nick overy

CHfather thanks for the the response . I will FB message Ainslie to see if she can tell me more about her experiences of treatment here in Scotland .

Just wondering what other peoples experiences are in Scotland in getting diagnosed with ch and if they were able to get oxygen prescribed on the nhs ? I have been having ch for over 4 years now and my gp's don't seem very proactive . They did refer me to a neurologist after a couple of years complaining but have never been diagnosed me with ch but just general migraine/headaches . I am on Zomig Nasal spray (zolmitriptan ) and verapamil . Would be very interested if anyone in Scotland gets oxygen on the nhs and how they got prescribed it.