Sorry to burst ur bubble...but, u r right that ur surgery was a success, in that ur syrinx is shrinking and that u feel well...that is most important....
: )
Keep us posted on ur travel plans
"selma"
Hi - thank you both for your prompt replies. I can see what both of you are saying re the C1 Malformation bit always being there........ I have thought about this a lot myself .......Don't know if you realise but I live in the UK. I am looking at getting travel insurance for a trip abroad and I just want to feel confident that I am covered should any medical emergencies/payouts arise during the trip (obviously, this can be quite costly). I just thought that perhaps I might now be classed as 'Chiari-free' now that I'm 7 months post decompression and that the aim of the surgery is obviously working/been successful, ie the syrinx in my cord is shrinking - if you see what I mean. Anyhow, nevermind - but thanks for the comments. Looks like once a Chiarian, always a Chiarian eh?
Yes, because the decompression is not a cure, but a treatment to alleviate the symptoms. I, too, have been rejected for life insurance and disability insurance applications. So I just gave up and just saved the money in the bank...I figured, at least I'll have some money if I need it. Don;t you have a travel insurance with your work benefits? I use that when we travel. Check with your benefits package.
Hi and welcome to the Chiari/Syringomyelia Forum.
From what I understand and believe once u have chiari u always have chiari...the surgery was only to open the flow of CSF...and give us some more room...but our skulls were malformed, and it was a congenital condition....u can not get rid of something like that...only treat it to help avoid further issues.
I am not sure about travelers insurance?.....May I ask Y u r getting it and y this is an issue?
We r happy to have u join us, but not happy for the reasons that bring u.
"selma"