Eagle Syndrome is a rare condition classified by the elongation of the styloid process or calsification of styloid ligaments.
Eagle Syndrome is extremely rare
Eagle Syndrome is extremely rare
I live in North Alabama. I was diagnosed with Eagles about 4 years ago. Mine had calcified and was sharp as a needle. It was causing neck and jaw pain and eventually it started poking me. I was referred to an ENT at UAB in the Kirkland Clinic. He removed my right styloid and tonsil. I have had no more pain once I healed.
Hi Angie. I just found this site and have just been diagnosed. I'm in the southern US. Can't find a surgeon to speak with about helping relieve this pain. What about you?
Hi there, My name is Angie. I've recently been diagnosed with Eagle Syndrome, & would love o meet others who also have it, or have had surgery to correct it. Looking forward to chatting. Cheers
I've also found that eating healthy, & getting daily exercise,9 even if it's just walking) really helps. Drinking lots of water, eating green vegetables, cutting sugar , bread, & margarine out of my diet has helped me to cope better with my ES pain & symptoms.
Hi there. I've had ES for almost 15 years now, although i've only recently been diagnosed with it. I've been on Norspan pain patches for about 8 to 10 years now. I'm on 10 mgs. The patch is effective for 7 days, & then you put a fresh patch on. Patches have helped massively with my ES pain. Occasionally i've forgot to put a new patch on after a week, & the pain has suddenly got worse, & i wonder why... then i realize that i've forgot to put a fresh patch on. I've foud patches to be really good, the only downfall is that they're addictive ( being opoid) I've chose to have surgery & am currently waiting to hear when my operation will be. Heat packs, i've found help with the facial pain & migrain due to ES. I hope i've been able to help you somewhat. Cheers :-)
I was hoping someone would have some kind of home remedy that would help with the discomfort of this problem. I have been applying ice packs to face and neck to try to obtain some relief. Because the styloid process is in such approxsimity to the caroid artery am very leary about having surgery. So much is still unknown about this.
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I have recently been diagnosed with Eagle Syndrome, After almost 15 years of misdiagnosis.
I'm a single mum of 6 , & i live in Victoria Australia.
My hobbies...
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Created by AussieEagle | Last updated 6 Nov 2016, 09:53 PM
Created by sissky | Last updated 28 Aug 2015, 10:56 AM
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