My daughter is 12 years old and was diagnosed with Tourette Syndrome when she was 5.\u00a0Despite being a psychologist, I did not recognize her symptoms as TS initially, and even after the diagnosis was terrified.\u00a0 I have since learned quite a bit about Tourette and am much more at peace with it.<\/p>\n
Then, at age 7, my daughter was diagnosed with OCD.\u00a0The OCD has become increasingly more of an issue than the tics from the Tourette.\u00a0 Despite being an A-plus student, my daughter struggles with intrusive thoughts and had much difficulty adjusting to middle school this year.<\/p>\n
Things are gradually improving now that she is on medication and has been receiving much support and accommodations from her school.\u00a0My daughter “graduated” from the Tourette Syndrome program at Rutgers University\u00a0after participating for one year in therapy for Exposure\/Response Prevention at age 8.\u00a0 She continues in Cognitive Behavioral Therapy (CBT) today.<\/p>\n
My younger son has been exhibiting more tics over the past year, although they seem to be primarily motor tics and are less severe.\u00a0I don’t believe he would meet the criteria for TS at this point, but surely he manifests some form of tic disorder.\u00a0 Nonetheless, we are keeping our eyes open.<\/p>\n
My son and I were at the Patriots game this past Sunday for Tourette Syndrome Awareness Day and saw the TS ceremonies before the game.\u00a0 I sought information at the NJCTS <\/a><\/strong>table at the stadium during the game, as well as purchased bracelets for both of my children.<\/p>\n I was impressed by the supportive connection I witnessed among the girls on the field after the ceremony.\u00a0I would love for my daughter to have a chance at that kind of support.\u00a0 I am looking into participating in Camp Bernie<\/a><\/strong> from June 8-10.\u00a0And I hope that I can both receive and contribute support to other parents of children with TS via this blog.<\/p>\n