Page 23 - Real Rochdale Issue 22 Summer 2024
P. 23

GEM Appeal marks 30


                                years of fundraising







          The GEM Appeal is this year celebrating 30
          years of fundraising and research into rare
          genetic conditions. Founded in 1994 by
          Karen Johnson, a mother-of-three who
          tragically lost both her young sons to rare
          genetic disorder Hunter syndrome, the
          charity has been a driving force in advancing
          support for families affected by this
          condition.

          To mark the charity’s 30th anniversary, the
          Diamond and Pearl summer ball was held
          at Rochdale Town Hall on 15 June, which
          will be followed by the Strawberry Sparkle                The GEM Appeal received the Queen’s Award
                                                                           for Voluntary Service  in 2019
          ladies’ luncheon on 21 August, and charity
          patron Denise Welch’s annual charity ball in         She added: “The medical team at the hospital
          November.                                            is optimistic about the future and is striving

                                                               for more rare genetic diseases to be included
          Karen’s sons, Simon and Mikey, were born             in the newborn screening programme heel
          with Hunter syndrome, a rare inherited               prick test.
          disorder where specific sugar molecules
          cannot be properly broken down in the body.          “There is still a long way to go to find cures

                                                               for these genetic disorders, but the GEM
          The condition, also known as                         Appeal charity will do all it can to help get
          mucopolysaccharidosis type II (MPS II),              there. We want to continue to be with them
          predominantly affects boys and leads to a            every step of the way.”
          range of health issues due to the
          accumulation of these sugar molecules in             For more information about the GEM
          organs and tissues.                                  Appeal, including how to donate, please
                                                               visit www.gem-appeal.co.uk
          Hunter syndrome can vary in its severity
          with symptoms including rapid and
          progressive learning and memory problems,
          and heart and lung dysfunction.

          GEM Appeal trustee Wendy Mills said:
          “Treatments have been life-changing for
          many families with children with genetic
          conditions; reducing symptoms, avoiding
          further complications, extending life
          expectancy and giving better quality of life.”




                    www.gem-appeal.co.uk



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