# Kaiser neurosurgy **URL:** \ **Category:** TN Discussion\ **Created:** [August 27, 2018, 1:56am UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034 "2018-08-27T01:56:08Z")\ **Posts on this page:** 8\ **Page:** 1
**Author:** ![ekay](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwithfacialpain.org/ekay/32/5840_2.png) [@ekay](https://forum.livingwithfacialpain.org/u/ekay)\ **Post date:** [August 27, 2018, 1:56am UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/1 "2018-08-27T01:56:09Z")
Has anyone here had MVD or other facial pain procedure from a Kaiser surgeon in the SF Bay area. If so, your experience and recommendation please. Also has anyone wanted to see an outside of Kaiser surgeon and were you able to manage that referral from Kaiser to an outside facility? ---
**Author:** ![Bunny1](https://avatars.discourse-cdn.com/v4/letter/b/90ced4/32.png) [@Bunny1](https://forum.livingwithfacialpain.org/u/Bunny1)\ **Post date:** [August 30, 2018, 6:02pm UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/2 "2018-08-30T18:02:53Z")
The husband of a friend had a MVD at Kaiser Redwood City…successful as far as I know. It was about a year and half ago and we have moved away from the area. Good luck. I have had 2 MVDs at UCSF. The first lasted about 5 years and my last was almost 3 years ago, keeping my fingers crossed!!! ---
**Author:** ![ekay](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwithfacialpain.org/ekay/32/5840_2.png) [@ekay](https://forum.livingwithfacialpain.org/u/ekay)\ **Post date:** [August 30, 2018, 8:25pm UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/3 "2018-08-30T20:25:38Z")
I had mvd at UCSF in 70s. One of the early ones that dr wilson retired now deceased did. Lasted 15 years. Kaiser surgeon cut nerve causing numbness top of head to chin. All left side. Now have TN on right side and don’t trust Kaiser surgeons two of whom said risk for numbness too great. Maybe true but I want an independent of Kaiser opinion. Want UCSF opinion ---
**Author:** ![ModSupport](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwithfacialpain.org/modsupport/32/5274_2.png) [@ModSupport](https://forum.livingwithfacialpain.org/u/ModSupport)\ **Post date:** [August 30, 2018, 8:42pm UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/4 "2018-08-30T20:42:39Z")
Hi ekay Have you tried searching using the magnifying glass tool near the top, just to the left of your avatar? (It’s grey and a bit hard to see on some monitors.) Seenie ---
**Author:** ![ekay](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwithfacialpain.org/ekay/32/5840_2.png) [@ekay](https://forum.livingwithfacialpain.org/u/ekay)\ **Post date:** [August 31, 2018, 12:11am UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/5 "2018-08-31T00:11:53Z")
Did this on my phone and full of oops… re do… I had my MVD at UCSF in the 70s. I was one of the first that Dr. Wilson now diseased did. It lasted 15 years. Kaiser surgeon cut the nerve causing numbness from top of my head to my chin on left side. Now have TN on right side and don’t trust Kaiser surgeons two of whom said risk for numbness too great. May be true but I want an independent of Kaiser opinion. I want UCSF opinion. ---
**Author:** ![Cj1419](https://avatars.discourse-cdn.com/v4/letter/c/f08c70/32.png) [@Cj1419](https://forum.livingwithfacialpain.org/u/Cj1419)\ **Post date:** [September 1, 2018, 7:15pm UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/6 "2018-09-01T19:15:08Z")
I don’t blame you for not trusting Kaiser. Had some bad experiences with them not related to TN. A co-worker’s spouse was sick and they had to get HR involved in getting Kaiser to let her go to another facility besides Kaiser. That was many years ago things may have changed. Do what you have to do that is best for YOU. Best! ---
**Author:** ![Keith](https://avatars.discourse-cdn.com/v4/letter/k/f05b48/32.png) [@Keith](https://forum.livingwithfacialpain.org/u/Keith)\ **Post date:** [September 2, 2018, 5:53am UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/7 "2018-09-02T05:53:50Z")
I had MVD surgery in Redwood Coty with DR Efron a few years ago. He is amazing. His bedside manner is “tell it like it is”, but I’m ok with that. He is highly competent. Now I have TN on the right side too. I don’t live in the area and there isn’t Kaiser where I’m at, but I’m trying to get the new insurance company to use him. Don’t have any worries. My experience was excellent. Feel free to pm me directly if you have more questions. He’s awesome. ---
**Author:** ![seattlesi](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwithfacialpain.org/seattlesi/32/6082_2.png) [@seattlesi](https://forum.livingwithfacialpain.org/u/seattlesi)\ **Post date:** [April 12, 2019, 6:59am UTC](https://forum.livingwithfacialpain.org/t/kaiser-neurosurgy/15034/8 "2019-04-12T06:59:26Z")
Hi Bunny, Where did you have your MVD? I had mine at Oregon OSHU. Unfortunately lasted only one month. I am reluctant to have i again unless I find a competent Dr, I am on Oxcarbazepene 600 mi daily seems to help 90% of the time