Hey all, I was wondering if anyone here has received a lidocaine treatment? "The supposed mechanism by which lidocaine works in clusters and migraines is by numbing the portion of the trigeminal nerve known as the sphenopalatine ganglion."
If it works, I'll get it again before I go on vacation. But I think it is too expensive to take it as often as they suggest.
Anyone familiar with this?
I am hyper sensitive to meds and am being treated for vestibular migraine. My neurologist said I can start with 100mgs of Gaba at night or break in half 300mg tablet of Gralise (Gaba ER). He is one of the top, well-renowned doctors that treats my migraine spectrum, so at first I did not question his option of breaking Gralise in half. However, after viewing the manufacturer's video on how it is processed, I am a little concerned (safety, processing, absorbtion, etc.) about this method. He does titrate patients up on Effexor by counting the beads, preferably using the brand version, and is creative with other ER versions of drugs. BUT, still apprehensive.
Has anyone tried Gralise, broken it in half and/or could suggest a best course (Gralise 300/half or Gaba 100) given the circumstances?
Thanks - C
Sorry to keep going on about side effects, I just want to know.
Has anyone had substantial (diffuse, all over perhaps) hair loss from any of the AED's, that upon quitting that medication, eventually that hair loss reversed and it regrew?
I know it sounds vain, and hair isn't everything to most people... but can it grow back - its diffuse loss for me right now. I am male, just turned 30. I don't have a recession or if I do its very mild. My hair had loss before, but it was controlled - and was due to Adderall just being on that a couple days actually (as strange as that may sound). BUT being on lamotrigine, years later - my hair no longer looks good, and is straw like and very thin. I had 80% of my hair and it looked amazing, as I started with a thick full head of hair. You could see expanded part lines and such when I had the incident on Adderall. ANd then I switched to Dexedrine eventually and used some Spironolactone cream at nights, to prevent shedding. When off Dexedrine I barely shed. Same with other meds. Dexedrine was less bad than Adderall. So that was my mid to late 20's hair and medication wise.
And in the last winter till April, I really tried to "get used" to the side effects of Lamictal, but I couldn't. I liked it and it did make me feel more resilient and grounded and calm and less depressed - but it simply wasn't good for me to have the side effects. They were affecting my self-esteem. I've been off of it since April 22 I think, and I hope hair regrows. I am now on Finasteride - and have been since January, but am taking a small break from that and then restarting it at a micro dose (as they have similar DHT inhibition anyways, and hopefully I can reduce side effects). I didn't even realize that I was losing hair on Lamotrigine, until at least a few weeks later or a month or so. I was more concerned with the death rash, and the other side effects.
EDIT: This is really disheartening... I guess it doesn't often reverse with Lamictal? I've read studies showing it's rare.
Hi, I'm new here and hoping one of you can help me out. I've taken Lamictal, 400 mg (max dose) for about 8 years. We added on Neurontin just 4 months ago ( 200 mg). 3 weeks ago I started itching. All over- even between my fingers. No rash but heat makes it worse. I've eliminated all obvious causes - lotions, shampoos, detergent, dryer sheets..so on. I've never been allergic to anything in my life (47). My Dr wants to titrate me off the meds, starting with the Neurontin. Last resort. Has anyone here had a reaction after being on a med for a long time ?