‘All I want is to save my son’ - mother pleads for drug to help her boy
Lewis Harte diagnosed with the muscular disease when he was two years old
In August 2017 Ann Marie Walsh Harte learned that her then five-year-old son Lewis would not receive a new treatment for his Duchenne muscular dystrophy.
Lewis was diagnosed with the muscular disease when he was two years old. “It’s a terminal condition, you’re looking from teens to twenty five maybe, and that’s with or without medicine” Ms Walsh Harte explained. “What we do know is that the drug (Translaran) would keep Lewis walking for at least seven to 10 years.”
Currently there are five children in Ireland who are suitable for the drug Translarna. The American made drug is available in 22 other European countries. And while it is not available in the Republic, the drug is available to those who need it in Northern Ireland.
Ms Walsh Harte and her husband Pádraig, who live in Co Mayo, first heard the HSE would not make the drug available in January 2017. They appealed the decision and it was rejected again in August . “That decision was not acceptable to us, when we were told it was like a death in the family” said Ms Walsh Harte. “Being a no decision is something that I can’t accept because my son is slowly dying.”
Lewis’s family has continued to campaign on his behalf and Ms Walsh Harte met Minister for Health Simon Harris on November 10th of last year. Mr Harris subsequently met members of Muscular Dystrophy Ireland. On January 24th of this year the issue was raised in the Seanad by Sinn Féin Senator Rose Conway Walsh. She said: “The HSE has come back to the drug company and said we need to start the process again, we need to make a new application.
“This really concerns me because of the length of time that it would take for that process to go from start to finish.”
“I would plead with the Minister to do a conditional approval. We’re not taking about about hundreds or thousands or even dozens of children. We’re talking about five children.”
To compound the issue for Lewis, his physio in Castlebar took a leave of absence last August and he has been without physio since. “We’re doing the best we can by doing the physio we know and keeping him up and active, but things can be missed and physio is paramount for the condition.”
Ms Walsh Harte now hopes that the decision by the HSE on Translarna is made quickly. “These kids do not have time on their side for 18 months, not even six or three months” said Ms Harte “Having that ray of hope that there’s a medicine there has kept us going… knowing we can save him from this, that’s all I want, to save my son”.
In response, the HSE said: “Given there is a High Court case pending the HSE cannot comment further on the previous application. The HSE has informed the company in writing that it will consider any new application received in a timely fashion in line with the statutory requirements which it is legally required to consider.”