Yes, he's had his ties lasered now and is about to get a brace to expand his palate and headgear to guide his orofacial growth in the right direction. Hopefully this will avoid him having to have teeth pulled when he is a teen.
Hope your dd is feeling better and back to feeding.
Come and join the Facebook Tongue Tie Babies Support group. You will get knowledgable information on there.
DS1 is 6yo and has had endless problems from his undiagnosed ties. We are just about to start orthodontics to correct his orofacial development as it has been badly affected by tongue and lip tie. This is as well as reflux, sleep apnoea, food allergies/intolerance, endless stomach bugs to name but a few of the problems.
Learn as much as you can about it and you will find that it's a much bigger issue than most people realise.
Dd is 1. We're in sw London and my GP has referred us onto a department at St George's in Tooting. I don't know who we will see but it's a starting point.
Thanks for the info re Dr Kotlow. I will read up on his articles and take some print outs with me. From the photos it looks as if it could be a class III tie. I'm glad you told me about the laser treatment, from other sites it was looking as though the choice was leaving it or an op under GA.
I haven't checked her for posterior tongue tie. She was checked at the hospital by midwives but unfortunately I'm not sure that means she's definitely ok.
We did battle with Breastfeeding for the first 4 months. Constant feeding (and I mean constant!) with lots of pulling off and crying, reflux, inability to sleep luring flat, colic type symptoms. I just kept going as after the first 2 weeks my nipples weren't shredded and weight gain has never been a problem. And I hadn't been on this forum so I didn't know better
Still feeding now but after every feed I have imprints from her top four teeth.
I'm worried the tie will cause her problems later and I don't want to wait for years to see if there's a safer way of treating it now. I'm happy to go private for this.