Did I have Lupus as a child?

During the Lupus Star Foundation (Lupus Star Website) peer support group meeting, I mentioned that I might have had lupus long before I was diagnosed.  Throughout my childhood I had several issues that were just kind of brushed aside and not paid much attention to.  For example, as a child I used to have chest pains quite often. The doctors always said it was just a pulled muscle, because of my sports and dance and such. Ummm, maybe it was pleurisy people. Also, I was very active, but when I ran it was quite painful for my ankles and feet.  I just thought I was slow and out of shape.  


When I got a bit older, like high school and my first year of college, I would sometimes have to stop dancing because of exhaustion.  I mean I just could not finish performances sometimes.  I would faint or come really close to it.  This even got me kicked off of the marching band pommerette team.  I would run out of practice because I felt so bad and I couldn't keep up.  I thought I just sucked.  Did I have lupus back then?  I probably did, but the doctors did not catch it.  They always put the symptoms off as something else.  


As an adult something finally brought the disease all the way out. Yeah thanks!! Now that I know all the symptoms and different ways to diagnose lupus, I think that I definitely had the lupus all along.  Lying dormant within this little girl, that had no idea what lupus was. 


It is important to take any change in your health seriously.  It may seem like nothing, but it could be very serious.  You have to take control and understand what is going on with your body. If your chest is hurting, it means that something is wrong.  You need to find out what it is.  It is not normal for you to have pain for months at a time.  Get it checked, and make the doctors figure it out.  Don't just believe what they tell you!!  They are "practicing", they do not know everything.  As my fellow lupus survivor told us "you have to be your own advocate"; he is absolutely right.  Get tested and checked out when your feeling "funny", it could save your life. :0)


With Love,

2 comments:

Petula said...

This is so true and I was just talking to my mother about this yesterday. With some of the Sjogren's disease symptoms like the dry mouth and eyes I've had that forever. I only drink water and have for years because I can never get my thirst quenched. Then my mother says, "Yea, as a child you always complained of aches and pains, but they could never find anything." Unfortunately, I probably was carrying that gene or whatever from the beginning along with the multiple myeloma. That in addition to the trauma of almost dying from my gall bladder situation, I think, brought on the fibromyalgia.

Simmi said...

Yes, the time that it takes to get diagnosed is just sad!!

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