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03-06-2014, 05:54 AM | #1 | ||
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Junior Member
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Hi special Arnold Chiari Members.
I live in South Africa. Do you know of anyone living in South Africa as well? Thank You, Take care Samantha |
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04-17-2014, 09:50 AM | #2 | ||
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New Member
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Hi
I live in South Africa, Limpopo have chiari malformation. |
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04-24-2014, 10:34 AM | #3 | ||
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Junior Member
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Hi
Great to hear from You Nicci I too live in South Africa, Johannesburg. How are You coping with Your ACM symptoms and condition? Would love to hear more about you and what you have been through. Have a great eve ahead. Take care Samantha |
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05-03-2014, 12:29 PM | #4 | ||
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New Member
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Hi.
Well I am doing ok. Just a problem getting medicine for these headaches. We are not so lucky as the people over seas. Had the decompression, Dr. J. Steyn at Wilgers did the op. Help me all the way but last year said he has nothing more he can do for me. Guess its just how it is. Wow someone in SA with Chiari |
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05-22-2015, 05:17 AM | #5 | ||
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Newly Joined
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Hi,
So glad im not alone! I was diagnosed 5 years ago, Type 1 with a 7.2mm protrusion. I was on strong pain meds for a year but have been going strong without them for 4 years apart from over the counter pills. I have been suffering with bad headaches the last 2 months and its just not going away! I have made an appointment but can only see the doc in 2 months. How have you been coping and have you gone for surgery? Take Care, Angelique - SA |
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05-26-2016, 07:21 AM | #6 | ||
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Newly Joined
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Hi Angelique
My wife has been diagnosed with a 5 to 6mm Chiari by DR Tuewen at the Olivedale. Would love to get in touch. |
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06-06-2016, 09:01 AM | #7 | |||
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Senior Member
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THERE IS ALSO A group on FB for sm in s africa which also has to do with chiari
Syringomyelia - South africans living with SM
__________________
Remember That Life Is Short!!!" break the rules, Forgive quickly, Love truly, laugh uncontrolably, And never regret anything that made you smile |
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08-09-2017, 11:32 AM | #8 | ||
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Newly Joined
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04-11-2018, 05:46 AM | #9 | ||
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Newly Joined
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Hi I am from Vredendal (West Coast) and have Syringohydromyelia of the cervicothoracic junction, C7 through T2 - don't have any other info and don't know what it is. Specialist is not concerned, I need to go back after 3 months.
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11-25-2018, 05:52 AM | #10 | ||
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Newly Joined
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Hi, are you still around on this group?
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