Guest guest Posted February 22, 2004 Report Share Posted February 22, 2004 Hi all, Glad to find this group.........My dh and I live in PA with our dd, Abbey, age 12. We have another dd who is currently serving in the US Air Force, stationed in Guam... Our dd, Abbey is diagnosed with PDD-NOS. She also has mild MR. Last School year we decided to enroll her in a virtual charter school here in PA. This has worked out for the most part. She is involved in many social activites and enjoys these alot. Currently they are mostly with other special needs children. The gap has really expanded between her and her typical peers. In Pittsburgh, as everywhere I suppose, girls in the spectrum are hard to come by. I look forward to hearing all your experiences and sharing information. Lynn in PA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2004 Report Share Posted February 23, 2004 Lynn, welcome to the group-glad that you found us! My name is Pennie and my daughter is Abby too She is 6 years old. She is very much an Aspergers kid. She also has Sensory Intergration and Epilepsy. We are from Michigan. Pennie Abby's Mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2008 Report Share Posted September 30, 2008 Hi Bo! Welcome to the group,,, hope you will find the support you are looking for, we're a group with world wide members,, please feel free to ask any question you might have and we'll try to help you find the answer hugsJackie Subject: New member introTo: Hepatitis_C_Central Date: Tuesday, September 30, 2008, 11:20 AM I am a 53 yr old SWM in W TN,non responder in good health still,I have psorosis but can't tell it from the way I feel.I have had this for about 30 yr's known about it for 4.My nickname is is Bo.I was bo in 1956 a long time before dukes of hazard lol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 2, 2008 Report Share Posted October 2, 2008 well we are here for you now Bo,, dont ever forget that!Jackie Subject: New member introTo: Hepatitis_C_Central Date: Wednesday, October 1, 2008, 10:44 AM Hello everyone,My name is bo(nickname yes but gone by that since birth)SWM 53 had this for 30 yr's,non responder(Could tolerate only 6 wks of tretment)I have psorisis but I feel normal.I work full time.I have 2 teenagers still at home.It did cost me my marriage my ex freaked out more than me so I can identify with the fear.Now after 4 yr's I'm just caosting along.I've watched my friends who don't have this disease run into problems a lot worse than mine,so now I'm just glad that this is all I've got to deal with.I will say that I wish I had been a member of this group before I started treatment and failed,I think it would have made a diffrence(BO Quote Link to comment Share on other sites More sharing options...
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