MDJunction - People Helping People
 

Why wear a ribbon?

 
"I am only 53 I am permanent disabled, my migraines don't go away" (MULBERRY8)

MDJunction to me

bmac"A place to communicate with individuals that share my
pain and joy and allow me to "vent" without being judgmental.. MDJunction helped me understand my condition when many did not.
" (bmac)

more testimonials
New Daily Persistent Headache (NDPH) Online Support Group
A community of patients and friends dedicated to dealing with NDPH and other chronic headache conditions together.
Join This Group
Group Home   Forums   Articles   Members (1244)   Diaries   Videos   Leaders   Guidelines
NDPH Group RSS Feed
NDPH ForumsGeneral & SupportGreater Occipital Nerve Injection
02/18/2008 11:59 AM
miffy
 
Posts: 16
New Member

Hi everyone

I had a Greater Occipital Nerve injection last friday my first and apart from leaving me bruised (which has now gone) it has not helped with the pain at all. I had it on the left side only at the back of my head.

My headache doc says it can take up to 2 weeks before any effect is felt. If there is no reduction in pain or frequency in pain after this time period, then another injection in more than one head location is tried.

Just wanted to know if anyone has had this and if they had any joy with it either immediately or some days after?

Reply

02/23/2008 02:39 AM  Top
MaryR
MaryR
 
Posts: 3862
Group Leader

I haven't had that done so I don't know. I think that might be the same thing that goonybgood had done a few weeks before she started the "I've been feeling remarkably good" thread in the general and support section. I don't really know enough about injections to know if it the same thing or not since I haven't had any. Hers took a while to work if I remember right. At first she thought they just hurt from the injections, but eventually they did help. You may be able to tell from reading the thread if it is the same thing as yours or not. Hope that helps.
Mary
NDPH support group leader
Dementia support group leader
Not a medical professional...just another patient with my own set of experiences to share.

02/23/2008 03:05 PM  Top
Sahara18
Sahara18
 
Posts: 134
Member

Hi Miffy, my daughter has been getting occipital nerve blocks for two years. She started out with Lidocaine/Solu-Medrol every 10-12 weeks. They only last about 6wks for her, but because of her age, her neuro said he can only give her the steriod that often. I asked him if he would give her Lidocaine only injections between the steroid ones- he said yes (they last about 2 wks). Now that she is almost 18 (in 4 wks) he can give her the steroids every 8 wks. That will relieve her of and extra set of injections! The first one took about 2 days to start working. Her scalp was sore...she wouldn't, and still doesn't, brush her hair for a day or two after. (She keeps it in a ponytail.) They seem to work pretty much immediately now. She gets 4 injections, it was just two - one on each side, but she asked for two extras near the crown of her head where the nerve ends. Her neuro withdraws the needle a little and reinserts it twice at each injection site to spread the meds around some. She said this is so much better than the migraines. She still gets the migraines in the front, but says they are not as debilitating. I would definitely give it another try on each side. I hope this info helps. Smile
Jennie

Previous discussions I participated in:
My head hurts help!!!!!
Triptans anyone?
migraine ? help

02/23/2008 03:21 PM  Top
Thyqua
Thyqua
 
Posts: 127
Member

Hi Miffy,

I had occipital nerve injections on both sides at the back/top of my neck a couple of months ago. Sadly they didn't work for me, just made me feel rather terrible for a week and then that area has hurt at times since.

Don't let me get anyones hopes down tho, I've heard this has worked wonders for some people. I was also told it would take a week or so to work so hold tight and I'm really hoping if it'll start working for you soon.

thyqua xx

"don't look back...something might be gaining on you"

07/26/2011 04:28 AM  Top
coachchalfin
Posts: 12
New Member

I went to a very caring neurologist and she wrote down a couple of names of the thing I have but I decided that it is occipital neurologia. I had tried everything. Currently I had two rounds of the nerve block on my left side. It worked for about 2 weeks. The second round didn't work. I think the doctor missed the vein. Please give me some advice if you can. I only get it on the left side of my occipital nerve. IT happens everyday! I wake up with it often in the morning. I feel I tried everything- 1/2 of an advil masks the pain for several hours. I take on every morning and one at about 5 PM at night. So I am taking only 200 mg of Advil a day. The headaches often engulf my though process and it is annoying. I am also taking 300 mg of Gabapentin every morning this is a anti-seizure drug that apparently treats chronic pain better than seizures (I never had a seizure). I live in NY and am going to Montefiore Headache clinic in the Bronx in September (don't take my insurance- Smilehttp://www.montefiore.org/services/headache_center/

Previous discussions I participated in:
Left Occipital nerve release surgery

07/26/2011 11:43 PM  Top
cmiller
cmiller
 
Posts: 860
Member
I'm an Advocate

I had only a ten day 50% relief when I had it done and the pain was so intense I decided not to have more. I believe they can easily miss the right spot with these injections also.

Hey Coach, I just wanted to let you know that the anti seizure drug gabapentin is an epileptic drug however it works by calming the nerves to stop seizures and because occipital neuralgia pain is mostly nerve pain it also can calm the nerves. I was on 2400 mg per day at one stage because I was having up to 300 electric shock type painful spasms a day. This is where gabapentin really works as it knocked down those painful spasms to about 30 per day but much less painful. I hope this helps.

I am not a medical professional. I sufferered Occipital Neuralgia and had right and left occipital nerve release surgery in 2010.
Before surgery I would throw up almost daily from the severe dizziness and had severe light and sound sensitivity. I stayed in bed, curled up in the fetal position wishing I had the courage to kill myself. If I didn't take a cocktail of antiseizure, opiates and muscle relaxers I suffered hundreds of electric shock type pains per day in my head and had a constant migraine type pain 24/7 from july 2008. I lay grieving for my life that once was the friends who once were and the void in my future.
Right surgery 100% relief; left surgery, scarring grabbed a crown nerve and I had surgery again to relieve that june 2011. Surgery really helped but was left with daily migraines triggered by certain sound pitches making living in this noisy world very difficult

07/27/2011 07:45 PM  Top
tortoisegirl
tortoisegirlPosts: 2786
Group Leader

Any chance you got into a rebound cycle with the Advil? Thought I'd mention it. Taking any amount more than 2-3 days a week could put you at risk, and you'd need to go off of it for a few weeks to break the cycle if so. Something to read up on and ask your doctor about as it can exacerbate your pain situation. Hope you get some relief soon. That you got such relief the first time is a good sign. I'd consult your doctor again and see where to go from here. Results can vary. Ideally, you want to keep getting the injections at greater intervals to try to get pain free or reduced pain. Yes, the nerve pain preventative meds are a good thing to try--Lyrica is another one in the same class. Best wishes.
Kate
a NDPH Group Leader
~I'm just another patient navigating the daily challenge of this chronic pain. Thankfully it has got easier over time,and it could always be worse.~

11/02/2012 12:10 PM  Top
fusion
Posts: 1
New Member

I have had two of these injections ....and the only relief I felt really was from the local for 2 to 3 hours...

11/02/2012 08:37 PM  Top
MaryR
MaryR
 
Posts: 3862
Group Leader

Hi and welcome fusion, Sorry to hear that the injections were not helpful in your case. I have heard of that happening sometimes, where the initial numbing stuff works, but then the injection really doesn't do anything. Frustrating. Has anything else helped you at all?
Mary
NDPH support group leader
Dementia support group leader
Not a medical professional...just another patient with my own set of experiences to share.

11/02/2012 08:56 PM  Top
tortoisegirl
tortoisegirlPosts: 2786
Group Leader

Fusion: Welcome! Thank you for sharing. Actually, sometimes the fact that you responded at all, even if only to the anesthetic portion (not the steroid which is typically added) can be helpful for your doctor in formulating treatment ideas, even if getting subsequent blocks is not likely to be helpful. For all three types of nerve blocks I had, I didn't even feel any relief from the anesthetic ....they actually caused me more pain (needle trauma).

I have had a few meds help though, as well as some lifestyle changes. Definitely frustrating. Feel free to start an intro thread (click "start a discussion" at the top of the page) and share as little or as much about your journey as you feel comfortable. It can take a lot of trial & error, but most of us do find something that gives us some relief. Best wishes.

Kate
a NDPH Group Leader
~I'm just another patient navigating the daily challenge of this chronic pain. Thankfully it has got easier over time,and it could always be worse.~
Reply

Share this discussion with your friends:
Members who viewed this page also read:

NDPHNDPH ForumsGeneral & SupportGreater Occipital Nerve Injection

Disclaimer: The information provided in MDJunction is not a replacement for medical diagnosis, treatment, or professional medical advice.
In case of EMERGENCY call 911 or 1.800.273.TALK (8255) to the National Suicide Prevention Lifeline. Read more.
Contact Us | Bookmark Us | FAQ | Awareness Ribbons
About Us | Terms & Conditions | Privacy | Spread the Word | MDJ Advocates | Advertise
Copyright (c) 2006-2013 MDJunction.com All Rights Reserved