The migraines have been pretty consistent lately.  I get 1-2 attacks a week with most of them responding fairly quickly to over the counter medication.  I talked briefly with my neurologist this week and he said if OTC is doing the job, then we don’t have to look at going back on to anti-seizure medications any time soon.  I don’t take enough of the NSAIDs for them to be an issue with my liver at this point.  I’d like to be on a prophylactic medication but the side effects from the ones I have been on aren’t really ideal for me.  Topamax had such a positive effect on the migraines but making me turn into a stupid idiot was difficult to handle.

School has been going well over the summer.  I’ve been making headway on my iPhone migraine diary and may even have something out there by the end of summer.  I have to remember I’m not doing this to make money on the iTunes store, but rather get a good grade for my graduate Capstone project.  Rushing to get it out to the market isn’t what I would consider a good idea.  However, if I got real world users to help with the process along the way, that could make for a very good final presentation.  On a good note, my neurologist is totally on board with helping me with the application!

Summer is FINALLY here in Wisconsin and we’re having our first 90+ degree day.  Can’t say I’m thrilled for the heat and high humidity, but it’s nice to have the body clock reset after a really long winter.

The holidays are nearly over and I can’t believe another year is starting.  Next year I’ll be turning 30, will have been together with Tazz for 13 years, had our house for 8 years, been diagnosed with migraines for 7 years.  I have typically established goals for myself in writing on this blog, but never really think about them in such a concrete manner again throughout the year.  To sum up this next year’s goals: be healthy & be happy.  Making a punchlist of dos and don’ts isn’t productive, for me at least.  As long as the choices I make maintain my health and happiness, I’m cool with that.

I’ve had a rash of migraines over the past month that hopefully I can just attribute to stress.  In the past, I would easily have 5-6 episodes a week that would respond to over the counter medication.  However, now I seem to get more frequent spikes of pain that last a few minutes and then go away for most of the day.  Taking any medication doesn’t make sense in these cases as the pain will probably subside before the medication has a chance to be absorbed into my system.  The number of instances of migraines that visibly affect my speech or thought processes are also on the rise.  I don’t normally get overwhelmed with pain to the point where I can’t think straight but at least once in this month I’ve had a migraine that made me feel drunk or like I was stroking out.

Next year my employer’s medical insurance is changing its deductible schedule for physician visits.  My family doctor will increase to $25 a visit and now specialty visits, like to my neurologist, will be increased to $50.  I may see if my family doctor can get my records from my neuro to help with managing the migraines.  I usually only see my neuro once a year but $50 is quite a bit of money to be given the next round of antiseizure medications that help the migraines but put the rest of my body through hell.  I’m sure everybody is going through this same type of change with their benefits, assuming you even have a job during this next year.

Happy New Year everyone.  Lets hope it brings more balance to our lives and a renewed sense of hope.

I’ve been on Topamax, Depakote, verapamil, triptans, melatonin, indomethacin, celebrex to name a few. None of them really worked. Is that strange? I’m not willing to stay on any more anti-seizure medications. I was not myself on Topamax and I’ve realized I’m probably better off not screwing with my neurotransmitters if I don’t have to. Ultimately, coming back to Tylenol and ibuprofen has proven more effective than any $50/month medication.

I’m not expecting some new miracle cure that developed in the past year to fix it all for me. I think at least I’d like to get another MRI done for comparison to the two others I’ve had. While I’ve been assured that nothing like a tumor or clot is responsible for the pain, I’d like to stay up on it. Maybe some day I’ll make a mobile made up of brain scans. I think that would be pretty.