life after brain tumour removal

Hi I wonder if anyone out there can help me, my mother has had her second brain tummour removed around january time this year, the second one was at the back of her head which affected her balance etc, so now she has had the surgery and check ups, the scan just show the scaring from the surgery. But she is still having a terrible time with feeling wobbly, dizzy etc, she has been on steroids then off them and no difference, its gettin her very low.. just wonder if there is any advice out there. 

thankyou in advance for reading my post

 

 

  • Hi cymru. Welcome to the forum.

    I'm not a doctor and I have no medical qualifications.

    My GP prescribes me Cinnarizine (also called Stugeron) following an attack of viral labyrinthitis some years back. This med is good for suppressing dizziness and nausea. However, I have absolutely no idea whether it would be helpful for your mother. 

    If you want to try something off the wall, but which might just help, she could try New Era Combination S tissue salts. Again, these might not help. 

  • Hi cymru, I know first hand how difficult it is to deal with dizziness and balance problems, though not for the same reason as your poor mum. I hope she's doing well in other ways.

    Here's a link to an article about coping strategies when dizzy

     healdove.com/.../seven-ways-to-cope-when-youre-dizzy

    Another tip, if you're watching TV and it makes you dizzy, focus your eyes on a fixed point just off screen, say the ON light, then use your peripheral vision to follow the action. 

    Do make sure the docs know how this is affecting your mum. You could ask if a referral to a balance clinic would be of any benefit. It's very draining and tiring to have balance problems. Unfortunately it can be depressing.

    Hope your mum finds a way to cope.

    regards, gamechanger

     

  • Hi,

    After having a brain tumour removal  (partial) a year and a half ago, steroids and the usual chemo and radiation,  I'm still unsteady on my feet, I cannot walk quick or my feet tie themselves together. 

    I did asked my consultant and this is very normal for several years. 

    I now take it slow and steady as the world rushes past me.