Drugged driving

I was watching Dr. Oz a couple days ago, because sometimes I like to pretend to pick up healthy habits.  Anyway, he was discussing drugged driving... something that is becoming a rising concern given the amount of prescription drugs we take.  It is a hot button topic for chronic migraine sufferers when there have been cases of people with treated migraines being changed with DUI.  Because it means Driving Under the Influence, which can include medication, which does include pretty much everything we take to abort a migraine.  And people also say we should not drive while having a migraine.  Thus, we should not drive at all.  Honestly, when you think about it, that is quite true. 

The police officer on Dr. Oz, and this would differ in Canada and various states, someone can be charged with a DUI, lose their license, get fined and have their car towed.  For using prescription drugs that we are taking as prescribed.  Some that were mentioned where blood pressure meds and anti-depressants, which are two migraine preventatives, both of which I am currently on, plus an anti-seizure med.  The problem with some of these meds is the sedation aspect, may cause drowsiness which effectively slows reaction time.  Not in all people of course.  And it does not say on the script not to drive.  Nor do our doctors tell us we cannot drive.  So that sucks for anyone charged with a drugged DUI for prescription meds, since apparently doing as our doctor said is not an excuse, nor is ignorance and nor is our personal idea of impairment.

I have had concerns over this myself, but there is no alternative transportation where I live, so I drive to work, but never anywhere else.  Obviously my doctor has not said I could not, even when I brought it up.  Nor has any pharmacist expressed concerns over a particular med, or the combination of them.  But you know, my reaction time could be affected without my being aware of it.  Since I live with moderate pain, it is only severe pain that concerns me.  And unanticipated side effects are only a concern while I am getting used to a medication.  And really when it comes down to it having a full blown acute migraine and driving seems to be far more dangerous than having a treated one and driving.  Think of how impaired we can get neurologically from a migraine, not even counting the pain... asside from the visual issues there are huge issues with clarity of thinking and reaction time.  However, migraine or not, our actual preventatives, which we may not notice a change to reaction time given we take them every day, could be counted as impairing us.  Sure would be a good thing to know.

I also tend to trust my doctors judgement over and above my own.  I don't make the decisions, or I would not be working or driving.  He has the power.  Yet, I would be the one suffering the consequences.  And sure as hell do not drink and drive, yet everyone seems to think it is fine when I have more than fifteen migraines a month, that I treat, and three different preventatives.  Most unfortunately is that since I do have to work, which does suck, and am not considered disabled and unable to work, the one form of alternative transportation open to people with disabilities is not an option.  Is it right that I must always in all aspects of this life live by other people standards of 'not sick enough'?  Tell me I have a disability and help me accommodate it, instead of bickering on what is a real disability and what is not.  If we are to be considered legally liable for driving under the influence, then there ought to be a way to help us get around.  And since these are prescription medications that we take on a regular basis shouldn't our doctors be legally obliged to state we cannot drive instead of making us guess?  I mean, if someone gets severe seizures they cannot drive, so for a chronic condition that might impair our reaction time, plus medications, plus combining medications, shouldn't there be guidelines for a doctor to follow?  It sucks that we are in this gray zone where people cannot even make up their minds about whether we have a disability or not, let alone thinking about how difficult that condition makes our every day living.
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