Occipital Neuralgia Headache: Terrible pain lasting weeks, what helps?
I suffer from occiptal neuralgia headachs. Three weeks usally @ a time. I do have trigger shots but medicare has cut my time to every
fours months, they do help. Hot Hot showers, massage, $$ on pillows.
Beginning to take VitB2?
A comment on Mayo chat they take Valium/Medrol dose? any other ideas?
Interested in more discussions like this? Go to the Headache & Migraine Support Group.
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@rnlorena I am wishing you a good outcome. In Nov. I had a terrible three week bout. Dr. were
out of town, I want something to help me get through. I plan on asking about Botox?
Amitriptyline for Pain? (Old Depressant w/nerve pain control). I go about two months after
shot and will have :Flair up simply awful Ice pick pain, started one side for long time, now
both sides. My Ice Pack slepted with me. I can't tell you how helpful this sight has been.
One person said a combo dose of Valium/seriod cured him complately? I have a list of questions.
@rnlorena I had an ablation no change. They said I could have another. My nerve shot is tomorrow, they usually last three months, but I am adding other tips so here goes, My Pain Dr. is great.
@suszy39 When I went to the second Neuro-Opthalmologist she questioned me for quite a bit. I have read all about Occipital Neuralgia. I am not having the symptoms like it calls for. Mine is different. She doesn't think I have Occipital Neuralgia. I don't think so either. This is mind boggling for sure. The Dr. I went to is a pain Doctor. They do more than just pain meds. I really don't know and will just have to wait till and see what is next. It could be another nerve block. @rnlorena
Hi!
Im 28 years old and have occipital neuralgia for the last 10 years. My symptoms are a-typical, slowly getting stronger until they reach 7-10 on the pain scale and last for 14-30 hours. I have those attacks usualy 2 times per week.
Im getting Oxcarbazepine. That helped me to get it down to 1 time per week. Also, for an attack im currently using morphine. Opioids are the only medication that helped me to be pain-free in an attack.
Hi @sinyaale - welcome to Mayo Clinic Connect. The attacks you have sound painful.
Hoping that here you can meet others taking about occipital neuralgia headaches, such as @suszy39 @rnlorena @pierwell @laura1970.
What would you say are you future hopes for your condition and your treatment, sinyaale?
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2 Reactions@sinyaale Welcome this is a great place to bring your thoughts, suggestions, to fellow folks
who totally understand where you are out. Many good tips, I am flyiing with all of them.
Concerned ON Person
@suszy39 Having had an ablation and they burnt the nerves I would be asking why it didn't help. That is truly strange. I will be sure and bring that up to my Dr. when I see her. My question will be this. If you do an ablation what are my chances of it not working? I definitely will be questioning those things. @rnlorena
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Thank you for the warm welcome!
Well, i hope that my condition will be managable in such a way, that it doens´t interfere every aspect of my life; from waking up, laying down. Doing the dishes wrong, beeing to stressed or to lose. Beeing able to set goals for oneself again without having to redefine them every week/month because the condition burns the bridge to the goal. Beeing able to chase the "mind-version" of yourself - how you see and what you´d like to become.
Treatment? A surgery that actually works. Had my third one last week and the overall chances aren´t high that it will help. So relief. I hope for some relief for the mind.
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Thank you!
Still hard to believe there´s someone currently writing understanding the everyday struggle with the condition.
How long do you have it? What´s in your opinion the hardest part ?
@rnlorena I’ve had two ablations with minimal effects.
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