Showing posts with label Chucky. Show all posts
Showing posts with label Chucky. Show all posts

Tuesday, February 22, 2011

Mornings

2/22/2011 0 Comments
Mornings can be really tough. There are days that Chucky is easy to get ready for school and then there are the days he is not cooperating. Days in which he won't take a shower or get dressed. How do I deal with these mornings? I am actually curious how you deal with rough mornings. I think it is a method of survival for us moms. I have had to accept the fact that my coffee is usually going to be cold before I finish the cup and I should probably put pants on under my robe so that I can run to the bus without forever tainting the poor children's minds with my legs.

I must admit that the television is a wonderful help in the mornings. He has a set morning routine and it includes some TV time. Chucky never used to watch TV and I loved that, but I can say that it does help to motivate him. I allow the TV on when he first wakes and he can watch it for about 15 min before I have to start getting him ready. Then it is time to shower and we have to struggle with all of the sensory overload induced during this task. There are days he loves the shower and there are days even the sound of the shower is overwhelming for him. I remember when he refused to shower because he referred to it as mosquitoes biting him. Now he just tells me it is too loud. If anyone figures out how to turn the volume of the shower down, please let me in on that!

After he takes a shower we have to deal with the cold feeling he gets when he steps out of the shower. We won't even discuss the meltdown that occurs when the rug on the floor gets wet. He then refuses to get dressed because he is cold. Umm... last I knew, putting clothes on when you are cold, makes you warm. So, he runs into the living room where I chase him down and dry him off. Then we fight to get him dressed. At times he will put his underwear and shirt on. Pants are still a little tough for him but he has done it on his own on occasion. It is a major improvement to where we were last year.

After getting dressed we make breakfast which goes really smooth, once he decides what he wants to eat. The little booger will eat the same thing for a week and expect that food until one day he doesn't want to touch it anymore. Then I have to figure out what he wants to eat. LOL.... This is where it gets tricky because unfortunately I did not get ESP when I had him and therefore I cannot read his mind. Sometimes it is easy and then there are times it is trying. So he finally eats and we wait for the bus. Whew... what a busy morning. How do yours go? What makes it easier or harder?
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Tuesday, February 8, 2011

Traveling Crocodile Companian

2/08/2011 0 Comments
My son Chucky has a Facebook page, where he has met many other children with Autism. The page is written and monitored by me. The whole thing started because my page had become all about him and advocating for him. I wanted my space back. I know that is selfish right? I don't care!! Every bit of my world revolves around my children and I wanted something of my own. So, his Facebook emerged.

Basically it is a page where people who were interested in knowing how he was doing and noting milestones could see them. No one can search for him. They can only request him through a friend of his's page. I am very selective about who I accept. My son loves his page. He enjoys reading everyone's comments to him and he really enjoys seeing the pictures of children that are like him. He has made a couple very close friends. This has given him some socialization. He wants to talk to his friends on the computer and he looks to see what is going on.

It is also wonderful for me. I can talk to other Mom's who understand. They know what I am going through and can give me reasonable solutions that they have tried with their angels. Well, I am not writing to justify my son having a Facebook page because I don't really care what anyone else thinks about it. I am not trying to be rude either just honest. My son met a little boy Jake on his page and has been communicating through pictures and their diaries for about six months now. Jake's mom and I are sure to read the comments to them and show them the pictures as well. We also have mail correspondence.

The other day Jake's mom and I had discussed sending a crocodile to stay in Australia for a month and during this month they would take pics of him in Australia. The thought is that after the month it would then travel to another special needs home with a note and spend a month there as well. They would also take pictures and post them either on a blog, Flickr or Facebook. Everyone's pictures would be on one site and added to by the carer of Mr. Crocodile.

My only thought about this is that he might get lost. What if it goes to someone who cannot send it forward? Does anyone have any thoughts or think they would like to join us in our adventure? I think it would be awesome to join our special needs children together in a special way. What do you think? Do you want to have special time with Mr. Crocodile?
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Sunday, January 30, 2011

Emergency Meltdown Kit

1/30/2011 0 Comments
My son is having serious meltdowns. It is so hard to just sit there through them seeing him so upset. This all gets harder when he is flailing his arms and screaming in my face. I start losing my patience and feeling overwhelmed. Anyone else feel like this? I think I have the solution. It may differ for different children but hey, it is a thought.

I think I am going to make a kit just for meltdowns.This kit will include some damage control, first aid, armor for me, and calming things for him. It just might work. You might ask how I came up with this idea and so I am going to tell you. Chucky had another meltdown today. It was really bad although I didn't get slapped today just kicked a little. Then I took a deep breathe and sat back. Every so often in a calm voice I said,"When you calm down we can talk" Eventualy after a lot of screaming and kicking, he calmed long enough for me to suggest an alternative calming tool. This worked wonders. Now I will share with you exactly what my son found so calming along with the other items I wish to include in my kit. 

  1. Bullion Cubes- It doesn't matter what flavor, they are pretty much harmless. But, if your child like to build they are amazing. I don't cook with them but instead I buy them for my son's fine motor development. He can stack them, unwrap them, build with them.. ect. They work wonders and when I really need him to take a breather I know I can rely on the trusty bullion cubes. 
  2. Comfy Stuffed Animal or Pillow- My son finds it soothing to have a comfy when he is upset so this might be something good to keep in the kit.
  3. Mouth Guard- to protect my teeth from those terrible blows to the mouth.
  4. Drum Set- This worked wonders. It was a perfect defuser. He got to hit something but not a person and he loved the reaction sounds. 
  5. A Padded Suit - This is to protect my skin from all the bruises that I am constantly getting. 
  6. Bandaids - Just in case we need one 
  7. Ice- most times after a serious melt one of us needs this
  8. Music - to calm him 
My son said this was his sister Chipmunk and him jumping on a trampoline.
The pile to the side is dirt he says. This is one of his creations after a meltdown.

I think this completes my list of items I shall include in my emergency kit. I am not so sure how to fit a drum set in a kit but I am welcome to any suggestions. Do you think an Emergency Kit would help you? What would you put in yours? 






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Meltdown Disruptions

1/30/2011 0 Comments
Cute ChuckyImage by ibtrav via Flickr Well, it has been a really rough week.. wait I meant month but I think today was the worst day all month. Chipmunk isn't feeling well, her belly hurt all day. I made her a warm bath and told her to relax for a little while and see if she felt any better.

I was talking to her for a little while when Chucky,started screaming my name. Which seems to have never ended since he woke up. I tried to ask him what he wanted he just kept screaming Jocelyn. So, I let him go into the bathroom but told him he had to stand near the door because his sister needed privacy. I figured this way he could speak to her and get what he needed. That didn't happen. This led to a screaming child in the bathroom with sick daughter in the tub. Did I mention that the bathroom echoes so we     hear this rant twice. Boy am I lucky.

 I asked him what he needed and got screamed at some more. Being as there was no consoling him, and he was winding up and flailing I decided to remove him from the bathroom. Did I mention there was a sick child in the tub? Well, removing him was not an easy task. AT ALL!!! He grabbed onto the door, shoved it closed almost catching my fingers and was kicking me. I really couldn't calm him down and he over powering me. It is at times like this that I feel completely helpless. I was overwhelmed and exhausted. We were only 10 minutes into this meltdown. I asked my daughter to ask a friend to help. I only got him to the hallway, which isn't that far, and he threw himself down on the floor. Then it got really bad. I know how much worse can it get? Trust me a lot!!

He continued to scream and I sat on the floor trying to calm him. BAD idea. Actually I should have stayed as far away from him as I could. As I sat down I saw an angry ranting child and I think his eyes were red at the time, shoving the back of his head into my mouth. I bit my damn lip. Ouch!!  Oh, let me remind you again, There is a sick child in the tub!!! Unfortunately I was not with her and she is staying there. Hey, think about it... at least if she pukes, which we all know I can't handle, it's an easy clean up!!  After all the head butts, I decided to ask him how he was feeling. Some crazy person actually suggested trying to get your child to recognize their feelings when they are in this state. It is supposed to help them calm down. Ummm.... word of advice...IT DIDN'T WORK!!

This made him worse. He slapped him in the face 4 times and was kicking the shit out of me. I was stumped. Anytime I spoke to him it got worse but after hit three, I grabbed his arms. Then I said hitting is not ok. Charlie is feeling very angry. He was possessed, really. Have you ever seen The Exorcism of Emily Rose? That was what my son looked like. Just to clarify, he is a sweet boy and I love him so much, but he was seriously off the wall!! I could not calm him. I tried showing him what he could do when he was angry. Then as I sat helplessly in the hallway with my possesed son, I thought about what I could do to reach him. It was at that moment that I noticed a metal popcorn tin. Hmm... Drumming, hitting.... this might work. My friend is a musician so, he started drumming on the tin and singing a bit as well. My son was still screaming but after a minute he seemed to calm. It was enough to talk to him. Wow, there is an end to this!

He calmed enough during the drumming that we could take him into our roommates room where there was a full drumset. He was in there for almost an hour drumming away. It really did calm him. I asked him what he needed from his sister and he told me!! He just couldn't verbalize his needs at the time. He was frustrated. He needed an outlet!! So, I guess we should all own a drum set?? I can't afford one but, it worked this time. That was not the end, it did happen again later on in the day actually, my whole day was filled with meltdowns. The final one, I just gave in. He wanted his sister and he was worried about her. I think this was part of his anxiety and he didn't know how to cope with it.
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Tuesday, January 25, 2011

Please Duplicate Me

1/25/2011 0 Comments
Do you ever wonder if you are failing as a mom? Is it your fault your child is coming home with poor grades when you know she/he knows the work? I am having those thoughts and they are eating me alive. When I started this blog it was meant to provide some insight into the life of my whole family. How it is for all of my NT children to live with a child with Autism. How it affected my children's relationship with me and vice versa.

I mentioned in a previous post about how I felt conflicted. I felt like I couldn't comfort Chipmunk when she needed me and monitor Chucky during his meltdown. Chucky needed me there to ensure that he didn't hurt himself, but Chipmunk needed me there to comfort her. This is really challenging. Am I the only Mom who has this struggle? Well, you are probably wondering what prompted this post.

Today, Princess brought home a 66% on her science test. It was about simple machines and I am certain she understands them. She loves Science. It makes me wonder if she is just having a tough time because of how much of my time is devoted to her brother. I really try to help her with things but it is so hard. I am constantly interrupted and she gets frustrated. I do try and I am trying different approaches. I just am not sure if this is her way of protesting or a teenage issue. I want her to do well. I don't want to have our days filled with one problem after another. I want to be able to enjoy my daughter again.

I have tried to do things with her before she goes to bed at night. We have played her favorite game and sometimes we just sit and talk. Well, she talks cause I can't seem to get a word in edgewise. I think I mentioned this in my Talk-a- Holic post. Does anyone know if there is a talk-a-holic anonymous group? We even started taking photographs in the morning before her brother woke up. She really seemed to enjoy this and so did I. But, unfortunately I think with all of the recent snow days and such things got off track. I am going to try to start this again.

Honestly I think if she did as much listening as she did talking she might actually be able to do the work correctly. Sometimes I think that I am too hard on her, but most of the time she just isn't doing what I know she can do. It bothers me though that I don't have enough patience, arms, legs, mouths, hands, or ears to give equal attention to all of my children. I guess tonight I just feel inadequate. Inadequate as a mother. Incapable to do this job that is in front of me. Can anyone relate? The job of motherhood with multiple children is hard enough but when you add special needs children to the mix, I think it can become overwhelming and very very challenging.
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Saturday, January 22, 2011

A Little Resolve

1/22/2011 0 Comments
Well, to ease my frustration just a little the school board called. I am not entirely sure if this means anything but, we shall wait and see. I explained, yet again, what my concerns and issues were and they pacified listened to me while expressing their understanding my concerns. I had already written out my letter regarding the problems I was encountering. I still have decided to send the letter out. Due to all the snow issues it is going in the mail on Monday. Actually I think I will drop them off at the district office and request that they be stamped as received. I have kept copies of the scripts from the pediatrician and the letter to ensure that there is a paper trail.

The school board stated that they were sending an email to the OT at my son's school demanding that he receive therapy immediately which is a step forward. While the Occupational therapist has been taking some time for Buddy, and I told the board this, he is not receiving the therapy that his 504 plan entails. The lady I spoke with said she didn't care that the therapist was helping him, she wanted them to abide by his plan which would give him individualized one on one OT. This made me smile. I felt like maybe, and I may be leaping into the dark abyss, I was not fighting this alone. I think I may have someone backing me that has authority.

I also took the time to explain the custody agreement and how we make this Co- Parenting work. While Buddy's father is good at some things, when it comes to advocacy and school meetings, I am more aware and I deal with those issues. I am not saying that he isn't trying to be involved in those areas but he doesn't understand them. I might add that sometimes I feel as if I am really going easy on him and his lack of participation regarding this.

He himself was totally unaware of the school problems. You would think that Buddy's report card, that was NEVER mailed to me, would reflect these difficulties. The teacher stated that she spoke to him several times on the phone, but he does not remember this. I am now changing the way I deal with it all and while my day is overflowing with the responsibilities for my youngest son, I am now taking full responsibilities for my oldest son as well. This might seem confusing as it really has always been my job as his mother.

Buddy and Chipmunk live with their Dad due to some issues with my youngest's father. I wanted to bring them back to my home but with all the issues surrounding Chucky it just didn't seem fair. Chucky was very aggressive as he was entirely non-verbal , so we decided to maintain their schools in his district and have joint custody. Buddy would visit and leave my house with bruises and terrorized by his brother. This has seemed to work although I miss having my babies home with me all the time.  When the children lived with me, I was responsible for all school issues. He didn't attend the meetings and he was totally uninvolved with the early intervention Buddy was receiving. Thia didn't concern or bother me because they were always with me and it was quite evident what they needed. I assumed that because they lived primarily with me it was my sole responsibility to ensure their needs were met.

I think I got so caught up in Chucky's needs that are right in my face that I tried to allow Buddy's father to take some of the responsibility that I was always liable for.  I see now that that may not have been the best thing to do. When it comes down to it, I guess in a round about way I am responsible for the lack of communication with the school. I could have been calling them and pushing for his needs. Instead I was communicating with their father thinking that everything was fine, but knowing how poorly he is with any form of advocating. I miss being as involved as I was and I am going to change that. I have called my children's teachers and requested to speak to them. I will make this work for the better. I will turn this around. It is my hope that maybe through observation he may learn how to do this and pick up a few skills, but in the end, I have to advocate for my children. I have to ensure they get what they need.  I am MOM.
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Monday, January 17, 2011

Sleepless Nights in Cottekill

1/17/2011 0 Comments
Now I know that when you have a baby you expect to have sleep deprived nights but I didn't think they would last almost 4 years. Give me a break!! My son was waking all night and he was not wanting to play either. In fact he didn't want to be touched, flailed his arms and legs and screamed at the top of his lungs. He banged his head, punched anyone within range and bit. He was a demon child!!!! Not really but man it was way more than I ever dealt with. 

Finally after three and a half years of complete hell and many bruises later my boyfriend grabbed the video camera and started recording the extreme difficulties I was encountering with my son. This opened the doors for my online video diary that I started for my son in hopes to find support and answers. I got great feedback from fellow parents and even professionals that expressed genuine and deep concern for the situation. With that I also received comments that were hurtful and ignorant but I was bound and determined to help my son. If this was the path I had to walk down then so be it. 

After recording a three night torture session, I brought the video to the doctor's office. The doctor watched it and immediately attempted to put my son on medication and told me it was a temper tantrum. This was not the case. My son would wake up in complete rage. The fact is that my son was having Night Terrors, which is common for most toddlers but destined to last longer with children on the spectrum. Chucky was not producing the Melatonin in his system and therefore was not getting restful sleep. I left the office in complete shock and disgust at how quickly they were to medicate the child rather than troubleshoot what was going on. 

I spoke to more parents and even saw another doctor. This doctor stated that I should try Melatonin and to start off at a low dosage. We tried 1.5 mg but that didn't do anything for him then we upped it to 2.5 mg which helped him sleep but he was still awaking three to four times a night in distress. The doctor said 5 mg every night at 7:30 for a month and a half. For most children this would reset their system and then they don't need it. We did this religiously and I must admit that I was scared to stop it for fear of the torture sessions to return. Regardless of my fears I did not want my son to rely on anything to acquire sleep and so I stopped the Melatonin. I must confess that it didn't last long. I kept him off of it for three days and it was horrible. The doctor and I agreed that it was best to maintain the Melatonin continuously. 

He was finally sleeping better. He also showed behavioral changes during the day. Now, don't blow this out of proportion, he was far from an angel. But, he had less melt downs and seemed cheerier. It was nice to see him smile. I am not sure if the Night terrors were because of lack of sleep or if it was because of  dental issues that I was unaware of, but when I stopped it he was having sleep issues again so either way it helps him.

 He complained that his tooth hurt and I scheduled a dental appointment immediately. We saw three dentists that refuse to see him again and he was referred out to a specialist in Catskill. It is a far drive but the Greene Pediatric Dentistry, is amazing with him. He had a lot of dental issues. Six teeth got pulled and two of them were capped. It must sound like I am a horrible mom, but he doesn't eat a lot of candy and hasn't drank out of a bottle since he was a year old. The problem was that like many children with SPD,Sensory Processing Disorder, he could not tolerate the taste of the toothpaste or the feeling of the toothbrush. Brushing teeth always led to a major meltdown. These ended in me almost losing a finger and that was if I was lucky cause he might just take my whole hand off. LOL.. 

I found a wonderful toothpaste,Natural Toothpaste - Kids Orange Wow with Fluoride   that works for him and after all that dental work I think he is more attentive. I am not saying he likes it but he wants to keep his teeth. While he still requires a lot of strength and patience to brush his teeth, most of the time he really tries to do it himself. 

Well, boy this this post get totally off track. Umm... what were we talking about? Oh, I remember, Sleep or lack of!!! The reason for my sharing all of this with you is because I am not sure what has been up lately but he has not been sleeping. The other night I wanted to sit down and write and I have been so tired. I just wasn't able to do it. At first he was waking and coming downstairs to climb in my bed, which is better then when he was on his 3 am wake up call kick. He would awake at 3 am, I think he thought it was morning time, demanding chocolate milk with honey in it warmed up. He would drink it and then I would explain that it was still night time. If I was lucky he would go back to sleep. If not, well, it was a very long day. 

Anyways, he started waking up in the middle of the night and climbing into my bed. No big deal right? About three nights later he was stirring and crying intermittently. I went in and checked on him but when I spoke he flipped out. It was a flash of the past. He was flailing and screaming. There was no consoling. I wanted to hold him but he wouldn't let me touch him and the doctor said to put him in a safe spot and not to touch him. I did that and it was horrible to see him in this state again. I think it is so hard to see your child so upset and not be able to console them. My daughter approached with caution and sat on the side of the bed. Chipmunk is amazing with Chucky and can usually calm him very quickly. 

This didn't work either and he swung his arms at her face and hit her. He didn't hit her hard but it really hurt her feelings. She ran off crying and while I wanted to console her I needed to ensure that Chucky remained in a safe situation. She calmed down and I grabbed the iPad. I never figured out what was wrong but he put on some classical music and calmed himself. This is a first!!! About five minutes later he started crying that he had to go potty. Was all of that because he needed to go potty??? I am not sure but he still wouldn't let me touch him and when I did, to help him get his pants down, he cringed and moved away from my touch. Not only did he cringe but he screamed as if my touch was hurting him. My eyes were burning as I was fighting back the tears that wanted to stream down my face. I cant describe my feelings that night as they were so mixed and conflicted.

I was angry at Autism for attacking my son. I was hurt that he wouldn't let me console him. I was happy that he found a way to calm himself and I was feeling uncertain about how I could continue handling him while not neglecting my daughter's need for comfort. Finally I was scared. I am not sure why fear arrived but I think it is because of the uncertainty of what is wrong and the fear of the unknown or how much damage he will do. 

Since this incident he has been sleeping well again. The only other incident was actually kind of funny yet scary at the same time. I woke up and the back door was open. Ok, Did your heart drop to your feet yet? Mine did.  It was freezing in the house which means that it was open for a while. I checked for all my children and they were in their beds. Whew!! So, why was the door open?? When I went to get Chucky up for school, he had no undies on. I asked him why not and he said,"Me go Pee in snow when you sleep!!" OMG... this is funny as he went outside to pee but scary cause it was like 2 degrees outside and he could have wandered farther. Time to barricade the doors!! 

Thanks for listening to my rant and I hope I didn't stray too far off topic. LOL... It has been a long week!!
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Monday, January 10, 2011

The Opposite of Ignorance is Awareness

1/10/2011 0 Comments

Last night as I was doing a little grocery shopping with Chucky and Pumpkin at Hannaford a woman approached me asking about the device my son was playing with. I explained that it was an iPad that he got for Christmas . She asked what it did and inquired if they were for children. I told her that we use it to help him communicate and also to teach him. They are not just for children but many children use them. I did NOT mention that Chucky had Autism. It didn't even cross my mind to tell her this.

I question myself about why I didn't take the opportunity to educate her about my son's diagnosis. Why not educate an open ear? Was it for fear of rejection or maybe just an avoidance of the topic? Although it may have seemed like a perfect situation, at that moment, I didn't need to. He was calm and was watching Curious George. I don't feel there is a need to point out to everyone that he has some difficulties. I want them to know him for who he is and his name is Chucky Cheese not Autism. The woman continued to chat about her son and Curious George and the iPad when my son began flapping and screeching.

It was at that moment that my heart dropped and I felt like I wanted to run in the opposite direction. Instead I tried to calm him and maintain the conversation despite my fear of a rude ignorant comment. I misjudged the woman and I am sorry for that. Instead of making a nasty comment or judging my son she calmly asked me if my son had Autism. Yes, you heard me right. She asked me about my son without coming to her own conclusions and without making false judgement.

This is the first time I have encountered someone that was able to question the behavior without judging my parenting and being critical. My offering the information wasn't needed. While I was cringing and looking for a quick exit she was connecting and inquired. Maybe she saw the instant fear of rejection in my eyes or the look of complete tenderness in my interaction with him, but she got it and was compassionate. I appreciate this and encourage anyone who is unsure about a situation to ask. It feels better than to have someone gawking or making rude comments.

This lady made my day. Not only was she open to attempt to converse with my son but she was also open enough to ask questions. She wanted to know more which is how we spread awareness and how we open the doors to acceptance. The story doesn't end there because she also looked at me and expressed how wonderful she felt I was doing with my son. This made me feel as if I was invincible even if that invincibility only lasted 5 minutes. It was worth it. So, to the woman in Hannaford I must say thank you. You gave me more than you could ever know just by asking a question and exchanging kind words and a smile.




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Wednesday, January 5, 2011

So Yelling is Out…umm..What can I do?

1/05/2011 1 Comments
I read an article today titled , I Have Asked You A Hundred Times!. It really hit home. I have been having a torturous time with my tween. She is just lazy, ridiculously lazy. It drives me insane.
I used to have her take a shower in the morning but she was never ready when the bus came and would be leaving with wet un-brushed hair. I now insist that she take a shower at night but, it is still a battle. Do your tweens argue about a shower? I mean you would think they would want to look their best right? I am so confused, so I decided to take the natural consequence approach.

I asked her to take a shower and if she chose not to that was her choice. I told her that I would not take her anywhere if she was not showered. Do you know the girl didn’t shower for almost a week. She didn’t care that I wouldn’t let her sit on the couch or at the table during meals. She didn’t even get the point when one of her friends told her she smelled.

The end of that was when the guidance teacher called me telling me that she had a smell on her. I explained the issue to the counselor and she assured me that this is a normal phase for tweens. Although she said it usually goes on with boys. I explained how I tried to allow her peers to influence her and it didn’t work. So, now I feel as if I have to be on top of it. I will not remind her anymore. It is now that she takes a shower by 7:30 or she goes to bed at 8:30 instead of 9:30. I think that is reasonable.

My sister recently wrote a post titled The Mom (Super Human) in Me -VS- The Human in Me. I encourage you to read it cause it is a great post. It really hit home for me. I too struggle everyday with my human form vs. my Mom form. Do You struggle with this too? Do you find yourself fighting the urge to say,”That was a stupid thing to do?” when your child trips over the shoe they left in the middle of the floor instead of asking if they were ok? It may sound mean but come on, I know she has brains and I wish she would use them.

I am only human and I am not trying to be mean. I love her so much but the arguing has got to stop. I hate yelling at her and I find myself so frustrated with her actions, or lack of actions that I cannot enjoy her presence.  Does that make me a horrible mother? She wants me to listen to her sing and while I would love that in the back of my mind all I can think about is the fact that I want her to clean her room and take a shower.

I can take a little of the blame for her behavior. I totally cringe in saying that when the going gets tough and I don’t want to fight with her, Mom gets going. Off to do something else, leaving her to do, not what I am requesting her to do, but what she chooses to  do. No, I don’t let her roam the streets, not that she would get far cause we live in the sticks, and I will not allow her to go out. Well, maybe I do … *cringe*. There are times that I am so annoyed and I justify her going out as we both need breathing room. This is just one more excuse.

I challenge myself to be more consistent but not to yell, ummm… or scream. It has to be possible, Right???? So, I shall state clearly what I expect of her and take the things that mean the most when she selectively goes deaf. LOL! Sometimes I find it so hard to try to get control of the situation because I have a special needs son. He takes up so much of my day and somehow… when things get tense with Krystal or I am trying to draw the line, in chimes Chucky and he needs me NOW!!!

How do other moms handle this? I think I might go crazy. I used to think that after you have three children, you can add more and it didn’t effect anything. For instance my “wife” as I call her, used to ask me to babysit “her” two girls, which are really mine, but she would always ask,”Are you gonna be ok? That is a lot of kids.” At that point I would respond with,”Are you kidding? After three extras don’t count. They all occupy themselves and whatever bickering could occur can’t be any worse than with three.” She always thought I was crazy, but now….. forget it. I cannot take on more than one more child.
My maximum child occupancy has changed from unlimited to five. I find myself doing Math and really scheduling things. If Chucky goes to his dad’s house I can have at least two kids over but.. if he is home the parents must stay. I do it at birthday parties too… I am such a wonderful host..LOL… I will see how many moms or dads can stay through the party and lend a hand. Most of them are well aware of the situation and are more than willing to help.

This overwhelming barrier of motherhood involving special needs lets my daughter ignore my requests and since my brain cells died after I had Charlie, I can’t remember anything.  Do you have the same problem? How do you juggle it?

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