Living with MS for 14 years in GuanDong Province, China
ayesha
Posted on March 19th, 2012
Kathy wrote to us to tell us about her younger sister Sarah who has had MS for 14 years.
At the beginning she recovered quickly from relapses and could have a normal life including going to work, but after 5 years, she couldn’t work anymore. Now she cannot walk very well and may relapse if she is tired or gets virus’ like the flu. She stays at home now but she is healthy and stable. We all love her so much, she is such a lovely sweet person.
This year, I will try my best to find campaign team around GuanDong province China, to raise awareness among Chinese people about MS and WMSD, and to get their support.
Categories: World MS Day 2012
I am from iran at the year of 2007 I went to china in hope of finding a cure for my ms but found out no body knows my sickness clearly
only at current time some doctors do stem cells in china but as i check it is not so verified as other countries like Ukraine do the same but with no result
Hi. I was diagnosed 2006. I know I have it at least 20 years prior to diagnosis. I
since stopped working and I have small trouble walking. but I get up every morning exercising volunteering at the national m s society this gives me something to do. I feel empowered. no m s does not kill you, I will not let it ruin my life.
Hello MS comrades,
I have what you guys have since 2007. I am doing fine and leading a normal life the best I can. Whatever happens: keep smiling!
Take it easy!
Any one want to be our friends, can add my QQ: 1048495934, or write to me via kathy.cq@foxmail.com.
Anyone want to be our friends, can add my QQ: 1048495934, or write to me via kathy.cq@foxmail.com
My name is Holly and I have had MS for 26+ years. Physically I rate as very progressed. Cognitive functioning is good. I\\\’ve raised, on my own, two very successful good kids (now 29 and 30 years old). As if they are grown and gone I am at a loss as to what to do with myself. With the help of my computer, I am writing children\\\’s stories, but not very successfully. I find it very difficult. I live alone which is the way I want it. My vision is poor and my hand coordination as well. I used to play guitar, recorder and violin. I also enjoyed woodworking. MS says not kill and take your life, it only ruins it.
Your sisters story scares me. My MS is just starting to interfere with my job. Mine is not physical but cognitive issues.
Hello, can i have the e-mail or qq or icq etc. contact of Sarah or Kathy, i’am have ms since 2007, also i love China and looking for a friends from there. I’am from Russia.
Thank you.
Andrew