I had SaH in `08 and am still in constant pain at the wound site and was left with an ABI.
I,d like to hear from antone else who has been through this and find out how they are dealing with this life changing (for me it was) experience !!!
I had SaH in `08 and am still in constant pain at the wound site and was left with an ABI.
I,d like to hear from antone else who has been through this and find out how they are dealing with this life changing (for me it was) experience !!!
i had my sah in 2007 however and you probably dont want to hea this but my head apart from a ridge in my skull is pretty tidy i until 2008 oct of suffered blinding headaches but with medication these stopped i sometimes get them now when i am dehydrated tired or stressed my only adise is to see a doctor or neurolygist life will change massivly i went from lots of money to benefits but i enjoy the support of family and friends having seen first hand the abject poverty in africa and india i am lucky i have a roof over my head food in my stomach every day if not family makes sure i do my pain was short lived sorry if this not helpfull but good luck with your further recovery neil
I have a scar the same as yours but from planned surgery to reduce he size of a tumour, I do not suffer from head aches, but it took a long time for the sensation of the skin on my head and right side of my face to recover, even now there is part of the skin on my head that I cannot feel. Worst was when I wanted to scratch and itch but could not feel my hand on my head. Fortunatly this has subsided
Hi
I had my SAH just over a year ago, the feeling on scar is still not completely back and the metalwork by my temple is always sore! Luckily I do not get many headaches.
Take care, Linda
Hi, The metalwork can be removed under local.
I had 2 of the 4 plates removed after a year but the back two seem ok to leave .
I begin a Pain management course Jan 4th which includes having tailored analgesia.
I hope some good will come of it and will post updates,
I have recovered pretty well except I have LHS paralysis. Hence I am in a wheelchair.
Fortunately it did not seem to affect my ability to talk, eat, think. I have a very supportive family and friends.