{"id":161226,"date":"2026-03-09T14:30:23","date_gmt":"2026-03-09T14:30:23","guid":{"rendered":"https:\/\/www.kidneyresearchuk.org\/?p=161226"},"modified":"2026-03-09T14:31:53","modified_gmt":"2026-03-09T14:31:53","slug":"i-had-no-idea-my-lack-of-energy-was-a-sign-my-kidneys-were-failing","status":"publish","type":"post","link":"https:\/\/www.kidneyresearchuk.org\/2026\/03\/09\/i-had-no-idea-my-lack-of-energy-was-a-sign-my-kidneys-were-failing\/","title":{"rendered":"I had no idea my lack of energy was a sign my kidneys were failing"},"content":{"rendered":"\n\n\t\t\n\t<p>A\u00a028-year-old lawyer was\u00a0left in disbelief after\u00a0suddenly finding herself in hospital and\u00a0being told\u00a0she&#8217;d\u00a0need\u00a0a\u00a0transplant or dialysis to\u00a0survive <a href=\"https:\/\/www.kidneyresearchuk.org\/kidney-health-information\/living-with-kidney-disease\/kidney-failure\/\">kidney failure<\/a>.\u00a0\u00a0<\/p>\n<p>Ellen Swarbrick, from Manchester, says: &#8220;In 2023,\u00a0I&#8217;d\u00a0moved to London to train as a lawyer\u00a0and it\u00a0was\u00a0a\u00a0really exciting\u00a0time in my life.\u00a0I&#8217;m\u00a0a very social person and was working hard. Slowly I\u00a0began to find myself getting home from work and feeling shattered.\u00a0I&#8217;d\u00a0lost the energy to do anything.\u00a0\u00a0\u00a0<\/p>\n<p>&#8220;I assumed it was because life was so busy and had no idea it was a sign of something more serious.\u00a0Being diagnosed with a type of kidney disease called <a href=\"https:\/\/www.kidneyresearchuk.org\/conditions-symptoms\/iga-nephropathy\/\">IgA nephropathy<\/a> the following year was\u00a0terrifying. I cried myself to sleep\u00a0every night\u00a0for about six months after that. It took some time to come to terms with the fact\u00a0I&#8217;d\u00a0need a transplant.&#8221;\u00a0<\/p>\n\t<h2>Warning signs of kidney disease\u00a0<\/h2>\n<p>Every day 23 people start treatment for kidney failure. However, many\u00a0are not aware of\u00a0problems with their kidneys until\u00a0only <a href=\"https:\/\/www.kidneyresearchuk.org\/conditions-symptoms\/dialysis\/\">dialysis<\/a> or a <a href=\"https:\/\/www.kidneyresearchuk.org\/transplantation\/\">transplant<\/a> will keep them alive.\u00a0<\/p>\n<p>This was the case for Ellen, who only discovered\u00a0she was living with kidney disease as she\u00a0was\u00a0entering\u00a0kidney failure. She is now sharing her experiences\u00a0to raise awareness of <a href=\"https:\/\/www.kidneyresearchuk.org\/conditions-symptoms\/symptoms-of-kidney-disease\/\">warning signs<\/a>\u00a0that could\u00a0help others get diagnosed at an earlier stage.\u00a0\u00a0<\/p>\n<p>Ellen says: &#8220;In hindsight, I can see there were\u00a0some signs before I\u00a0ended up in hospital. I\u00a0just never put two and two together. I\u00a0didn&#8217;t\u00a0know anybody around my age who had gone through anything like this with their health.\u00a0<\/p>\n<p>&#8220;I attributed\u00a0my\u00a0tiredness to being busy. I noticed puffiness in my face but assumed it was\u00a0weight-gain from being in a desk job and not exercising as much.\u00a0I&#8217;d\u00a0been taking antihistamines for hay fever because of my puffy eyes, but it\u00a0wasn&#8217;t\u00a0helping.\u00a0<\/p>\n<p>&#8220;On a work trip\u00a0abroad,\u00a0I felt nauseous and\u00a0my ankles became swollen, but I thought it was because of the heat.\u00a0I remember sending photos to my friends and laughing about the size of them. I just had no clue that swollen ankles were a dangerous sign of health problems.\u00a0\u00a0\u00a0<\/p>\n<p>&#8220;When I got home, I\u00a0still\u00a0wasn&#8217;t\u00a0well.\u00a0I felt like I was developing the flu.\u00a0The next day I woke\u00a0with\u00a0patches in my\u00a0vision.\u00a0It was\u00a0really scary. I called 111 and was told to go to the eye emergency centre at St Thomas&#8217; Hospital.\u00a0I could barely see where I was going.\u00a0<\/p>\n<figure itemscope itemtype=\"https:\/\/schema.org\/ImageObject\">\n\t\t\t\t<img decoding=\"async\" class=\"lazyload\" src=\"data:image\/gif;base64,R0lGODlhAQABAIAAAAAAAP\/\/\/yH5BAEAAAAALAAAAAABAAEAAAIBRAA7\" data-src=\"https:\/\/www.kidneyresearchuk.org\/wp-content\/uploads\/2026\/03\/IMG_5464-scaled.jpeg\" alt=\"Ellen in hospital\" height=\"2560\" width=\"1178\" title=\"Ellen Swarbrick\" onerror=\"this.style.display='none'\" loading=\"lazy\" \/><noscript><img decoding=\"async\" class=\"lazyload\" src=\"https:\/\/www.kidneyresearchuk.org\/wp-content\/uploads\/2026\/03\/IMG_5464-scaled.jpeg\" alt=\"Ellen in hospital\" height=\"2560\" width=\"1178\" title=\"Ellen Swarbrick\" onerror=\"this.style.display='none'\" loading=\"lazy\" \/><\/noscript>\n\t\t<figcaption>Ellen Swarbrick<\/figcaption>\n\t<\/figure>\n\t<p>&#8220;My blood pressure was\u00a0really high\u00a0and that had\u00a0caused\u00a0fluid to leak into my eyes. I was sent to A&amp;E and spent two days in ICU before moving to the high dependency ward. I was on a drip to manage my blood pressure and\u00a0had\u00a0loads\u00a0of tests and scans.\u00a0\u00a0<\/p>\n<p>&#8220;I was told my kidneys were &#8216;pretty bad&#8217; but until that point,\u00a0I\u00a0didn&#8217;t\u00a0realise my kidneys were related to my high blood pressure or other symptoms. I assumed it would be something\u00a0I&#8217;d\u00a0recover from, but then I\u00a0got the news\u00a0from\u00a0my biopsy\u00a0that\u00a0I was at stage four chronic kidney disease. It\u00a0was so strange finding out\u00a0I&#8217;d\u00a0need a transplant or dialysis.&#8221;<\/p>\n\t<h2>Living with chronic kidney disease<\/h2>\n<p>Ellen&#8217;s <a href=\"https:\/\/www.kidneyresearchuk.org\/kidney-health-information\/stages-of-kidney-disease\/\">kidney function<\/a> continued to decline and within ten months her kidneys had completely failed.\u00a0\u00a0<\/p>\n<p>She\u00a0says: &#8220;After my diagnosis my\u00a0mental health went down the toilet. It\u00a0massively knocked my confidence.\u00a0I felt like nobody understood me and\u00a0I\u00a0withdrew socially. It was difficult to join in with work socials when I\u00a0couldn&#8217;t\u00a0drink.\u00a0I felt so tired all the time anyway.\u00a0I became a lot less outgoing and went into myself.\u00a0<\/p>\n<p>&#8220;I\u00a0didn&#8217;t\u00a0want people to know that I was unwell. I remember going back to work and pretending everything was fine. I\u00a0hadn&#8217;t\u00a0come to terms with\u00a0my diagnosis. I\u00a0didn&#8217;t\u00a0want to accept the fact\u00a0I&#8217;d\u00a0need adjustments, it felt very isolating.\u00a0<\/p>\n<p>&#8220;What made me feel less alone was listening to other young people sharing their\u00a0experiences on social media. I realised that kidney disease\u00a0doesn&#8217;t\u00a0only affect older people. Learning\u00a0about how other people were dealing with their\u00a0own\u00a0diagnoses was a huge help.&#8221;\u00a0<\/p>\n<figure itemscope itemtype=\"https:\/\/schema.org\/ImageObject\">\n\t\t\t\t<img decoding=\"async\" class=\"lazyload\" src=\"data:image\/gif;base64,R0lGODlhAQABAIAAAAAAAP\/\/\/yH5BAEAAAAALAAAAAABAAEAAAIBRAA7\" data-src=\"https:\/\/www.kidneyresearchuk.org\/wp-content\/uploads\/2026\/03\/IMG_5515.jpeg\" alt=\"Mother and daughter sitting on a hospital bed together\" height=\"1686\" width=\"1284\" title=\"Ellen Swarbrick\" onerror=\"this.style.display='none'\" loading=\"lazy\" \/><noscript><img decoding=\"async\" class=\"lazyload\" src=\"https:\/\/www.kidneyresearchuk.org\/wp-content\/uploads\/2026\/03\/IMG_5515.jpeg\" alt=\"Mother and daughter sitting on a hospital bed together\" height=\"1686\" width=\"1284\" title=\"Ellen Swarbrick\" onerror=\"this.style.display='none'\" loading=\"lazy\" \/><\/noscript>\n\t\t<figcaption>Ellen and her mum<\/figcaption>\n\t<\/figure>\n\t<h2>A transplant from Mum<\/h2>\n<p>As Ellen&#8217;s kidney function deteriorated, her parents, brother,\u00a0partner\u00a0and friends all put themselves forward to donate a kidney.\u00a0<\/p>\n<p>Ellen says: &#8220;It was a race against time to have the transplant before I needed dialysis.\u00a0I was scared, although I have developed a more positive view of\u00a0dialysis\u00a0having\u00a0seen the experiences of others.\u00a0We are lucky to have a treatment\u00a0option\u00a0which keeps us alive after organ failure, and I know I may have to rely on it in the future.\u00a0<\/p>\n<p>&#8220;I\u00a0was fortunate to escape dialysis\u00a0this time, as\u00a0I was\u00a0being\u00a0prepared for treatment\u00a0at the same time my mum was having her final tests ahead of donating a kidney. She was the best\u00a0match,\u00a0and our\u00a0amazing transplant nurse arranged the surgery\u00a0to happen ten days later.\u00a0\u00a0\u00a0\u00a0<\/p>\n<p>&#8220;The transplant itself was such a blur, it all happened so quickly. I was excited and scared. It was emotional thinking about mum doing something so incredible for me.\u00a0The doctors were brilliant at keeping me informed and I knew her surgery had gone well before I had mine.\u00a0\u00a0<\/p>\n<p>&#8220;The thing that had worried me most was immediate transplant rejection and my mum going through\u00a0surgery\u00a0for nothing, so it was a massive relief\u00a0when I woke up\u00a0to find that the kidney was working well.\u00a0There were concerns about Mum\u00a0for 24 hours\u00a0post-surgery, but\u00a0since then her recovery has gone\u00a0well.\u00a0She&#8217;s\u00a0completely back to herself now.\u00a0<\/p>\n<p>&#8220;The transplant was the start of me being able to live again. I feel like\u00a0I&#8217;m\u00a0getting my personality back and\u00a0I&#8217;m\u00a0enjoying being at work again.\u00a0I see my friends more often and have started running. I have so much more freedom. My mind feels peaceful again.\u00a0Whether my transplant lasts for two or 25 years, I want to make sure\u00a0I&#8217;m\u00a0making the most of that time.\u00a0\u00a0<\/p>\n<p>&#8220;I hope that by sharing my story, more people are diagnosed sooner so that their kidney function can be protected. That way they may not\u00a0need a transplant until they are older, if they do at all.&#8221;<\/p>\n\t<h2>Kidney health check<\/h2>\n<p>There are estimated to be 7.2 million people in the UK currently living with <a href=\"https:\/\/www.kidneyresearchuk.org\/conditions-symptoms\/chronic-kidney-disease\/\">chronic kidney disease<\/a>, more than 10% of the entire population. However, symptoms can often remain undetected or attributed to other causes.\u00a0\u00a0<\/p>\n<p>Knowing your risk of kidney disease could help you and healthcare professionals to protect your kidneys, preventing or delaying the need for life-altering treatments such as dialysis or a transplant.\u00a0\u00a0<\/p>\n<p>Our <a href=\"https:\/\/www.kidneyresearchuk.org\/kidney-health-information\/kidneyhealthcheck\/\">kidney health check<\/a> is a quick and easy online tool which you can use to help you understand if you are at risk.<\/p>\n\t<h2>Take your FREE health check today<\/h2>\n<p>Did you know that every day over 20 people start treatment for kidney failure?<\/p>\n<p>Several things can increase your risk including diabetes, high blood pressure or being overweight.<\/p>\n<p>Take our quick and easy online test to see if you are at risk.<\/p>\n\t\t\t<a href=\"https:\/\/kidneyresearchuk.org\/kidneyhealthcheck\/\"  target=\"_self\">\n\t\t\t\t\t\t\tTake kidney health check now\n\t\t\t\t\t<\/a>\n\n","protected":false},"excerpt":{"rendered":"<p>A\u00a028-year-old lawyer was\u00a0left in disbelief after\u00a0suddenly finding herself in hospital and\u00a0being told\u00a0she&#8217;d\u00a0need\u00a0a\u00a0transplant or dialysis to\u00a0survive kidney failure.\u00a0\u00a0 Ellen Swarbrick, from Manchester, says: &#8220;In 2023,\u00a0I&#8217;d\u00a0moved to London to train as a lawyer\u00a0and it\u00a0was\u00a0a\u00a0really exciting\u00a0time in my life.\u00a0I&#8217;m\u00a0a very social person and was working hard. Slowly I\u00a0began to find myself getting home from work and feeling shattered.\u00a0I&#8217;d\u00a0lost&hellip;<\/p>\n","protected":false},"author":3,"featured_media":161223,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_searchwp_excluded":"","footnotes":""},"categories":[30],"tags":[],"class_list":["post-161226","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-patient-stories"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>I had no idea my lack of energy was a sign my kidneys were failing - Kidney Research UK<\/title>\n<meta name=\"description\" content=\"Ellen Swarbrick was left in disbelief after being told she\u2019d need a transplant or dialysis to survive kidney failure.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, 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