{"id":65883,"date":"2021-09-20T13:40:00","date_gmt":"2021-09-20T03:40:00","guid":{"rendered":"https:\/\/hudson.org.au?post_type=hdsn_news_post&p=65883"},"modified":"2024-10-17T12:54:32","modified_gmt":"2024-10-17T01:54:32","slug":"jesss-story-hidden-pain-of-pop","status":"publish","type":"hdsn_news_post","link":"https:\/\/hudson.org.au\/news\/jesss-story-hidden-pain-of-pop\/","title":{"rendered":"Jess\u2019s Story | Hidden pain of POP"},"content":{"rendered":"\n

Six months after the birth of her third child, Jess*, 35, felt something wasn\u2019t right. As she was walking 200 metres to the beach one day with her baby in a carrier, she felt an uncomfortable dragging sensation in her pelvis and had to sit down.<\/p>\n\n\n\n

Jess visited her obstetrician and a pelvic floor physiotherapist and, after a 4D ultrasound, was diagnosed with severe pelvic organ prolapse (POP)<\/a>.<\/p>\n\n\n\n

\u201cI could not believe this was happening to me,\u201d Jess says. \u201cI went from feeling so happy and content in life to so scared about my future health and depressed.\u201d<\/p>\n\n\n\n

Jess wears a cube pessary to support her uterus which needs to be put in place and removed every day. While it helps with the dragging feeling, she finds it embarrassing, humiliating, and by the end of the day she is in pain. The pessary also limits many of her usual physical activities. \u201cI still feel like I can\u2019t run or jump and do high intensity exercises,\u201d she says.<\/p>\n\n\n\n

Her medical advice is to wear the pessary for as long as possible, because without it, surgery is the only other option and despite this, the prolapse can recur\/ reoccur.<\/p>\n\n\n\n

\u201cWith the current surgical options available, things are looking bleak. I am tired of constantly thinking about it and worrying about it. I just want it fixed so I can move on and enjoy life with my beautiful babies and husband,\u201d says Jess.<\/p>\n\n\n\n

Jess says it was only after confiding in friends that she discovered two others in their mid-thirties had also suffered pelvic organ prolapse and had surgery. \u201cIt\u2019s a very embarrassing thing to have happen, especially in your thirties. That\u2019s why people don\u2019t talk about it.<\/p>\n\n\n\n

\u201cThe only thing that is keeping me going is reading about Professor Caroline Gargett\u2019s<\/a> team\u2019s research into a potential stem cell treatment for POP,\u201d Jess says. \u201cI am desperate for a better treatment option. The thought of having to live with a pessary for the rest of my life or having surgery now only for it to more than likely come back and need more surgery, is just not good enough. It makes me sad that this is my life now.\u201d<\/p>\n\n\n\n

\u201cI hope the stem cell team have all the funding they need to continue their very important work to find a treatment for this condition and make it available sooner rather than later.\u201d<\/p>\n\n\n\n

Jess says the research investigating solutions soon after birth trauma occurs is especially important. \u201cIf there was a way to repair the damaged muscles after birth trauma, that would be absolutely ideal. It would prevent future prolapse and a lifelong battle with a chronic condition.\u201d<\/p>\n\n\n\n

*Jess has chosen to remain anonymous<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

Six months after the birth of her third child, Jess*, 35, felt something wasn\u2019t right. As she was walking 200 metres to the beach one day with her baby in a carrier, she felt an uncomfortable dragging sensation in her pelvis and had to sit down.…  Read more<\/a><\/p>\n","protected":false},"featured_media":57936,"menu_order":0,"template":"","issue":[132],"tag":[],"story-type":[],"treatment-type":[],"class_list":["post-65883","hdsn_news_post","type-hdsn_news_post","status-publish","has-post-thumbnail","hentry","issue-winter-2021"],"acf":[],"yoast_head":"\nJess\u2019s Story | Hidden pain of POP - Hudson Institute of Medical Research<\/title>\n<meta name=\"description\" content=\"Six months after the birth of her third child, Jess*, 35, felt something wasn\u2019t right and tells her story of the hidden pain of POP.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/hudson.org.au\/news\/jesss-story-hidden-pain-of-pop\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Jess\u2019s Story | Hidden pain of POP\" \/>\n<meta property=\"og:description\" content=\"Six months after the birth of her third child, Jess*, 35, felt something wasn\u2019t right and tells her story of the hidden pain of POP.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/hudson.org.au\/news\/jesss-story-hidden-pain-of-pop\/\" \/>\n<meta property=\"og:site_name\" content=\"Hudson Institute of Medical Research\" \/>\n<meta property=\"article:modified_time\" content=\"2024-10-17T01:54:32+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/hudson.org.au\/wp-content\/uploads\/2023\/07\/Jesss-Story-e1649771230781-edited.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"666\" \/>\n\t<meta property=\"og:image:height\" content=\"666\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/hudson.org.au\\\/news\\\/jesss-story-hidden-pain-of-pop\\\/\",\"url\":\"https:\\\/\\\/hudson.org.au\\\/news\\\/jesss-story-hidden-pain-of-pop\\\/\",\"name\":\"Jess\u2019s Story | Hidden pain of POP - 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