Andy and Diane – Cleft lip and palate
Andrew and Diane were informed by a sonographer that their son had a cleft lip at their 20-week scan. When their son was born it was clear that he also had a cleft palate.
Andy and Diane were informed by a sonographer that their son had a cleft lip at their 20 week scan. The couple were then sent away with little information and told to come back the next day when a consultant would be there to confirm the diagnosis. In the meantime Andy and Diane looked on the internet to try and find out more information and were overwhelmed by the range of experiences reported on the web. The consultant who confirmed the diagnoses had delivered the news to the couple in a blunt and negative manner, and it was suggested that their son may be born with other syndromes and have potential breathing problems. Most distressing for Andy and Diane was the fact that were asked to consider a termination and were left to consider the options over a weekend without knowing the full context of the situation. Andy and Diane were deeply upset and responded by asking for a second consultant’s opinion. The second consultant confirmed the presence of a cleft but was much more positive and explained that there were many things that could be done about it.
The couple went on to have appointments with specialist cleft nurses. The care pathway for cleft was explained to them and they were shown pictures of before and after; surgery. The couple began to feel more reassured and now felt able to ask the professionals questions about their son’s future care and treatment.
Andy and Diane’s son was born with a unilateral cleft lip and palate and had to be fed with special squeezy bottles as he was unable to breastfeed. A positive aspect of bottle-feeding was that Andy could be involved with feeding his son. Following their son’s cleft lip repair the couple were able help healing by massaging and rubbing Vaseline on his scar, and they also had to put stents in his nose to help shape the nose. It took a while for Andy and Diane to adjust to the look of their son and also the new sounds he made when he laughed. As cleft babies can often have glue ear he will also have his hearing and speech monitored regularly alongside sessions of speech therapy.
Having a child born with cleft means that there are a lot appointments, and the travelling involved impacts on the family’s financial resources. Although they have accommodating employers they often have to use annual leave allowances, which means spending time together as a family is also compromised.