I have known about my basilar artery aneurysm for 10 years. It was considered unremarkable even just within structural mean. I have had stable serial MRA's since discovery; until of course as a birthday present; notification that it had enlarged enough to require intervention. I am being referred to a radiologist for coil embolization. Has anyone out there had the surgery and willing to share the details?

We've been watching my inter-cranial aneurysm for nearly five years now, so I have some idea of just what getting that "birthday present" must have felt like. Since we've already determined that my aneurysm isn't appropriate for coiling, & since i believe in being prepared, I am now awaiting an appointment with a neuro-surgeon who works with lasers. I'm not trying to send you off in a different treatment plan direction--just thought you'd be interested in what else is being done in the field: http://cbst.ucdavis.edu/research/aneurysm-treatment

You can start a thread in NT's Aneurysm Forum by reposing this introduction there if you'd like. That's where you'll meet people who've been through it. Here's the link: http://neurotalk.psychcentral.com/forum7.html

Also, in case you haven't seen them, several top hospitals have developed patient educational material on
What to Expect:
http://www.massgeneral.org/condition...ion.aspx?id=87
http://rhodeislandhospital.org/adam/.../1/007372.html
http://www.jeffersonhospital.org/Tes...r-coiling.aspx
http://www.muschealth.com/gs/TandPco...?pageid=P08768

This is a great place for information-gathering; not a bad place for making the acquaintance of some pretty remarkable people too. They've been where you are & can tell you what it was like from the perspective of the far side of healing. I'm sure you've heard some of the horror stories. I felt better, lurking over there, hearing the voices of many experiences.

One day at a time, Robert Taylor. And--always--let us know when we can help.

I am a recent graduate from Probable MS to Absolutely Positive MS, so I guess I should celebrate. Actually, it's a relief; being in limbo is frustrating.

I am currently trying to decide whether to treat the disease or treat the symptoms and I'm hoping to find some good input in these support groups.

Thank you so much for being here and providing this wonderful resource.

Yes, I can understand that it would be a relief. But obviously you spent your limbo time learning; good for you! Here's the link to NT's MS Forums: Multiple Sclerosis: *http://neurotalk.psychcentral.com/forum17.html
Stumble Inn: *http://neurotalk.psychcentral.com/forum102.html

Stumble Inn is for social, non-medical discussions. If you go to the Ms forum & start a thread, then copy your post over to it, you'll soon be in touch with many, MANY folks with informed opinions. This is one of the most active boards here.

Do take care, & I hope to see you around here (or there) making friends!