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Tuesday, 2 July 2013

7 Things You Don't Know About A Parent of Children with Additional Needs

Annotated from some text I came across on another blog about parents of children with additional needs -

1. I am tired. Parenting is already an exhausting endeavor. But parenting a child with additional needs takes things to another level of fatigue. Even if I've had a good night's sleep, or have had some time off, there is a level of emotional and physical tiredness that is always there, that simply comes from the weight of tending to those needs. Hospital and doctors' visits are not just a few times a year, they may be a few times a month or week!! Therapies may be daily. Paperwork and bills stack up, spare time is spent researching new treatments, positioning her to sit a certain way, advocating for him and her in the medical and educational system. This is not to mention the emotional toll of raising a child with additional needs since the peaks and valleys seem so much more extreme for us. I am always appreciative of any amount of grace or help from friends to make my life easier, no matter how small. 

2. I am bitter - I can't help it - I find it extremely difficult to listen to other people's melodramas and patiently listen to them go on about how hard they have it. Since having my baby girl I see life through a different lens and I have lost patience for other people's petty problems - I find it hard to listen to anyone, even my poor husband as my mind is constantly whirring with thoughts of how I can make things better, how I can do things better and which hospital appointment I have to attend next and what preparation I have to do for it. I plough my every last bit of energy into doing the best I can as a mum and falling out with professionals on a daily basis because I cannot merely take their word for it when the subject of debate is my child's life and wellbeing. It is exhausting not being able to trust even the professionals to get things exactly right for your child and to constantly question their decisions, I do not do this for a pass time and I do not like coming to blows with people but when my children are in the equation, I would cut my arm off if I knew it would benefit their lives in a positive way.

3. I feel alone. It's lonely parenting a special needs child. No matter how much I try to explain the difficulties we face as a family, few manage to actually take this on board and think that telling us everything will be fine and "she'll be alright because she smiles a lot," will make it all better - I feel comments like this trivialise the daily worries we face and also do not allow us as parents to voice our worries concerns and fears to the person saying "everything will be fine". It's been a sanity saver to connect with other special needs parents with whom it's not uncomfortable or shocking to swap stories about medications, communication devices and therapies. Even within this community, though, there is such variation in how every child is affected and I feel humbled by every family's unique difficult experience. 

4. I am scared. I worry that I'm not doing enough. What if I missed a treatment or a diagnosis and that window of optimal time to treat it has passed? I worry about their future, whether she will ever drive a car, or get married, or live independently. I am scared thinking of the hurts she will experience being "different" in what's often a harsh world (not to mention that I fear for the physical safety of the person who inflicts any hurt upon my son). I am scared about finances. Finally, I fear what would happen if anything were to happen to me? No one fights as hard for my children as I do - its a full time soul destroying job at times 

5. I wish you would stop saying, "as long as it's healthy, or tell stories of how worried you were that your child may have had something wrong with it and you're so relieved it's normal, " I hear a lot of pregnant women say this. Don't get me wrong, I understand and share their wishes for healthy babies in every birth, but it's become such a thoughtless mantra during pregnancy that it can feel like a wish against what my children are. "And what if it's not healthy?" I want to ask. (My response: you will be OK. You and your child will still have a great, great life.) no life should be worth less because it is not just how you expect or want it to be - you get what you are given and every life is as valid and special as the next. 

6. I am human. I have been challenged and pushed beyond my limits in raising my son and daughter. I've grown tremendously as a person, and developed a soft heart and empathy for others in a way I never would have without them.  I look at children and adults with additional needs in a completely different way - they used to be from a world I found difficult to connect with but now I am part of that world and have no choice but to dive head first into it. I'm just like the next mum in some ways. Sometimes I get cranky, my son and his demands irritate me, and sometimes I just want to flee somewhere quiet and dark.. Which leads me to the final point...

7. I want to talk about my son but find it still very difficult to because of the comments i receive "he seems fine to me" and "oh my kids do that all the time" and "well thats him just being boisterous" It's hard to talk about my son. Its hard to talk about my daughter. She is not what i expected in a daughter - she is more than i could have ever imagined and i truly believe she was sent to me to save me from myself (a sufferer of lifelong depression and anxiety disorder) My children are the most awe-inspiring things to happen to my life. Some days I want to shout from the roof tops how funny and cute my son is, or how he accomplished something in school. Sometimes, when I'm having a rough day, or have been made aware of yet another health or developmental issue, I might not say much. Sometimes i forget to even update their daddy on an evening because i am often so exhausted or overwhelmed by the information i have received that day. I don't often share with others, even close friends and family, the depths of what I go through. Usually if a friend or family member asks "how are you?" I just respond, "Good." Its easier and who really cares or wants to know the long drawn out in depth answer about how we are struggling to cope and feel a deep despair most of the time even though things appear fine on the surface. And if I'm not sharing, don't think that there isn't a lot going on underneath, or that I don't want to. Sometimes I just don't have the energy to share or I fear the response I will get back.
Raising a special needs child has changed my life. I was raised in a family that valued performance and perfection and unconsciously I'd come to judge myself and others through this lens. Go to university, get a successful job. Nothing breaks this lens more than having a sweet, innocent child who is born with impairments that make ordinary living and ordinary "performance" difficult or even impossible. All I want for my children is for them to be satisfied with their lives and feel comfortable and happy with themselves. 
It has helped me understand that true love is meeting someone (child or adult, special needs or not) exactly where he or she is -- no matter how they stack up against what "should be." Raising a special needs child shatters all the "should bes" that we idolise and build our lives around, and puts something else at the core: love and understanding. The definitions of beauty, perfection and happiness are questioned and re-evaluated. So maybe that leads me to the last thing you don't know about a special needs parent... I may have it tough, but in many ways I feel really blessed. And to not realise the blessing is to not survive the challenges we face. 

Monday, 8 April 2013

Zumbathon and Family Fun Day

If you follow Hallie's Story on Facebook you will already know I am organising a charity event which I am hoping will attract hundreds of people on the day. As well as raising money for Sturge Weber Uk I hope the charity event will help spread awareness across sheffield of the rare condition and help educate hundreds of new people. It will be a fantastic day for all ages whether you're taking part in the zumbathon or bringing the kids for a fun filled afternoon playing games, taking part in craft activities and saying hello to Beartie the sturge weber mascot bear!

Monday, 14 January 2013

facebook

Hallie's Story is now on facebook too : )

fund raising info

http://www.justgiving.com/Yvette-Hughes1    http://www.justgiving.com/yvette-hughes1               

please visit Yvette's just giving page and pledge your support to Sturge Weber UK.

Yvette is running a half marathon on 10 February to raise money for Sturge Weber UK and needs your support : )

I am touched that she and others have chosen to raise money for Sturge Weber UK, it gives me the motivation to try and spread awareness even more about the rare condition to get others involved in raising money for the charity.

Please also take a look at http://www.justgiving.com/david-needham1 - Hallie's Grandad is raising money for Great Ormond Street Hospital as they have, amongst other amazing specialist services, a Sturge Weber Clinic - the only one in the UK.

Also...! My husband (Hallie's daddy) Graham has a just giving page http://www.justgiving.com/graham-davidson (you can find his page by typing in Hallie Davidson) Graham is raising money for Sturge Weber UK

There are more fund raising events coming up this year that will be raising money for Sturge Weber UK - I'll keep you posted! xxx

Saturday, 22 December 2012

video - useful to know seizures come in all different forms

Hallie's first seizure on Monday 17 December 2.20pm.  She is 7 months old. Her seizures start in her left foot and move quickly up her left leg into her torso and then into her left arm.  They last approximately 5 to 10 minutes.  Hallie only has unilateral port wine stain on her brain (the right side only) affecting the frontal and parietal lobes.

Going home!

I'm very happy to say we have managed to get out of hospital for Christmas! And Hallie's christening tomorrow : ) I had planned a Christmas going back and forth between Hallie in hospital and Isaac and Seth at home (which I would have made work as you have to work with whatever situation you are presented with) but having Hallie at home Christmas Day is something I certainly won't be taking for granted.

After being nervous about the doctors and nursing staff at the beginning of Hallie's admission, I have left feeling a lot more positive and the nurses were very caring, cheerful an attentive. I hope Hallie goes back to S2 again if she gets readmitted - although hopefully this won't be for a long while!

xxx

Friday, 21 December 2012

Hallie is hospital - photos

Our stay in hospital: part 2

After my chat with the neurologist (in which I blubbed and told him I didn't mean to offend him or question his expertise, I just wanted to fight for Hallie and ensure she was looked after properly) he apologised and said he had actually treated SWS patients before which made me feel a lot better. He agreed to treat after 5mins of a seizure starting instead of 20mins, which was concerning me. But only as a one off treatment and not repeatedly every time she had a seizure in clusters as this could send her into a deep sleep and affect her breathing.

So, Hallie was given another loading dose of sodium valproate and had her carbemazepine medication increased. The neurologist told me he was increasing Hallie's carbemazepine much faster than he normally would to try and get on top of the seizures.

Hallie's last seizure was 8.30am Thursday 20th - fingers and toes crossed (words of the neurologist) that the seizures are under control for now and Hallie can go home for her christening on Sunday and of course have her first Christmas at home!

Our stay in hospital

Well, it's been a long week of which half the time I haven't known what day it is or time! So, I haven't had the opportunity to update hallie's blog.

She was admitted on Monday 17 December to Sheffield Childrens Hospital. I had fed Hallie her usual bottle around 2pm and we were sat watching tv having a cuddle when I noticed Hallie wasn't kicking her leg normally, it was rhythmically twitching. I didn't panic as I have been waiting for this for the last 7 months (although I must admit I wasn't expecting it all to happen the week before Christmas!) I lay Hallie down on her change mat to have a proper look at her body. She was very happy in herself as she lay on her mat watching me. The twitch moved up the left side of her body and into her left arm and hand. I recorded this on my phone as evidence just in case she stopped before the ambulance arrived. I phoned 999 and explained what was happening saying my baby girl was having a seizure and that she had Sturge weber syndrome and it was her first seizure. The ambulance arrived within a few minutes and I explained all this once again to the two medics who had never heard of SWS surprise surprise and I didn't want them to think she wasn't fitting. But, even though the seizure was stopping, they could see her left side was completely paralysed so said they were going to take her in with the blue lights.

At A&E Hallie continued to fit every few minutes. I was so unbelievably worried because at this point I didn't feel they were taking the situation seriously or treating it with urgency. Hallie was fully alert and wide awake throughout her seizures - she was responding and moving her eyes following the doctor's light. Because of this, they thought she was okay and she was coming out of each seizure after a few minutes. I didn't count but I would say Hallie had approximately 10 to 15 seizures in the two hours she was in A&E. finally she was given a drug (I cannot remember which one) and she was transferred to the neuroscience ward.

Hallie was given Carbemazepine and a loading dose of sodium valproate to kick start the levels of drug in her system. The nurse explained that because little ones' livers work so efficiently they tend to get rid of the drugs really quickly out of their system so need high doses to keep levels up.

Hallie kept fitting I would say 3 to 4 times a day, each fit lasting 5-10mins - the neurologist visited a lot and I had an emotional conversation with him about my concerns that he wasn't treating aggressively enough. It was so difficult because on the one hand I didn't want my baby girl to be pumped full of all these chemicals but I also wanted to ensure she was getting the treatment she needed to prevent brain damage. The nurses were a little stubborn when I kept insisting SWS seizures needed to be treated differently to other epileptic seizures. They kept telling me they had treated many patients with epilepsy over many years to which I replied "how many children have you had on this ward with Sturge weber syndrome?!"

Monday, 17 December 2012

Seizures have started

In hospital A&E - Hallie has started with seizures

She is fine in herself. The seizures started in her left foot and leg and moved rapidly into her torso and then into her left arm. They have been on and off for the past couple of hours

I will update my blog in detail later

Thursday, 6 December 2012

Marlcliffe School Christmas Fayre

Wow what an afternoon!! I haven't managed to count the money we've raised yet as every time I try my little boy Seth says he wants to "help"! But I think it's over £100 : )

We had a guess the bear's name and a lovely young boy (around 7 years old) won by guessing the name Buddy - he was very pleased

We raffled a chocolate house and I made Christmas cards and bracelets which sold well. The Marlcliffe art club Christmas cards didn't sell as well as I had thought but I will try again next week!

Hallie got sleepy half way through the Fayre and wanted a snooze bless her but the hustle and bustle was all too much. She wore her Christmas outfit especially and sat in her pram while mummy and grandma were busy on the stall.

Most importantly I managed to hand out a lot of leaflets and hopefully this will help spread awareness - I chatted to quite a few parents and explained the syndrome. The first parent I chatted to told me her son had recently passed away after having a brain tumour - this made me even more aware of how lucky I am to have Hallie in my life and how precious life is and how easily it can be taken away from us.

There were a few people who approached the stall to just give a donation without buying anything - you could see by the look on one elderly man's face that he had experienced Sturge Weber Syndrome some way in his life. All in all it was a great event and I would love to do more : )

I handed out leaflets asking parents to contact me if they would like me to organise a book party (in which I will link fundraising into the ordering of Usborne children's books)

Hallie is going on her first train journey next Tuesday, tickets are booked, we're finally off down to London to see the consultant in the specialist clinic at Great Ormond Street. I'll keep you updated on what is said.

I'm now going to have a well earned glass of wine with Graham and most likely fall fast asleep on the sofa!

X

Monday, 26 November 2012

Some recent photos of my Hallie x


Development of the central nervous system

The port wine stain - cluster of blood vessels - develops in the first few weeks of development in utero - so by the time I was 8 weeks pregnant with Hallie, her condition was already present and the blood vessels were on her tiny brain and what would be her skin eventually!

(Picture taken from google source)

Fund raising

Hello, just a quick update while I'm up with my coughing children!

My husband graham is raising money for Sturge Weber UK by doing a triathlon "iron man" event in June 2013. He has a just giving page on www.justgiving.com (type in Hallie Davidson and you'll find him) - donations welcomed please :oD

I'm also trying to do as much as I can too to raise money and awareness for the charity - I have a stall at my son's school Christmas fair on 6.12.12 - I'm going to be selling Christmas cards, raffling a very special cake donated by a very kind friend Hazel and I'm going to raffle a big cuddly bear : ) marlcliffe school have also kindly agreed to ask a few pupils to design special Christmas cards which will get printed up hopefully next week so I'll be selling those on my stall too along with the Sturge Weber UK wristbands and sweeties and children's wooden jewellery too : )

I'm also organising an Usborne book party for 1.12.12 for all the parents in my son's class YR DR and 10% of book sales will go to Sturge Weber UK - any parents who are interested please contact me ASAP as at the moment I don't have enough to hold a party unfortunately : ( - I'm planning on providing wine and food as a thank you for coming x

I've spoken to Jenny Denham this weekend just gone about my fund raising ideas - she is the first person I have chatted to from the Sturge weber Facebook support group and she is the chair of the committee of Sturge Weber UK - it was lovely speaking to her and I'm so glad there is a support group and the Internet in general these days as it provides such a useful and supportive resource for me and parents alike to share experiences and offer guidance. I know people criticise emails and texts as being impersonal but I find them a godsend for asking quick questions and getting instant answers - even from consultants!

Anyway, as the coughing seems to have died down now in our household I best try and get some sleep! Night : )

Thursday, 15 November 2012

Neurology appointment finally!

After spending the last four weeks worrying about what the scans of hallie's brain might show, today we got a proper chance to view the numerous scans and put our questions to the neurologist. Although to be honest I don't feel I have learnt much more about hallie's condition other than where on her brain she has the birthmark (patch of blood vessels/stain) whatever you want to call it!

Hallie has a patch of blood vessels on the right side of her brain, underneath where the port wine stain on her scalp is. You can't really see the port wine stain on her scalp because of her beautiful mop of hair : )

The neurologist then did a few physical tests on Hallie to rest her reflexes and how she used each side of her body, particularly her hands. Hallie wasn't that co-operative but that's not surprising since she woke up with a stinking cold this morning. He said he wasn't too worried about how she was using her hands at the moment but she would need to be checked regularly as these things usually become more obvious as a child reaches 12 months.

He didn't really put a plan in place and said the usual "it's a case of waiting to see" which is extremely frustrating. I wish I knew exactly what was going to happen Hallie and when.

Now we have the Great Ormond Street appointment in December to look forward to - I am looking forwards to meeting the consultant at their Sturge Weber Clinic as my friends in the Sturge weber UK Facebook support group have sung her praises many times and I'm hoping she will provide us with a lot more information (which will hopefully make things a lot clearer as I feel a bit fuzzy at the moment)

Thanks for reading : )

Thursday, 25 October 2012

Nightmare

I had my first nightmare about Hallie last night. She was sat in her high chair and I thought she was cold because she looked like she was shivering uncontrollably but then I realised she was having a seizure and her face looked really distressed and I couldn't soothe her : (

Still haven't heard from the neurologist regarding the details of Hallie's MRI scan on her brain - I'm eager to know exactly where the stains lie on her brain and what the next steps are for treatment etc. we have an appointment on 15 November to discuss the brain scan but I had actually requested that the consultant phone me before then - he's obviously too busy as I've left him three messages! Hmm might phone again today and leave another message for him..

We've got Hallie's eye appointment on 1 November so hopefully that won't be too traumatic for her and her eyes won't have worsened.

X

Tuesday, 16 October 2012

Sturge Weber Syndrome

I thought I'd try and write a post to say a bit more about Hallie's diagnosis (if my two mischievous sons will allow me!)

Last week Hallie was diagnosed with Sturge Weber Syndrome (SWS) - this was not a complete shock as we had been forewarned the week Hallie was born by the neonatal consultant who came to visit me at my bedside.  He had written it down on a piece of paper and told me briefly a list of possible complications Hallie may have if she did have SWS. 

For those of you that read my blog because you want to know more about SWS - here comes a detailed explanation taken from various resources (including my head)!

Sturge Weber Syndrome occurs in the first weeks of an embryo's life.  It is an abnormality of the central nervous system (I think) and is not hereditary.

Symptoms of SWS include:-

  •  A Port Wine Stain of the skin (usually around the eye and forehead area as this is near the trigeminal nerve which is connected to brain activity). 
  • A layer of blood vessels touching the surface of the brain called an angioma (these blood vessels can irritate the brain causing seizures).
  • Glaucoma - raised pressure in the eyes caused by increased level of blood vessels in the back of the eye.
  • Developmental delays and learning difficulties - this is more likely to occur when a child with SWS has the epileptic seizures.  When the blood vessels on the brain (angioma) are on both sides of the brain this is more likely to cause severe learning disability.
  • Sometimes the child will have weakness of limbs on the opposite side to that which is affected by the angioma on the brain.
Hallie is due to go back for her second eye appointment on 1 November - her eye pressures measured at 16 - 19mmHg in her right eye (the one completely covered with PWS) and 12mmHg in her left eye on her first appointment aged 4 weeks old.

An appointment has been pencilled in for Hallie to be seen at the specialist SWS clinic at Great Ormond Street in December.  We will hopefully get a chance to chat to Dr Aylett, the specialist who is very knowledgeable with the syndrome. 

Hallie is also pencilled in for her first laser treatment in January at Leeds.  I haven't changed this as a few parents on the Sturge Weber Facebook Support Group have reassured me that Hallie would be treated in a children's ward which made me a little happier.

I have found it invaluable having the SWS support group on Facebook and am so thankful for modern technology - I would feel so alone and helpless without the internet and Facebook and the numerous people I have become connected to via support groups.  The same can be said for the autism support groups I am connected to on Facebook too (that's another story though!)  Contacting the consultants is so quick and easy and I can get in touch with a few of them via email and get reassuring replies a few hours later.  All this support and information helps keep me calm and collected which allows me to continue fighting for Hallie's referrals and appointments etc.

I still haven't seen the neurologist regarding the results of Hallie's MRI brain scan.  He has been away.  I am hoping to contact him this week and ask where on the brain Hallie has the angiomas.  I am guessing it isn't extensive otherwise her behaviour wouldn't be as it is - but I don't know how it all works.  I am under the impression the parts of the brain where the angioma touches are the only parts that are affected when the child is having an epileptic seizure - which is why sometimes a child can carry on playing normally whilst having a seizure... this worries me and makes me anxious I will miss a seizure or not notice her first one straightaway (if she has any at all that is)  The symptoms above do not all occur in every child with SWS. 

Most symptoms occur in the first year of life.

Epilepsy:

approximately 80% of people with SWS have epilepsy - in most cases the epilepsy starts in the first two years of life and if by age 5 Hallie has not had a seizure she isn't likely to.

I am to watch out for twitching or jerking of the limbs on one side of the body, or jerking involving all limbs with loss of awareness.  Absence seizures (where child appears "not there"), drop seizures where the child will drop to the floor and episodes of limbs becoming stiff. 

The seizures I am worried about are the subtle ones where the child may just have a change of breathing or just a slight twitch of the hand or foot for example.

{I have taken a lot of this information from a booklet on SWS written by Dr Sarah Aylett from GOSH}

PLEASE SEE www.sturgeweber.org.uk FOR MORE INFORMATION ON SWS AND HOW TO SUPPORT THE CHARITY.