<script src=""></script>{"id":134,"date":"2012-09-09T15:25:56","date_gmt":"2012-09-09T15:25:56","guid":{"rendered":"https:\/\/lupusmalaysia.org\/index.php\/2012\/09\/09\/the-child-with-lupus-pslems-theme-for-world-lupus-day-2009\/"},"modified":"2012-09-09T15:25:56","modified_gmt":"2012-09-09T15:25:56","slug":"the-child-with-lupus-pslems-theme-for-world-lupus-day-2009","status":"publish","type":"post","link":"https:\/\/lupusmalaysia.org\/bm\/the-child-with-lupus-pslems-theme-for-world-lupus-day-2009\/","title":{"rendered":"\u201cThe Child with Lupus\u201d &#8211; PSLEM\u2019s theme for World Lupus Day 2009"},"content":{"rendered":"<p>Persatuan SLE Malaysia (PSLEM) has chosen the theme, \u201cThe Child with Lupus\u201d, for World Lupus Day 2009 next month to raise awareness of the challenges faced by children suffering from lupus as well as the difficulties faced by their parents, caregivers, medical professionals and friends.<\/p>\n<p>PSLEM Vice President and Consultant Rheumatologist Dr Yeap Swan Sim explained that while lupus is generally known as a condition that affects young women of child-bearing age, lupus can also affect children as well. Lupus often goes unrecognised because its primary symptoms \u2013 joint pain, fatigue, skin rashes, and fever \u2013 mimic many common illnesses, which can cause people and children to receive treatment for conditions they may not have.<\/p>\n<p>\u201cDiagnosing an adult with lupus is difficult, but diagnosing a child is even more so as they often do not know how to describe their symptoms. Caring for a child with lupus also places tremendous stress on any family,\u201d Dr Yeap added. \u201cAfter the diagnosis, the first step for every parent is to understand as much as possible about juvenile lupus and the special needs of a child with the disease.<\/p>\n<p>\u201cPresently, there is no known cure for lupus. The medications used to control lupus depend on the severity of the disease and these medications have side effects that could affect the child physically, emotionally and psychologically,\u201d she explained. \u201cThus parents face the challenge of educating the people who the child will be relating to almost daily \u2013 siblings, other family members, school teachers, classmates \u2013 so that they will be sensitive to the needs of the child with lupus.\u201d<\/p>\n<p>World Lupus Day 2009 Organising Committee Member Ms Chee Siew Lian emphasised that this year\u2019s focus on young lupus patients was in response to the increasing number of parents of children with lupus who have sought out the association\u2019s help and support network.<\/p>\n<p>\u201cWe would like to get more parents aware of the signs and symptoms of this disease so that they are aware of it and will seek medical attention for their child early. With proper treatment, the prognosis for children with lupus is good \u2013 in fact, among our association\u2019s Committee Members are patients who have battled lupus since they were eight, nine, 12 years old, \u201d Ms Chee said.<\/p>\n<p>\u201cThe message we wish to convey to parents of children with lupus is that there is hope and a future for their children, especially if the disease is detected early and the treatment regime is closely followed. We have seen that parents and children cope better in living with lupus if they are in a support group and this is where PSLEM can help by connecting them to counsellors and survivors,\u201d she added.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Persatuan SLE Malaysia (PSLEM) has chosen the theme, \u201cThe Child with Lupus\u201d, for World Lupus Day 2009 next month to raise awareness of the challenges faced by children suffering from lupus as well as the difficulties faced by their parents, caregivers, medical professionals and friends. PSLEM Vice President and Consultant Rheumatologist Dr Yeap Swan Sim&#8230;<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[14],"tags":[],"class_list":["post-134","post","type-post","status-publish","format-standard","hentry","category-articles"],"translation":{"provider":"WPGlobus","version":"2.12.2","language":"bm","enabled_languages":["gb","bm","cn"],"languages":{"gb":{"title":true,"content":true,"excerpt":false},"bm":{"title":false,"content":false,"excerpt":false},"cn":{"title":false,"content":false,"excerpt":false}}},"_links":{"self":[{"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/posts\/134","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/comments?post=134"}],"version-history":[{"count":0,"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/posts\/134\/revisions"}],"wp:attachment":[{"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/media?parent=134"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/categories?post=134"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lupusmalaysia.org\/bm\/wp-json\/wp\/v2\/tags?post=134"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}