Guest guest Posted August 2, 2010 Report Share Posted August 2, 2010 , Talon's birthday was on the 31 st. It was my daughter that really wanted to do a small party. She loves to bake and wants to do it for him. We do not have a zoo or aquarium anywhere close by here...southern indiana in the middle of corn fields!!! We do have a rather large play system in the back yard so the cousins love to come here and play. My 2 year old loves it when they come too. I think Talon likes having them over but just not close to him. I hope to get the pics developed from it so we can talk about it and use them for social stories. Bless my mother in laws heart...she is here lying in bed with Talon and our 2 year old reading every book that Talon gives her and singing her grandma heart out. Talon loves for someone to sing him nursery rhymes and tho she would never sing out loud, she has begun to step outside her comfort zone and sing just because he loves it so. Happy Birthday to Dar too!!!! Hope he enjoyed his special day! It was HOT around here and HUMID!!! We love summer tho! kw To: From: rcjacobs4@... Date: Mon, 2 Aug 2010 02:57:50 +0000 Subject: Re: Can I please vent..if only for a moment...? Happy Birthday Talon! My son turned 14 also on July 26. When was Talon's. We went to the aquarium. I just planned something small. I was afraind to plan a party and disappoint myself when no one came to see Dar. His twin was away for their Birthday and normally everyone ignore's Dar at their party. He doesn't react so they stopped trying. I think I did good keeping it real. Making it Dar centered and NOT depressing myself. Mrs at Church always makes me smile. She does cards for everyone in the congregation on their Birthdays and she always gets my son a little toy too. I should message her reall quick because it really does make my day. > > > I cried as I read these 2 posts. I just sat here at the kitchen table to check my mail and now I have eyes full of tears that I am fighting back so no one sees me crying. I too have a son with DS/Autism. He turned 14 yesterday. We had a small party for him with a few of his cousins over. He did not attend the party but instead rode the golf cart with his grandma. He seemed to like having the kids around and would look at them playing on his swings and in the sandbox but he does not like to be around all the chaos and loud noises. My daughter (21) made gluten free brownies and put a candle in each one for all the children to blow out but Talon did not get a candle with fire. He did eat about 3 brownies. His grandma drove him all around the yard and would pull up to the party for brief periods. I should be used to this by now but it is still difficult. It is hard when he yells out and all the kids stop to stare......even his relatives. They are not mean to him but they do stop what they are doing and stare at him when he lets loose on a part growl and part howling sound. Anyhow, he did have a party and he had his bucket filled with various items he finds and then he carries it with him everywhere.....missing a phone charger??? go check Talon's bucket! Missing your belt???? go check the bucket. We try to laugh about it. He is walking around the house with one hose tubing from the nebulizer wrapped around his wrist and a whole ball of cords and chargers that he has found and somehow made a huge entangled ball out of. I am trying to focus on all the positives and be very thankful that he keeps bringing me his birthday cards and say " happy birthday " (you would not know what he is saying but we do.....very rough approximation of those words) and he claps and smiles so big. That is good and I am grateful. I think he wants another party. > I agree that getting used to the DS was difficult but then when he quit speaking and regressed into this world they call autism, I was devastated...... > > > > To: > From: amybanta@... > Date: Sun, 1 Aug 2010 13:48:19 -0400 > Subject: RE: Can I please vent..if only for a moment...? > > > > > > > Hi Jenn, > > I was the one complaining about not being able to travel. Trust me, that is > not really the major thing I am concerned about! When things get bad, and > they are pretty much always bad around here I start thinking about what > could have been. After Quinn was born I pictured myself as a retiree > traveling the world with my grown son who had DS. He would be a happy > comfortable young man who could mostly take care of himself and was just a > little slower a little different. That sure isn't ever going to happen, it > is only one of many things that is never going to happen. And if we want to > talk about not fair, I am a mother of two.Quinn has DS/ASD and obviously > something else since he is so far behind even the kids on this group; > is two years younger than Quinn he has ASD. is four years old and > can't speak in complete sentences. I have to prompt him to say " Hi Mommy " , > he has lots of other issues too but he isn't even the child I worry about! > In my ridiculous little world is a rockstar, he can do so much more > than his brother that I think every word he says is amazing. I know it is > crazy, but that is how I have to look at things to survive. I have also > stopped going to our local DS group events. Not only is Quinn so unlike > their children, but they all had babies around when was born and they > of course are all fine. I feel completely isolated as the mom of two kids > with special needs, I know that even the parents of much more severely > disabled kids feel sorry for me, because of course they only have the one > child. If I hear one more person tell me " Oh my, you have your hands full " > I am going to scream. > > So please understand if I feel the need to look forward to going to Europe > someday in the far far future. My life is very difficult right now. All > our lives are very difficult right now. We all need to do what we can to > get through it. Personally, I feel more comfortable knowing that if I need > it there are group homes for Quinn to live in when he grows up. When I > start panicking I remind myself that if it gets to be too much there are > options, I may never use those options but it makes me feel better knowing > they are there. > > I am not writing this to be mean and I hope it didn't come off that way. I > just want you to have all the information before you judge me again and I > want you to know that you are not alone in feeling that it isn't fair. It > really isn't. Most of all I want you to focus on your other three children > and truly appreciate how lucky you are to have them. When it comes right > down to it we are also lucky to have our extra special extra challenging > children, it is just harder to see that sometimes when things get so hard. > > Amy > > _____ > > From: [mailto: ] On Behalf > Of Jenn > Sent: Sunday, August 01, 2010 3:28 AM > To: > Subject: Can I please vent..if only for a moment...? > > I sincerely hope I do not offend anyone with what I NEED to say, but I hope > that you all may at one time or another been there and know that there are > days when we just feel hopeless, tired, and alone. > I am fairly new to the group and I had come across someones post > " complaining " about not being able to travel, etc. I'd like to first > apolgize to that person for my judging them (personally, in the privacy of > my own home, but never the less still judging them.) > I truly believe that we have all been there...thinking of our futures, of > what could have been or may be, > A few weeek ago when I joined I told everyone that I am a mother of 4. The > second born, who is 7 is our precious boy with ds. I was 24 when was > conceived. 25 when he was born. I knew about when I was 5 months > pregnant. I was scared, I didnt know much if anything about ds or any other > condition. As a lot of us think...it will never happen to me. Out of sight, > out of mind. > However, coming from a christian background and a divorced family I have > always been a fighter. Looking at the positive things in life and nurturing > that. > After a few days of self pity, I started researching everything and anything > to do with ds. I read EVERY available book in the library, made calls, > connections, etc. I felt prepared and ready to help my child achieve his > potential. After all, I thought, they are known to be caring and loving. > After he was born I was determined to get him into all therapies, prgrams > available. I joined local parent gropus, attended seminars and seeked out > the local pediatrician known to deal with special needs children with a > compassionate attitude. > But,...things changed. My once smiling caring, giggling toddler was gone. > His sparkling eyes now tend to just stare out in space...I felt/feel grief > for my little boy. Dont get me wrong, I do not love him any less. If > anything I love him that much more, but I cant help but feel " cheated " . I > accepted the ds diagnosis. I was positive and dreamt of his bright future, I > did not however, think this would happen, > It has been a year since his dx, but it still hurts. I still feel alone and > feel that I need to do more to help him. I am still a member of our local ds > group. They just sent me a link of pics from the ds meeting they attended in > Orlando. As I browsed the 200+ ics posted I first smiled seeing their > participation, but the smiles turned to tears...thinking to myself, " its not > fair " , " thats what I thought it would be like. I expected delays but I also > expected him to be part of a special group, one who he could bond and feel a > part of. I dod not expect him to prefer to be alone in his dark closet > rather than playing with his sibligs. I did not expect to miss his smile and > warm eyes, the connection.... > What is hard is not being able to voice me feelings with anyone, Rather > keeping them bottled pretending to be strong only to crumble into sobs at > night when everyone is asleep. This is when I think, :its not fair " \ > Thanks to all who read this. Sorry it was so long but if I cant talk, themn > at least I write...I need to just....sigh and let it ou. > Good night to all and God bless.... > Jenn > > Quote Link to comment Share on other sites More sharing options...
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