This past Monday I took Harvard to his first occupational therapy evaluation. I wasn't surprised I kind of could see the news coming. As any parent you want what's best for your child you don't want them to experience hurt or shame because they learn differently.The therapist suggested Harvard might have slight Hypotonia and low muscle tone. The therapist suggested he needs a hearing check also the therapist said he shows signs of development of a 9 month old by not speaking or walking he's not able to stack cups or place wood squares in a bowl just throws them down on the ground.The last suggestion the therapist recommends that Harvard go to a Developmental Pediatrician up to when he's 18 years old. Part of me feels torn for my precious boy . I asked myself Did I do this? Did the hospital Do this? Could it be from him rolling of the couch ? Is it from when my husband wouldn't let me give him formula when I wasn't producing enough breast milk ? Am I stunting his growth? Am I not letting him do things on his own? When I got home I just broke down sobbed held my son in my arms and sobbed some more . My dreams for Harvey were crushed I wanted and hoped he'd be able to go to Harvard University to study Harvard Law I wanted the best for him I still do Harvard deserves the best care for whatever he's got has or can work through. I hope this can be manageable possibly he can outgrow but it could just be wishful thinking .I just wish he wouldn't have to go through what I went through from knowing my learning adversities. Maybe this doesn't have anything to do about me but something bigger all on its own.The "Hurt & Mad" side of me would like to blame the hospital for not calling the doctor when they should of but hours later fully dilated 10 cm no baby coming out his nose hooked on my Pelvis Bone finally they made the call . Harvard wasn't breathing when he came out from the c-section. Harvard could be brain damaged from lack of oxygen for who knows how long . The "What If" side of me wonders did I pass this on to my son do I carry a faulty gene central nervous system due to a faulty hereditary gene? Could Harvey be brain damaged from rolling of the couch 7 or so times? I feel horrible. I just want Harvey to be okay !! I know this is in God's hands and that its going to be okay. I still think deep down maybe it's because I need to interact with him more maybe he doesn't get enough. If that's the case I feel ashamed again. I know he's getting help and I am grateful he is. I wish I could take this away I want to know what I can do to fix it. I am going to remain strong even if part of me is sad, mad,and hurt. Last thing, Harvey is a extremely happy baby which sweetens the future obstacles and heavy loads we will face together. I have joy that my son is extremely happy despite everything going on. I find I am lucky than most parents.
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