Hi Beautiful People..
My apologies for the long delay in response to you (Been working all week!).
Thankyou Vikki, Maureen, Suu, Annx, TJ, Clarice and Hendi51.
With all the fantastic Advise which you all have kindly given
Current Update!!
ENT has sent me his report from last Friday and he have grave concerns about the cause of my symptoms..
He fears that I might be worse off to have Radiation or Surgery.
As one other lady who had identical symptoms to me had surgery and was worse off.
He is referring me to another neurologist and would like me to trial medications to see if the symptoms of imbalance, dizziness and headache might give some relief to me. ENT would prefer to have a more leisurely approach to the management of the AN.
I think I shall go with ENT'S Advise for the time and see if they can help my symptoms with medications.
As I have expressed my thoughts to you before on how I feel,
I'm happy If the symptoms go away.. Just would like the symptoms to be gone! with meds to have a better quality of life!
Fingers crossed!!!
I Have another MRI on my head in two weeks to see how much the AN has grown.. then back to the neurosurgeon.
If I have to have surgery ever.. then I'm going to Melbourne!! as the ENT down there has done over 1000 operations on the head and is clocking around one a week...
So that's makes me feel like he's my man!!
I want to play with my brain!!
If anyone is going to.
I spoke to his PA the other day, and she gave me his email address so I can tell him my story and ask more questions on the surgery as I'm more than 2000km away he is more than happy to correspond with me in this manner.
How Fantastic!!
I will continue to read everyone posts, learn, and keep you all updated with whats happening to me.
In the hope that maybe I can help and give other people like ourselves the ability to learn from my experiences and yours!
Keep you posted..
Chat soon!!
All the best.
Melinda