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Prolonged post concussive syndrome: help!
Hi! I have post-concussive headaches due to a car accident 4
years ago. I've currently moved to the Fort Wayne, IN area and I'm looking for a doctor. The process is never fun, and I'm treated like an opiate junkie after repeatedly asking to find non-narcotic medications, or better yet: a treatment plan. (What a concept!) I'm disabled due to this condition. I have several symptoms, but the headache, depression, anxiety and noise/light triggers are keeping me close to home. Nice to find a home here. QUESTION TO GROUP: Has anyone with similar symptoms found relief on anything non-narcotic? Current dr wants to do Botox shots, and not feeling comfortable with it. Please share your experiences as I formulate a new plan of action. Thanks, Laura Hanlin |
Welcome, Laura Hanlin. May you find what you seek while here.
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Hello Laura,
Welcome to the NeuroTalk Support Groups. We have a Traumatic Brain Injury and Post Concussion Syndrome Forum here. (edited to add: I see you've found it already ;) ) You might like to repost over there to get some information and support from the members there. You'll find you're not alone with your symptoms. take care. |
Welcome Lhanlin. :Wave-Hello:
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Welcome Laura!
Botox is turning out to be a good option for various pain issues but I can understand your reluctance. I take a low dose of nortryptiline for nerve pain and find it very helpful. It is dispensed frequently for migraine. A plus is my mood seems to be better even though I only take 20mg at bedtime, much lower than the antidepressant dose. I can honestly recommend the TCA family as an alternative for opiate pain meds. I hope you find relief soon. Sending Healing Love, Littlepaw. :hug: |
Great to meet you!!
Laura,
:Wave-Hello: Hello and welcome, happy to see you have come to be with us, it a great place to be. As you can see we have a great number and caring fellow members here, where you have find a supportive and relaxing place. Have fun looking into the different forums. Our shoulders are here for support in many ways. Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
Quote:
Lafayette Indiana here! My daughters neurologist has recommended botox as well, if IF physical therapy doesn't work. She is currently taken topamax and baclofen for the headaches. We had to play with the doses a little bit but at this point her headaches are tolerable. She hasn't ever used a narcotic for pain as it can make you dizzy, nauseous and tired. So we are thinking along the same line that you are and making a treatment plan. We are 4 months post concussion and it is work every day to deal with it. I do not allow her to drive anymore and she has to be home bound for school. I think every one keeps saying it takes time. I hope that you can find some pain relief. |
Nice to meet you!!
Smayotte,
:Wave-Hello: Hello and welcome, happy to see you have come to be with us, it a great place to be. As you can see we have a great number and caring fellow members here, where you have find a supportive and relaxing place. Have fun looking into the different forums. Our shoulders are here for support in many ways. Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
Welcome Smayotte. :Tip-Hat:
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Torodol
Quote:
Torodol was a godsend for me the last five years of my cluster headaches. After 15 years of morphine, Demerol, Nubain and egotomine with oxygen treatments someone offered me Torodol. It worked for about 80% of my events |
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