Friday, 20 August 2010

Amazing Last Day Go Gracie

Well we had our last physio session with michael today and Gracie had her post op video done and she did amazing her rangein her ankles and legs is now so much better than it was before and she has really evened out.

Grace Amazingly managed to walk about 20 feet today in the walker with adam not really doing much at all it was over a few goes but she still did the distance just the same we are really proud of her just 4 weeks ago she couldnt of done a step in the walker without a lot of support, she really has done an amazing job here we still have a long way to go but we are so happy with her progress so far.

at the end of the session we said goodbye to michael and i have to say it was very emotional and i did have a little cry these guys have been just so amazing to us here. we cant wait to come back next year and show them what she can do by then.

so thats it we are all done here for now we are having a bbq tonight to say goodbye to everyone and then have the weekend to get packed reasy for coming home on monday , this has been an amazing experience and we have met some really lovely people along the way that we will keep in touch with thankyou everyone for making this possible and to those of you who continue to support us and Grace to get her through the next 12 months we are so very gratefull..xxxxx

Thursday, 19 August 2010

Last Physio with Beth and Giant Cookies



Well we had Physio today and we said goodbye to Beth as she is going to be off tomorow it was really sad we gave Beth and Michael a thankyou card each and a giant cookie cake to say thanks they have been so brilliant with grace its such a good hospital here and we are going to miss it.


Grace had another go on her favourite bike and pedalled around the physio room with help we are hoping to have enough left over too get her one before we go we are just waiting on the cost of shipping.


Grace also went on the total gym today and did 33!!! really good reps with her legs she is doing so well we just have to keep up all the good work when we get home.


last physio tomorow and then we get discharged cant belive we have been her over a month now and its nearly time to come home .






Tuesday, 17 August 2010

Meeting with Dr Park and todays physio WOW

We had our last appointment with Dr Park yesterday he said that Gracie is doing really well, he expects her to be walking with her walker within 6 months and then work toward Crutch/ stick walking after that there is a quite good chance that she will walk independantly providing she can isolate her foot movements which she can but wouldnt for Dr Park typical...lol....

we asked about the surgery and he said that she now has no signs of spacticity in her legs at all which is brilliant as she grows she may need some heelcord stretching or hamstring lengthening withing maybe 3-5 years time, which we expected at some point but basically as longas we keep stretching her ankles out all should be good there may be some need for serial casting at some point if the stretches and splints dont work but that we will not know yet.

he had to cut 60-65% of her nerves to release her spactisity but that is quite common as she is young she has the best chance of a bright future, we have to send videos of gracie to him every 6 months to be reviewed and will return next year to see Dr Park and to have some more physio and a splint change.

we are absolutely over the moon with this outcome with all the improvements she has made already such as her straight sitting being able to sit crossed legs her right arm improvements and her general awareness that i am positive has improved we are just excited to see what she will be able to do next.

We had a really good physio session today with beth too and grace was brilliant in her walker and only needed some minimal support around her hips which is amazing, she also got her new splints today some lovely day ones with ladybirds and flowers and some butterfly ones for the night.

we are really please with Gracies progress in just a few weeks and have many things that we hope to do over the next few months to help her such as a trip to Bobath in London in November and lots of equipment to help her, she is onlymaking this progress because of each and every one of you that has helped us get her here thankyou so much xx




Friday, 13 August 2010

Gracie make a model of michael

Gracie did really well at therapy again today some assisted crawling but she is moving her legs herself when she wants too, and also some walking in her walker she can only manage a few steps at a time and still need some help holding her hips but she proved to us today what she can do when she wants too.......





she made a face on the dress me Elmo and then turned round the Beth (physio) and said it Look like Michael ( the other Physio) it was so funny we decided to get her to walk in her walker to show michael and she was so excited she was practically running.



Grace is doing really well here and im hoping by the end of next week she will be a lot stronger i am worried that she is not going to get the level of care back home as she is getting here if she was staying in St Louis she would get physio everyday for 3 months we have had just under 4 weeks and we are going home to twice a week of physio, im hoping the gym equipment will help and we will be working her hard and liasing with america for the next year or so but i do wish we could give her physio everyday but its just not possible .....

we have the weekend off physio now and are hoping the weather is going to cool down from sunday next week is looking a lot cooler being in the 88's so hopefully we will be able to get out and about a bit more , we will be saying goodbye to the last of the original residence inn sdr families that were here when we came on sunday Debbie and Sophie and Pete which will be sad but then next week it will be our turn to go home .......

Tuesday, 10 August 2010

Monday post op day 15 Brilliant day video of Gracie in her walker



we had the morning free today so we went to the science museum down the road before therapy which as always over here is free, the kids had fun and really enjoyed the dinosaurs.




















After this we went to the hospital we dropped chloe and Harvey and Evie of at the playroom which has been brilliant for them they have been using it every day when we have therapy with Gracie, and it means that both Adam and I are free to be with Gracie and see her sessions without worrying about the kids.
we then went up to therapy with beth Grace was brilliant she did some walking in her walker with help and also some crawling as well as tall kneeling she worked so hard today and i cant wait to see what she is like in 6 months if she is like this after 2 weeks.

Monday, 9 August 2010

Monday post op day 14

I cant belive we have been here 2 and a half weeks already !!!!! And i cant belive Gracie is 2 weeks post op her back has healed beautfully and she is trying really hard she is doing her streches well and although she is still very weak in her legs i can see improvements in so many things for her, she seems to be a lot more aware of her surroundings and a lot more chatty she is holding herslef in sitting brilliantly and is so much better with her hands her clumsiness has reduced greatly, she is also walking with support and getting better all the time.

We got up and said goodbye to cath and rees and Elodie and Lucas this morning as they were leaving for the airport we have met some really great people here and will be keeping in touch with them when we leave we were very sad to see them go.

We had therapy today quite late in the afternoon so we visited the magic house first where the kids got to let off a bit of steamit like a childrens science museum but fun at the same time.

We got to physio with michael and was hoping that Gracie was going to be good today and she was she did great she started the day in her walker doing some supported but not too much at all walking then moved on to the total gym and did great with her leg presses doing about 20, she then went on to a wooden trike and managed to push herself along which she has never been able to do before it was only about 5 pushes but this is amazing for Grace , she also had a go on the tread mill but was not quite ready for this yet im hoping that when she gets her splints she will be more able to this but all in all a really good session.........

we are now starting to see the things she is going to need when we come home to get her up and around and will be hoping to raise the funds to buy her a leg press bench as this is brilliant for her strength and also a wooden trike, as well as raising the money to bring her back next year for her post op appointment we would like to raise about another £10,000 -£15,000 to achieve everything she needs so will be continuing with her fundraising to finish the job and get her up and around so if anybody has any ideas or would like to help please let me know thanks xxxx

Saturday and Sunday



We have no Therapy on the weekends so after waving Callum and Family off to the airport which found quite emotional in the morning we decided to have a day out so we visited st louis zoo with little Elodie who had the surgery 2 weeks before Gracie and Lucas and their mum and dad cath and Rees who were also leaving St Louis on Monday.




What is Brilliant about Here is that all the attractions are free, so the zoo cost us nothing we had a lovely day and managed to get most of the Huge zoo done seeing all the animals although it was very hot and sticky but we are slightly getting used to the heat now.




After the zoo we decided to go back to the cheescake factory for dinner which was again lovely we had a really good day and will miss cath and rees loads when they go.




2 new SDR families arrived this weekend we have ruby who is having surgery next friday and little Dom who is having his surgery on tuesday so we all met up downstairs on Sunday night to say Hi and introduce ourselves we found it so helpfull when we got here talking to all the other families that had already been through the op i hope we can be as helpfull to them we also had another family who are staying at the metrolofts who have a little boy called Logan who is also having his surgery on Tuesday come over which was nice too.