I just thought I would post an update as I have had a few alerts regarding new posts since I wrote this.
My son is 8 now and we seem to be in a wax & wane situation regarding the severity of his tics. The Paediatric Consultant we had at Derriford left and went to Exeter hospital (I think) and a new one took over. Thankfully the new consultant is also going down the same route as his predecessor.
If you type p.a.n.d.a.s. syndrome into google ( full stops inc.), a whole lot of new research comes up
including a recent white paper (type in 'p.a.n.d.a.s. syndrome white paper) by Dr Swedo 15/02/12. There is also a site that I have used called pandasnetwork.org.
It is compelling reading suggesting that even peripheral contact with a strep b infection say in a classroom or social setting can trigger P.A.N.D.A.S. kids symptoms.
My son has never had a positive throat swab and the updated research doesn't say that a daily on-going penicillin dose is as effective as I was led to believe 3 years ago.
It is positive for us all that at least research is being done and that Dr''s presumably can't go on
disregarding the condition affecting our kids. The information is invaluable for printing off and handing to Teachers, cub/beaver leaders and Dr's because it explains why our kids are the way they are sometimes.
Our new consultant said that if my son is aware of any differences, or is teased, he just has to say, ' oh, that's just a tic I have sometimes, it's just part of who I am' which is a good way of putting it into perspective. He also put in writing to my G.P. & school that my son has no more chance of stopping the grunts, blinks & twists than he could a sneeze.
One thing I have noticed as a parent is that computer games, wii games etc.. and tiredness all greatly increase the severity of the tics and they increase at the end of the day when I believe fatigue sets in.
Like most parents on here, I am hoping that at around 13, the symptoms will disappear. I have hope because I found out that my cousins son had the same symptoms which disappeared as he grew up. A child of a cousin is a pretty tenuous relationship to imply a genetic link, however it was never diagnosed in this child and the similarities are very striking. Ask around within your family to see if you also have a tenuous link.
We have learned to cope, live with and ignore the symptoms as advised by our consultant. There was a much larger increase in Jan 2012 including regression where our 7 year old went back to baby programmes, poor writing and a total inability to imagine or be inspired to think about anything not there in front of him. The worst symptoms lasted approx. 2 weeks and as school noticed, we referred once again to the consultant. The tics gradually reduced but still haven't totally gone. Stress seems to trigger increases too inc. new school year, holidays, xmas and all the excitement and the lead up to birthdays.
1st diagnosis of this condition is very hard and scary, but as parents, we have to try and deal the hand we are dealt and I promise, it does get easier. It also means that we celebrate the good days and times and tolerate the bad as best we can. I am sorry if I can't answer your questions, but I am just a mum who's son has some weird condition that not many have heard of. We do cope as I am sure all parents of kids with P.a.n.d.a..s will learn to do as best they can.
I don't want to patronise, but at least it isn't life threatening and there are kids certainly a lot worse of than ours. Please keep strong and don't take no for an answer if someone is trying to palm you off.
Kindest regards to all of you.
Tracey