Roberts Family
I started searching for PANDAS specialists, only to find there were 3 in the state of Georgia and 2 of them were not taking new patients. Only 1 was taking new patients, but they did not accept insurance.
I started searching for PANDAS specialists, only to find there were 3 in the state of Georgia and 2 of them were not taking new patients. Only 1 was taking new patients, but they did not accept insurance.
Unfamiliar with PANDAS… I had no idea there was a possible connection between his strep and his OCD symptoms. Upon our return, we finished up his antibiotic and within days he was exhibiting his OCD behaviors again.
In spring 2014, our family underwent a massive change. We had no idea what was happening, how it was happening or why it was happening. All we knew was that our beautiful, smiling, playful, energetic and affectionate, loving son had morphed into a child who could not walk out our front door, communicate with us or even eat a simple meal.
It’s one thing to have three physically sick kids, it’s another level to add the stressful neuropsychiatric symptoms of PANDAS/PANS. The financial burden . . . led us to file bankruptcy. For us, the financial burden is times three.
Georgia lacks doctors who understand PANDAS and can treat it. We had to travel to NJ, NC and IL to find PANDAS doctors who confirmed the diagnosis.
In seven years, we spent $280,000 on schools, doctor and psychology visits, medicines, tonsillectomy and IVIG treatments that would have been unnecessary had my son been correctly diagnosed.
In the next year, new and more severe OCD symptoms and tics emerged. An integrative doctor gave a rapid strep test and said it’s not PANDAS. We now know blood work is necessary to show heightened strep titers.
We are trying to beat this dreadful disorder. I figured out that when he is aggressive, loud and out of control, his body is being attacked by a virus causing inflammation in his brain.
If we had a pediatrician who was knowledgeable about PANS/PANDAS, we could have treated him sooner. My son suffered for two years because of the medical community’s ignorance to this dreadful disorder.