MG
Hi
My name is Christina and I have been going to the doctors since 2012. I had woke up one morning on step. 3, 2012 having trouble seeing. I had double visionfor two weeks and it did not go away. The doctor acted like he could not help me. He said it should go away after two weeks and it lasted a little after two weeks. I did not have double for a while but in 2013 in April I started getting the double vision again. It only lasted a week and then went away. Then in may I got the double again I had changed doctors because the last one was really not helping me. I had since so many doctors to find out what was going on. I was told I need glasses and put $400 dollars into them but they did not work at all. Then one of my doctor had some blood work done and I had found out in 2014 I had My as then Gravis. I would have trouble grabbing thing or even holding a cup in my hands. Then I was positive for RA in my joints. I have seen two doctors down in UCSF.
I been having trouble dealing with finding out about having MG. I have trouble working or just doing things I like to do. I have been telling my family that I needed to find a support group. They doctors have been telling me about looking into one too. I don't know anyone that phase this disease and even when I talk to people about it they don't even know what it is. I just been hurting a lot from all this I just being having more trouble grabbing things.
My name is Christina and I have been going to the doctors since 2012. I had woke up one morning on step. 3, 2012 having trouble seeing. I had double visionfor two weeks and it did not go away. The doctor acted like he could not help me. He said it should go away after two weeks and it lasted a little after two weeks. I did not have double for a while but in 2013 in April I started getting the double vision again. It only lasted a week and then went away. Then in may I got the double again I had changed doctors because the last one was really not helping me. I had since so many doctors to find out what was going on. I was told I need glasses and put $400 dollars into them but they did not work at all. Then one of my doctor had some blood work done and I had found out in 2014 I had My as then Gravis. I would have trouble grabbing thing or even holding a cup in my hands. Then I was positive for RA in my joints. I have seen two doctors down in UCSF.
I been having trouble dealing with finding out about having MG. I have trouble working or just doing things I like to do. I have been telling my family that I needed to find a support group. They doctors have been telling me about looking into one too. I don't know anyone that phase this disease and even when I talk to people about it they don't even know what it is. I just been hurting a lot from all this I just being having more trouble grabbing things.
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