
Cutting-edge medicines hoped to transform treatment of incurable skin condition
Debra, which supports 300 people living with epidermolysis bullosa (EB) in Ireland, said the entry of Filsuvez into the Irish market will ease the extreme pain endured by those with 'Butterfly Skin'.
The disease is caused by the absence of proteins between the skin layers, making the skin ultra fragile and easy to wound.
The charity insists that the expected introduction of the prescription medical gel before the end of the year could pave the way for gene therapy treatments, such as Vyjuvek.
Sinead Hickey, head of research at Debra, said: 'Where Filsuvez is a promising start, as it can offer temporary pain relief, we hope it will mark the beginning for the treatment of rare disease in Ireland.
'Vyjuvek has the potential to provide life-changing wound healing for people living with Dystrophic EB, it has already proven to be very effective in the US.'
The topical gel delivers new COL7A1 genes directly to skin wounds to promote wound healing.
Ms Hickey said it does not have to be applied by a medical practitioner but can be done by a trained individual or family member.
'Unfortunately, Ireland is one of the slowest countries in Europe to move from recommendation to market and it could still be between seven and 12 years before we see Vyjuvek available to people here,' she said.
Filsuvez, meanwhile, is applied to a sterile non-adhesive wound dressing or directly to the skin to ease the extreme pain of wounds caused by EB.
Debra made submissions to the NCPE (National Centre for Pharmacoeconomics), which has recommended the HSE provides the gel once agreement is reached on pricing.
A timeline has yet to be announced but Debra is optimistic a resolution will be found by the end of summer.
The charity's chief executive, Jimmy Fearon, said its entry into the Irish market is a step in the right direction.
'The treatment for EB hasn't advanced much over time, so new treatments always bring hope,' he said.
'This is not a cure but it may reduce the equivalent of a bandage change every two weeks, providing some pain alleviation.
'What this primarily represents is hope, breaking through the glass ceiling would hopefully mean that others will follow.
'Debra and other EB charities around the world support and invest in important research but, ultimately, it's the pharmaceutical companies and venture capitalists that run the breakthrough.'
Ireland is in the lowest quartile in Europe for introducing new drugs to the market, the chief executive said.
'It's an arduous process to bring a drug to market and this is a positive step,' added Mr Fearon.
'What we really need is faster progression from recommendation to market – time is of the essence for the 300 people in Ireland living in pain due to this condition.'
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Determined Ava Gardiner, from Tarbolton, Ayrshire, is taking on a full year of gruelling challenges for TEAM EB in the battle against the painful condition, also known as Butterfly Skin. Celebs and everyday Scots are signing up to join TEAM EB with the Daily Record by taking on a challenge for DEBRA this summer. But determined Ava Gardiner is going even further with a full year of gruelling missions for the charity, dedicated to the two sisters she never got to meet. The 21-year-old's family, from Tarbolton, Ayrshire, have been deeply impacted by EB, or Butterfly Skin, as her older sisters Georgia and Freya tragically lost their battles against the condition. Ava is determined to help other families find hope of a cure. She said: 'I will forever be connected to DEBRA and will continue the good fight in memory of my sisters for as long as it takes to eradicate this horrendous condition. 'I chose to dedicate my 21st year to pursuing several personal challenges and raising awareness of EB. They have not been without pain but that's my challenge. 'I can now tick off Edinburgh Marathon, May 2024, Aintree half Marathon, February 2025, Kelpies Supernova, March 2025 and Barcelona Hyrox, April 2025. 'This week, I will attempt Tough Mudder Scotland for TEAM EB. 'If one person in every town and village is inspired to take on their own challenge, however small, then together, the Daily Record and TEAM EB will achieve something wonderful. 'I know how proud my Mum is of all three of her daughters and she is my biggest supporter. 'My family will be forever grateful to DEBRA for its care and support and that is why I will continue to fight so that families in the future never go through the pain of losing a child to EB.' Ava's parents, Kirsteen and Sam, had never even heard of EB until their first daughter Georgia was born with the rare form, Severe Junctional EB, 25 years ago. She said: 'This is fatal in infancy due to such severe blistering across the whole body and internal organs, making it difficult for infants to feed and digest food. 'Born after a normal pregnancy, Georgia arrived into the world with significant damage to her skin and immediately struggled to breathe. She was very quickly taken to special care and my parents were told that Georgia would be unlikely to survive to night and were supported to say their final goodbyes. 'Georgia miraculously survived her first night in this world although my parents knew her life could end at any moment. Doctors liaised with experts at Great Ormond Street Hospital (GOSH) in London and the family learned the full extent and horror of EB. 'At that time DEBRA did not have a dedicated team in Scotland and advice for practitioners came from specialists in London. Georgia died aged four weeks old. Ava said: 'In that short time she made a massive impact.' Join the Daily Record WhatsApp community! Get the latest news sent straight to your messages by joining our WhatsApp community today. You'll receive daily updates on breaking news as well as the top headlines across Scotland. No one will be able to see who is signed up and no one can send messages except the Daily Record team. All you have to do is click here if you're on mobile, select 'Join Community' and you're in! If you're on a desktop, simply scan the QR code above with your phone and click 'Join Community'. We also treat our community members to special offers, promotions, and adverts from us and our partners. If you don't like our community, you can check out any time you like. To leave our community click on the name at the top of your screen and choose 'exit group'. If you're curious, you can read our Privacy Notice. DEBRA reached out to Ava's parents and began a relationship that sadly would be very much needed again and less than two years later they were pregnant with their second child. The charity had expanded its services in Scotland and in 2002 co-ordinated pre-natal testing and pregnancy support for the couple. A foetal skin biopsy sadly confirmed that, like her sister, Freya also had EB. Ava said: 'My Mum's experience carrying and delivering a baby with EB was hugely different second time around. Although the outcome was inevitable, Mum's understanding of EB together with the healthcare team's approach ensured Freya's arrival was unique. 'DEBRA provided guidance and advice for everyone involved in Freya's care and early in 2003, she was born into this world inside her amniotic sac, a rare occurrence but one which kept Freya's skin perfectly protected and unblistered for her precious first moments in the world. 'Like her elder sister, Freya was a fighter. Her battle with EB lasted for three months.' When the couple got pregnant for a third time they again travelled to London for testing. Thankfully, doctors were able to confirm that their third daughter, Ava, did not have EB. Ava grew up with her family campaigning to raise funds for DEBRA to help stop other families facing the ordeals they had – but insists more needs to be done to educate. She said: 'I have many early memories of my parents fundraising for DEBRA at our village gala days. They did anything from selling homemade tablet to braving zip slides. Mum's friends donated proceeds from their own events over the years, all to raise vital funds for research and ultimately a cure for EB. 'My local community is aware of EB because of my family's experience and that will be the same in other towns up and down the country but the reach needs to be greater in order to make the difference the EB community deserves. 'The Daily Record's support of Team EB this year will help to do this, sharing our message across the whole country – thank you to them and to everyone who wants to help.' Former Gers boss Graeme Souness swam the Channel this month for DEBRA while charity ambassador Scott Brown, who starred for Celtic, is also urging Scots to join in. Join Team EB by signing up for any challenge you choose, from marathons or swims to short walks or extra steps each day.


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