If you are on Social Media at all, then you have seen the multitudes of posts about PANS PANDAS Awareness Day today.  Some posts have just the facts. Some posts are personal.  NEPANS is made up of both professionals working and those who are parents to with children with PANS and so we try to cover both points of view. I myself am a Mom who wants to support families and help provide resources to professionals so little kids like my own are helped quickly and thoroughly.  Below is a short view into what it was like when our son first had PANS symptoms. It is not the full story. But a glimpse into our life with PANS. After you are done, please share at least one of the resources on this website.  Awareness really does spread one person at a time. It was one person that told me to look into PANDAS. You never know who you can help by sharing what you know. And last but not least, tomorrow might not officially be PANS Awareness Day but the sharing should not stop. Thank you for help. Thank you for reading.

Best,
Gabriella True, NEPANS Board President

The month of August has always been a month of celebrations, trips, parties, and friends.  August 2009 was no different – A trip to Camden Yards, a visit with the Orioles in their clubhouse, a meet and greet on the field with Red Sox, a game of wiffle ball with Orioles mascot on field in front of fans, a camping trip with friends, a deep sea fishing trip, an amazing party with friends, family, and new neighbors.  I always had friends laughing and hanging without any anxiety.  I was excited for school, alert, outgoing, and absolutely no behavior issues or anxiety.   

September 2009 - I missed the first week of school because I had strep throat and an ear infection.

October 2009 – I had H1N1 and was quarantined – it was very scary.

November 2009 – I was required to get the H1N1 vaccine to return to school.

December 2009 – Symptoms started to appear.  Gazed look, large pupils, blank stare, no expression, pale coloring, puffiness, sleepiness, anxiety.

February 2010 –  After my first Grand Mal Seizure - The beginning of tests.  EEG, CAT Scans, MRI, Spinal Tap.

During the summer of 2009, after divorcing my husband, my son and I moved into our new home.  Shortly thereafter we experienced many losses, including his 19-year-old babysitter and “big brother” to a car accident and his 21-year-old cousin to cancer.   My son was already in therapy to help get thru the divorce and move. According to his therapist he was engaged and accepted the losses. 
 
The Day it all Started
Suddenly in February 2010, during school vacation, life significantly changed.  TJ was attending zoo camp as he had several times previously.  When I picked him up on Thursday, the counselor who had known TJ since he was two, pulled me aside and said he acted very strangely in camp today. He was withdrawn, hid under the table, wouldn’t eat, and wasn’t his usual happy go lucky kid; she was very concerned.  I explained that he was going through a lot and maybe it finally caught up with him. His grandmother watched him that night while I worked. At 8:00, she called me very concerned and asked me to come home right away, “Something was wrong with TJ”.    TJ had cornered himself in a fetal position, soiled himself and was violently jerking. It was very scary.  Friday, my good friend agreed to watch TJ while I had some appointments.  He told me that he thought TJ maybe having seizures; he jerked all morning and wouldn’t eat or get off the couch. 

My Son Bradley was born in 1998 with Down Syndrome. He was and still is everyone's special boy. He has made amazing strides in life and continues to amaze us today. He verbal skills are very limited so he could never tell me when he was sick. It was very difficult figure him out sometimes. 
 
Sudden Onset OCD and TICS
Back In 2007, when he was nine years old, things changed suddenly. He developed behavioral issues, OCD and Tic disorder. Because of his disability, the psychiatrist would blame his Down Syndrome instead of looking further to find the root cause. As a parent you are desperate to help your child with these issues. We decided to try anti-psychotic medications. However, things got worse over time so in 2011 we decided to change doctors because I was tired of all the horrible medications and side effects. We started seeing a pediatric neurologist when he was 13 years old. He was still going to school but we were noticing more sporadic meltdowns and aggression, more panic and tics, The Neurologist diagnosed him with ADHD, OCD, ODD, IED, with possible Tourette Syndrome, GAD, and Panic Disorder. One thing we pointed out to the Neurologist was he had been treated with numerous antibiotics for different surgeries and infections mainly in his sinuses and ears and after those rounds of antibiotics he had wonderful behavior so much so it was like he was a different child. She looked at me like I had two heads and I was the crazy one.