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Cluster Headache Help and Support >> Getting to Know Ya >> New member http://www.clusterheadaches.com/cgi-bin/yabb2/YaBB.pl?num=1427784812 Message started by Ron B on Mar 31st, 2015 at 2:53am |
Title: New member Post by Ron B on Mar 31st, 2015 at 2:53am
Hi y'all. I'm new here. Diagnosed with CH in February of this year. No idea how long I've had them though. I've dealt with migraines since I was 15 (I'm 24 now). Also have bilateral Trigeminal Neuralgia and acute intermittent porphyria. Just got my oxygen dose put at the correct level by a neurologist (hospital doc did it originally). That's about it.....
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Title: Re: New member Post by AussieBrian on Mar 31st, 2015 at 3:05am
G'day Ron, and welcome. It's good news you've already got your oxygen happening and there's the Oxygen Info button on the left of your screen that may let you get an even better result.
Having any luck with the other therapies available? There's plenty to choose from and we're only too happy to talk about them. The best of times are ahead, Brian down under. |
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