Wiskott Aldrich Syndrome is a immune and blood disease that effects the immune system the B and T cells, you have an increased susceptibility to Infections, Bleeding and Cancer,aswell as delevoping an autoimmune disease without a transplant, Wiskott Aldrich Syndrome (WAS) is potentially fatal.
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Saturday, November 10, 2012

Getting There Slowly... Happy Times

10th November 2012
Day Plus 1676+

It has been a hard few months for me and what written is never to upset or hurt it is my feelings and thoughts. I make no comment that I am perfect or Right this is how it is said to me and I put into words the best I can. As for my whinge below it has to be said Sorry sometimes I need to get it off my chest too but it is not at anyone I just needed it said is all so Don't read and think it is at you because it is not it is all about ME LOL...

I am Grateful for my children and for what I have I never walk around saying that my children are worse never because I know they are not. I never ask for anybody to make comment and I don’t make comment other than this Blog or Face book sometimes.  I will not and Do not EVER speak about my children medical problems to any of my friends other than Best Mate as I don’t want to bore people with the same tale or be the one who has problems to tell or the feel sorry looks if they want to know read my Blog I say plus I really hate when they say they look NORMAL Did I ever say that they Don’t ... I am told I am a hard person not really I just think there are time and places for things. I am told I am hard on people and friends No I don’t take Crap and I will tell it how it is so if you ask me do I like or am I fat I will always answer you the truth No I don’t like or Yes you are Fat No I am not being RUDE I am being a Friend by telling the truth and if you not like it Don’t ask me Simple as that. It is hard to not tell the the truth living inside my world is different to yours and as much as I want to be there for you I also have alot going on. Sometimes Just Sometimes I say WHY ME WHY MY KIDS why because I am human and Normal and even though I am grateful for my children when is enough is enough... I do not wish anything on anyone and I would never want to see a Mother, Father or Grandmother or Children be Sick or watch being Sick.

After almost 10 years in and out of hospitals and Therapy Two Children going through 2 perm Babies and 2 Transplants and Heart and Lung and Kidney and Liver failure ICU Adminission for Months at a time and being told to pull the plug on your Child life and Hold your Child who is Died but thankfully the doctors got back to life and Many Cardiac Arrests Drug overdose from the Hospitals and a child that is drug addicted from  the drugs he was on in transplant and Operations that could not count on mind and my husband’s Toes and hands being the one that had to put the feeding tube down your child nose over and over every time it came out or the nurse that is in tears from doing the Blood test and gives the mum the needle to do because she can do it anymore. Sitting in a HOSPITAL for 12 months my only visiters where my and troys beautiful Family members and my mother and mother inlaws and inlaw fathers sister inlaws but no friends no calls  . People say they understand OMG Please Dont if you not seen it or lived something like it Don't comment or better they say I was in hospital for 2 days OMG I understand well OMG Don't Hate me when I snap I find that Rude Just Rude . People who did not visit but Say I was so busy I wanted to visit or I really should have I dont know Why it must of been a busy time for me but I wonder if there child or children were sick would they expect I visit them well Don't hate me if I don't and Don't turn around and say I should be visiting you.. I do want to help everyone I love I just cant be everywhere all the time and I have to remember that. All the problems they get from side effects of the Chemo Grrrrrrrr and then told your Childs has metal problems not one but Two Thanks Transplant Oh better when they tell you it is from the Transplant... PLEASE Do Not tell me that I should be used to it HOW please explain How or Transplant is finish so you should be lucky Really you don’t think that I am lucky I count my blessing everyday for both my beautiful children but you do not forget and the scares are always there and sometime I wish I had your life..Please dont tell me that I have to get over it move on your talk to someone NO you dont get over the battle the Fight and the Fear life goes on but it is there deep with in... Over it so over it enough is enough and I am sorry but when do my children get the left alone... That is My Whinge for the Day LOL OVER IT!!! Breathe Now Breathe....

Okay!!!

James Got into the IM Support Class we wanted... Yes this is great news hopefully he will settle in well. James Anxiety is going okay still some highs and lows but getting there. Slowly sorting it out Hopeful we will get there one day. James still not doing any sport does not like anything. James Asthma has been not good and they have now perm move him onto Singulair everyday which we have seen a difference in him. James still getting the bone pain and they put this down to the bone marrow regenerating itself. James has put on a little weight and Height Not much but some this is great news for him.
James Had his Anniversary on the 24th October for Transplant 9 years one Big Brave Boy Love him to bits Love Him around the world and back... His Smile makes my day..

We were shown everything in details so here James in a Nut Shell this is not everything but basics...

Diagnosis
Aspergers
IM... Mild to Moderate Intellectual disability
Asthma
Bone Pain
Glasses
Growth Problems
Global Development Delay
Scarred Lungs
Testicle Problems
Anxiety disorder
Sensory Processing Disorder (SPD)

Zac is a different kettle of fish he has been all over the place. We got Zac a weighted Blanket they are not cheap this has helped with settling Zac and Sleeping there has been a very small improvement with his sleeping from this blanket we love the blanket okay Mum does anyway LOL. We got Zac eyes tested turns out he needs Glasses so we brought and paid for them and came back for his 2 months check up turns out his eyes are worse and we need to go up in strength and we have been advised that we may have to go up in strength every 3 months over the next year  but because his eyes are getting worse the lens have got more expensive. Thanks a lot there.  On a Bright note Zac got into the IO/IS Support Class which is good for him but I saw the class and it made me sad for him Glad he gets helps Sad thought both my kids needs these classes and that they just can’t have a Normal. On a not a happy Note the doctors believe Zac has Autism which I am not so happy about and the test is $1200.00 OMG Lovely. I tell you I did not see this Autism one coming oh well so we are waiting to find a doctor to do the test my doctor could sign it off but wants to have him tested as Zac has so many problems he does not want to be mixing it up with them but he said all the other problems still stand so my god this is just added to the stack the stack of problems is huge. I am so sorry but Transplant might have done the Wiskott Aldrich part but it has given me so much more back in return Over it.
Zac had a birthday he turned 5 Yes the big 5 all grown up my little monster is all grown into a Big Monster ... LOL.. I love him to pieces Both my boys make my day everyday..

We were shown everything in details so here is Zac in a Nut Shell this is not everything but basics...

Diagnosis
Small Section Permanent Collapsed Lung will not heal could very much get worse and the whole lung Collapse.
Fibrosis of the Lungs
Reactive airway disease
Asthma
ADD
Deaf in one Ear
C.A.P.D. processing Disorder of the Brain
Sensory Processing Disorder (SPD)
Hypervigilance Disorder
Non Sleeper
Global Development Delay
Moderate to Severe Intellectual Disability
Speech stuttering

Bad Eyes Glasses
OCD Obsessive-compulsive disorder
Anxiety disorder
Waiting on Test but believed from Doctor
Autism

Remember though all these problems my children are Normal, Normal with a difference but normal they Talk and Walk and Run and Laugh and look good too they may have problems but they are no different to yours they just have extras that make them extra special...

To top my week off the boys had bloods they are back and tests are not Bad but not great.

James Blood is-
RCB is Low and PCV Low so waiting on Doctors... His EOSINOPHILS are High but this is okay as he has Asthma and Allergies and we know he has had flare up there so we would see that this would be higher..

Zac Blood is-
Hemoglobin is High and protein is High and Albumin is High and I also believe the Salt is high not sure on the salt trying to take in all info. So we are waiting on Doctors. Zac drinks a lot of milk which is also a lot to be worried about he has around 2 liters a day or 2000mls sometimes more.  Because Zac has had organ failure and he has a small Collapsed lung higher Hemoglobin is not a good at all for him. So now waiting on what the doctor wants to do with him and how to handle as he not in till Monday. Anyways Heres hoping it turns out to be nothing and life can be peachy clean for once I hate when they put you through all these tests and turns out nothing big after they think big… Really you know Doctors are Bad Men LOL Make a Big Deal out of Nothing Just like there down stairs Parts Bahahahahaha Okay Needed that Joke… Sorry Boys!!! Bahahahahahaha Feeling Good Now…

On a Good Note for me I gave up Smoking on 21st May 2012 which has been 174 days and Yes I still feel like a smoke I do all the Time Oh Hmmm.. LOL. I have also Joined the Gym I forgot to say I gained weight from giving up so trying to get fit again.I also was blessed with a niece in October 2012 she is beautiful.
I’m Tried very Worn Out and Broke the doctors cost a bomb and more but at least we have each other and I’m tried did I say that so very tried LoL. Yep just add Tried Again LOL
Sometimes I think which I know is so wrong of me that how come some people go in hospital get fixed up and walk out no problems to follow on No Nightmares to go through No Nightmares to sleep through but every week there is always something new for my boys I would not wish it on no one but over it over worrying over the nightmares.

SMILE Right SMILE because there is always so much worse in this world and so much worse happening right now and I don’t really have the right to be feeling like that when I have my Boys?

 To My Lovely Beautiful WAS Friends I hope for you that things improve and some normal starts for you all Transplants Goes quickly and well Bloods stay good Our children stay healthy and happy so we to can have great family lives with our beautiful children.

Sending out my Heart Soul and Thoughts to some special WAS Mums and their Children.

 
I have a New Song from Guy Sebastian performing Battle Scars I love this song and feel it . True Though this Battle Scars Lyrics ... The wound heals but it never does That's cause you're at war with love
You're at war with love, yeah.......These battle scars, don't look like they're fading Don't look like they're ever going away They ain't never gonna change This battle...

 
 
 
 
 
 

 
Happy Listening Everyone Great Song Sang by our Aussie Guy Sebastian Battle Scars Ft Lupe Fiasco ..

Be Safe and Be Happy Everyone to Next Time Take Care xxx

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