{"id":1065328,"date":"2012-02-28T04:59:49","date_gmt":"2012-02-28T04:59:49","guid":{"rendered":"http:\/\/www.longevitymedicine.tv\/rare-disease-strikes-family\/"},"modified":"2024-08-18T11:11:23","modified_gmt":"2024-08-18T15:11:23","slug":"rare-disease-strikes-family","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/ataxia\/rare-disease-strikes-family.php","title":{"rendered":"Rare disease strikes family"},"content":{"rendered":"<p>ALEXIA JOHNSTON          <\/p>\n<p>      RARE CASE: Joanne Illingworth, 46, has NARP, a disease that      attacks the nervous system. Despite its rarity, it is      hereditary and her three siblings also contracted the      disease.    <\/p>\n<p>    Timaru woman Joanne Illingworth is likely to be one in a    million, if not more.  <\/p>\n<p>    Ms Illingworth, 46, suffers from neuropathy ataxia and    retinitis pigmentosa (NARP), a disease that affects very few    people in the world.  <\/p>\n<p>    A report suggests the condition is so rare that its prevalence    is unknown.  <\/p>\n<p>    NARP, which is in the multiple sclerosis \"family\", attacks the    nervous system, causing muscle weakness, numbness, tingling or    pain in the arms and legs, and loss of balance and    co-ordination.  <\/p>\n<p>    Ms Illingworth had a normal start to life. As a young girl she    would run around and play like other children.  <\/p>\n<p>    However, at 13 all of that changed.  <\/p>\n<p>    \"I was sick in bed with the flu. I got out of bed and I    collapsed on the ground because I couldn't feel anything.\" She    was admitted to hospital, but then sent home without a    diagnosis. It took another 17 years before she found out what    she was suffering from.  <\/p>\n<p>    Despite the rarity of NARP, it was to become a common condition    in Ms Illingworth's family after her three younger siblings,    including a half-sister, also contracted the disease, all    within about three years of each other. Ms Illingworth was the    first in the family to get the disease, a hereditary condition    passed down by females.  <\/p>\n<p>    Her brother has since died of NARP. Her two younger sisters    live in Oamaru. The family does not know anyone else with the    condition.  <\/p>\n<p>    NARP affects people differently, depending on the severity of    their case.  <\/p>\n<p>    \"It affects your eyes, your speech and I shake quite a lot,\" Ms    Illingworth said.  <\/p>\n<p>    Her life had been full of frustrations. People often assumed    she was drunk because of the way she talked. Ms Illingworth had    lost count of how many doctors she saw before getting a    diagnosis, but she hoped her determination would inspire    others.  <\/p>\n<p>    Rare Disease Awareness Day will be marked tomorrow \u2013 leap day \u2013    one of the rarest days of the year. For more information about    the day visit rarediseaseday.org.nz  <\/p>\n<p>    - \u00a9 Fairfax NZ News  <\/p>\n<\/p>\n<p>See the original post here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.stuff.co.nz\/timaru-herald\/news\/6489786\/Rare-disease-strikes-family\" title=\"Rare disease strikes family\" rel=\"noopener\">Rare disease strikes family<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>ALEXIA JOHNSTON RARE CASE: Joanne Illingworth, 46, has NARP, a disease that attacks the nervous system.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/ataxia\/rare-disease-strikes-family.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":64,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[1246881],"tags":[],"class_list":["post-1065328","post","type-post","status-publish","format-standard","hentry","category-ataxia"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1065328"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/64"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=1065328"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/1065328\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=1065328"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=1065328"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=1065328"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}