I'm 7 years old. I'm going into 2nd grade. I love to read,draw and make up games to play. I have 6 pets. A dog,two cats and 3 fish. I also have a brother.
One day my feet got swollen and they hurt really bad and they had spots on them. I didn't know why. We went to the doctor and she told us to go the hospital and they did some tests and then they said I had HSP. I didn't know what that was. One day after that my stomach started to hurt very badly. It would not stop. I threw up a lot! And I had to go to the hospital. I have had to go there 7 times. Not counting the blood tests.
I met a friend at the hospital named Shaun. He's very nice. We got to meet the Falcons together. He is funny. He has Cystic Fibrosis.
It hurt because I had to get so many blood tests at the hospital and IV's. I had to get a PICC line. It's a line that goes to your heart to give you medicine. It's like an IV that stays in my arm all the time. The good thing about getting a PICC line is that I don't have to have a needle when I get blood tests. I don't have to take yucky medicine when I have it because it goes through my PICC line. I had to get it taken out a little while ago.
I don't like HSP and I don't like my steroids. It makes me tired sometimes. I would like to stay up later, but mom says I have to listen to my body cause I'm sick. The steroids make me have a special diet and a bigger appetite. Sometimes I get headaches because of the steroids. I have to take SO MANY medicines. I can still run and play and I can do everything I usually do. My cheeks are puffy because of the steroids.
If you have HSP and you want to talk, just post on here and I will email you back.
