Hi there.
I recently found out my 2.5 year old has glue ear, following a NHS hearing test. She also has a speech and language delay which why she was referred for the test.
At the time, when they told me about it, I was a bit in shock and didn't really ask any questions, so I'm hoping you lovely lot here can help and share your experiences.
They have asked her see her back in 3 months to assess the situation. If she still has glue ear, is it likely they will refer her for surgery for grommets?
If this is the case, it it still a long waiting list? I saw someone had posted previously saying because of COVID it is a really long wait.
If that's the case, how do I go about finding a private ENT specialist in my area?
I also read that someone said they saw a private ENT who was able to tell them how much fluid was in their child's ears (so the level of hearing loss) and also how long it had been there (which indicated if it was likely to clear in 3 months).
If I'm honest, I feel like I've massively let my daughter down by not trying to get this sorted for her sooner, and I feel bad that she hadn't been able to hear properly for a really long time.
She is such a happy little girl and I don't want her lack of S&L to hold her back.
I'd just really appreciate someone's take on the situation and to know all of the information I possibly can. Thank you for taking the time to read and respond xxx