Logan's Journey

Ok, so I know I promised updates more regularly and I am already slacking but hopefully you will all forgive me!  :) We had some good news recently and I wanted to share it with you all...as I may have mentioned, the doctors believe that ideally Logan should be having professional therapy almost daily with a mixture of physical, occupational and speech.  My insurance however only allows us to have 20 a year and even then we are still responsible for the $50 copay.  This was making it difficult to really get all of the therapy in place that can help Logan make the most progress. There is a program called Katie Beckett that actually allows you to apply for Medicaid for a child with disabilities even if the parents do not qualify for it based on income.  I had to fill out / put together about 350 pages of documentation about Logan's condition, get it signed from multiple doctors and deliver everything in a perfect packet to the Katie Beckett offices.  This was quite an underta

Happy Boy!! First I want to say I am sorry it has been so long since my last update but I am going to try to find the time (somewhere between working full time, the doctors appts and traveling to see clients) to keep you all updated on Logan's Journey, as it is quite a unique one.  I have realized that this journey can be very lonely at times and that is my doing by not sharing as much as I could but hoping that this might be an outlet to get our story out there to the friends and family that love us so much and possibly anyone else going through the same thing.   My first birthday...the cake was more fun to smash than eat!! Anyways, so I guess I have a lot to update everyone on, so bare with me on this first post!  :)  Ever since the Infantile Spasms stopped in July, Logan has been seizure free...WOOHOO!!  He takes seizure medication twice a day to keep them at bay but from what we are able to tell they have stopped which is great news.  Since getting past the spasm