Exhausted from parenting/ASD children/Welcome to Schmolland!

I think the new title is perfect, we all have our moments where there is just not enough energy to do what we want to meet the needs of our kids.

bookwormde
 
I am very sorry for your loss. As you will see, everyone here is very compassionate. The title was even changed to avoid any confusion.

Like you, we belong to a club (land) no one would ever chose to join (live in). Most days are good but some days are very difficult. When we feel like no other person could possibly relate, we can come here and often find a friend who has been there before or can atleast share our frustrations without judgement. Grief can eat you up if you do not share it with others who understand where you come from. Unfortunately, there are always others who have been there before and have shared the same pain... whatever club (or land) that may be.

Well said... I was up most of the night thinking about this part of the thread... and am very troubled by it... this is one of those outsiders walking into Schmulland and saying, "I see nothing wrong here." and making judgement on us as parents and quickly exiting before anyone has time to invite them in for dinner or just coffee... grieving or not... sit down, chat and read ALL the posts before judgement.

Stepping away from the mic before I say too much... no fire allowed in Schmulland!
 
I can completely relate to what people say on this thread.

Our son is 13, non verbal and Autistic, we are finding as he gets older & we do too there are regular times where we are just so tired.

My wife and I work full time but get little free social time to ourselves, in a way our Florida holidays are our relief from the day to day stress.
We find we can relax a little more when on vacation, and feel younger, more energetic too.

Best wishes to all of you from the UK. :hug:

Welcome to Schmolland! I must say, I love the quote under your name... that is beautiful!
 

:grouphug: Hi Johnny! Welcome to Schmolland! I am quite sure that we accept dual citizenship here (since you mentioned the UK) ;)
My DS9 is currently obsessed with Doctor Who. I am using this to talk him into eating bangers and mash in the UK at Epcot... fish (though he's fine with the chips) was nixed fast but sausage has been open for dicussion, so there is hope.

:)

Doctor Who is very popular over here (I prefer the X files!).

Glad to be accepted, we are all friends on here. :grouphug:
 
:)

Doctor Who is very popular over here (I prefer the X files!).

Glad to be accepted, we are all friends on here. :grouphug:

Hi JohnnySharp2! I'm glad you're here, too!!!:thumbsup2 I also love the x files! My sister has a completely non-verbal son, too, who is 12. I watch how hard that is! I hope you stay around and share some of your UK advice!;)
 
Well said... I was up most of the night thinking about this part of the thread... and am very troubled by it... this is one of those outsiders walking into Schmulland and saying, "I see nothing wrong here." and making judgement on us as parents and quickly exiting before anyone has time to invite them in for dinner or just coffee... grieving or not... sit down, chat and read ALL the posts before judgement.

Stepping away from the mic before I say too much... no fire allowed in Schmulland!


I thought the same thing when I read his post. I got an awful feeling in my stomach because 1) I felt so bad for him and 2) I felt so judged. It made me even more grateful to everyone here for being so supportive! Looking back on that first post I wrote I realize I could have been flamed right off the disboards! Instead I was accepted and we've all become like family!:lovestruc Amazing what "understanding" does to people and situations!
 
/
Well said... I was up most of the night thinking about this part of the thread... and am very troubled by it... this is one of those outsiders walking into Schmulland and saying, "I see nothing wrong here." and making judgement on us as parents and quickly exiting before anyone has time to invite them in for dinner or just coffee... grieving or not... sit down, chat and read ALL the posts before judgement.

Stepping away from the mic before I say too much... no fire allowed in Schmulland!
EXACTLY! I wasn't sure how to feel attacked or understanding of their perspective.. but they werent understanding of ours :confused3 guess thats one of the drawbacks of the internet but every parent with an ASD child understands the thread completely!:grouphug:
 
Hi JohnnySharp2! I'm glad you're here, too!!!:thumbsup2 I also love the x files! My sister has a completely non-verbal son, too, who is 12. I watch how hard that is! I hope you stay around and share some of your UK advice!;)

Hi, sure I will :)
 
A question for y'all...

Has anybody had a "microarray" done on your child? They can now take the DNA strand down farther and are finding deletions in many children with autism. A microarray is bloodwork. I guess doctors are being told this is to be one of the first things they order when asd is suspected. My sister just had this done on her child (12 yr. old boy w/autism) and they found a deletion in shank 3. She said this area is responsible for language and social skills. The exciting thing is they are already in testing phase with a mouse to fill in the deletion. I haven't had this test done on my boys but I was thinking it might be interesting to do. Just wondering if anyone else has heard of doing this in your area. My sister is in Texas. I don't think doctors are routinely ordering this test in my state yet. Just curious.:scratchin
 
Checking in to Schmolland. Schmolland was very agitated at my house this morning. We had a rocky start with shredded wheat flying around the dinning room while I was in the shower and ended with storming out of the house angry because they couldn't behave for 10 minutes.

So my respite today is to go to my job as a special education teacher of middle school students and deal with their problems. :rotfl:

We have cub scout stuff to do tomorrow and it is visiting historic places around town. I hope we Schmollandites can blend in with the rest of the towns people, if not it is going to be a long day!

Good luck today to everyone!

Daisy
 
Disney Bishops I'm so sorry for your loss.

I wanted to say hello all.

Daisy & Max I commend you for going to the dr. My hubby and dm have suggested many times I go too, I'm now going next week.

We started out the week pretty crappy but seem to be mellowing out some as the week has progressed. We did cancel part of our vacation for June but have kept the wdw vacation. My schmutch does not do good with the unknown. WDW she's knows.
 
Daisy&Max and Elan, I'm sorry you're having a rough week! :hug: Mine hasn't been the best either but it's Friday and I'm hopeful for a better weekend for us all! :grouphug:

Elan, I'm sorry you had to cancel part of your trip. At least there's still WDW and, really, what more do you need? (Except maybe some help from your local pharmaceutical company!;)) Hang in there and let us know if your doctor gives you something that helps. Right now my stress buster is taking my dogs on very long walks! Usually that helps but there are days when my dogs (I refer to them as my prozac) aren't enough!
 
I would like apply for a Schmutch passport :goodvibes

I have been living in Holland, er, Schmolland, for about 9 1/2 years. My DS was diagnosed with PDD-NOS when he was 2 1/2. He's in Middle School now, doing pretty well. But some days....:scared1:
 
This made me think. I would love to hear everyone's diagnosis story. How and when did you find out you were moving to Schmolland? Anyone else want to share your story?

I'm still reading the thread from the beginning but I found this one and thought I'd throw mine out here.

My DS10 was born 4 weeks prematurely after losing 40% of his blood volume when his cord tore from his tummy and then the placenta abrupted (kid got a double whammy). He was on a vent for the first hour of his life but because he had been without o2 for 17 minutes before they could get him on the vent, he was likely going to be blind, deaf, severe cp, and cognitively impaired. Two years later he was a more or less normal kid, although he had quirks about food, loved staring at fans, and would only be held long enough to nurse. When he turned 2 he became this hellion that could never be consoled or placated. He cried every time we left the house, he never slept, and he was easily frustrated. I took him to the ped and she said it was the terrible twos. So we waited. At 3 I asked her about ADHD. She said lets wait and see a little longer.

When he was 4 I gave birth to a 6 week early premie who couldn't hold his temp or his weight after birth...but could breathe. DS began throwing even worse fits, would hit and hurt anyone he could get his hands on, he would destroy things, and I was miserable. I did some research on Autism and felt like he was a spectrum kid. So back to the ped who dxed him with ADHD and gave us a referral to a developmental ped.

The developmental ped said it wasn't a spectrum thing but bad parenting. :( Recommended we get counseling, try some anti depressants on him for the anxiety, and work with the behavior mod. I went home even more depressed and resentful of the kid.

Six months later he is running away in school, hiding under furniture, barking at people and having to be restrained by school personnel so he couldn't flee. So back we went to the developmental ped. Saw a nurse practioner and she increased the anxiety meds and the adhd meds and we waited. A few months later we went to WDW and while we were in the room napping DS got a hold of my mother's leatherman tool (it was in her purse) and cut his hands all up. They were superficial cuts but, bled nonetheless. Oh and he ran away one day too and it took us 45 minutes with MK security to find him. He was happily wandering around Frontier Land all by himself.

We got back home, I took him straight back to the nurse practioner, cried to her and told her she had to fix him. I started telling her why I thought he was autistic and she saw the light. She gave me a screening form and it was blaringly obvious that he was on the spectrum. So we went for a huge battery of psych tests and 2 months later we had our dx.

I thought I would be happy with my dx because now i knew what it meant. I had read the new books on Holland and thought I could handle it. I'm a special ed teacher, how hard could this be. :lmao: yeah well, that soon turned to more depression and angst for me and I'm still lving that.

He is now on concerta (no holidays for him), Risperdone, Clonidine, and Zoloft. He's not great but he's better. It took almost 4 years to get the dx but we now have it and are learing better to navigate the terrain. Unfortunately, I have it stuck in my head that it should be easier for me since I can do it with other people's children. Its not.

I am finding so much strength from this thread. I can't believe how much of your stories sound like mine. I've spent all my planning time today reading...laughing, almost crying, and the like.
 
Since Daisy & Max has better focus than me and has been actually going through the thread :lmao: I'll share mine as well which is very short

At around 6 months I noticed my son was not smiling and was unusually quiet for a baby, he didn't laugh or squeal or babble. So at his 6 month check up I asked the doctor about autism and she told me it was too soon to tell, but to keep an eye on him and let her know in the future. At 9 months I brought it up got the same answer. When he turned a year old he was making a lot of changes he laughed and smiled and babbled,and could even say a few words: No, Hello,Stop.
Then at 15 months he got a flu shot got very sick, 103 fever, throwing up, totally out of it, and when he got better he was a totally different child. He wasn't babbling anymore or trying to talk, and less than 2 weeks later he had what we believe was a mild seizure. It was on Christmas Eve he had just woken up and passed out after eating he was cold and clammy, and grayish.. I took him to the ER but by the time we got there he was back to normal and the nurse refused to believe me,so we waited in the ER for 4 hours for them to call us but they never did,I guess they just didn't believe anything was wrong so we left because he seemed fine.
At his 18 month check up I took him back to the ped for a check up and brought up autism she took one look at him and said he was not autistic he was just a little delayed because he was a boy, I told her that I wanted a second opinion and almost had to make her write the referral. At 20 months he had three diagnosis: the first with Infants & Toddlers who found that he was extremely delayed speech 0-3 months which made me want to cry, his second was with a Neurologist at Children's who told me without a doubt he was autistic, our third was a 2 day test with a Speech Pathologist, OT, and developmental ped who concluded that he was autistic.
I had know all along but it took about a year for anyone else to confirm it, not as long as I know some people went through but frustrating nonetheless especially with his father telling me that I was wrong and just wanted something to be wrong with him (what kind of mother would I be?) and that I was just crazy. He never conceded to that.. and I may be a little crazy :laughing: but not about that!!!
 
I would like apply for a Schmutch passport :goodvibes

I have been living in Holland, er, Schmolland, for about 9 1/2 years. My DS was diagnosed with PDD-NOS when he was 2 1/2. He's in Middle School now, doing pretty well. But some days....:scared1:

:grouphug: Welcome!!!
 
You go less than 24 hrs. without checking in and end up 4 pages behind! Took me forever to catch up! Bunch of chatty cathies you all are! :laughing:

I am so sorry for your loss... and so new and so raw... I, too, lost a child (two to be exact). I mourn them every day... one would be 20 this year and the other would be 8.

We love our children to the ends of the earth and would never stop loving them or doing what is best for them... but please understand that some days we are very tired... not of being a parent but parenting for that day... we always get up the next day and resolve to make the sun shine and the day be happy.
I hope this makes you understand us a little bit better... we love our children VERY much...

I love this quote. I don't know how it could've been said any better! I am sooo sorry. I had no idea and cannot imagine what that must be like for you.

Thank you for the welcome. This looks like the kind of support group I can use!

I don't know about the situational since I have to take it daily so it builds up in the system. I'm hoping it will make me better able to deal with my kids' quirks. I've been so depressed that I've found myself wishing my kids were more "autistic" so that people would realize they aren't just weird or strange and that I'm not a bad mother. Then I feel so guilty about wishing for that.

I'm so glad I found this thread. I'm going to try to read through as much of it as possible. Thank you for the welcome!

Daisy

You're welcome for the Welcome! We've become kinda like sisters here. We all "GET IT". I love that I can be completely open and honest about what I am going through at the moment without fear of being judged. Occasionally a passerby may make a misguided statement out of their own grief or experience, but we can overlook that. They have their own cross to bear.

I know you didn't mean it to be funny but when you said sometimes you wish your kid appeared MORE autistic so people would know there was a prob and he was not just weird, I cracked up. I used to feel the same way when DS was a little younger. Be careful what you wish for....now I find myself wishing the opposite. DS LOOKS perfectly normal, but the autism really shows now more than it used to, so now i find myself wishing he appeared more normal so people wouldn't look at him like he was weird. I don't believe the grass is greener on either side. In schmolland it's all the same shade.

I just had to say we had a doozy of a night with our 17 yr old ASD son. It's so hard to know what is typical teenage behavior and what is asd! Tonight a minor incident at the dinner table escalated into him being really mad and somehow it's everyone else's fault! We don't even know how it starts half the time! My DH and I just end up looking at each other thinking WTH just happened? I definately see the Schmolland landscape when I look out my window tonight! It makes me want to close the blinds, though! I know many parents say they wouldn't change a thing about their asd child but I'm just not there yet. I love my child unconditionally but if I could take his struggles away I would!

Thought I was the only one who used the word "doozy". :laughing: Sorry about your rough night. I have a pic of one of my rough nights...I just may have to post it sometime! Don't worry, I'm not there either iwrbnd. I'd have my U-Haul pack in 20 minutes if I knew a way out of Schmolland. I will always strive to help him become as normal as possible and at the same time embrace who him for who he is. :grouphug:

I can completely relate to what people say on this thread.

Our son is 13, non verbal and Autistic, we are finding as he gets older & we do too there are regular times where we are just so tired.

My wife and I work full time but get little free social time to ourselves, in a way our Florida holidays are our relief from the day to day stress.
We find we can relax a little more when on vacation, and feel younger, more energetic too.

Best wishes to all of you from the UK. :hug:

Hooray! A Schmutch DAD! I believe you're our first dad! Welcome aboard. I have a cousin, once removed (she was married to my cousin), who is British and has a darling on the spectrum....she says she is from Schmengland! :rotfl:

Believe me...we all relate to the no social time, worn out and tired sort of feeling.

Amazing what "understanding" does to people and situations!

All I can say to that is AMEN sista! My friend and former Assoc. Pastor once said "Condemnation never set anybody free!" Criticism and finger pointing only worsen the situation and don't offer any encouragement or solutions. I am so thankful for this thread and all my new friends.

BTW, I LOVE THE NEW TITLE!!!!!!!! PERFECTAMUNDO!!!!!!!! :thumbsup2

We have cub scout stuff to do tomorrow and it is visiting historic places around town. I hope we Schmollandites can blend in with the rest of the towns people, if not it is going to be a long day!

Good luck today to everyone!

Daisy

GOOD QUOTE! I LIKE THE PART ABOUT BLENDING IN WITH THE REST OF THE TOWNSPEOPLE! :rotfl:

I would like apply for a Schmutch passport :goodvibes

I have been living in Holland, er, Schmolland, for about 9 1/2 years. My DS was diagnosed with PDD-NOS when he was 2 1/2. He's in Middle School now, doing pretty well. But some days....:scared1:

:welcome: I think we need an official seal for our ID cards! ;) We don't have passports. Once you're here....you're here to stay. You may move back and forth from the country to the city...or even closer to the border, but you're still here in Schmolland. Glad to have you!
 
Well said... I was up most of the night thinking about this part of the thread... and am very troubled by it... this is one of those outsiders walking into Schmulland and saying, "I see nothing wrong here." and making judgement on us as parents and quickly exiting before anyone has time to invite them in for dinner or just coffee... grieving or not... sit down, chat and read ALL the posts before judgement.

Stepping away from the mic before I say too much... no fire allowed in Schmulland!


I thought the same thing when I read his post. I got an awful feeling in my stomach because 1) I felt so bad for him and 2) I felt so judged. It made me even more grateful to everyone here for being so supportive! Looking back on that first post I wrote I realize I could have been flamed right off the disboards! Instead I was accepted and we've all become like family!:lovestruc Amazing what "understanding" does to people and situations!

EXACTLY! I wasn't sure how to feel attacked or understanding of their perspective.. but they werent understanding of ours :confused3 guess thats one of the drawbacks of the internet but every parent with an ASD child understands the thread completely!:grouphug:

I stepped away from my keyboard for hours last night before responding. I was worried I'd sound harsh with the things I wanted to say... even though they were not flames by any means.
I felt awful for feeling offended but I was... 1) There was nothing wrong with the original title except for picking apart wording and 2) Every parent has been tired of parenting at some point and in denial if they claim otherwise. Telling others their feelings are not valid does a great disservice to those who are struggling just to make it through the day.
The Good citizens of Schmolland are not inclined to kick anyone when they are down no matter what their citizenship status. We are crusaders who will teach you our national dance instead. Quoting our national anthem:
I get up, and nothing gets me down.
You got it tough. I've seen the toughest around.
And I know, baby, just how you feel.
You've got to roll with the punches to get to what's real
Oh can't you see me standing here,
I've got my back against the record machine
I ain't the worst that you've seen.
Oh can't you see what I mean ?
Might as well jump. Jump !
Might as well jump.
Go ahead, jump. Jump !
Go ahead, jump!
 
Don't know if I am offically a member, but I am a dad also (and and Aspie)

bookwormde
 

PixFuture Display Ad Tag












Receive up to $1,000 in Onboard Credit and a Gift Basket!
That’s right — when you book your Disney Cruise with Dreams Unlimited Travel, you’ll receive incredible shipboard credits to spend during your vacation!
CLICK HERE














DIS Facebook DIS youtube DIS Instagram DIS Pinterest DIS Tiktok DIS Twitter

Back
Top