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I have chiari malformation
Hello everyone. I'm Sarah, in my 30's and was Diagnosed with Chiari malformation 9mth ago. just had surgery and seeking some enlightment on Post chiari surgery. Thanks for support:)
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Hey,
Welcome to NT. this is a great place to find answers. I don't know too much about your condition but there are many who come here with it. Try using the search feature above. I'm sure there's tons of info here for you. Glad your surgery is over. Take care... |
Great to meet you!!
Sarah,
:Wave-Hello: It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place. Sad to hear you your situation. Here is a great forum to check into for some wonderful friends to help you out. Arnold Chiari Malformation & Syringomyelia: http://neurotalk.psychcentral.com/forum71.html Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: |
Arnold chiari
Hi I'm Natalie, I was diagnosed with a chiari malformation 2 years ago, my doctor isn't taking me seriously and I could really use some advice as where to go from this
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Nice to meet you!!
Natalie,
:Wave-Hello:It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place. Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: |
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