Thursday, January 5, 2012

Thankful..





This christmas Im Thankful..I realized it today, during a mini sad moment..I was standing outside emmas class room looking at the pictures and I realized she's the disabled one in the picture every picture was in a differnt piece of equipment and I thought omg my child is disabled really..here's were I feel guilty.

growing up I lived 2 blocks from the library I lived there not always to read but crafts and such.. well when I was about 10 a class of older special needs came in. well not being the understanding, not so scared person i am today.. one of the boys took a liking to me, I didnt realize that then but he chased me all through the library yes I was scared I didnt understand why he was the way he was or why he was chasing me. fast forward to my 1st job another special needs boy blurted out I had zits and use medicine..lol.. so growing up not really being around the special needs community I was hurt.. so getting to my point..

I was looking at my lil sweet innocent angel sitting in all her equipment and said so what.. SHES FREAKING ALIVE AND THRIVING, MY GIRL IS SMART..tHE MEDICAL community and the world has deemed her as SEVERLY MENTALY RETARTED> NOPE SHE CANT TALK MAYBE THE OCCASIONAL YEA OR A JUMBLED ILOVEU.. BUT RETARED, MY GIRL CAN WATCH A SAD MOVIE CRY WHEN THE SAD PART, BE HAPPY WITH THE GOOD ONES AND SCARED DURING THE BAD TIMES.. that shows alot of inteligence.. To this day I have guilt and am still afraid I will freeze with older disabled children, but I dont! My girl has changed this whole family.

we rejoice in small miracles such as touching mommy or daddy with her ipad.. we rejoice emma falling in love with Rapunzel, I have longed for the day for her to love an object and just not beat it.. she can push a baby stroller a couple feet at a time of course with us holding her under her arms.. but shes doing it.. shes taking a liking to food recently we rejoice.. dont under estimate your child I know theres alot more she can learn and do and I will fight for it..

So my realization on my own life is that I love to help others find equipment or resourses.. so mama must save for a new computer so that I can help..I cant believe my life is like this growing up, NEVER would I have dreamed of being in these shoes but yous know what I fill them well.. yes life is hard but thinking back of all my friends, i was probably the most sensitive honestly I think this life was chosen for me.. all i want to do is get along with everyone, love and be happy..SO HERE IT IS THANK YOU GOD FOR BLESSING ME WITH MY 2 ANGLELS ON EARTH AND THE 2 IN HEAVEN. I KNOW LIFE IS LONELY, STRESSFUL,JOYFUL, HEARTBREAKING BUT I WILL TRY MY BEST TO BE THE BEST MOM AND ADVOCATE FOR MY CHILDREN .THANK YOU FOR TECHNOLOGY THAT HAS KEPT MY CHILD ALIVE FOR ALMOST FIVE YEARS, SOMETIMES i FORGET WITHOUT A FEEDING TUBE MY CHILD WOULD NOT BE ALIVE.I WILL FIGHT BEG WHAT EVER IT TAKES TO HELP MY CHILD even if i do get on my FB families nerves. THANK YOU GOD FOR LETTING MY CHILDREN BE ALIVE AND HAPPY AND HEALTHY, YES EVEN WITH A GTUBE..IM GRATEFUL IM GRATEFUL EVERYNIGHT WHEN I LAY IN BED AND CUDDLE THE PRINCESS, I THINK OF ALL MY DEAR ES, MITO, ETC FRIENDS THAT WISH FOR ONE MORE DAY.. I HAVE SO MUCH TO SAY TO YOU ALL THAT MY HEART BREAKS FOR YOU, I DONT KNOW HOW YOU GUYS DO WHAT YOU DO BUT IM THANKFUL YOUR IN MY LIFE BECAUSE I CHERISH ALL THE MOMENTS NOW.. SO KNOW THAT MY SILENCE IS JUST I DONT KNOW WHAT TO SAY.. KEEP FIGHTING FRIENDS..

SO BE GRATEFUL WEATHER IT BE YOUR NORMAL LIFE OR YOUR LIFE FILLED WITH GRIEFE WE ARE ALIVE AND WE ARE BLESSED.. I KNOW WITHOUT MY ES FAMILY I WOULD BE LOST IN THIS WORLD..

Tuesday, July 19, 2011

BOOOOO

Well we had our big appointment at childrens.. im conflicted on how i really feel.. There are no words on how I feel about my lil princess.. To me she is so smart and funny... everything she does is truly a miracle.. dare I say I asked the dreaded question.. Do you think Emma is considered severe MR like her diagnosis says..Yes.. she says.. well did I cry no really I wanted to just booo her.. not my princess..
My girl is smart.. why do I have blinders on I dont know why.. She loves to read, interact with others plays ipod, goes potty.. is this really the brain of an 8 month old baby..
So a foundation has paid for emmas and mine new bike were just waiting to pay the 300 for shipping I feel so blessed to have people help us.. but at the same time feel like a forever begger.. Some people may be conflicted on weather to help emma with an ipad.. should a lil one have an ipad is for just for fun will mommy steal it..lol.. no mommy is getting a new computer the 1st week of august..
honesltly to beg for donations is in a way demeaning.. but with special needs being 3 times the cost what choice do i have but to beg and plead for help.. My child doesnt walk talk or eat.. she has so many hurdles in life.. why do we have to fight tooth an nail for everything.. will this life be all about begging for help.. I guess so..
My girl finally got a kidwalk she is crusing like nothing.. my heart has been telling me for 2 years that emma needs this.. and I was right.. so when someone like me asks for donations.. were not going shopping.. My girl is fighting for her life to walk, to eat, to learn to prosper in this life she needs help.. please donate to help emma get an ipad.. please give my girl the chance she desperatly needs..

Sunday, July 17, 2011

Friday, March 18, 2011

Friday, February 11, 2011

under construction

if your missing on my page you will be back..lol.. underconstruction.. thanks..

Tuesday, November 2, 2010

Pray for alayha


Need urgent prayers tonight for baby alayha.. shes new to our emanuel family and I feel very connected to her and her mother. its amazing how one lil syndrome can bring so many families together. her mother is so young it just breaks my heart so please even if you dont know her just say a simple prayer.. you can do it baby alayha we are all praying and loving you from afar..
My second prayer is for another emanuel family.. one friend is getting ready. to fight breast cancer and has surgery soon.. please keep linda in your prayers..

love your family and hold them tight.. this world is crazy.. :(

Wednesday, August 18, 2010

summer update



life has been slow this summer I had big plans to live at the pool all summer and be tan.. here I am vampire white as ever an only been to the pool 2 times.. for all that doesnt know I had breast reduction surgery this summer something ive wanted since the 9th grade.. they took almost 10pds.. I know wow..well Ive had alot of setbacks, stiches poppin open I mean wide open, staph infection..its been a fun summer.. on top of that emma had phemonia twice this summer. Nick off his meds has been nuts. . although george lopez on tv taught what an upstair outsidey is and hes very excited for the future..lol hes been on his meds for 2 weeks now and so far I dont like them he just seems so sad. im sure they will kick in and hell be back to his normal fun loving temper tantrum self..
Emma is doing really good right. Her standing is awsome but she still relies on us all the time to catch dont know how to break that bad habbit. She is getting more personality everyday. I still dont feel she will ever talk, although I dream all the time of hearing mama from her mouth.. I even day dream what her lil voice would be like..she is still getting all her therapies which can be tiring for all of us.. school is going great with her she doesnt even know i excist once we reach the class. Its almost like she throws her arms up ready for her toys and she knows nothing else. horse therapy starts next week for nic so add another day to add my schedule..fun times people..

Thursday, April 22, 2010

overwhelmed

You know somedays I handle my life really really well..somedays..most days I guess.. but this week..wow..am I over whelmed..I long for the normal life..

I am depressed..
My husband is bipolar/crazy..lol
Nick is asbergers/adhd and now being tested for an auditory processing disorder..plus he has my gene and will probably have an emanuel baby.
Emma emanuel syndrome, 1 ear, tube fed..

can we see why I'm stressed and depressed..

Today me and my big ole GENES are depressing me..I love my children more than life and sometimes it really bothers that my genes have done a number..I dont regret having them but today I want more for them.. I want them to be normal..

So today..I dream of mexico..no drs and specialist..daily just one normal freakin day..

MAKE A WISH

MAKE A WISH
Toes in the sand

Bahama's princess

Bahama's princess
make a wish 2013

GROWN UP

GROWN UP
MY BOY

i love u

i love u

Emma in the nicu

Emma in the nicu