\r\n<blockquote>I didn\u2019t think I had any symptoms of lung disease - just a cough and feeling lethargic, which my doctor put down to my lupus and the flu.<\/blockquote>\r\nI was getting more and more tired all the time and had two seizures due to pneumonia.\u00a0 I couldn\u2019t walk anywhere because I was always out of breath and this is when they diagnosed me with Pulmonary Arterial Hypertension (PAH). Now I\u2019m still tired all the time but I make myself go to work as this is the only way I deal with what I\u2019ve got.\u00a0 I have a great husband who supports what I do and a great boss who does his best to make sure I am fine.\r\n<blockquote>When I was first diagnosed, I was numb.\u00a0 I had no information about lung disease and no idea where to get it from.<\/blockquote>\r\nAfter a while I realised there were people out there that were worse off than me so I just dealt with it by throwing myself into work.\u00a0 This worked for a while until I got more sick and realised that I had to cut back work as I doing about 60 to 70 hours a week.\r\n\r\nWhen I was diagnosed with PAH I thought, \u2018why me, what have I done to deserve this?\u2019. But I kept going and I still am.\u00a0 I know there is nothing they can do for my conditions as none of them are curable and I am classed as severe but I still have my family and my work. For how long I can work, I don\u2019t know - my boss said as long as I want to come to work he will have me there. I will just keep going till the end, which is all anyone can do in this day and age. There is no point in getting down with it as there is nothing that can be done.\r\n<blockquote>I experience stigma all the time from people saying, \u2018you should not be doing this or doing that\u2019 but I see it this way, if I can do it, I will - simple. I am a very stubborn person so to tell me I cannot do something doesn\u2019t sit well with me.<\/blockquote>\r\nLiving with PAH affects what I do day-to-day, even when I sleep, as I cannot breathe properly.\u00a0 I am trying to access my superannuation to get the oxygen machine to be able to work, exercise and sleep better. At work I have two flights of stairs to walk up which is difficult, but I do it.\u00a0 I get out of breath walking from one part of the house to the other and I am always tired and sore, but this is a part of life now for me so I deal with it the best way possible.\r\n\r\nWhen I was first diagnosed there was nothing and I looked for five years before I found the support from Lung Foundation Australia. When I was first diagnosed not even the doctors could tell me anything, only that is was from my lupus.\r\n<h4>Sharing your personal experience with lung disease is a compelling and inspiring way for others to learn about and cope with their diagnosis. Your story may also encourage people to identify and act on symptoms they are experiencing, which may otherwise have been ignored.<\/h4>\r\n<h4><a href=\"https:\/\/lungfoundation.com.au\/get-involved\/how-you-can-help\/share-your-story\/\">Share your story, here<\/a>.<\/h4>","post_title":"Patricia's story","post_excerpt":"","post_status":"publish","comment_status":"open","ping_status":"closed","post_password":"","post_name":"patricias-story","to_ping":"","pinged":"","post_modified":"2018-10-18 15:06:45","post_modified_gmt":"2018-10-18 05:06:45","post_content_filtered":"","post_parent":0,"guid":"https:\/\/lungfoundation.com.au\/?post_type=story&#038;p=440","menu_order":0,"post_type":"story","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":12110,"post_author":"85","post_date":"2021-01-12 11:12:39","post_date_gmt":"2021-01-12 01:12:39","post_content":"<!-- wp:heading {\"textAlign\":\"center\",\"level\":3} -->\n<h3 class=\"has-text-align-center\">For Tegan, research means&nbsp;longer life expectancy,&nbsp;more effective treatments and to one day find a cure.&nbsp;<\/h3>\n<!-- \/wp:heading -->\n\n<!-- wp:paragraph -->\n<p>Aged&nbsp;just five,&nbsp;Tegan&nbsp;was diagnosed with Pulmonary Arterial Hypertension.&nbsp;Her heart was roughly the size of an adult male athlete.&nbsp;&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Her&nbsp;mum was told her daughter&nbsp;had five years to live.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Tegan&nbsp;had been&nbsp;suffering seizures, losing&nbsp;consciousness.&nbsp;Shortly after, she developed a persistent cough that would not go away.&nbsp;\u201cWith my doctor finally deciding to send me for an X-ray, it became apparent all too quickly that something major was wrong,\u201d she says.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Five years later,&nbsp;aligning&nbsp;with&nbsp;her doctor\u2019s&nbsp;timeline, Tegan\u2019s symptoms began to worsen.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:quote -->\n<blockquote class=\"wp-block-quote\"><p><strong><em>I deteriorated so much that I was placed on the heart\/lung transplant waiting list. My seizure activity increased dramatically&nbsp;\u2026&nbsp;I was placed on oxygen and used a wheelchair for all activities outside the house.<\/em><\/strong><em>&nbsp;<\/em><\/p><\/blockquote>\n<!-- \/wp:quote -->\n\n<!-- wp:paragraph -->\n<p>Pulmonary Arterial Hypertension (PAH) is a progressive disease caused by narrowing or tightening of the pulmonary arteries that connect to the right side of the heart to the lungs.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>When&nbsp;a new medication became available,&nbsp;it was&nbsp;effectively&nbsp;Tegan\u2019s&nbsp;last option while&nbsp;she&nbsp;waited for a transplant.&nbsp;It&nbsp;meant&nbsp;inserting&nbsp;a permanent line into&nbsp;her&nbsp;heart to deliver medication&nbsp;frequently;&nbsp;she\u202fwould have to carry around a pump and\u202fher\u202fmum and\u202fher\u202ffriends\u202fwould\u202fhave to\u202fhelp\u202fher take the\u202fcomplicated medication\u202fevery day.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>But within a month, she saw dramatic&nbsp;changes. The right side of&nbsp;her&nbsp;heart returned to normal,&nbsp;Tegan could&nbsp;walk more&nbsp;unhindered&nbsp;and&nbsp;she&nbsp;eventually&nbsp;came off oxygen, no longer&nbsp;needing&nbsp;a \u201ctruckload\u201d of medications.&nbsp;&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Now 31 and working as a full-time nurse, Tegan exercises&nbsp;regularly and&nbsp;can&nbsp;enjoy her hobby \u2026 travel.&nbsp;She has travelled solo for three months across Europe and Scandinavia during winter, taking with her three&nbsp;months\u2019 supply of medications and supplies weighing&nbsp;60kgs.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p><strong>For&nbsp;Tegan, research means&nbsp;more effective treatments and&nbsp;hope of a cure&nbsp;one day.&nbsp;<\/strong>&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>\u201cMy life requires planning and preparation more so than most, but I make it work.&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>\u201cWhen I was a child, my prognosis was poor, no longer than five years. Technology and medicine keep advancing, improving my chance of long-term survival \u2026 it\u2019s now been (almost) 25 years since my diagnosis.\u201d&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Tegan&nbsp;is thankful&nbsp;for what research&nbsp;has been able to do for her&nbsp;condition but&nbsp;hopes that more research can provide more stability and certainty for the future.&nbsp;&nbsp;<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:heading {\"textAlign\":\"center\",\"style\":{\"color\":{\"text\":\"#45b749\"}}} -->\n<h2 class=\"has-text-align-center has-text-color\" id=\"block-978d7c46-dc0b-4961-84e4-6811968526df\" style=\"color:#45b749\">Research saves lives and gives hope for a cure.<br><strong>Give hope. Give to research today<\/strong>.<\/h2>\n<!-- \/wp:heading -->\n\n<!-- wp:buttons {\"align\":\"center\"} -->\n<div class=\"wp-block-buttons aligncenter\"><!-- wp:button {\"style\":{\"color\":{\"background\":\"#45b749\"}}} -->\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-background\" href=\"https:\/\/lungfoundation.com.au\/donate\/\" style=\"background-color:#45b749\">Donate today<\/a><\/div>\n<!-- \/wp:button --><\/div>\n<!-- \/wp:buttons -->\n\n<!-- wp:separator -->\n<hr class=\"wp-block-separator\" \/>\n<!-- \/wp:separator -->\n\n<!-- wp:media-text {\"mediaId\":12521,\"mediaLink\":\"https:\\\/\\\/lungfoundation.com.au\\\/stories\\\/ethans-story\\\/oyo200924_30-reasons_afaf-and-elizabeth_outro-thumbnail-small\\\/\",\"mediaType\":\"image\"} -->\n<div class=\"wp-block-media-text alignwide is-stacked-on-mobile\"><figure class=\"wp-block-media-text__media\"><img src=\"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2020\/10\/OYO200924_30-Reasons_Afaf-and-Elizabeth_Outro-Thumbnail-small-1024x576.jpg\" alt=\"\" class=\"wp-image-12521 size-full\" \/><\/figure><div class=\"wp-block-media-text__content\"><!-- wp:heading {\"level\":4} -->\n<h4>30 Reasons for Research<\/h4>\n<!-- \/wp:heading -->\n\n<!-- wp:paragraph -->\n<p>In celebration of our 30th anniversary,&nbsp;we are highlighting 30 Reasons to donate to life-changing lung disease and lung cancer research.&nbsp;For the millions of Australians impacted by lung disease and lung cancer, research means more precious moments with loved ones, a chance to experience their&nbsp;next life milestone, and independence to do&nbsp;the&nbsp;day-to-day activities that many of us take for granted.&nbsp;<\/p>\n<!-- \/wp:paragraph --><\/div><\/div>\n<!-- \/wp:media-text -->\n\n<!-- wp:heading {\"textAlign\":\"center\",\"level\":5} -->\n<h5 class=\"has-text-align-center\"><strong><span style=\"text-decoration: underline\">Click&nbsp;<a href=\"https:\/\/lungfoundation.com.au\/get-involved\/campaigns\/30-reasons-for-research\/\" target=\"_blank\" rel=\"noreferrer noopener\">here<\/a><\/span>&nbsp;<\/strong>to find out more&nbsp;about the research being done courtesy of generous donations.&nbsp;&nbsp;<\/h5>\n<!-- \/wp:heading -->","post_title":"Tegan\u2019s story","post_excerpt":"","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"tegans-story","to_ping":"","pinged":"","post_modified":"2021-03-05 15:45:11","post_modified_gmt":"2021-03-05 05:45:11","post_content_filtered":"","post_parent":0,"guid":"http:\/\/lungfoundation.com.au\/?post_type=story&#038;p=12110","menu_order":0,"post_type":"story","post_mime_type":"","comment_count":"0","filter":"raw"}]},{"acf_fc_layout":"cta_horizontal","heading":"Become a member","copy":"Join Lung Foundation Australia to stay up to date with services, events and information that will help you to live well with your lung condition. Membership offers access to a range of benefits, including access to a hard copy of our quarterly LungNet newsletter. ","link":{"title":"Sign up now","url":" https:\/\/lungfoundation.com.au\/become-a-member\/","target":""},"link_icon":"none","background":{"background_type":"Image","image":{"ID":3099,"id":3099,"title":"membership_1920x450","filename":"membership_1920x450.jpg","filesize":480225,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","link":"https:\/\/lungfoundation.com.au\/patients-carers\/living-with-a-lung-disease\/pf\/support\/membership_1920x450\/","alt":"","author":"12","description":"","caption":"","name":"membership_1920x450","status":"inherit","uploaded_to":1274,"date":"2018-09-25 09:36:02","modified":"2018-09-25 09:36:02","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":1920,"height":450,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-300x70.jpg","medium-width":300,"medium-height":70,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-768x180.jpg","medium_large-width":768,"medium_large-height":180,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-1024x240.jpg","large-width":1024,"large-height":240,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","1536x1536-width":1536,"1536x1536-height":360,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","2048x2048-width":1920,"2048x2048-height":450,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-1920x450.jpg","xxlarge-width":1920,"xxlarge-height":450,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","xlarge-width":1280,"xlarge-height":300,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-480x450.jpg","header-navigation-width":480,"header-navigation-height":450,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":70,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":94,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/membership_1920x450.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":141}},"colour":"#ffffff","overlay":"None","repeat":false}},{"acf_fc_layout":"helpful_links","heading":"Helpful links","image_display_setting":false,"links_list":[{"image":false,"title":"Pulmonary Hypertension Association Australia ","description":"<p>PHA Australia brings hope and a better understanding of pulmonary hypertension to many families throughout the Australia and the world. <\/p>\n","link_url":"https:\/\/www.phaaustralia.com.au"},{"image":false,"title":"Pulmonary Hypertension Society of Australia &amp; New Zealand ","description":"<p>The Pulmonary Hypertension Society of ANZ operates with a commitment to supporting sustainable models of care for patients in the future.<\/p>\n","link_url":"https:\/\/www.phsanz.org"},{"image":false,"title":"Pulmonary Hypertension Association (USA) ","description":"<p>PHA (USA) works every day to end isolation, provide education, involve our constituents in everything we do, and find a cure for pulmonary hypertension.<\/p>\n","link_url":"https:\/\/www.phassociation.org"},{"image":false,"title":"Scleroderma Australia","description":"<p>Scleroderma Australia exists to promote scleroderma awareness on a National basis and advocate for improved and ongoing support for scleroderma patients.<\/p>\n","link_url":"https:\/\/www.sclerodermaaustralia.com.au"},{"image":false,"title":"PHuman","description":"<p>PHuman is a collection of educational information and real stories for people living with PH.<\/p>\n","link_url":"https:\/\/au.phhuman.com\/"}]}],"subtitle":"Pulmonary Arterial Hypertension","disable_header_overlay":false},"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/pages\/1389","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/comments?post=1389"}],"version-history":[{"count":10,"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/pages\/1389\/revisions"}],"predecessor-version":[{"id":91184,"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/pages\/1389\/revisions\/91184"}],"up":[{"embeddable":true,"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/pages\/1376"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/media\/3272"}],"wp:attachment":[{"href":"https:\/\/lungfoundation.com.au\/wp-json\/wp\/v2\/media?parent=1389"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}