By Teresa Conrick
Teresa Conrick is a Contributing Editor to Age of Autism.
March 2, 2011
Two years ago, I wrote about my beautiful, vaccine-injured child, Megan, turning 16. March 2nd marks her 18th birthday and boy, has she gotten some horrible gifts! The Supreme Court of our United States declared on February 22nd, (HERE), that she would be unable – EVER – to receive compensation for her childhood vaccine injuries that have detoured her from a healthy, and pain-free life. Her vaccine injuries happened 16 years ago, yet we were never told by any of the professionals back then that autism symptoms can be medically related to brain, gut or mitochondrial injury from vaccines. We are unable to go to those companies who made her vaccines and prove, to a judge and jury, that they were dangerous to her and injured her into “autism.”
Now some false autism advocates will try to convince you that autism “just happens”, that it’s “just genetic”, that “we are better at diagnosing it”, or that it’s such an intense diagnosis that “parents WANT to get their child labeled” for all of the perks and benefits. PERKS & BENEFITS? What a crock! How about this perk- severe medical issues, many of which continue to be ignored or dismissed by the US Medical Establishment.
So back to Megan — innocent, injured, nonverbal, and now ….. seizures. In August, Megan had a seizure, first in 2 years. She had an initial one back after her 16th birthday and we tested, consulted and waited as her EEG showed no seizure activity. Two years, nothing, thankfully, until this past August of her 17th year. Now like many of the symptoms of autism and many of Megan’s medical symptoms, nothing is NORMAL and there always seems to be a puzzle piece begging to be solved. She had that seizure on August 22nd, then the next on September 27th, then October 24th, November 23rd, December 25th, January 27th and now yesterday, February 28th. Do you see the pattern? First, I have to say how thankful that these are a monthly experience as SO many children have numerous, daily and even hourly seizures. They are though of the grand mal/tonic clonic type and so we did initially have her neurologist recommend and start her on anti-seizure medication. She was on this for much of this time while the monthly seizures were not stopped and instead she began to have erratic and concerning behaviors AND also develop a BAD RASH. That was a huge concern and we had to stop the medication, which had unfortunately shown no benefit for her anyway.