Sunday, September 9, 2012
Talking about Migraine Disease-My support group is limited
What can I say. It's getting harder over the past 20+ years to talk about migraine disease to my spouse and extended family. They have become less supportive. I have a few close friends that I can rely on. I get most of my support online through Migraine.com and other outlets. It's helpful to have others that share the same experience you have and have gone through what you have and you can always learn more since we are all on this same journey that shows no end in sight. We can make the best of it or we can groan and moan and make the worst of it. After going through all the posts I've read today and seeing the fighting spirit of everyone I have decided it's not time to give up the battle but to puff my chest out (as small as it is) and strut my stuff about (yep, stick my bit butt out and heaven help the poor soul behind me, LOL) and carry on the fight and not let it get me down.
My spouse and some of my extended family may be of no support, but I have God and a few others that will not let me down and I know there are some great people on this Blogger site that have great input as well.
So my questions is has anyone tried oxygen for abortive to migraine/cluster headaches? My neurologist just prescribed that to me last week. And also Sprix.
Take care and be well. God Bless you all.