{"id":39054,"date":"2026-05-24T11:07:12","date_gmt":"2026-05-24T11:07:12","guid":{"rendered":"https:\/\/pickbydoc.com\/?p=39054"},"modified":"2026-05-24T11:07:14","modified_gmt":"2026-05-24T11:07:14","slug":"dairy-farmer-was-misdiagnosed-with-lyme-disease-it-was-lupus","status":"publish","type":"post","link":"https:\/\/pickbydoc.com\/?p=39054","title":{"rendered":"Dairy Farmer Was Misdiagnosed with Lyme Disease. It Was Lupus"},"content":{"rendered":"<p> <br \/>\n<\/p>\n<div data-testid=\"tabbed-article-section\" data-section-id=\"_noHeaderPrefixedContent\"><span style=\"font-size:0;line-height:0\"\/><\/p>\n<div>\n<div>\n<p class=\"css-mnvj0k\">When dairy farmer Brie Hyde began experiencing chronic fatigue and joint pain, doctors treated her for Lyme disease. After years of worsening symptoms, she was diagnosed with Lupus.<\/p>\n<\/div>\n<\/div>\n<div>\n<p>As a child, Brie Hyde dreamed of being a veterinarian.<\/p>\n<\/div>\n<div>\n<p>\u201cI\u2019ve always been an outdoorsy person, very animal fascinated,\u201d she told Healthline.<\/p>\n<\/div>\n<div>\n<p>While attending the University of Vermont, she fell in love with dairy farming and started her own farm in Connecticut in 2004.<\/p>\n<\/div>\n<div>\n<p>\u201cI was a first-generation female farmer,\u201d she said. \u201cFarming is crazy active and very strenuous on your body and time, and that\u2019s what completed me. That\u2019s what makes me whole.\u201d<\/p>\n<\/div>\n<div>\n<p>However, early on during her farming days, she began experiencing intense hand pain that she initially attributed to the physical demands of her job.<\/p>\n<\/div>\n<div>\n<p>\u201cThere\u2019s pictures and videos and things that I look back at now, and I was constantly rubbing my hands,\u201d said Hyde.<\/p>\n<\/div>\n<div>\n<p>The pain eventually spread to her feet, ankles, knees, and hips, and during the summertime, she developed fevers.<\/p>\n<\/div>\n<div>\n<p>At first, doctors attributed her symptoms to <a href=\"https:\/\/www.healthline.com\/health\/lyme-disease\" class=\"content-link css-kxhged\" target=\"_blank\" rel=\"noopener\">Lyme disease<\/a>, a bacterial infection transmitted from ticks.<\/p>\n<\/div>\n<div>\n<p>\u201cSo they\u2019d put me on prednisone and antibiotics, and 10 days on prednisone, you\u2019re feeling better. So then it would go away, and I would push through,\u201d she said.<\/p>\n<\/div>\n<\/div>\n<div data-testid=\"tabbed-article-section\" data-section-id=\"Signs-and-symptoms-that-lead-to-a-lupus-diagnosis\"><span style=\"font-size:0;line-height:0\"\/><span style=\"font-size:0;line-height:0\"\/><\/p>\n<div>\n<p>Hyde\u2019s symptoms persisted and progressed.<\/p>\n<\/div>\n<div>\n<p>\u201cI\u2019d be in the shower, and my feet would be purple,\u201d she said.<\/p>\n<\/div>\n<div>\n<p>She also noticed a lacy pattern appearing under her skin and a strange reaction to sunlight.<\/p>\n<\/div>\n<div>\n<p>\u201cI would go out in the sun, and it would feel like I was burning from the outside in,\u201d said Hyde.<\/p>\n<\/div>\n<div>\n<p>She also experienced extreme <a href=\"https:\/\/www.healthline.com\/health\/fatigue\" class=\"content-link css-kxhged\" target=\"_blank\" rel=\"noopener\">fatigue<\/a>.<\/p>\n<\/div>\n<div>\n<p>\u201cThe crazy fatigue that I was getting and the pain in my hands had gotten to the point where I was like, \u2018This is not right. There\u2019s something not right,\u2019\u201d she said.<\/p>\n<\/div>\n<div>\n<p>She went back to her primary care physician, who ordered blood tests. Her doctor noticed Hyde had a high Antinuclear Antibody (ANA) test result and suggested she see a rheumatologist to screen for <a href=\"https:\/\/www.healthline.com\/health\/lupus\" class=\"content-link css-kxhged\" target=\"_blank\" rel=\"noopener\">lupus<\/a>.<\/p>\n<\/div>\n<div>\n<p>\u201cI honestly remember, I said, \u2018What the hell is lupus?\u2019\u201d she said. \u201cI had no clue. Not on my radar. No idea what it was.\u201d<\/p>\n<\/div>\n<div>\n<p>Hyde\u2019s challenging journey to diagnosis isn\u2019t unique. In fact, <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0003496724548038\" target=\"_blank\" rel=\"noopener noreferrer\" class=\"content-link css-kxhged\">research<\/a> indicates that it takes an average of nearly 6 years for a person to receive an accurate lupus diagnosis.<\/p>\n<\/div>\n<div>\n<p>\u201cSymptoms can overlap with those of other conditions and are often present at onset. Combined with test results that vary from person to person, this can make the path to diagnosis complex and far from straightforward,\u201d <a href=\"https:\/\/findcare.ahn.org\/Susan-Manzi\" target=\"_blank\" rel=\"noopener noreferrer\" class=\"content-link css-kxhged\">Susan Manzi, MD,<\/a> Chair of the Allegheny Health Network Medicine Institute, told Healthline.<\/p>\n<\/div>\n<p><span class=\"css-ryxryr\"\/><\/div>\n<div data-testid=\"tabbed-article-section\" data-section-id=\"Even-after-diagnosis-finding-effective-treatment-can-be-challenging\"><span style=\"font-size:0;line-height:0\"\/><\/p>\n<div>\n<p>Hyde\u2019s treatment journey involved a long process of trial and error.<\/p>\n<\/div>\n<div>\n<p>Doctors first prescribed prednisone and <a class=\"content-link css-kxhged sl\" href=\"https:\/\/www.healthline.com\/health\/drugs\/hydroxychloroquine-tablet-side-effects\/\" target=\"_blank\" rel=\"noopener\">hydroxychloroquine<\/a>, a common medication used to treat lupus, but she developed a severe allergic reaction.<\/p>\n<\/div>\n<div>\n<p>The next medication made her \u201cviolently ill,\u201d while another biologic treatment did nothing to improve her symptoms.<\/p>\n<\/div>\n<div>\n<p>As she tried different treatments, lupus slowly altered her daily life and that of her husband and children.<\/p>\n<\/div>\n<div>\n<p>\u201cMy husband was taking on more, and the kids were taking on more,\u201d Hyde said. \u201cThere were definitely changes. I couldn\u2019t be outside in the sun as much as I used to.\u201d<\/p>\n<\/div>\n<div>\n<p>At one point, the emotional and physical exhaustion became overwhelming and she hesitated to try more treatment.<\/p>\n<\/div>\n<div>\n<p>\u201cI was like, \u2018I don\u2019t want to take anything anymore,\u2019\u201d she said. \u201cEither I\u2019m taking too many medications to take the side effects away, or these medications are making me sick and I\u2019m not getting any better.\u201d<\/p>\n<\/div>\n<div>\n<p>But her doctor urged her not to stop treatment.<\/p>\n<\/div>\n<div>\n<p>\u201cOne of the things that\u2019s crazy about lupus is as bad as you feel on the outside, my doctor said, \u2018You have to realize what it\u2019s doing inside. You\u2019re trying to save your organs for the long haul,\u2019\u201d said Hyde.<\/p>\n<\/div>\n<div>\n<p>That perspective changed how Hyde viewed the disease.<\/p>\n<\/div>\n<div>\n<p>In March 2023, her rheumatologist suggested she try Saphnelo infusion.<\/p>\n<\/div>\n<div>\n<p>\u201cThat was a monumental moment in our lives,\u201d said Hyde. \u201cI remember I called my husband and I was like, \u2018I didn\u2019t realize how sick I was until now because I feel better.\u2019\u201d<\/p>\n<\/div>\n<div>\n<p>Today, she has regained parts of her old life. She works on the farm, vacations with her children, and participates in the life she once feared she might lose.<\/p>\n<\/div>\n<div>\n<p>\u201cI\u2019m able to be a normal person,\u201d Hyde said.<\/p>\n<\/div>\n<\/div>\n<div data-testid=\"tabbed-article-section\" data-section-id=\"How-lupus-care-and-management-is-improving\"><span style=\"font-size:0;line-height:0\"\/><\/p>\n<div>\n<p>Manzi said newer options like the recently FDA-approved <a href=\"https:\/\/www.astrazeneca-us.com\/content\/az-us\/media\/press-releases\/2026\/SAPHNELO-approved-in-the-US-for-subcutaneous-self-administration-as-a-new-autoinjector-for-the-treatment-of-systemic-lupus-erythematosus.html\" target=\"_blank\" rel=\"noopener noreferrer\" class=\"content-link css-kxhged\">Saphnelo Pen<\/a>, a self-administered, once-weekly treatment for SLE, bring hope to patients like Hyde. Although she is not currently taking this.<\/p>\n<\/div>\n<div>\n<p>On top of standard therapy, Manzi said self-administered biologics will help improve access and convenience of treatment while offering better disease control and reduced complications.<\/p>\n<\/div>\n<div>\n<p>\u201cTreatment is increasingly moving in this direction,\u201d she said. \u201cWhile approximately half of patients already receive biologics at-home treatment, access can still be challenging, with some needing to travel long distances for care. Self-administered options are helping to change that.\u201d<\/p>\n<\/div>\n<div>\n<p>Giving patients more choice, in collaboration with healthcare professionals, is essential to achieving better outcomes in SLE, she added.<\/p>\n<\/div>\n<div>\n<p>\u201c[It] empowers patients to manage their lupus in a way that best suits their individual needs and lifestyles,\u201d Manzi said.<\/p>\n<\/div>\n<p><span class=\"css-ryxryr\"\/><\/div>\n<div data-testid=\"tabbed-article-section\" data-section-id=\"Lupus-changed-how-she-lives-but-hasn-t-stopped-her-from-thriving\"><span style=\"font-size:0;line-height:0\"\/><\/p>\n<div>\n<p>Hyde still experiences flares, but she said her condition is under control.<\/p>\n<\/div>\n<div>\n<p>\u201cYou have to know your limits so that you don\u2019t push yourself too much,\u201d she said.<\/p>\n<\/div>\n<div>\n<p>She carefully plans social events, workdays, and travel to avoid triggering flares. Sun exposure remains a major concern.<\/p>\n<\/div>\n<div>\n<p>\u201cToo much sun, no matter what, will put me into a bad flare,\u201d she said.<\/p>\n<\/div>\n<div>\n<p>\u201cYou\u2019ve got to second-guess [whether] this large event is really going to be something that\u2019s worth putting myself at risk of getting sick,\u201d she said.<\/p>\n<\/div>\n<div>\n<p>She also deals with the emotional and mental strains of lupus.<\/p>\n<\/div>\n<div>\n<p>\u201cI always identified myself as a very strong, very active, independent woman,\u201d said Hyde. \u201cAnd all of a sudden, lupus took that all away from me.\u201d<\/p>\n<\/div>\n<div>\n<p>For a time, she even wondered whether she would have to give up farming altogether.<\/p>\n<\/div>\n<div>\n<p>\u201cThere was definitely a time where I thought, \u2018This is it,\u2019\u201d she said. \u201cThe pain and the fatigue [made me think] I have to find something else in my daily life.\u201d<\/p>\n<\/div>\n<div>\n<p>Questioning her identity is also something she faced.<\/p>\n<\/div>\n<div>\n<p>\u201cYou definitely go through the question of, \u2018Who am I? What can I do? What do I need to take away from my life right now?\u2019\u201d<\/p>\n<\/div>\n<div>\n<p>However, surviving lupus has reshaped her understanding of resilience.<\/p>\n<\/div>\n<div>\n<p>\u201cI feel like I\u2019m even stronger because I\u2019ve gone through this,\u201d she said. \u201cI\u2019m even more independent. I\u2019m even more resilient.\u201d<\/p>\n<\/div>\n<div>\n<p>She hopes sharing her experience helps others feel less alone when they\u2019re experiencing symptoms, medication failures, and uncertainty.<\/p>\n<\/div>\n<div>\n<p>\u201cThere were days when I was so sick, I physically could not get out of bed,\u201d she said. \u201cSo, to actually be able to enjoy life and enjoy what makes me happy and makes me feel fulfilled, if I can help somebody else find that, I think it makes it worth it.\u201d<\/p>\n<\/div>\n<p><span class=\"css-ryxryr\"\/><\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/www.healthline.com\/health-news\/dairy-farmer-misdiagnosed-lyme-disease-lupus\" target=\"_blank\" rel=\"noopener\">Source link <\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>When dairy farmer Brie Hyde began experiencing chronic fatigue and joint pain, doctors treated her for Lyme disease. After years of worsening symptoms, she was diagnosed with Lupus. As a child, Brie Hyde dreamed of being a veterinarian. \u201cI\u2019ve always been an outdoorsy person, very animal fascinated,\u201d she told Healthline. While attending the University of [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":39055,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[171],"tags":[],"class_list":["post-39054","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-health-conditions"],"jetpack_publicize_connections":[],"_links":{"self":[{"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/posts\/39054","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=39054"}],"version-history":[{"count":1,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/posts\/39054\/revisions"}],"predecessor-version":[{"id":39056,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/posts\/39054\/revisions\/39056"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=\/wp\/v2\/media\/39055"}],"wp:attachment":[{"href":"https:\/\/pickbydoc.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=39054"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=39054"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/pickbydoc.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=39054"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}