Jaal Posted June 26, 2013 Report Share Posted June 26, 2013 Ds7 is 7 weeks post ivig. Interesting pattern...1st week he was actually very good....the following 3 weeks very bad (tics, behavior, sensory). The last few weeks he is only exhibiting symptoms he had when he was 4-5 years old (lots of sensory and OCD, no tics or fire (our name for excess energy and movement). I have read some posts that said Dr. K refers to this as peeling back the layers. Has anyone else experienced this or read about it? Link to comment Share on other sites More sharing options...
nicklemama Posted June 26, 2013 Report Share Posted June 26, 2013 Yes we've experienced this.....twice. It's a typical post IVIG reaction for my son. Slowly, the symptoms/behaviors fade away. Link to comment Share on other sites More sharing options...
norcalmom Posted June 26, 2013 Report Share Posted June 26, 2013 In Brain on Fire, a book about a young woman with NMDA encephalitis ( where rouge antibodies to a specific receptor on neuronal tissue get through the BBB and attack the brain- usually after an illness and sometimes assiciared with ovarian cancer) the doctor and author describe "getting better in reverse order if symptoms". I like Dr Ks - turning back the pages annalogy better! And- this disorder is also treated with IVIG. Many similarities to pandas. EAMom 1 Link to comment Share on other sites More sharing options...
Mary M Posted June 29, 2013 Report Share Posted June 29, 2013 This was very much our experience. It can be painful to relive the symptoms...however, it is reassuring to know that the IVIg is working. Link to comment Share on other sites More sharing options...
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