Any parents of special needs kids??
lisah180
Posts: 69 Member
My son is 3 diagnosed with autism at 20 months, I fell into a depression after his diagnosis and just felt lost and turned to food for comfort. These days he is doing well and I am getting healthy to be the best version of me for him! Anyone else out there who can relate?
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My son is special needs (general developmental delay but they don't think he's on the spectrum) and it has been hard here too. He's 3 now and just started preschool. Hugs mama! I'm trying to get healthy for him and our new baby girl as well.0
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I have2 Children on the spectrum. My son has autism and he's 12, my daughter has aspergers and she's 10. You can add me for support if you like0
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My son was born with Congenital Heart disease and has had 3 open heart surgeries. He also has had feeding issues and seizures. He is now seizure free but suffers from Mild cognitive delays. He will still need to have corrective surgeries on his heart throughout his life. I also have a daughter who was diagnosed 2 years ago with ADHD. After my son was born I was and have been so consumed with taking care of him and my other 4 children that I completely let myself go. I to sought comfort with food. I want to loose the weight so bad it is just so difficult to remain motivated when life gets you down.0
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I wanted to offer my support. Autism is hard. I have a daughter that is on the spectrum on top of ADHD, Anxiety, depression, and learning disabilities. I'm at a different stage because my girl is a senior and we're trying to help her find a way to survive the real world. I also grew up with Autism, my 46 year old brother was diagnosed in the early 70's right when autism became an official diagnosis and before schools were required to offer education.
It makes taking care of yourself extra challenging. Good for you on making the effort.
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I have a son with 18p- (he's missing part of a chromosome). It's pretty rare, and affects him physically and with speech, and possibly some behaviorally (hr's almost 4 and with almost no speech, so it's hard to tell if it's just age plus frustration, or more than that). I also have a close friend who has a daughter his age and another who is 2 and both are on the spectrum.
I understand the depression and looking to food for comfort. There is a grieving process that follows any sort of diagnosis (not grieving that he is on the spectrum, but there is some sense of loss for the potential you expected, the hopes and dreams you had, etc. and it's totally normal and okay). Allow yourself to move through this process ... be angry if you need to, cry if you feel like it, and if possible, talk to other parents who have been through the same thing. It helps! And then, try to exercise for stress instead of eating, and start logging your meals again.
HTH0 -
I have to boys that have autism. Ages 6 and 4. My 4 year old is more serve then my oldest. He also has alot more health problems too0
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BHey there! I have 3 kids, 2 ASD(and ADHD & epilepsy) the baby is showing significant development and physical delays. I too have battled depression and feeling of failure for the last 10 years, since the first diagnosis. But life is awesome and the kids continue to amaze me (and break my heart) every day. It is a roller coaster for sure.
I use calorie counting and exercise as my "me" time and hobby, with the fact in mind that they need me even more and for as long as possible. I also need to be able to physically keep up with them and keep them safe. It will get better, some days. It will feel worse, some days. But this is our life. Make the best out of it for yourself and your family.
(Ps, between appointments and therapies, I have lost ~65lbs in the last year and can do things I never thought possible. You totally cam too).0 -
I have a 21 yr old son who has aspergers &ocd. as a 2yr old he was diagnosed. i busted tail to get him ready for school. we were told to put him in a home or medicate heavily, of course that was our LAST visit to that dtr. when started kindergarten he was only in speech therapy by then. he excelled all throughout school taking college course final 2 years of hs. he joined the navy & excelled, do in part im sure to the structured nature. because of his speech issues my daughter whom is 4years younger also had speech issues, which were corrected by 2 nd grade. this can be done!!! i am in medical field working with physical/mental challenged people everyday, have worked for our school district helping to structure ieps for other children. u ARE ur childs best & sometimes ONLY advocate!YOU need to stay healthy & make time for urself! otherwise these issues will overtake ur whole familys life, which is good for NOONE!!!keep your head above it& breath;) you can add me if ud like.0
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I think we should start a group, anyone know how to do that?
My middle kid has autism, he'll be 4 years old in a couple weeks and was diagnosed just after his 2nd birthday. I also went into a depression where I didn't take care of myself. I still get emotional talking about it, but instead of using food I jog and cry if I need to during my run. I am so grateful I moved to a school district that gives him a lot of services and I love his teacher, but we still have rough moments at home.0 -
My youngest son has a speech delay and fine motor deficits. He just began Kindergarten and is 5. He has oral sensory issues which is challenging for our family. He has trouble with some social cues, especially with regulating the volume of his voice and understanding physical boundaries.
When he was born I gained a lot of weight. He had severe reflux and screamed for hours each day. On top of that, my older son was only 16 months when my younger guy was born. It was stressful and I began having a lot of problems with anxiety and depression. After the reflux he had severe constipation, speech delay, social/emotional delays, and fine motor deficits.
Right now is very stressful for me as he begins Kindergarten. So far, he seems to respond quite well to the social demands and the structure.
I should also add that I'm a school psychologist. I do a lot of testing for special education. If we had our own group I would love to join, both for personal support and to maybe be able to offer professional advice?
It's nice to meet you all.0 -
I would love to start a group as well!! I don't know how either! It's so nice to meet you all!!0
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I figured it out and created a group! Let's chat, talk about our kids and offer support!
I made the group private so everyone feel comfortable talking about whatever without judgement! Let me know if you would like to join and I will send you an invite!!
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Me please. I posted my situation above somewhere.0
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I sent you an invite to join last night0
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Let me know if you didn't get it0
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Yep0
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I have a 25 yr old son with Down Syndrome. I'd love to join the group!0
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I was a late bloomer. I saw the first signs of a later confirmed diagnosis of Schizophrenia when my son was twelve. After the confirmed diagnosis in his twenties, I grieved for a couple years. I've reconciled myself to the diagnosis, the most scary for me is the statistically shortened lifespan, usually by suicide.
He's in his thirties, in a sheltered group home, works sometimes, and is engaged to be married. He's a humble, gentle man who never fails to call his mother. He also sometimes manages to beat a Master at chess. I've forgotten his score. All I know is that he nearly always beats me!
I wish you much joy as you find the challenges and treasures of raising a challenging child.0 -
I have two special kiddos. Daughter 13 Epilepsy and Autism, Son 9 Autism and Seizures. Is this a group? I'm newer to this and would love support from parents who understand.0
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I have two boys with special needs. The oldest is 16, and has severe autism and moderate intellectually disabled. We were told he has the mentality of a 4 year old. Our other son is 8, and was diagnosed initially with intellectually disabled, but was rediagnosed with autism and a learning disability. It's hard, and I turned to food as well because it was always there. Mindlessly eating and always on the go made for bad food habits. But I wouldn't change my boys for anything in the world.0
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I have three kids, and the oldest has ADHD type II, he's being evaluated for possible spectrum placement. He had speech delays that weren't treated until he was3.5 years. The youngest also has ADHD type II. It's been a struggle, especially as I deal with most of it myself, on top of a full time career and being a farmwife. Because we use extra-curricular activities to burn extra energy off and increase social interactions, I really have to watch what I eat while on the road.
When there aren't many parents willing to be open about the challenges and sheer crappiness of raising kids w mental/developmental disorders /delays, I found myself eating my feelings. Bad bad habit!0 -
I didn't get an invite!0
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My son has autism (mild), but his primary diagnosis is intellectual disability. In some ways, he's like any other 12 year old. In many ways, he's still a toddler.0
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I want to join!0
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I'm also an autism mom. My son is 11 and on the spectrum. His primary issue is speech, he's verbal but has significant delays. He also has sensory issues. I myself as far as myfitnesspal- I had WLS 2.5 years ago and am struggling to maintain a 160 lb loss. Nice to meet everyone- add me to the group if possible- thanks!0
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Hi! I just read this. I have a son who will be 2 in October. He has special needs. They have ruled out several disorders and recently had a muscle biopsy in July. We are still waiting on the results of that. He gets PT/OT/&DT once a week. With the help of braces we have gotten him walking and he just got measured for new taller braces to hopefully eliminate his crouched stance. He has low muscle tone. The doctors are so surprised to see he is walking because his tone is so low. He doesn't talk much, outside of Mama and Dada. We've recently added speech therapy to help get him going on that. He does sign for things though, so that helps. He screams alot though when he's frustrated and we can't figure out hat he's wanting. Hopefully the biopsy will provide some results. I'd love to join the group! It's great to have something like this on here.
I can definitely relate to the stress eating that comes with it. I recently decided to make it better though by becoming the best me I can be for myself and my kids. ☺0 -
arkowalyshyn wrote: »I didn't get an invite!
That's so weird, I definitely sent you one..I just checked its still saying invitation sent. Haha I'm probably doing something wrong!
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I named the group special needs parenting if I miss sending invites I think you can search for groups
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Thanks, I'll poke around some. Anyone else have bites? My 8 yo stopped for a long time, but has started again. She is non verbal asd.0
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kelleybean1 wrote: »I have a 25 yr old son with Down Syndrome. I'd love to join the group!
Hey there @kelleybean1 ... I have a beautiful 25 year old son with Down syndrome as well0
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