母亲主张在儿子的罕见病情治疗后,对血液紊乱给予平等支持。 Mother advocates for equal support for blood disorders after son's rare condition treatment.

Sophie Hodgson-Smith 是 7 岁 Jasper 的母亲，她患有一种称为 APDS 的罕见血液疾病，她正在倡导为血液疾病提供更好的支持。 Sophie Hodgson-Smith, mother of seven-year-old Jasper with a rare blood disorder called APDS, is advocating for better support for blood disorders. Jasper接受了骨髓移植手术,类似于癌症治疗,但与癌症病例相比,家庭得到的慈善支持有限。 Jasper underwent a bone marrow transplant, similar to cancer treatments, but the family faced limited charity support compared to cancer cases. Sophie搬到纽卡斯尔接受贾斯珀的治疗, 希望提高对于必须平等支持血液失调的认识, 并纠正对干细胞捐赠年龄限制的误解。 Sophie moved to Newcastle for Jasper's treatment and hopes to raise awareness about the need for equal support for blood disorders and to correct misconceptions about stem cell donation age limits.