Systemic Lupus Erythematosus
Systemic Lupus Erythematosus is an autoimmune disease that can affect any part of the body. This disease is ccharacterized by the immune system attacking the body’s cells and tissue. This then causes inflammation and tissue damage. As a result disease harms the heart, joints, skin, lungs, blood vessels, liver and kidneys. This disease is very unpredictable and has periods which are called flares. SLE mostly affects women around the child-bearing years ages, which are ages 15-35. It is more prevalent in African American women. SLE is treated with immunosuppresants. This disease can be fatal and there is no cure for this disease. I did not know anything about this disease until a few years ago when a very close relative of mine was diagnosed with it. After seeing the effect that it had on her I wanted to become more educated on this SLE. I interviewed my cousin Natasha Boyd.
ME: How would you describe how your living experiences have been with Systemic Lupus Erythematosus?
Tasha: Things have been completely different for me since I was diagnosed with SLE. I am limited to doing things for myself now. I can't not perform certain daily activities that are necessary. I can not drive any more. I have to have one of my older son's take me to the places that I need to go. I can't live alone. I need to have some one living with me and constantly checking on me. I can no longer take care of my daughter anymore who has special needs. I have to have caregivers help me with her. I am have a really tight budget because I have to survive off of social security income. Which is less than the income I was making when I was able to work.
ME: What are you trying to do to maintain your health inspite of the disease?
Tasha: I am trying to stay as healthy as possible. I take my medications on time. I go to my scheduled Doctor's appointments when I am supposed to. I also get enough rest, sleep and do limited exercises when I can. Living with the disease can be depressing at times, As far as my mental health goes I meditate and pray to keep me from feeling down all the time.
Me: I can understand how challenging it may be to go from being able to do things for yourself and all of sudden not have that ability anymore. It is a blessing that you have people in your life such as your sons and your caregiver's to help you care for yourself and your daughter.
References
location:. "Systemic lupus erythematosus - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 17 Nov. 2012. <http://en.wikipedia.org/wiki/Systemic_lupus
Systemic Lupus Erythematosus is an autoimmune disease that can affect any part of the body. This disease is ccharacterized by the immune system attacking the body’s cells and tissue. This then causes inflammation and tissue damage. As a result disease harms the heart, joints, skin, lungs, blood vessels, liver and kidneys. This disease is very unpredictable and has periods which are called flares. SLE mostly affects women around the child-bearing years ages, which are ages 15-35. It is more prevalent in African American women. SLE is treated with immunosuppresants. This disease can be fatal and there is no cure for this disease. I did not know anything about this disease until a few years ago when a very close relative of mine was diagnosed with it. After seeing the effect that it had on her I wanted to become more educated on this SLE. I interviewed my cousin Natasha Boyd.
ME: How would you describe how your living experiences have been with Systemic Lupus Erythematosus?
Tasha: Things have been completely different for me since I was diagnosed with SLE. I am limited to doing things for myself now. I can't not perform certain daily activities that are necessary. I can not drive any more. I have to have one of my older son's take me to the places that I need to go. I can't live alone. I need to have some one living with me and constantly checking on me. I can no longer take care of my daughter anymore who has special needs. I have to have caregivers help me with her. I am have a really tight budget because I have to survive off of social security income. Which is less than the income I was making when I was able to work.
ME: What are you trying to do to maintain your health inspite of the disease?
Tasha: I am trying to stay as healthy as possible. I take my medications on time. I go to my scheduled Doctor's appointments when I am supposed to. I also get enough rest, sleep and do limited exercises when I can. Living with the disease can be depressing at times, As far as my mental health goes I meditate and pray to keep me from feeling down all the time.
Me: I can understand how challenging it may be to go from being able to do things for yourself and all of sudden not have that ability anymore. It is a blessing that you have people in your life such as your sons and your caregiver's to help you care for yourself and your daughter.
References
location:. "Systemic lupus erythematosus - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 17 Nov. 2012. <http://en.wikipedia.org/wiki/Systemic_lupus