Casey Ryan Fero died in his sleep in
		the early morning hours of July 4th, 2005. He was 23 years
		old. I explained his Chronic Fatigue Syndrome history to the coroner,
		but she said it “wouldn’t make any difference.” She collected a bag of
		supplements and assumed that Casey’s death was from steroid use.  Casey
		did not use steroids. Samples sent to a toxicology lab specializing in
		substance and steroid abuse, showed all negative results.
		In September, a Madison
		forensic pathologist determined that Casey had Viral Myocarditis, that
		is, viral infection of the heart muscle. His heart tissue showed
		fibrosis indicating past infection. 
		I want people to know that
		life was good for Casey when he died.  He was proud of his recently
		awarded Associate degree. So typically Casey, he had no idea if he
		graduated, was afraid that he did not and only called the school
		counselor because we insisted. Yes, he graduated with one credit to
		spare! In addition, the last semester, he made the Dean’s list. Casey
		burst out of the chair and in a joy filled rant; he talked about getting
		his Bachelors degree and maybe even a Masters.  (He planned to major in
		history, his great love and sports science, a second love.) Then he
		said, “Let’s order Chinese,” A third love…
		
		Casey was diagnosed
		with CFS at age 9 and again at age 15. It caused him to feel weak,
		unable to think, and exhausted. He was plagued with headaches, stomach
		problems, and had major sleep disorder among a list of daily symptoms. 
		Casey persevered and did not want people to know his condition. Early
		on, he knew that medical help was unavailable and furthermore, he was
		met with disbelief in the school and in the doctor’s office.  
		
		Casey’s
		diary – mom’s journal of Casey’s day is a testament to loss of
		childhood. As parents, we created every opportunity we could for Casey.
		We loved him unconditionally and worked for years at helping him
		maintain self esteem though this illness. However, when a child’s
		basic needs are not met ,parents are powerless.      
CFS is a brutal
		illness for children.  
		Casey
		was a remarkable child and a wonderful young man.