Lindsay was born on the morning
of August 14, 1991 in Rockford, Illinois. She was the typical child who enjoyed swimming
and being with her friends. Lindsay took dancing lessons and performed in dance recitals.
She was looking forward to learning to ride a "two-wheeler" bicycle, losing her
first baby tooth and starting first grade.
During late fall of 1994, Lindsay
complained of her head hurting and started to exhibit easy bruising. After having a sample
of bone marrow taken in December 1994, leukemia was ruled out and Lindsay was diagnosed
with Aplastic Anemia.
Aplastic Anemia is a condition where a
persons body does not produce enough blood cells. Low red blood cells will prevent
the body from getting enough oxygen, low white cells allows infection easier, and low
platelets allow the body to bruise or bleed easier.
After several monthly blood samples and
semi-annual bone marrow biopsies,
Lindsays blood and bone marrow showed a sudden decrease. In
July 1997, Lindsays diagnosis was changed to Myelodysplastic Syndrome, or MDS. MDS
is a condition where the body all but stops making blood.
Lindsays options for treatment of MDS were
either a bone marrow transplant, or chemotherapy in hope of restarting her blood
production. Chemotherapy was the option and Lindsay started treatments in July 1997.
Lindsay breezed through her chemotherapy treatments, but had trouble fighting off
infections. After chemotherapy, her body no longer had white blood cells to fight
infections, so Lindsay received antibiotics on a regular basis.
Lindsay lost the battle to
infection on a stormy evening, September 17, 1997.
Towards the end, the only thing that Lindsay
wanted was to "get better," which is the desire of all children who endure this
very difficult treatment. A memorial fund has been established in Lindsays name to
support the expense of blood and bone marrow donations, in the hope of helping all
children get better.