Hi everyone, I'm back after a long break, unfortunately not along break in the pain just a long break from here. Well after 8 years now I'm still the same CCH and Chronic migraine ... Sometimes I get mixed up with them both but still trying to sort them out. I've know Dr M at Queens for so long I've seen his hair go from black to grey lol. I've had the ONS for 3 years now and I have to sadly say that I'm not shouting from the roof tops about how great it is but it has improved things a bit. I'm having regular nerve blocks and hopefully will be having Botox in a few weeks as long as I can manage without too many injections in the next few weeks. Having said all that I have no social life, work is killing me and I'm still in pain most days. I'm really looking forward to meeting you all in October, I think the only other person I have spoken to since I first joined here is Mike.
have had 2 very bad years and now I'm hoping I can open up and discuss this illness without feeling I'm going mad.
Regards. Angie




Joined: Wed, 04/15/2026 - 17:47
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Submitted by Val on Mon, 08/25/2014 - 11:31
PermalinkAnd me? Val.
And me?
Val.
Joined: Wed, 05/27/2026 - 18:25
Last seen: 2 months 2 weeks
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Submitted by Dorothy on Tue, 08/26/2014 - 10:25
PermalinkHi Angie Sorry you're
Hi Angie
Sorry you're suffering so much. I hope meeting others at the London meeting will give you a boost. There's nothing like mixing with your CH family!
Dorothy