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Cluster Headache Help and Support >> Cluster Headache Specific >> Radacliffe seeks medical help for headaches
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Message started by Joshua on Jun 21st, 2012 at 11:03am

Title: Radacliffe seeks medical help for headaches
Post by Joshua on Jun 21st, 2012 at 11:03am
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London, June 20 — Actor Daniel Radcliffe was forced to cancel his commitments and seek medical attention after his headaches became extreme.

The 22-year-old was diagnosed suffering from a condition known as cluster headaches which causes intense pain on one side of the head and is experienced by just one per cent of the population, reports dailystar.co.uk.

"I was in the middle of these weird things called cluster headaches. It's very rare evidently, but it's exceptionally painful. I was taking 12 strong painkillers a day and going, 'Why do I still have a headache?'," he said.

IANS


Title: Re: Radacliffe seeks medical help for headaches
Post by Guiseppi on Jun 21st, 2012 at 4:36pm
I fired off a couple e-mails to his fan club...he needs to find this board! :)

Joe

Title: Re: Radacliffe seeks medical help for headaches
Post by AppleNutClusters on Jun 21st, 2012 at 8:39pm
A wizardly lightning bolt to the head is well-known to cause cluster headache in susceptible individuals.  I wish someone would go all expecto patronum on my CH!  :P

Title: Re: Radacliffe seeks medical help for headaches
Post by Katherinecm on Jun 22nd, 2012 at 7:47am
hehehe, me too!

Title: Re: Radacliffe seeks medical help for headaches
Post by aprildawn on Jun 22nd, 2012 at 1:18pm
If more celebrities that have the media's attention would come forward about this condition, maybe the media would give cluster headaches some attention.

Title: Re: Radacliffe seeks medical help for headaches
Post by kika on Jul 13th, 2012 at 11:39pm
I agree. Although I feel badly for Daniel,  I would love to see CH come out of obscurity.

Title: Re: Radacliffe seeks medical help for headaches
Post by metoo on Jul 14th, 2012 at 8:31am
Many people avoid sharing their stories of suffering, especially when the malady is poorly understood, as is ours. 

Thank you all for your patience with us who are finally finding out that there are others out there.  Lots of bright people on this site, and that bodes well for CH sufferers. 

TJ

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