I have my ENT appointment next Thursday 18th. I hope who ever I see will listen. It might be the consultant I saw years ago or one of his team. I wrote a list of symptoms I believe are caused by my styloid processes which have been growing steadily since their discovery in 2004. My symptoms have gradually been getting worse since then too with them ramping up over the last 12 months. I am glad I don’t have to wait much longer because I am honestly scared something bad will happen soon. I pass out, have permanent severe headaches, eye pain, blurred vision, neck pain like I have tonsillitis, (I have no tonsils) bradycardia, tachycardia, ear pain, jaw pain, etc etc.
Is there anything I can do that will help me get them to take me seriously? In 2004 I was told to be referred back if my symptoms (clicking, slight neck pain, and pain in swallowing) got worse. I’m I’m the UK and I know for a fact that the consultant that I am under knows about ES but has never performed a styloidectomy. I especially need my left one out as it’s now growing under my tongue and almost pushed through the skin.