I Don’t Want To Be An Autism Parent Anymore

*Preface: have you ever felt overwhelmed with life? I have. Of course I love my son with all my heart, I should never need to even justify that, but living with a child with severe autism is hard. I do not need threats made to my life or my child’s because I find some days hard. Comments like that will not be approved.

And for the record I don’t always feel like this but I am human and some days this is exactly how it is. *
The day started far too early. There was no sweet cuddles in bed or a little voice asking for a drink; no I was woken as usual by screaming. I have had day after day, month after month, year after year of being woken by screaming and I don’t want that anymore.

I don’t want to wake up to a smell that would make you want to vomit and bedding that is fit for the bin more than the washing machine, because yet again it is covered in something that ought not to be seen by anyone else. I am so tired of that now.

I don’t want to sit on my couch in the middle of the night looking at my child and wondering what I did to have a child who sees no point in sleeping, who at 8 still can’t say ‘mama’ and who still thinks the world revolves around his needs only.

I love him more than words could ever convey but I don’t want to be an autism mum anymore. 

I want to be a mum who has fun with her child rather than doing therapy with them.

I want to walk my son to school and talk to his friends instead of sending him in a taxi to a place where I am a stranger to them.

I want to be able to talk to my child about the fact it is his birthday soon and discuss what he would like to do to mark that day.

I want to be someone who takes my child to bowling, teaches them to ride a bike or even goes to the movies with them. Instead the only place I ever take him to is hospitals or respite.

I am tired of missing out on everything. I am tired of never having party invites, knowing nothing about his day at school, having to still dress him, having to take adult nappies and wipes with me wherever I go.

I don’t want to be an autism parent anymore.

I am tired of holding my child as he screams in public again.

I am tired of the never ending judgement, the stares and the horrid comments.

I am am tired of carrying around my broken heart as a result of the interventions and therapies having achieved nothing.

I simply can not bear the thought of my child as an adult knowing what society is like.

I am tired of meetings.

I am tired of phone calls from his school.

I am tired of fighting for everything but then being accused as having an attitude or people thinking I act like I am entitled. 

I don’t want my child to have autism anymore. This is not a ‘different way of seeing the world’ that he has, or ‘a wonderful gift’. This is a child about to be 9 years old who can not say ‘mum’ or use a bathroom himself. This is a child almost my height who still can’t put his own clothes on, brush his own teeth or dry himself after a bath. This is a child who can never ever be left alone, who has to have everything the same all the time, who self harms and wanders. This is a child still with the mind of a toddler who will require others to look after him his entire life.

Who would want that for their child?

Who would want that as a parent?

Today I don’t want to be an autism parent any more.

The problem is I have no choice.

So I strip that bed, bath that child, cook him that breakfast as I always do and let him sit on my knee while he rewinds the same ten seconds of video on you tube he did yesterday and the day before that and the day before that.

Nothing changes much in my house, except my feelings. 

Today I am tired. I don’t want to be an autism parent today the same way any other parent may feel about not wanting to be the mum of a toddler who tantrums daily or a baby who has reflux or the partner to someone with Alzheimer’s. We all have days when we are just down about the life we have.

Yet we carry on. We dust ourselves down, search for some positives or listen to some music.

Tomorrow is a new day. It will probably start off with screaming again too., but maybe tomorrow I will be stronger, more hopeful, more upbeat.

Maybe tomorrow I will want to be the autism parent I need to be. 

Maybe tomorrow. 

375 thoughts on “I Don’t Want To Be An Autism Parent Anymore

  1. On the really bad days I try to comfort myself by thinking of all the other amazing Autism parents out there all battling on with little or no support.
    It helps me to feel a little less isolated.
    You are strong
    You are important
    You are loved
    You are doing a amazing job
    Much love and respect to you
    Thank you for being so honest

    Liked by 1 person

  2. Reading this makes me wish I lived nearer and I could pop in to share a cuppa, or give you a hug, or let you go and have a lie down…. in fact I wish I lived nearer to everyone in the comments. And then I realised I do live near to so many parents of children with autism; we have a local tribe who are there to share the good and bad times, online and very occasionally out, and it makes a huge difference. I’m desperately hoping you do have some local support who will think about who else they can gather and how they can best help xxx

    Liked by 1 person

      • Thank you for being real!!! Thank you for sharing that unconditional love that we know we will give them isn’t easy or desired!!! Thank you for reminding me it’s ok to be human and not super mom 100% of the time with a fake smile or shroud remark! Thank you! Some days are harder than others and some
        Weeks and sometimes months….. and it’s ok to not be excited prepared or content about it! Thank you!!

        Liked by 1 person

  3. This post touched me beyond words. I started a Facebook group.( fathers coping with autistic children) only 2 days ago for this very reason. The sacrifice you/we make every day can not be explained.
    Thanks for sharing.

    Liked by 1 person

  4. I respect your honesty. I have got a beautiful boy that is on the spectrum. I’ll be honest with you we have our good and bad days. Just remember how far you have come and you wouldn’t be the person you are today without your gorgeous boy. Your doing a amazing job. You’re strong. You Are important It’s good that you’re getting this off your chest and talking about the bad days. I respect you.

    Liked by 1 person

  5. oh wow. i am incredibly lucky to be the parent of a NT child, and i have days on which i think i’m being tested. reading this helps me to realise how wrong i am. thank you so much for being so honest. depictions of people with autism always show the ones who can just about fake being NT – never the ones with nappies, who are non-verbal. your story broke my heart but opened my eyes.

    Liked by 1 person

  6. Felt this last night….angry at fighting for provision rather then enjoying just being a parent….Feels like you can’t talk like this as once again you will be judged x

    Liked by 1 person

  7. Thank you for your honesty. My heart breaks for you and yes, I’ve been there, too, and we carry on because we love our children and they need us. My daughter is now 20 and lives in a home for autistic adults in Notts. My husband and I visit every two weeks and Steffi comes home for a few nights every 3 months. Her problems are complex and severe but I feel guilty about her being there every single day. Do you get any respite or practical help? This is so important because you SO need it. You need to recharge. You need someone to take the pressure off you on a regular basis. Am always ready to listen if you want to message me. In the meantime you can be assured of my prayers. It WILL get better eventually but you need help. Much love.

    Liked by 1 person

  8. Your honesty is your strength! It’s never going to be easy…but you will always find that extra bit of stamina to stay one step ahead. Never shy from asking for help, never bother about being judged, and never give up. Love and hugs from one A Mum to another A Mum.

    Liked by 1 person

  9. Miriam, this makes me very sad to read this. And I know how hard this would have been for you to write.
    I hope today is a better day for you. I miss your boy and think of him often.

    Liked by 1 person

    • He misses you so much too! Thankfully not every day is like this but holidays are just so tough! This shows how different a child can be at school and home too.
      We never even made parents night as no-one will look after him 😦

      Like

      • I know, he is the most extreme case of displaying different behaviours in different places I have ever come across.
        Such a pity you missed parent’s evening. I hope today has been a better day, I imagine holidays are very difficult.
        Please give the boy a huge hug from me.
        Have you started s1 placement procedure?

        Liked by 1 person

      • Not started high school placement yet. The last few days have been great and we have had so much fun! Today we are off to pottery painting and to ten pin bowling and Isaac will love both of these.
        We only missed parents night as clashed with his sisters so have another appointment scheduled and so excited to see what he has been up to in school. I know he loved his recent horse riding session!

        Like

  10. This brought tears to my eyes my son isn’t autistic but has a profound learning disability and I find days so hard you have wrote this with pure honest and made me feel I am not the only one

    Liked by 1 person

  11. Oh yes, I am so there. My son is almost 20 and the days and years just drain you. As you said, I love him dearly, but I don’t want him to be autistic and I don’t want to be an autism mum anymore. I want the joy of a 19 year old boy who has just left school and is beginning his journey as an adult, not one who is still like a small child. I am sick of people talking about autism being ‘just a different way of looking at the world’. Fine for those who are aspergers, and high functioning ones, but not for those lower down the spectrum. He cannot live a full independent life; that is not another way of looking at the world, that is a disability. It is just totally heart breaking, and we should be allowed to say it. Not admitting it is just hiding a secret and pretending everything is fine. We need to be honest. Sure, some days are good, but some are just horrrible.

    Liked by 1 person

      • It is bizarre people reacting like that, not accepting what you are saying. Firstly, it is your expression of how you feel about your life, so what does it have to do with them anyway? Secondly, are they feeling some sort of fear that if they express an ounce of regret over having a child with some sort of issue – and let’s face it all kids have their moments – then they think they are saying they don’t love their child. I love my son completely. My son’s autism is not him. If I had a blind child and I could cure his blindness, I would do it at the drop of a hat. So why not autism?
        (To say having a disabled child is’ great, wonderful, a blessing, it has shown me so much in life’, is like saying you are glad your child is disabled, like you want him to be be disabled because it has made your life so much better.)
        Thirdly, I think perhaps possibly some of them are somewhat new to being a parent of a disabled child. After years and years of it you get exhausted, burnt out. The novelty wears off.

        Liked by 1 person

  12. Reblogged this on Eirene Hogan and commented:
    Oh yes, I am so there. My son is almost 20 and the days and years just drain you. As you said, I love him dearly, but I don’t want him to be autistic and I don’t want to be an autism mum anymore. I want the joy of a 19 year old boy who has just left school and is beginning his journey as an adult, not one who is still like a small child. I am sick of people talking about autism being ‘just a different way of looking at the world’. Fine for those who are aspergers, and high functioning ones, but not for those lower down the spectrum. He cannot live a full independent life; that is not another way of looking at the world, that is a disability. It is just totally heart breaking, and we should be allowed to say it. Not admitting it is just hiding a secret and pretending everything is fine. We need to be honest. Sure, some days are good, but some are just horrible.

    Liked by 1 person

    • 1. The feelings of parents of autistic people are valid.

      2. If parents of lower-functioning autistic people didn’t say anything, no one would know that either of them exist. It sucks that such autistic people lack agency in how they are discussed, but there isn’t a better option if a person can’t speak, type, or sign.

      3. It makes sense that lots of higher-functioning autistic people are upset by this piece. First, there is a ToM element to understanding how devastated a parent or caregiver could be. Second, a lot of higher-functioning autistic people (I fall into the highest-functioning end of this category) fear that discussions about how challenging autism can be will lead to “cures” and other attempts to make everyone “normal.” The fear is valid, but the lashing out at caregivers is uncalled for. IMO, the anger should be directed at health insurance companies and at big organizations that only look at ASD in one way (i.e. Autism Speaks).

      4. I always tie discussions like this back to thinking intersectionally. Several factors contribute to a person’s difficult situation, as well as a person’s privileged situation. It seems that very few people try to think intersectionally (and I go to a liberal arts school, so if my classmates can’t do it…). We all have to self-advocate, but if we are able to, we have a responsibility to advocate for others, ya know?

      5. Okay, I’m back down from my high horse. Your feelings are valid, you are brave, and I support you from afar.

      Liked by 1 person

      • Thank you. I have no issue with healthy disagreement or debate but I draw the line at blogs slating me or comments that threaten my life or my children’s lives. I have had to involve the police this week as many comments (which have never been approved as per instructions from the authorities) crossed a line that should never be crossed.
        I never threaten anyone nor would I use my blog to publicly slate another person. There is professionalism like you have demonstrated incredibly above and then there is those who sadly may now find themselves in trouble from the law.
        Thank you for your support and for your we’ll I formed comment too.

        Like

  13. The day started when I cried for my “autism mom” because the world is a scary and overwhelming place to be when your brain processes sounds and touches and smells so differently from most people.

    I wish my “autism mom” would not tell people about my most private and embarrassing moments when I need her support the most.

    I don’t want to sit on the couch with a parent who is annoyed and angry that my brain races and is on high alert so that sleeping sometimes seems impossible. I don’t want to have an “autism mom” who only wants me to speak when I am able to communicate in so many other ways. But she will not listen.

    I want an “autism mom” who does not resent me for having more complex needs than she understands.

    It is so hard to love someone who wishes you were not yourself.

    I want a mom who has fun with me instead of turning everything into therapies and “teachable moments”.

    I want my mom to know that I am valuable and have every right to be included with everyone else.

    I want my “autism mom” to listen even when I do not communicate with spoken words.

    I want a parent who presumes competence and believes that with the right supports, I can do so many things. I want a parent who does not resent me when my disabilities make doing some things impossible.

    I am tired of missing out on my childhood. I am tired of my “autism mom” telling the world that I have no value and am too hard to love and my needs are too great as my autistic self and then being surprised when everyone follows her lead.

    I don’t want an “autism parent” anymore.

    I am tired of being forced into situations that are too overwhelming and not being given the tools to manage sensory overwhelm or advocate for myself when I have had too much.

    I am tired of the never ending judgement, the bitterness and the horrid things my “autism mom” says to other people about me.

    I am tired of being subjected to therapies and interventions that seek to make me a non autistic version of myself. I am tired of forced compliance and being rewarded for pretending to be a version of myself that hurts.

    I simply cannot comprehend how society could ever break my heart more than not being accepted by my parent.

    I am tired of people having meetings about me, without me.

    I am tired of being in a hostile sensory environment and being punished for not being able to handle it.

    I am tired of my “autism mom” fighting autism instead of confronting ableism.

    I don’t want an “autism mom” anymore. I don’t want a parent who cannot appreciate my gifts and only focuses on the things that are harder for me. This is an adult woman who expects me, a child, to have the tools to navigate a world that is not set up for people with my kind of brain. This is an adult woman who tells people that I have the mind of a toddler and thinks that if I need intense supports now and when I grow up that my life can’t have value.

    Who would want that for a parent?

    Today, and every day, I don’t want an “autism mom”.

    The problem is that I have no choice because only my “autism mom” can decide to love me, accept me, and treat me like a person who belongs and who loves me unconditionally, even when I am not the kind of child she expected to have.

    Tomorrow is a new day and I will still be autistic then. I can only hope that my “autism mom” can love me like I deserve.

    Liked by 2 people

    • I can’t believ how unkind you must be to post something like this to a mom who is trying to do her best, year on year and is tired and frustrated and just needs to be truthful and share her struggles. Her child is loved and cared for, do not judge this mom.

      Liked by 2 people

    • that is describing a high functioning aspergers child, not the child that was described in this post. A child with severe autism will find life as an adult difficult. They cannot fit into the neurotypical world but will need to in order to be independent. Ignoring that need will condemn them to be isolated, without any social support. Accpeting their autism doesn’t mean we will not help them to function independently as best as they can. It is also assuming the ‘autism mom’ is cold and heartless every single day and spends no special time with her son allowing him to be who he is. It doesn’t feel as if you have really listened to what the post is saying at all. Mothers of all children have days when it gets difficult, that does not mean they are cold and heartless and do not love their child, it simply means they are tired.

      Liked by 1 person

    • I think you missed the point of this post. I’m am almost certain that all parents of a disabled child, be that autism or any other disability, have days where they are tired and so run down they can’t think…and wish, at that moment, that their child was NT. My son is autistic, has ADHD, Sensory Processing Disorder, Tourettes, GDD and a Learning Disability. For the first three years of his life he slept in ten minute snatches until he was prescribed melatonin, which meant I slept in ten minute snatches. Even with on the maximum dose he wakes during the night and isnup playing in the night. He’s now 11, and has to be watched ALL the time because the ADHD means he is unpredictable and impulsive. He could actually kill himself doing something like sticking a knife in the toaster while it’s on. At least twice he’s nearly been killed trying to play tag with cars, managing to wriggle away from me and out of his wrist strap. We live in a state of hypervigilance, constant exhaustion and almost complete isolation. Our 15 year old daughter feels forgotten and left out because our lives revolve around our son. Not to mention the constant meetings and fighting to get services for him, to help him lead a decent life. We’ve just come out of a four month fight over his EHCP just to get him the help he needs at school, to get CAMHS to do regular medication reviews for his ADHD meds….
      My husband had a breakdown two years ago due to the extreme stress of having a child like our son, I live on antidepressants and have been suicidal due to stress and bone numbing exhaustion. So, yes, there are days that I wish with all my heart, that our son didn’t have autism, or ADHD or any of the other things that limit him. When I wish we too could go on holiday wherever we wanted, without worrying about what obstacles there may be, go to a restaurant to eat and do things that people with NT children take for granted. Does it mean I love my son any less, NO! I love him more than life, I nearly lost him at 21 weeks and spent three days expecting him to arrive, having been told he wouldn’t be saved. Does it mean that there are days that I am sick, tired and feel like I can’t go on, yes. And our son is verbal, relatively continent and has some understanding, nothing like the child described above.
      Just because someone has a bad day and feels like they can’t do it again, doesn’t mean they don’t love their child, or don’t accept that they’re autistic…it means they are tired, they have reached a point of exhaustion that makes the world a dark place. And during those times they wish they had a NT child.
      I think your comment is really unfair…maybe you are a supermum who can handle everything this mum handles every day (and will handle every day for many years), and is not exhausted and beaten down.That’s commendable, remember that not everyone is like you…some of us find it difficult to keep going when we are scraping the bottom of the barrel. Like anyone you’re entitled to an opinion, but writing a response like this equates to kicking someone when they’re down.

      Liked by 2 people

    • Wow! It’s Mother’s like this that paved the way for Autism to be recognized. They used to just intitutionalize the lower functioning children and do nothing to help the high functioning but kick them out of school. My great Uncles came home with a note simply stating they were not able to learn…do not send them back. With no recourse possible.

      This is a Mother that works tirelessly for her child without even being able to converse with him. This is a Mother who does not expect this child to have tools to navigate the world but fights for help so THEY can navigate the world together. It’s unkind to say her personal feelings (on a bad day) means she does not love her child. Most Mom’s feel the weight of the world on their shoulders and it’s okay to say ‘today I’m not handling it well’.
      It’s not easy being human. Empathy, compassion, and a helping hand or word go a long way.

      With all of the horrible, abusive, and neglectful Mom’s out there, let’s pick on this one. He’s a very lucky boy to have this Mother. And either you’re not a parent (of any child, much less a child as large as you that can’t do anything for himself) or you are up on a very high horse. I’m sorry you do not like the way she worded her exhaustion.

      Liked by 2 people

  14. I’m in this boat, I’m strong today. It helps to have support. I didn’t always have it. Get more help now then before.

    Well said mumma. Stay strong 💪

    Liked by 1 person

  15. Thank you for sharing the reality of living with autism you are an amazing Mum and to the outside world people haven’t got a clue what life is really like my son also has autism

    Liked by 1 person

  16. I think the saying ‘A different way of thinking’ really suits only those who are seen as ‘high functioning’. While I am not always happy with the functioning labels this is what sets aside your son from my daughter who is definately dealing with her own struggles daily however can communicate quite well. We have tough days too where i wish her struggles away. I wish she could cope at parties, wish she could be happy at school, understand things other kids do but i still love her with all my heart. Thank you for writing such an open blog on such a tough day. Many don’t share those feelings with others and this will most likely be read by another parent feeling guilty about these feelings and realise they are not alone. 💚

    Liked by 2 people

  17. I live in Zimbabwe, Africa, with my husband, my 17yr old son and 22yr old son, who has cerebral palsy and autism. He is wheelchair bound and completely physically dependent. We do not have the facilities that first world families with special needs have, so I have learnt o do it myself and, boy, does that work out great!!! NOT!!!!!! It is a battle of epic proportion if i suggest we do, or eat, something new! You know the story! i have huge respect for any family with special needs and need you to know that you are always welcome to look me up on fb or email me if you ever need to let off steam to someone who lives it too! email… wlhzim@hotmail.com

    Liked by 2 people

  18. When you decide to have a baby, you are unconditionally agreeing to love, support, provide and do whatever is necessary to meet the needs of that Baby/child. When you become a parent you do not get to decide what you do and do not want it is not all about you it’s about meeting the needs of that baby/child. Its about becoming in tune with your baby/child, it’s finding ways to support your baby/chD to communicate the way they decide, to have the supports that suit them, to have to freedom to decide what they want to have done to them and their bodies.

    Liked by 2 people

    • I am quite sure Miriam is fully aware of all of that. Do you honestly think she does not do all she can for the child she loves? That does not take away the exhaustion, the pain, the sorrow. You cannot be happy by pretending to be happy.

      Liked by 1 person

  19. What a brave and powerful post. I’m sorry to hear that some higher-functioning adults are disapproving – I’m one, and I think yours/your son’s is an important and valid experience. I admire you for being willing to describe the difficult times, and doing so in a way that is both moving and matter-of-fact.

    Like

  20. Wow I don’t have a child with special needs but let me tell you reading this honest piece has made me appreciate what I do have. I am a single mom of 2 boys and sometimes the challenges can be overwhelming but nothing compared to what you have to face every single day. Today I will try and appreciate what I have. I have the outmost respect for each and every one of you. You are doing an amazing job and to write with such honesty shows that you are only human but yet here you are still doing what you do because of the unconditional love that you have. Well done parents I honestly salute each and every one of you xxx

    Like

  21. I understand your pain. You are still a great mom, and your little boy is lucky to have you. But I know its hard. Every day. Wishing you could be like other families. Wishing it could have been different. Some days not wanting it at all. Its ok to feel that way. Sending you a prayer, from a fellow autism mom.

    Liked by 1 person

  22. Yes I cryed. God will help you…was my daughters coment. Today I to wanted to give up. After your your comments I’m not alone. Not the first time. Thanks I have to go fight for services. God has this.

    Liked by 1 person

  23. Thank you for writing this.

    Please know, although I don’t know you at all, that as an autism mum too I’m there with you. Please know your strength comes from a place others do recognise. Please know you’re an amazing mum. Know that your love, even on the worst days where you can’t see it or feel it, is deeper than anyone could even begin to imagine.

    Autism mums draw strength from a place seldom visited by mortal men, it is a place of warriors and guardians. When you need to crawl through one more day, we are all there in that realm, spinning the wheels and keeping the light going so that you can make it through.

    B

    Liked by 1 person

  24. I do appriciate your honesty but I would love to have my son here with me. He passed away 30 months ago. I miss him every day. I miss his quirky ways I miss watching the same bits of video over and over. I would give anything to be running round after him. I still get up between 4am and 5.30 ( that would have been a lay in). Thomas was non verbal but knew enough words to get his needs met.

    Liked by 1 person

      • Yes, being frustrated and overwhelmed and burnt out does not mean we don’t love our children. I often think, when I have difficult days, just how devastated I’d be if my son were to pass away. It must be very hard for you Wendy, I am so sorry to hear of your loss.

        Like

  25. I’m sorry you are having a hard time and I can see that you are genuinely struggling. It’s not nice to mentally burn out and not have the right supports in place. I hope someone can put their hand out and offer you some guidance and help make things easier for yourself and that beautiful boy of yours. You need each other, you can get through this. There are brighter days ahead.

    Like

  26. Love this! When I am really down I think about all the other autism parents out there doing the same as me and it makes me feel less isolated. We are all amazing – even on those days we don’t want to be an autism parent anymore.

    Liked by 2 people

  27. My son now resides at his fathers. I had a breakdown. The judgements and looks by my family are pretty harsh but if I don’t get well then I will never be if any use to him. I still do the medical spots and he stays once a week. His father has unfortunately poisoned my sons mind against me but hey…that’s life…I have enough guilt to raise the titanic but I must remember I’m ill too.

    Liked by 1 person

    • omg, I’m so sorry to hear about your husband’s reaction. That is just awful. You do all you can, you work until you break, and that is the thanks you get. Maybe his turn will come …

      Like

  28. Lots of love to you. I hope you can be guided to someone who can help you change his behaviour in some ways. Try Metamorphosis – free on you tube- to help him be calmer and you. Very best wishes for a better future and things to change for the better. I married as Apergers person and even he was hard going. It is not your fault. Not in any way at all.

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  29. Thank you so much for your brutal honesty. My son functions highly, so I don’t want to suggest that I struggle with the same challenges, but I do have days when I feel like this too. I was woken by screaming every day for years, he’s only really grown out of it in the past few years for some reason. Now it’s more waking up with tantrums every now and then. Until I had my daughter (when he was 4) I thought all children woke in this way for the first years of their lives. Now I can appreciate how stressful and exhausting it is for the first moment of the day to feeling like this everyday. How bleak and lonely and relentless it feels. It colours the day from the out. It’s not something I’ve heard other parents talk about. Now I realise how much of a luxury it is to wake to general happy/quiet/calm noises. Just one of many little pieces of a jigsaw that make up the daily battles of a mum to an autist. Thankyou for your honesty. X

    Liked by 1 person

  30. So very sad because it’s so real I have been there with daughter and I’m afraid it doesn’t get any better in adulthood she 25 with the mind of a 5year old in some way & pre school everyday life. She can’t wash herself she can’t dress herself choose anything day to day living She can however flick & flap anything that is not glued down At the moment it’s a block of wood and a long piece of wood My heart breaks she will never marry but she is oblivious to everything & she is the happiest person I’ve ever met she loves music and sings along with her own words 😊🙉 Keep going It’s hard but where would they be without us. Many a day as far away as possible 😊 Sending hugs 🤗 & strength to you xx

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  31. you may think you not a good mum and think your not doing a good job but just think its you who see to your kids on hes good days and not good days so in my eyes your the best mum and i no how you fell as my kid is the same but she is my kid and i am her mum so its my job to love her xxx

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  32. Thank you for you blog, thank you for being you. Your son knows you are there for him no matter what & he appreciates it; even though he cannot say so.
    My brother-in-law is high-functioning autistic, lives with parents age 42. I worked in a School wiv autistic base for 4 years, with high functioning through to non-verbal autistics. What you & other parents do is amazing!
    Your sons know you do it, they love you.
    You are valuable & valued. I loved your post. Always here if you need a listening ear.

    Liked by 1 person

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