Ann

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When Ann was thirty years old, she noticed that her walking began to bother her while working. In a few days, Ann could not walk and went to the hospital where she was diagnosed with MS. She regained the ability to walk after a course of intravenous steroids and returned to work. After relapse, Ann was concerned about having children, but was cleared by her doctors to become pregnant. During both of her pregnancies, she had mild flare-ups, but her symptoms resolved after the births. Over the years, Ann’s flareups impacted her vision and decreased her ability to focus and read. She has taken cortisone to treat these flareups, but she has never taken any other medicine, nor was she offered any other medicine to treat her MS symptoms. Currently, Ann’s symptoms include eye issues that come and go, and incontinence. Ann has been using catheters to manage her incontinence for close to 30 years and feels fortunate that Medicare provides them so that she can use a new one every time. Ann also experiences fatigue and some difficulty walking.
Ann worked for the government in community corrections for over thirty years helping released prisoners integrate into supportive environments. Ann was reluctant to tell people about her MS because she worried that they would use it to deny her advances at work. Ann did not tell people at her work because she didn’t want to be seen differently in her workplace.
When Ann first received her diagnosis, she expected to become crippled and die soon or die prematurely. However, she wishes that she had known from the beginning that many people do have easier times with MS than she was expecting. Ann feels that her MS is part of her, part of who she is but not a big part or not an important part most of the time. Ann believes that the most important and the hardest part of an MS diagnosis is dealing with uncertainty. Ann is surprised to be as old as she is because she never expected to get there. She sees herself as someone who has had an interesting career, done some great things, been in some interesting places. Ann notes that “it has been a good life, in spite of the MS, or because of it, or who knows.” Now, Ann is retired, very happy and content.
Ann is also diagnosed with Chronic Obstructive Pulmonary Disease (COPD) unrelated to her MS. Generally, she uses a cane or walker to walk outside because she has to carry her oxygen equipment and purse which is just too much to carry.
Ann identifies more as person with COPD than MS.
Ann identifies more as person with COPD than MS.
INTERVIEWER: So, given this idea that MS, as you said, is sort of your body against itself, how does having MS make you think about yourself as a person, in your sense of who you are?
I'm a person with MS, among other things, at this point. But right now, I'm much more person with COPD because I have the oxygen tubes to remind me all the time.
Ann did not disclose her MS diagnosis to coworkers.
Ann did not disclose her MS diagnosis to coworkers.
Given the kind of places that I worked, I don't think I was comfortable, nor did I feel any need to tell them. That was the big thing. If something serious had happened where I couldn't get around as I did, I might have told them, but I probably wouldn't. But since I could get around, there was no need to. And I didn't want to be different. I guess that bit. I didn't want to be seen differently and that sort of thing.
Ann talks about her pregnancies in relation to MS flare ups.
Ann talks about her pregnancies in relation to MS flare ups.
Well, I had a flare up-- after I was diagnosed, I was in my late 20s, I think. Yeah, it was just before my birthday. And my husband and I were married. Had been for about four years. But did not have any children, but we were always planning to. And so, basically, I got concerned. Well, my doctor initially told me, because of the cortisone, I guess, not to continue to use birth control. And I was cleared to become pregnant about a year later. And our son was born in November of '72. As it turned out, early in '72, what would have been about the time of implantation of the fetus, I had another flareup from walking, et cetera. But then I had my baby, and we came home. And life continued. Then two years later, we decided to have another one. I had another flare up, again, what, in retrospect, is about the time of implantation. And so, I then had my tubes tied. So that solved that problem.