{"id":449,"date":"2021-06-21T07:34:53","date_gmt":"2021-06-21T05:34:53","guid":{"rendered":"https:\/\/www.amyloidosisalliance.org\/events\/world-amyloidosis-day\/testimonials\/long-days-march-to-clarity\/"},"modified":"2021-06-21T07:34:53","modified_gmt":"2021-06-21T05:34:53","slug":"long-days-march-to-clarity","status":"publish","type":"aa_testimony","link":"https:\/\/www.amyloidosisalliance.org\/fr\/events\/world-amyloidosis-day\/testimonials\/long-days-march-to-clarity\/","title":{"rendered":"Long day\u2019s march to clarity"},"content":{"rendered":"<p class=\"wp-block-paragraph\">My father was diagnosed with hattr in the late 70\u2019s and died a couple of years later &#8211; at the time I was 12 years old, meaning old enough to understand some things about the disease &#8211; in particular the severity and hereditary nature of it. When I was about 20, I decided I wanted to know whether or not I carried the gene and I got tested. When I went to my doctor\u2019s office to learn about the result, he asked me if I really wanted to know, given that I was so young, and that even if I had the gene I might not develop the disease and if I did, there was not much to be done about it (this was back when liver transplant was pretty much the only treatment), and so I decided I didn\u2019t want to know the result of the test. I guess this stuck in the back of my mind for years &#8211; I mean, if you\u2019d have had a perfectly healthy 20-year old in front of you, whom you knew didn\u2019t carry the gene and hence would never develop the disease, would you even ask if she really wanted to know the result?<\/p>\n<p class=\"wp-block-paragraph\">Anyway, years later, in 2017 when I was in my forties, I started experiencing numbness and pain in my heels, and I decided I wanted to learn the result from the test, so they dug it out of the (probably) basement of some hospital archive and lo and behold, I do carry the gene. I had a fat pad biopsy and I had in fact developed the disease, however the feet issues turned out to be \u201conly\u201d heel spurs and ever since they healed I haven\u2019t had any issues\/symptoms until now, 4 years later. I\u2019ve been on Tafamidis\/Vyndaqel since 2017 and it has worked until now, when I\u2019ve lost a bit of sensation to my feet\/experience numbness plus increased faintness.<\/p>\n<p class=\"wp-block-paragraph\">Getting the diagnosis and learning about this disease was a really rough and intense ride and it took the better part of a year to come to terms with it. Now, I\u2019m so forever happy and grateful that we live in a time when there are treatment options and I\u2019d like to think that I\u2019ll be able to live a full and satisfying life for a long time, seeing my kids grow up and get families of their own. That\u2019s really all that I want.<\/p>\n<p class=\"wp-block-paragraph\"><a href=\"Amyloidosis: Our family's curse\">Long day&rsquo;s march to clarity<\/a> &#8211; Britta &#8211; Sweden<\/p>\n","protected":false},"excerpt":{"rendered":"<p>My father was diagnosed with hattr in the late 70\u2019s and died a couple of years later \u2013 at the time I was 12 years old, meaning old enough to understand some things about the disease \u2013 in particular the severity and hereditary nature of it.<\/p>\n","protected":false},"featured_media":1196,"template":"","class_list":["post-449","aa_testimony","type-aa_testimony","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Long day\u2019s march to clarity - Amyloidosis Alliance<\/title>\n<meta name=\"description\" content=\"My father was diagnosed with hattr in the late 70\u2019s and died a couple of years later \u2013 at the time I was 12 years old, meaning old enough to understand some things about the disease \u2013 in particular the severity and hereditary nature of it.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/events\/world-amyloidosis-day\/testimonials\/long-days-march-to-clarity\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Long day\u2019s march to clarity - 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