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Jennifers Elizabeths very Special Page 
Jennifer was born with Septo-Optic-Dysplasia ( Totally blind & missing part of her brain, The Septum Pellucidum & The Corpus Callosum ).She was also born with Turner Syndrome ( stunted growth )and anomilies of her arms and feet. She has thyroid deficiency, adrenial deficiency,cortizol deficiency,lipid problems, advanced osteoperosis,scholiosis,bronchial asthma,chronic sinisitus,chronic ear infections,migraine headaches,female hormonal problems, high blood pressure , salt deficiency,severe reflux,severe psorasis, chronic pain and muscle spasims.In other words, though she may be young, her little body is aging rapidly and she suffers ( painfully ) what most people take a life time to feel in old age.She is currently taking several different medications daily. Parents are George & Cheryl Weaver and sister Bonnie, twelve years old.Your our precious angel and gift from God Jennifer & we love you more then words can express.We are truly blessed to have you in our lives.Thankyou Lord for this precious child!!!!! You are a true insperation to us all Jennifer!!!We are very proud of you.October 2007, diagnosed with a somatrophin deficiency.::::::::::::::::::::::::::I Have Hurt A Thousand Times, But Smiled Away The Pain. I Am Courage.
I Have Faced Impossible Odds, And Won. I Am Determination.
When No One Would Listen To Me, I Trusted In God. I am Faith.
I Have Put My Life, In Others Hands. I am Trust.
I have Shared My Story, To help Others. I Am Inspiration.
I Have Fallen Many Times, But I Always Get up. I am Strength.
I Know That A Day Will Come, When My Pain Will Be Gone. I Am Hope.
I Am Courage I am Determination I am Faith I Am Trust I Am Inspiration I Am Strength I Am Hope
I AM JENNIFER!!
Birthday is 03/20/1985
WE LOVE & MISS YOU JEFFERY,REST IN PEACE www.caringbridge.org/fl/jeffery
REMEMBER: If this is your first time visiting or your 100th, please sign the guest book. Jennifer LOVES to read and keep all the messages in braille.THANKYOU & GOD BLESS YOU!!
CHECK OUT THESE WONDERFUL SITES!
www.online-angels.org www.angelsofdestiny.net www.netwish.org www.blanketministry.com/prayerblanket.html
FOR FINANCIAL ASSISTANCE WITH MEDICAL BILLS,TRY:
http://groups.yahoo.com/group/getorgivemoney/

PLEASE VISIT THE PHOTO PAGE TO SEE A PICTURE OF JENNIFER'S ROSARY'S,THAT SHE HAS LOVINGLY HANDCRAFTED.THEY HAVE BEEN BLESSED BY A PRIEST & ARE AVAILABLE UPON REQUEST TO ANYONE WHO REQUESTS ONE.MAY GOD BLESS YOU.
****HAPPY HAPPY 23rd BIRTHDAY JENNIFER**** ( MARCH 20th )
Journal
Sunday, January 27, 2008 11:46 PM CST I know that it has been a while since the last update, so let me appologize for that.2007 was a difficult year for Jennifer, for all of us, both physically and emotionally.It has been a true test of our faith.Which I think that we passed.
As of now, Jennifer seems to be stable. We managed the change over from pediatric doctors to adult doctors.So that is finally taken care of.We settled the insurance issues.For those of you that don't know, when Jennifer turned 22yrs of age, our insurance company considered her an adult and removed her from our insurance plan. she was not covered for a while. We had to prove to the insurance company that she was handicapped and had special needs.We found it to be very strange, because we have had the same insurance for seven years and they we're billed from her doctors all those years. yet, we still had to prove it to them.
Last October, Jennifer was diagnosed with a somatrophin deficiency.After all the tests were in, what that means is that she has no growth hormone in her little body.The tests shhow she doesn't simply have low growth hormone, she has NONE at all.She is a miracle child.She should have not made it to be an adult. As we already know, she also has no steroids. Thank God for watching over her.
The treatmeny for somatrophin deficiency is a daily injection of Humatrope ( synthetic growth hormone ),Again we went a few rounds with the insurance company and also the doctors office and the pharnacy this time.Humatrope is injected with what is called a pen.The pharmacy finally got the medication,but it came without the pen and they had no idea where to get one.The insurance company told us we we're suppose to get it from the doctors office. The doctors office said it was suppose to come from the pharmacy.Now you can see a picture of what we went through.AGHHHHHHHHHHHHH, VERY FRUSTRATING. I finally contacted the old pediatric endocronologist and they put us in touch with a representative from Lilly, the company that makes Humatrope. They met us at the doctors office and brought a pen.They showed us how to mix and administer the medicine. Jennifer was shown how to do it herself.She is really amazing,being totally blind, she manages to measure the correct dose, load the syringe onto the pen and using an alcohol wipe, she cleans the pen and the injection site on herself,She gives herself a shot every night before bed.I will say that she has stuck her finger by mistake a few times and she is quickly getting tired of doing this everyday.She is always supervised and either Bonnie, daddy of myself are always with her.Considering that she will have to do this the rest of her life,she absolutely must know how to do it herself. As her mom, watching her do this every night is very difficult.
Anyway, we are just waiting to see what affect if any,the new medication will have on her health.
I will not take so long in updating this page next time.Also, at the bottom of the page is our new address and phone number.Like I said, it was a difficult year.
PEACE oxo
********QUICK UPDATE************* *******03/06/2008***********
Jennifer is profoundly sick. Took her to the doctor, day before yesterday.She had been really complaining about being very dizzy and nauseaous for a number of days.All she wanted to do was stay in bed and try and sleep.Turns out that she has a massive sinusitis infection. SOOOOOOOOOOOOOOOO, here we going again.Ten days of strong antibiotics ( 1000mg of augmentin ), which makes her even more nauseaous. Along with lots of fluids and bed rest.She is such an amazing kid and we are so truly blessed to have a wonderful, kind,caring doctor.He just adores her and so do all the nurses.She always has to give the doctor a hug and a kiss before we leave the office. He said that his goal is to keep her as happy, healthy and as comfortable as possible.He actually talks to her and asks her what would make her feel better,And he really listens to her.Thankyou and God Bless you Dr. Rahman for taking such good care of our baby girl.
peace oxox
FROM OUR FAMILY TO YOURS, HAVE A BLESSED EASTER ALL!!!!
Read Journal History
Hospital Information: Patient Room: PLEASE SEND CARDS & LETTERS TO: Miss Jennifer Elizabeth Weaver 1152 South Confederate Drive Lake WildWood, Macon, Georgia,31220 478-477-8044
Links: http://smilequilts.com/jenniferw.html ***********************PLEASE STOP BY AND CHECK OUT JENNIFERS LOVE QUILT******************* http://www.specialchild.com/archives/dz-037.html Learn all about Jennifers blindness. http://www.turner-syndrome.com Learn all about Turner Syndrome.
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