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hmmm.
i've had botox twice and did not have any side effects from it, but my pn is in my feet. i also had it before i was diagosed! :winky:
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Hi-
I have had juverderm, Restylane, and Botox several times since I have had symptoms of PN. None of them appeared to have made a difference in my symptoms. The neuro that dx me was also the one who gave me the botox for my migraines. Actually made my headaches worse, and after 2 treatments discontinued the use. I will say that I did like it for wrinkle prevention in forehead! I also loved the results from restylane and juverderm done in the nasal fold and lip augmentation. Mrs. D points are excellent-so it would be a hard choice now as to whether or not I would use them again. I think with me, if I had the $$, vanity might win out. :( |
I have read on a site that they will take my medical history and if there is a history of any autoimmune illness like RA, MS, or autoimmune thyroid they will not proceed anyway.
Since I have clinical Graves Disease I would be knocked back and they would refuse to inject me most likely. If they are truly diligent to ask me in the first place. At this stage I am going to give this procedure a miss. Thank you for feedback/opinions. |
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I'm jealous...but I'm too chicken to give it a go. I'd have a panic attack as soon as I sat down in that chair.:( |
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