{"id":3758,"date":"2021-12-02T09:33:43","date_gmt":"2021-12-02T09:33:43","guid":{"rendered":"https:\/\/www.specialeffect.org.uk\/?p=3758"},"modified":"2022-02-17T09:46:29","modified_gmt":"2022-02-17T09:46:29","slug":"can-you-help-find-a-bone-marrow-match-for-olcan","status":"publish","type":"post","link":"https:\/\/www.specialeffect.org.uk\/news\/can-you-help-find-a-bone-marrow-match-for-olcan","title":{"rendered":"A bone marrow match for Olc\u00e1n!"},"content":{"rendered":"

Olc\u00e1n’s a fantastic seven year-old boy who\u2019s in medical isolation, and we\u2019ve recently brought his school and his friends back into his life via a little BubbleBuster<\/a> robot that takes his place in the classroom.<\/p>\n

He has Aplastic Anemia, a very rare and serious condition. He\u2019s currently relying on regular blood transfusions to stay alive and urgently needs a bone marrow transplant but, as he\u2019s a rare tissue type finding a match for him was always going to be a struggle. But the good news is that a match HAS finally been found<\/a>, and we send Olc\u00e1n and his family all best wishes in his continuing treatment.<\/p>\n

<\/p>\n

Below: Olcan and his family<\/em><\/p>\n

\"three<\/p>\n

The story in full<\/strong><\/p>\n

In September 2021, then six-year-old Olc\u00e1n Wilkes was diagnosed with a one in a million blood disorder called aplastic anaemia. Due to the severity of his condition, doctors can\u2019t be certain on how long Olcan can live without a transplant as any potential illness could be fatal. The average death rate for those with the condition is 70% within one year.<\/p>\n

To beat his life-threatening condition, his family are appealing for as many members of the public to become bone marrow donors as possible. A transplant is the only known cure.<\/p>\n

As he waits to find a match, Olc\u00e1n undergoes two-three platelet transfusions a week, blood transfusion every couple of weeks, and attends school remotely via a \u2018robot\u2019 from his home or hospital bed.<\/p>\n

Living between Newent, Gloucestershire, and County Antrim, Northern Ireland, Olc\u00e1n Wilkes was a normal six-year-old boy who loved football, playing with his friends and his four-year-old brother, Hunter. In August 2021 his life changed forever after his parents noticed severe bruising over his body.<\/p>\n

Following a number of tests and treatments, in September 2021, and at just six years\u2019 old, Olc\u00e1n was diagnosed with aplastic anaemia.<\/p>\n

Aplastic anaemia is a life-threatening blood condition and a form of bone marrow failure, affecting just one in a million people*. The incredibly rare condition was the cause of death for Eleanor Roosevelt, the former First Lady of the United States, and Marie Curie, the famous physicist and chemist. The average death rate for those with the condition is 70% within one year and 80% within five years for those under the age of 20, if untreated.<\/p>\n

As well as his aplastic anaemia diagnosis, doctors also found traces of paroxysmal nocturnal hemoglobinuria (PNH) in Olc\u00e1n\u2019s blood. PNH is another rare blood disease which commonly can be caused by aplastic anaemia, leading blood cells to break apart.<\/p>\n

Olc\u00e1n\u2019s parents Sam, a farmer and former retained firefighter, and Genevieve Wilkes, a senior project manager in the healthcare sector, are appealing to the public in their desperate hope to help Olc\u00e1n and others like him.<\/p>\n

Olc\u00e1n has a rare bone tissue type, meaning he falls into the small percentage of people with no donor match. After his brother, family members and the global register were found not to be a match, the family decided to try immunotherapy to prolong his life. The treatment, called ATG, kills specific cells in the immune system that are attacking bone marrow stem cells. In mild to moderate cases of aplastic anaemia, ATG has a 60% success rate meaning that patients will no longer be transfusion dependent**. Due to the severity of Olc\u00e1n\u2019s condition, just three weeks after his ATG doctors are confident that the treatment is unlikely to be successful and as they usual wait is three-six months to determine the success, Doctors have decided to keep searching for a transplant as Olc\u00e1n doesn\u2019t have that long to wait.<\/p>\n

Willing to do anything to keep their son alive, Olc\u00e1n\u2019s parents recently investigated the option of IVF so they could use a cord blood transfer from a selective embryo, a process that means having another baby might provide an identical bone marrow match for Olc\u00e1n. Almost immediately after considering this, doctors informed Sam and Genevieve that their son does not have nine months to wait.<\/p>\n

As he waits to find a match Olc\u00e1n must undergo two to three platelet transfusions a week and two blood transfusions a month to keep him alive. Since being diagnosed in September, he has had over 25 platelet transfusions and five blood transfusions in total<\/p>\n

Despite having to live in between his new home and hospital in Northern Ireland, with the support of charities Specialeffect.org, Olc\u00e1n has been attending school remotely via the use of a robot. \u2018Sitting\u2019 in a classroom back at his old school, St Joseph\u2019s in Ross on Wye, England, the robot follows the teacher and class around for the day, allowing Olc\u00e1n to continue with his treatment, without missing out on his education and interaction with friends. His family have also received support from Angel Wishes, a local charity who offer emotional and financial support to all children in the family.<\/p>\n

Sam Wilkes, Olc\u00e1n\u2019s dad said,<\/p>\n

\u201cAfter Olc\u00e1n\u2019s diagnosis, it took a while for the severity of it all to sink in. We are desperate to encourage as many people as possible to take the two minutes it takes to register for the free swab, for Olc\u00e1n and others like him. Those two minutes, and the time spent returning the swab, could quite literally save his young life.<\/p>\n

\u201cEverybody that gives blood is making an enormous difference, too, watching Olc\u00e1n go through multiple transfusions weekly. He\u2019s just the most wonderful boy, who misses football, his friends and play fighting with his brother – and our abiding hope is that we can find a donor match in time.\u201d<\/p>\n","protected":false},"excerpt":{"rendered":"Olc\u00e1n’s a fantastic seven year-old boy who\u2019s in medical isolation, and we\u2019ve recently brought his school and his friends back into his life via a little BubbleBuster robot that takes his place in the classroom. He has Aplastic Anemia, a very rare and serious condition. He\u2019s currently relying on regular blood transfusions to stay alive… View Article<\/a>","protected":false},"author":3,"featured_media":3760,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[16],"tags":[],"class_list":["post-3758","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-other"],"acf":[],"yoast_head":"\nA bone marrow match for Olc\u00e1n! - SpecialEffect<\/title>\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.specialeffect.org.uk\/news\/can-you-help-find-a-bone-marrow-match-for-olcan\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"A bone marrow match for Olc\u00e1n! - SpecialEffect\" \/>\n<meta property=\"og:description\" content=\"Olc\u00e1n’s a fantastic seven year-old boy who\u2019s in medical isolation, and we\u2019ve recently brought his school and his friends back into his life via a little BubbleBuster robot that takes his place in the classroom. 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