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Occipital Neuralgia and other Cranial Neuralgias For discussion of Occipital Neuralgia, Glossopharyngeal Neuralgia, Nervus Intermedius (or Geniculate Neuralgia), and Vegal and Superior Laryngeal Neuralgia. (Trigeminal Neuralgia has its forum below.) |
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#1 | |||
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Well, I've just had my latest nerve block. I had it done on Wednesday by my neuro. It's just starting to work now, just on 2 days later.
![]() I can feel my pain level dropping and my mood lifting already! ![]() ~Jaime~
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. My Poetry Site - . |
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"Thanks for this!" says: | Nik-key (08-13-2008) |
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#2 | |||
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That is wonderful news Jaime! How is working now? Hope you are still getting relief
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******************************************** More Than One Soul Dies In A Suicide . ******************************************** . |
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#3 | |||
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Quote:
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. My Poetry Site - . |
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"Thanks for this!" says: | Burntmarshmallow (08-09-2008) |
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#4 | |||
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Senior Member
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Fantastic! Glad to hear it. My last block was a total disaster, I haven't been brave enough to try it again. But, so glad it is bring you relief~ Nikki
__________________
******************************************** More Than One Soul Dies In A Suicide . ******************************************** . |
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#5 | |||
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If you go to youtube and search ON, there is a 2 part vidoe of a guy with ON getting an ONS. It's interesting how well he did.
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#6 | ||
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So, I watched the video and I must admit, it kinda scared the crap outta me. I have been referred to a guy who does the ONS and will probably be getting it done soon after exhausting many other techniques (and mind you, I'm only 20). Anyways, I'd appreciate any advice, guidance, etc. about the procedure. Thanks! |
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#7 | ||
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My cousin, female 32, has RSD. It is localized to her right foot and leg. She says
it flares every few months. It is flared now. It burns, she says. Most of the pain is in the foot she broke two years ago. When she had her first nerve block, she experienced her first seizure. Now she has seizures every couple months. She doesn't jerk. She just seems to pass out briefly, then, she doesn't know who family is for a few minutes. Her speech is usually slurred too. Do you think this is from the nerve blocks? Also, how intense is the permanent nerve stimulator? She is afraid to get one implanted. Thank you |
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#8 | |||
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While I would be glad to have the pain be gone permanantly, I am starting to feel a bit scared at the idea of having wires in my head and a battery pack in my abdomen. ON is not for wimps! *laughs* I am only 37 and I think I'm too young to be dealing with the crud too! Especially since I was also diagnosed with MS this spring. How much more can a girl take? I spend far too much time at the hospital. I am hoping if I do end up getting this ONS, it would mean LESS time at the hospital. |
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#9 | ||
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![]() Quote:
Hi Jaime are you still doing o,k with your blocks ? pain specialist has taken me off versitis patches as they were not doing any good. i am now back on nerve blocks, had one today he is trying to get aeneasetic right into lft side of my face my pain being all in lft of head & face. just had 5 docs watching & nurses trying to hold my hands as though i hadn`t had them before. not feeling good tonight & can`t lie down hopefully will be o.k in another couple of days. regards jane |
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#10 | |||
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Yes, my ON block is still working. It's almost 2 months now, and I'm still getting good relief. The warmer weather seems to help too.
I hope the block you had soon starts working. Quote:
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. My Poetry Site - . |
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Thread | Forum | |||
Nerve Blocks for RSD/ CRPS?? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Nerve blocks | Medications & Treatments | |||
Vegas Nerve Stimulator | Depression | |||
Sympathetic nerve blocks | Peripheral Neuropathy | |||
Sympathetic Nerve Blocks | Reflex Sympathetic Dystrophy (RSD and CRPS) |