moonlite

Hi Thank You all for your kind words well the doc gave me codeine phosphate to try for a week if still persists then take another action, so time will tell I've been taking them since lunch yesterday but there still there so time will tell, but i will not dwell on this life is too short. it is nice to know people do care. xxxxx Again thank you.

Thank you just booked doctors appointment fir tomorrow will let you know.

Hi I had my SAH clipped & coiled in July 2011 then the a non ruptured aneurysm cliiped In april/may last year but my headaches are really getting bad really gripping the hospital Has discharged me, not too sure what to do.

Hi Pete i had a sah in July 2011 it wasnt until 6 months later that i suffered a fit then again twice more until they sorted my meds out, all i can say is dont panic about it it might not happen not everybody sufferes all you can do if she does fit is be there for here and call an ambo as they need to check the brain again. Good luck

Hi I had a seizure after my op then again 6 months later they gave me epilim which didnt work so they increased the strength but gain did not work so put me on lamatrogine slowly but now having a lot of partial seizures so on another med so far is working but ive gotta see the neuroligist this week so dunno wot hes gonna say but its hard for the benefits people to understand this.

Hi I will have a word with cab its worth a try thank you all Regards Moonlite

Hi i dont know all the benefits i can get I had my sah in July 2011 but now have epilepsy since dec 2011 I do get esa and had to fill in the medical formi also get dla so only on low rate wating to get middle for my husband as my carer as i dont feel safe going out on my own my doctor did say i shouldnt be left alone did tell dla but im not sure what else i can get probably nothing but you never know Thanks Moonlite

I get min at the back of my head ive had my MRI last month and everything was fine but i also get a pain across the topp of my shoulders.

Hi i had my SAH in July 2011 grade 1 with a complex mca bifurcation aneurysm I still suffer the headaches and tiredness but glad to be alive, then in December last year I started having fits so more time in hospital and CTs with angos and lumber punctures i feel though I wasnt given much support no groups etc.. when i came out in July then to try and see nero for epilespy as been a nightmare ive had to do all the ringing around etc.. and then things seems to be going slow as the tablets dont work theyve had to change them but im also having partial fits, so feel im still suffering from the sah and dealing with epilespy as well. Sorry to moan.