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A support thread for the undiagnosed, hand holding through the wilds and wonders of the unknown(50 Posts)
As one year draws to a close and we get ready to welcome in a new one, it seems fitting that we're in need of a new thread to continue what has become a lovely supportive thread for those of us with children who have no clear diagnosis.
Lots of our children are SWANs which stands for Syndrome Without A Name, having multiple and sometimes complex difficulties but neurological and genetic testing is yet to find a cause.
Hoping that some us us may be blessed with some answers in the year ahead, and looking forward to sharing the good times, celebrating little achievements, helping each other to negotiate the obstacle course of testing, therapies and community support, and offering each other a shoulder and a hug when things get tough.
link to the old thread here
Gah, typo in para 3. That's going to irritate me all year isn't it?
Ooh,how exciting,a new thread!
I have to admit, I was putting off posting because I didn't want to have to come up with a new title!
Good news about the dla, firsttimer. I can't believe I am going to have to fill out the forms again next year, I am struggling enough with the form for ds's statement, which I have to get done for a meeting in January.
I am typing on our new iPad (ds's new iPad!), it is an amazing thing, very excited about hunting down apps to use with ds.
Also looking forward to mumsnet ting in bed, of course!
Ooh ipad! We have one that is rapidly becoming the kids' domain... There is a whole list of brilliant apps on the swan facebook page I think. I'm yet to explore it as Orange is happy playing with his keyboard app. Can't remember what it's called <useless> but it's a free app and turns the whole screen into a piano.
I sometimes MN in bed on my iphone, in fact I might do that right now. Fresh clean bedlinen is calling me
Ah,me too (fresh bed linen) and a hot water bottle and a snoozy cat...I am going to go up now.Yes I have seen the piano thing,it looks great. There is a communication app (using pictures/symbols) that was recommended on the Kleefstra FB page, that I want to look into, but the one that ds loves at nursery is one where he gets to hit a cat in the face! He thinks it is hilarious.
Try SMULE app. Piano music but you just hav to tap dots so very good for fine motor skills and sharpening reactions
Here's a site for apps you can have a look at.
App city here too. I'm sure DH trawls through app stores instead of doing any work.
We have list writer that is voice activated - could be good for verbal timetable, particularly if the day is going to be a bit different.
DS3 use a good app last year when he was struggling to learn how to write the letter shapes. It also moved him along with phonic sounds and blending..
If anyone knows of a good paediatrician app, that makes judgements based on the evidence, rather than personal
lack of opinion, I would be very grateful
Hi can I join? I am at the 'is there something wrong or not' stage, so I don't know if we fit in here? I have read through a lot of the previous thread, but was unsure about joining in, so now seems like a good time, since it is a new thread?
I have 3 dc. My youngest is a year next week, and appears to be quite behind with her physical development. She does not sit up at all, though very recently has started to push back into an almost kneeling position from her tummy - but she is still not upright and cannot lift either hand off the floor or she will tip over. She does not weight bear at all, so no pulling up to stand or anything, but has in the last week or so started to 'commando crawl' briefly - it seems to exhaust her.
Her birth was a little complicated - she was breech but born vaginally, undiagnosed IUGR - she weighed 5lbs 1oz at 38+6. She required full resus twice and was in SCBU for a week. She had feeding issues - dx with reflux whilst still in SCBU, shortly after she was dx with a milk intolerance. She was quite slow in holding up her head, much slower than my other children. She didn't start weaning until 8 months as when I tried at 6 months, she choked, retched and threw up everytime. She rolled at 9 months and gradually learned to roll around the room :-)
She has recently learned to clap her hands and just today she waved for the first. She makes plenty of noises, and is sociable - though she is very upset when handled by docs etc, which I presume is normal to be fair to her! She seems to have good use of her arms, can feed herself finger foods (and non foods lol).
Due to her history, she has regular paed reviews, the next one is in a couple of weeks. They expressed oncern at her last appt and have said she may be referred to physio at this next appt. I went ahead and took her to a private paediatric physio who said her tone seems ok - though dd was hysterical everytime the lady came near her, so she wasn't able to examine her much! So I don't know whether to be reassured or not.
I worry a lot about her, but I realise there is every chance that she is just taking her time with things.
This worry is not helped by the fact that my 8 year old girl has been referred for an assessment, as her teacher suspects aspergers. So all of this, combined with the fact I am due to return to work soon, is causing me many tears, sleepless nights and constant worry!
So I hope you don't me joining in as I am sure you will all help me learn to cope with this worry!
Sorry, just wanted to add that I think it is the incessant questions on her development at the paed reviews, the fact that they can never tick very many boxes, combined with her history that makes me worry about this - I honeslty don't believe that I would have worried at all had this been my son, who had a very straightforward birth!
count me in my ds2 has no dx hes 6 now, have been going on for 5 years .
Can I join too please, my son is 5 no dx, been concerned about him since 6 weeks old due to poor eye contact, has never been formally assessed for aspergers but I will be pushing for this soon. Also have a dd age 3.5 with possibly a milder version of aspergers.
Oh, I jumped in here without reading previous posts and properly understanding what the thread was about. Sorry. I think both my kids have Aspergers just haven't been taken seriously yet to get a dx.
My apologies again. X
Hope you don't mind if I join in aswell, DS is 7 in January and although he has many prof's involved and is statemented he still has no formal Dx. He has, at last, been referred to CCDS but the waiting list is huge and he is a complex little so and so who just doesn't seem to fit nicely into any little box so not sure if it will do any good anyway.
I have to say, after over 5 years I thought I would know one way or the other, it does upset me that I can't say 'well, DS needs this help/acts like this/can't do this because...' if that makes sense.
At any rate, he is a darling boy and extreemely cheeky
Hello lovely new people, welcome . Great to have some new faces for the new year x
Hello everyone, new and old faces
Hope everyone had a good New Years Eve.
We were with the best of friends in London, and it was lovely, despite 2 of the 6 children there being ill, and none of us making it to 12!
My new years resolutions are to read more, eat less and have more fun with my children (not doing so well on the eating less so far, but have started a book and have spent the last 2 days making pillow mountain in the girls bedroom, so 2 out of 3 isn't bad!)
Ds starts the year with a ton of appointments - opthamologist, cardiologist and a pathfinder meeting to sort out a statement. He is doing well though, and touch wood, has shrugged of a couple of colds without them turning into pneumonia (keeping everything crossed)
Lots of love and luck to all of you and all your dcs in 2013.
Happy New Year to everyone, I hope the year has started peacefully and 2013 we can all make more moves forward than backward or standing still.
We've been a bit head in sand about DS over the last couple of months and since we moved. He's 14 months now, sits well but has no saving reactions and still not really able to weight bear. But, he is reaching out loads and pressing buttons and page turning like mad. For so long he just wanted to be read to so I think him observing thousands of page turns has enabled him to learn that skill, albeit crudely as he still has no real grip of any sorts.
I wanted to come and rejoin the thread if I may as I need to keep focused on working hard to help him, when he makes these leaps we get so excited and relax and head back into the world of 'he's fine, just taking his time'. But the gap is pretty big now so I have to make sure I am banging on doors to get some help. NHS physio is so hard to access in our new area so we are going to dig deep and try and access some private sessions. I'm trying to get some work I can do from home as feel DS needs me here but what have you all done about work? We are very lucky in that we can just afford our bills on DH salary but I had always envisaged trying to keep some kind of connection and the money would help us not having to spend each month worryiing abut it but just don't think that is possible at the moment, not least because we seem to have at least one appointment for DS each week at the minute. I do worry that I am being too over protective about DS though and maybe a decent nursery could help him progress. So hard to know.
Not sure if anyone has tried it but DS had some osteopathy sessions before Christmas, I was sceptical before hand but I swear it has helped. He does seem more relaxed in himself and I think that has enabled him to develop a bit more, certainly he's made more advances in the month of osteopathy than he had in the previous six months.
Anyhow just wanted to come back and say hello and to wish you all the best, hoping it is the start of a better year for us all.
Hello, may I sneak in?
DS (8) has had an initial meeting with a psychologist at CAHMS who said he thought DS was HF but on the autistic spectrum, and would diagnose him 'properly' at the next appointment. So we've had a month or so of feeling relieved and looking forward (such as it is!) to a label other than that of a naughty child.
His next appointment (where he is supposed to be diagnosed) is only an hour long - which doesn't sound right to me. I was expecting a longer assessment for a formal diagnosis.
His behaviour over the holidays has been textbook quirky, obsessive, over-stimulated
Oh, and would you mention his suspected hypermobility at this next appointment?
I don't have any experience of the autistic spectrum but I do think you should mention hypermobility. My DS is globally delayed with hypermobility and sensory seeking behaviours. We don't know yet how much his hypermobility affecting his gross and fine motor development is in turn having a knock on effect with his cognitive development.
It could well be totally unrelated but good for everyone to know about it just in case it is affecting any of your DS behaviours.
Best of luck with the appointment.
Hi. I am a regular, but don't post often. DD is diagnosed with extremely rare
genetic disorder, which is associated with learning and physical disabilities. (So technically I have dx and shouldn't post here ...). She is now 3 and doing extremely well. Besides being tiny and officially failing to thrive, she is meeting her developmental milestones (albeit on the slow side). While I am extremely pleased - obviously - the last years have been very stressful for me. I constantly check her hearing/speech/vision and am waiting for more severe delays to show up. One OT said she had substantial OT issues, but when we went to see another OT, we were told she is fine (or OT bad?! - First one couldn't provide services because she has assessed DD.). Anyway,
I guess I wanted to post here, because we all share having to deal with the
uncertainty in our children's development. This has become a 'me' post.
Wave to those I met 2 years ago...
Oh yes, she is definitely sensory seeking!!
Could I sneak in with you all for my adoptped daughter, we are undergoing assessments too, been seen by camhs for the last 12 months they feel she displays either foetal alcohol, autistic spectrum, attachment disorder, learning problems and sensory problems or there could be more than one condition but now on a waiting list for a psychiatrist/psychologist assessment by camhs, just been seen by a paediatrician who felt foetal alcohol spectrum as she has a very small head circumference, thin lip and philtrum and now referred to a geneticist to decide if it is or not, just been referred to see an educational psychologist for her school problems, our little girl is 6 in year two
hi all! is it really two years wow! I actually think we are about to get an autism diagnosis although I won' t believe it till we have it and two years ago I would have been utterly shocked as I thought autism had been ruled out. I am already buying books and reading up on it and can totally relate to wanting to put a name and have info on things.
Hello everyone, just checking in after the holiday season and theres a lovely new thread. Thanks Starfish. (I really need a new name on here too)
Im just glad xmas etc is over without any major dramas. DD absolutely loved staying with my H's folks who are adorable with her. Shes v v cuddly at the moment whcih makes it even better, drool-y kisses for everyone
Start of the year was a bit crap with me and DD down with nasty flu and H having a bout of MS fatigue. So the 1st was rubbish and that made me really weepy - Ive been saying to myself 'next year will be better' like a mantra and then just thought 'who am I kidding?' Need to keep hoping we get through this somehow and life will get there someday.
MissDuke really sympathise with where you are at, I found the 'is there isnt there' something wrong stage very hard. Such an emotional rollercoaster.
Ouch I find the work thing very hard, I work freelance and its hard to find the discipline for it when so much of my head and time is taken up with worry about our DD.
Hazey like your resolutions. Hope the years appts start well for you.
My resolutions for the year are to try to enjoy DD as much as possible and focus on being her mother not her therapist. Try to get back into a work frame of mind, obsessing about the home front wont help anything. Stop wasting time watching TV/DVDs and spend time on home/hobbies/relationships instead.
Ah, found you all again! Hi to all the new people and happy new year to everyone.
Our Christmas has been a bit crazy, as after 6 months of waiting, we completed on our new house the week before Christmas - great timing! So we are now all moved to the countryside and very glad to be here. Whilst I am braced for a nightmare in getting services transfered over, we just met with our lovely key worked from the borough (we had nothing like this in London) and feeling confident that this move was the right thing to do.
To complicate our Christmas, our lovely boy went from 'he needs a muscle biopsy at some point' to 'he needs a muscle biopsy asap.' So he has an open muscle biopsy on 21st Dec. He has dealt with it fantastically and despite some nasty looking stiches up his thigh he has been a little star. We now have a hideous wait until March to see what the result are re: mitochondrial conditions. Trying not to think about it, but its tough.
All in all we are ok though and just trying to enjoy our new home. Feeling a but guilty about that lack of physio etc that I have been doing, but as DS experiences periods of regression (prompted by illness) it really is one step forward, two steps back for us. I just need a break from it. He is at the same developmental level he was nine months ago (despite having moved forwards during this time, only to go back again). Still feeling guilty though!
Hope everyone had a lovely Christmas.
Oh smiles, nothing to do but keep going. Am hoping for good news for you.
Just wanted to say a quick "hello and happy new year" to my chums from the old thread and "hello, welcome, look forward to getting to know you" to new posters. No real news here, we've all be well the Christmas and had a good one so doing better than last year! Will post properly when I haven't got to run out to collect DH from the train. Bye!
Picking brains here please.
DS2 had a transit marker test for his bowel. It's part of the 3 pronged attack we have at working out why all 3 DS have problems - each has a paed working on different theories. DS2s paed is looking at muscular dystrophy.
Long story short - of 18 markers, day 5 xray shows at least 10/11 still inside, at what looks to be predominantly in the colon (not very scattered). I am no medic, so I could be wrong, but I know basic what's where anatomy.
Appointment is not for months.
Anyone been through the same? What might be next?
Congrats in the move smiles, hope you are settling in well. And hanbee glad you are keeping so busy, hope its a good busy?
Interesting that you freelance firsttimer. It's hard to work out what do about personal satisfaction fom work / long term career but also ensuring DS has what he needs on a day to day basis. I took redundancy just before DS to give me some flexible working options and have picked up a bit of work to do at home but its not consistent. I think we could really do with me working a bit as we currently have no OT provision and DS needs both OT and PT. We saw a private physio yesterday who was horrified at the lack of treatment he has had. We need to keep going with her until we can get the NHS to start helping properly, am going to stop fretting about getting a job and just focus on DS and trying to get some work I can do from home to help pay the bills.
Hope everyone else is ok.
auntevil I am not in the UK, but gastric motility is probably Bee's #1 forefront problem (and DS has motility issues as well). I have to get Bee off the bus, but I have become a bit of an unfortunate "pro" over the last 14 years on these topics. I will be back, if you can think of any specific questions, please ask (or if you would rather ask privately, feel free to message me).
Auntevil - dont know anything about your ques so sorry but cant help.
Ouch - freelancing has been tough and to be honest I spent the first half of last year digesting everything going on with DD rather than getting any work done. I now do freelance interviewing on large scale surveys as the regular bit. Its something I can do flexibly weekend and evenings and I can do it with my eyes shut plus the organisation sources the work which makes it easy. So that ticks away in the background and pays for a large proportion of childcare month to month. For the rest I do something more competitive and niche. Its lucrative but scary and sometimes Im just not up to it - I need to be on the ball for it and over the last few years 'on the ball' isnt how I would describe myself! Im hoping to do more this year as we are in a better place overall. Its an area of work that I hope will still be my career long term but I found it impossible to focus on career type work on my own when we were on such a learning curve regarding DD. I do find it helps me to have another focus apart from DD, otherwise I obsess over her progress/lack of progress and get very down. Its a really hard balance so please do post about how you are organising it. Im really interested in how people combine paid work/careers with having children with SN.
More generally we had a great team around the child meeting just before christmas and the plan regarding SN placements/additional support for DD is coming together in a way I think Im really happy with. Theres still a way to go with the Ed Psych needing to do an assessment but if that chimes with my overall thinking I think we will opt for her to stay in her current MS nursery with one to one support funded from 3-5. I think we've been really lucky to have some very good NHS therapists and an ed psych who seems thoughtful, intelligent and experienced - but it has taken a lot of time and thinking to get to this point.
It's hard isn't it firsttimer. I have realised in the last few days that me not working really is the right thing for DS and until we can't afford to pay the bills that will have to be the case. In itself really not a big deal but I think it's just another part of life where you realise DS needs have changed everything we thought would be etc. I am still massively struggling with where we are, at 14 months he still appears NT to most people and few people spend enough time with him to really grasp that he doesn't sit up unaided let alone crawl or walk or even more worrying, doesn't play with objects in an age appropriate way. So it's kind of easy for me to want to act as other parents if NT children do and exercise choice based on a typically developing child. But knowing I can't leave the house for my old type of job forces the huge realisation that DS isn't NT and that this is having a massive impact on our lives and decisions. In theory we'd be trying for another child now but I just can't see how it wouldn't send me onto a pit of depression coping with a pregnancy, a needy immobile baby and all his therapies plus fighting the bloody system to access them.
So work, which appears to a catalyst for lots of feelings.... I feel fortunate that there are aspects of my old job that I can do at home but its hard trying to reposition myself and drum up the work, I have organised a coaching session that was offered as part of my redundancy and am hoping that will give me some inspiration for how I can diversify. I really think DS benefits from me having something outside the home and his needs. Like you I just dwell on his needs and the future if I don't have work to occupy my mind and force me to up the ante of how much to pack into a day.
In good news though DS is finally sleeping past 5am, scared to say it out loud in case he reverts but am finally having a bit of decent sleep and not putting him back to bed when most people are rising.
Ouch - sounds like I was in a very similar position to you when DD was 14 months. Really struggling to understand why everyone else's lives were falling inot place and moving on but we just seemed stuck and increasingly exhausted (she slept terribly for ages). Getting some childcare just to rest and regroup really helped - altho it made me worry about money horribly. We havent had a second yet (wasnt a definate that we'd want two) but it was sad to watch other mums have their seconds and, right now, its really hard to watch those second children overtake our girl in terms of development. Its also really hard when its not immediately apparent to people why your child still takes up so much of your time. They are off doing soft play and running around stuff while we still only managed the occasional venture out for a coffee - I felt really left behind.
My tips for what they are worth are:
-Give yourself a break however you can. Whether its from expectations (your own and others), from activities with NT children or from your own child.
-Apply for DLA as soon as possible. I and a huge block around doing this but we got highest rate awarded just before christmas and the extra cash is a big help - I wish I'd done it sooner. Its also helped me realise that the are objectively good reasons why we are struggling so much and its not just down to my laziness/depressedness/disorganisation etc
-Tell people whats happening in detail - the tiredness, the extra work and worry involved, that you want to get back to work at some point but not sure how etc and see who out of friends and contacts can come up with good suggestions both workwise and lifewise. Maybe just the odd project will materialise that helps you realise the doors still open for that magical point in the future when you may again be able to walk through it. At strategic points that realisation that people dont think I am completely redundant in terms of my work filed has really helped keep me sane. I sometimes feel totally swallowed up by having a child who needs so much from me. Balancing it is really important for me at least.
Sorry such a huge essay. Take what sounds helpful to you from it. Its just I recognised so much of what I really got very down about in what you wrote that I wanted to feed back my experience from a little furtehr down the line - my DD is turning 3 soon and life really is coming together again now but it was awfully bleak for a while.
PS: the coaching session sounds like an excellent plan. I hope it proves useful
firsttimer can't begin to thank you for your words and time to write them. It's awful to be greatful there are other people in the same position but so totally stress relieving to know there are. I sincerely hope you have been fortunate to have had someone give you some words from experience along your journey.
At the moment I am having so many experiences that are validating why I have been such a mess during his first year, the continual attempt to be normal when you have a child kicking against every every action you do. I don't know if I feel good to know its not just my poor parenting /depression/disorganisation (!) or bitter to now be recognising it has always been a differetnt journey.
It's amazing how much other people's perceptions are still part of my choice on what to do. I plucked up the courage to take DS to a SN playgroup, we needed to get out of the house, it was on and I thought it would be a refreshing change to be with mums who don't look puzzled and stop talking when you answer the perennial 'opener' "how old is he?". My SIL was horrified that I took him, "he's not SN just behind", we'll I don't know what he is but he's not fitting into the NT world so I thought I'd dip my toe somewhere else. All arbitrary anyhow as there was no-one at the SN group!
Quick question, when did friends / colleagues etc get that you weren't just being a neurotic mum and that your DD did have valid issues? (Sorry I know that's not worded well but I hope you know what I mean). I had to turn down some work as the hours would have been dreadful and I fear that my colleague would perceive me as just being clingy mum. In my line of work women who have children generally retrain if they don't go back to long hours and talking about kids is a bit of a dull subject so childcare issues are kept firmly private.
Thankful for mumsnet and this board / thread, it's pretty isolating and it's good to find people who completely completely get it.
Ouch - Its really nice to be able to share experience and not feel like you are the only one for whom everything is so oddly different. I think starting to use the terms disabled and SN was huge for me. It took me a long time to start using those words and longer to feel confident about them but these labels helps me feel legitimated and gives me a useful shorthand when dealing with people who have little understanding of whats going on with us. I did have friends who took a sharp intake of breath or even queried that 'is she really disabled' 'she looks so normal' etc.
My family are sadly convinced that Im just a drama queen which is really hard to take. Most others have fallen into line and as shes gotten older her disability has become more noticeable as her peers race ahead of us. Thats got both good and sad sides to it. Having a visible disability helps not having to explain things that you can sense people think are strange, esp when youre tired and overwrought and yet another raised eyebrow at using a buggy, taking your child into the under 12month section at soft play etc is more than you feel up to. Plus more support and SN placement options start to become available. I think the bit until 3 is a really tough bit
With work I think it must depend a lot on the culture of a field. Ive found Im lucky in that even though I was very much someone who made their rep by being on the ball, etc, my field is actually a lovely one and I remember going to a work related event when she was two - tearing up lots as I tried to tell various people why I hadnt been around much etc, and realising that they like and value me anyway - even if I am not currently up to date and firing on all cylinders. Support can come from the most unexpected places, just like you can get horribly let down by people you thought would be there for you come what may. People have offered projects, kept me in mind, and been really nice when Ive appraoched them and just asked if I could do stuff more to keep my hand (ie: non essential stuff without strict deadlines). I just keep trying to find teh friendly helpful people out there - altho often I lose my nerve and the will to keep at it.
Hi Ouch. I have some understanding of how you feel - DS is 17 months and to look at him, he looks NT. It is only when people realise that he can't sit for more than a few minutes and cant crawl, or even transition from lying to sitting etc, that it is clear something is wrong. In a group environment, when I am holding him, I have to tell people for them to know that there is a problem.
As we have had issues like seizures and a movement disorder, it has made it easier for family/friends etc to accept that something is wrong. However, I still constantly get the stories of 'so and so didn't walk til he was two and hes fine, so and so had odd movements and hes fine.' Trying to explain that combination of symptoms that we have mean that DS is pretty definately going to have additional needs sometimes falls on deaf ears.
Personally, I have gone through phases with it all. I had a big stage of denial, then total heartbreak (this was when I found it very hard to be around NT children). Now I have reached a sort of acceptance and I tend to be very upfront about DS challenges around new people. I have to watch myself sometimes, as I need to remind myself that things that are now my 'normal' are still quite shocking for other people. I joined a couple of SN groups and they really helped me to find that 'normal'.
I really hope things start to feel better for you and that this thread helps you to know you are not alone!
There's also the emotional rollercoaster to factor in. I found I was all over the place everytime someone said anything along the 'she looks so normal lines'. Partly furious at having my worries and the work of it all dismissed but also achingly hopeful. Part of me desperately wanted to be the neurotic mum just so everything would pan out fine in a year or two.
I try harder now to acknowledge how much energy this takes up. As well as realising how awfully sad I was/am, heart broken and scared and grief stricken and that it was ok not to be able to just bounce back and be all proactive about organising work and life stuff and to just need time to process it all and thats actually just a normal reaction not a sign of how incompetent I am (I tend to think its all my fault somehow)
This thread has been a real lifeline for me over the past 2 years, theres so much support on here as well as all the practical help and knowledge.
It's such an all consuming roller coaster of emotions and practicalities. I just still can't really believe this is actually our reality and not just a little phase. I suppose it's just getting accustomed to seeing his peers transition to their next phase and not find it so eye wateringly painful. I guess its all part of the readjustment process. he has an 8 month old cousin who is starting to overtake him, god i love her to death but i am finding myself staying away as I just cant bear it. I also find it a bit odd that people, outwardly at least, don't acknowledge that even if there are no long term issues where he is at now is so far off the mark that that might be gut wrenchingly hard to deal with. But, saying that, I realised over Christmas that people maybe don't want to say what they feel, even though I am kinda feeding them the lines they don't want to agree, are they trying to protect me somehow? Maybe I've just got a rubbish set of friends! Only one, only one has recognised it must be hard.
Sorry, having a real moment of acceptance this week, I think it's because since we moved he's received no therapy and it was seeing the private PT on Tuesday that made me realise we have to start fighting his corner so much more vociferously. He is being let down hugely at the moment and I have to start battling harder.
Reading your comments genuinely gives me confidence that we will be fine and we will get used to our world, I've never been jealous before and I should be so greatful to have DS when other cant be blessed with children but I find myself looking at other people's kids and feel like we are missing out. Odd emotions.
Where are you both with diagnosis? Does the attempt to find a reason stop if the standard tests come back clear?
I sometimes stay away from my friends with NT children because it hurts. I also realise that often people want you to reassure them 'so it is going to be ok?' etc when you just dont know. Used to make me angry nowadays I see it more as how frightened people are of the bad things that can happen without rhyme or reason and so they either try to say its cos of something you've done/neglected to do or that its just a blip because 'bad things dont happen to good people' (thats just my theory)
In terms of diagnosis its become less relevant to me as time goes on. Not sure why, partly because Im starting to understand that a diagnosis wouldnt make it easier to know how to help her (maybe with autism that would be different but we are pretty sure its not autism). Im sure in the future a diagnosis would be of practical help in terms of accessing funding and SN provision. Its also that anything that can be diagnosed from bloods etc at this age is the kind of thing you wish you didnt know existed so theres this strange thing of wanting to know what it is but knowing that any clear answer would probably be a really 'bad thing'.
Whats getting easier with our girl (35 months old, GDD) is that as she develops its getting more fun for us all as she is able to interact more. She can walk now (unsteadily) but loves walking about and we can go out and explore even when its wet now. She initiates more play (her play is the level of a 9 month old say) so theres laughing and giggling in our house whcih is wonderful. We have massive kiss and cuddle fests - drool-ly kisses is a special skill she has def perfected - I dont think NT 3 year olds really want to cuddle as much as she does. She actually enjoys her bath and plays in it, it used to be a stressy rub down at best. In the last 6 months her communication is improving and we have a better idea of what she wants even tho she doesnt point/gesture really so the screaming has eased off too. I realise now how weepy that made me. Ive found that as we start to have more of the lovely fun bits of having a child the urgency of needing an answer to solve our problems has waned. We are worried and things dont look good in terms of catching up but we are adjusting in a way I couldnt have imagined and her differentness has brought new people and priorities into our lives that feel magical at times and would not have happened otherwise.
Your DS sounds totally adorable and I hope I am right in thinking you might be starting to come out the other side now in some way. Its funny yiu mentioon the park, i want nithing mire than to see him toddling around the park, wrapped up feim the cold with a big smile on his face, funny its the small things yiu year for.
I am sorry that your family aren't supportive, it is incredible how much people can ignore what is right in front if them. I can imagine it is hard to deal with.
I hope you've had some lovely sloppy kisses today, we are exhausted after rotten night of screaming but have realised enough is enough and I am no long going to pretend everything is normal and start seeking the real support we need. 14 months of rubbish sleep has done me in and I am throwing in the towel!
Here's to a good nights rest for us all.
Bloody Nora, DD, am blaming the tiredness!
You are right in saying I am coming out the other side - was convinced for a long time that would never happen for me but it has and life is starting to right itself somehow and that feels great.
It is a long hard slog, especially if you ave sleep trouble. Lack of sleep made me feel insane at times. Dont underestimate how hard it is to function normally with too little sleep - emotional reactions, decision making everything just goes off kilter. Get help, anyone you can think of, put your name down with charities and anyone else who can offer support and try to get sleep and rest in. I couldnt solve anything when I was so tired, I just ran in circles.
Oh and tell people, your friends maybe just dont know what to say and are taking their cue from you. Talk to them, tell them whats going on in detail and ask for help and suggestions. My family are a nightmare but some friends have been so supportive.
Diagnostically, we are no closer despite numerous tests. I was obsessed by diagnosis, as DS suffers from terrible muscle spasms and pain - without a diagnosis, no one knew which medication, if any could help. Now, after a couple of trials, he is on a medication which has reduced his episodes by about 70%.
I had began to acccept that we wouldn't get a diagnosis and we less worried, as we had found a way to help his pain. However, we then saw a period of regression, meaning that progressive conditions were a concern. This makes diagnostic testing critical for us. Not nessesarily getting a diagnosis - but ruling out the more terrifying options.
We would also love to have another baby and with no clue about what condition this is, the odds of it recuring and the long term prognosis - that is out of the question.
It really is a rollercoaster. DS has made no developmental progress in 8 months. I am starting to fear that it will never happen.
Personally, I have found that keeping busy and developing as much of a network as I could really helped. We used to go to 2 NT groups per week and 2 SN groups per week. Having that structure and being around people who knew DS and his challenges was a great help.
However, we moved about 2 weeks ago and I am feeling a bit lost now. We sit on the border of 3 local authorities which is making our support services a nightmare. I am sure it will all come together, but its easy to feel isolated. We have moved from London and whilst I have no doubt that moving was the right thing to do - I miss being able to put DS in his pushchair and walk for miles with loads of people around.
Oops, pressed post by mistake.
I meant to add - we also have horrendous sleep issues. It makes everything feel so much worse and I really feel for you.
From what I understand, it seems quite common for children with neuro issues to have sleep problems. We are waiting on a referral to the sleep team at Evelina Childrens Hospital at Guys and Thomas's. The charity Cerebra also offer sleep advice over the phone and may be worth a try.
I used to get really frustrated at myself with the sleep issues as I felt I was contributing to 'bad habits' and that he couldn't self settle. However I have recently accepted that we are in an unusual situation and we need to just do whatever it takes to get some sleep - from rocking him in his pushchair to co-sleeping. Since we were told his condition could be progressive I have tried to make the most of the night and turn the negative into a positive even when I am so exhausted I just want to cry.
There is something special about holding him in the middle of the night when the rest of the world is asleep - its bit of extra time together that only we share.
Great advice firsttimer thank you. I think you are right that people are taking their cues from me. I do feel a certain shift change and am more accepting of where we are now and the reality of an uncertain future.
smiles I am so sorry your DS experiences pain, that must be an added trauma for you at such a difficult time. I can only being to imagine how horrid it must feel to experience the regression and the pause in delay. It sounds like you have some wonderful moments together and he is very lucky to have you treasuring those nighttime cuddles, my poor DS could do with a bit if that I think at times! I hope you are settling in to your new home, we also moved from London a couple of months ago, like you I miss the crowds to walk and wander in, and the decent coffee shops, but I could feel the stress falling away as we got in the car and drove away. Having some space has made all the difference but it would be nice to start getting to know some people locally, am sure these things just take time.
Hello, just thought I'd bump the thread out of the nether regions of special needs!
Having a fairly shit week here, with ds ill since Saturday with a raging temperature, febrile convulsions and now a rotten chest infection. I have a horrible feeling we are heading for the hospital in the next couple of days.
We saw a cardiologist today, who discovered that ds has a small hole in his heart, where a duct that normally closes at birth is still open. Congential defects like this are consistent with Kleefstra syndrome, and it is on the milder end of heart issues, so we are relieved and concerned at the same time. He will have a 24 hour ecg in a few weeks time to see whether there are any arrythmias present.
Next appointment is a learning disability nurse coming to assess ds tomorrow. this feels huge, and I can't quite think about it properly.
We are also in the middle of the statementing process - so it is all fun here!
How are you all? Hope you and your dcs are ok.
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