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Left for her to lose. nala�*s mld progressed too far for her to be treated. but it meant the condition was picked up in her sister teddi before damage was done. she�*s at royal manchester children�*s hospital having stem cells removed from her blood, the first stage of a ground—breaking gene therapy. so, when they told us that there was treatment available for teddi, it was kind of like, a bit like a bit of a bitter pill to swallow because nala can't be helped, so you know, we are extremely grateful in one sense and then really sad on the other. two months later, teddi�*s personalise...

Available for teddi, it was kind of like, a bit like a bit of a bitter pill to swallow because nala can't be helped, so, you know, we are extremely grateful in one sense and then really sad on the other. two months later, teddi's personalised therapy, called libmeldy, is ready. scientists have added a working copy of the faulty gene which causes mld to teddi's cells. they're your cells. libmeldy costs more than £2.8 million, though the nhs has agreed a confidential discount. this one—off infusion aims to stop teddi's disease in its tracks. teddi will need to spend several more weeks in hosp...

She's at royal manchester children's hospital having stem cells removed from her blood, the first stage of a ground—breaking gene therapy. so, when they told us that there was treatment available for teddi, it was kind of like, a bit like a bit of a bitter pill to swallow because nala can't be helped, so you know, we are extremely grateful in one sense and then really sad on the other. two months later, teddi's personalised therapy, called libmeldi, is ready. scientists have added a working copy of the faulty gene which causes mld to teddi's cells. they're your cells. libmeldi costs more tha...

Ground-breaking gene therapy. when the told us ground-breaking gene therapy. when they told us there _ ground-breaking gene therapy. when they told us there was _ ground—breaking gene therapy. when they told us there was treatment available for teddy it felt like a bit of a bitter pill to swallow. natalie can't be helped. we're extremely grateful in 1's sense and really sat on the other. tum extremely grateful in 1's sense and really sat on the other. two months later teddies _ really sat on the other. two months later teddies personalised - really sat on the other. two months later teddies ...

What it is like for families to have to receive news that one of their children has an incurable disease — and the other child is also affected, but we can offer a treatment for that child. it's june 2022. teddi will be the first patient to receive libmeldy on the nhs. she can be helped because, unlike nala, mld was picked up before irreparable damage was done. she's taken it in her stride. she obviously hasn't been great when getting all of the needles and things in her. but to be fair, she's actually dealing with it quite well. hold on... it's a personalised treatment. teddi's blood is bei...