Tuesday, March 31, 2009




God is great!

It has been a great few weeks. Carter has made great strides and is doing well on hi flow. He was moved to the intermediate side of the NICU yesterday and I am soooooo proud of him!!! They always say that God doesn't give you anything you can't handle. I hope I have made him proud. I truly believe our little Carter is meant for great things!!!

Andy's parents came in this past weekend and unfortunatly my Mother in law was to sick to come to the hospital to visit Carter. My Father in law came though along with Uncle Tommy and we got some cute photos. Grandpa held Carter for the first time.

This is a wonderful and exciting week for us. I am looking forward to visiting with good friends this weekend.

Much love and MANY thanks for all the prayers.

Carters Mommy:)

Tuesday, March 24, 2009



Today I am writing with GREAT EXCITEMENT! Carter is doing very well!!!! It is so exciting to see the progression when there have been so many days of nothing but tears. I bathed him yesterday and he was able to breathe room air without desatting. He is so cute and was just looking around. HE HATES THE CPAP but hopefully he will be on hi flow next week. I have nothing but wonderful news to share.

Andy and I feel so blessed for all the love and prayers that have come our way. It is the power of God that has really pulled him through everything.

Today is also my wonderful husbands BIRTHDAY! So to my husband....I LOVE YOU each and everyday just a little bit more. You are my world, my sunshine and my BABY DADDY!

Much love and prayers- Deanna

Friday, March 20, 2009



I was so excited and honored today when we recieved this certificate from the Secretary of the Army and the Army Chief of Staff, along with an Army lapel pin!

We also feel so blessed that the military is taking such wonderful care of Carter.

Many blessings to our Doctors & Nurses and all who continue to serve daily.

Thursday, March 19, 2009

Which way does the diaper go? Help Clarence! (Clarence is one of Carters favorite nurses and ours:)
Are you serious...I can do this on my own!

LOVE BRANDY!

We have been so blessed this week and thank you to the doctors and nurses at the National Naval Medical Center.

Carter had a good week. For the first time, I cried happy tears....He apparently decided yesterday ENOUGH and today he is on CPAP. This is great news for him and he is in an open crib! Clarence, Anya & Brandy have done such an amazing job this week and I just want to say THANK YOU!

Daddy changed his diaper today and held him for the first time!

As a follow up, I am doing the March of Dimes walk in April. I hope you can join me. Information is listed below.

http://www.marchforbabies.org/teams/CarterThomasLinz

Much love...many thanks and MANY blessings-

Deanna, Andy & Carter (and Halo, Josie & Jack :)

Thursday, March 12, 2009


Last week I was sitting in the NICU and I looked over and found my self upset that another baby had made it onto the CPAP and Carter had not. This beautiful blessing was born about 4 days after Carter so had been there as long as us and gestationally just as challenged. On Saturday, we could tell he was having a bad day but this to me was just what Carter had gone through. On Sunday, he wasn't there. Please pray for him and his family. My heart breaks for them.

Carter's nurse asked me today why it would bother me if Carter passed away. "Was it because he has been through so much?" I am pretty horrified by this statement because he is my son. Regardless of the challenges we may face...HE IS OUR SON.

People aren't perfect, I am not perfect and life is not perfect. I am married to one of the greatest men I have ever known with a beautiful son and soooo blessed to have the love of friends, family and God with me daily.

Carter's eye surgery went well. We won't know for about two weeks as far as the outcome. We know he will have some vision challenges but it could just be him being near sighted. I pray for a positive outcome so he can see just how special he is.

Please pray for the joy in the NICU that has been with Carter, the children who struggle everyday,our doctor who is deploying and our neighbors in life who live a life we may never know but are heroes in everything they do.

God bless our angels in waiting.

Tuesday, March 10, 2009

Today we met with Carters opthamologist team. He has ROP. Yes, I feel at times like he has hit every issue in the preemie book. He is having surgery tomorrow on both eyes. Scared, yes but out of everything Carter has been through, I want him to see. On some level, it hit me in a different way because I want him to see the beauty in life, smell the flowers and hear the sounds of life.

Many have asked what ROP is: Retinopathy of Prematurity
The eyes of premature infants are especially vulnerable to injury after birth. A serious complication is called retinopathy of prematurity (ROP), which is abnormal growth of the blood vessels in an infant's eye. About 7% of babies weighing 1,250 grams (2.75 pounds) or less at birth develop ROP, and the resulting damage may range from mild (the need for glasses) to severe (blindness). The cause of ROP in premature infants is unknown. Although it was previously thought that too much oxygen was the primary problem, further research has shown that oxygen levels (either too low or too high) play only a contributing factor in the development of ROP. Premature babies receive eye exams in the NICU to check for ROP.



He is our joy, our blessing and my little fighter.

Today he is 3lbs 3 oz and 15 inches.

Much love-

Deanna, Andy & Carter

Monday, March 09, 2009

Andy and I have been working with America Supports You for over 4 years. As a military spouse, I am so proud and now as a mother touched by it all.One of Carter's attendings is being deployed to Afghanistan. She will be gone for at least a year. My heart aches for her and I pray for her safe return. I think it is so easy to forget but the war continues and our military family continues to deploy.

We have had very bad days and days filled with so many blessings. I never thought my life would be as it is at this moment but feel so blessed for all God has given us.

Much love to all- Deanna, Andy, Carter, Halo, Josie & Jack

Monday, March 02, 2009

Please log onto :

http://www.marchforbabies.org/teams/CarterThomasLinz





As many know, Andy and I were blessed with the birth of our son, Carter Thomas Linz on January 2, 2009. He came into this world at 23 weeks weighing just 1 lb, 8oz..
He has been through pulmonary blebs, IVH, NEC and heart surgery for his PDA. He continues to be our little "rocky" and beat the statistics. We are so proud of him.
This walk is for him....


Join us in the walk that helps all moms and babies.
The money we raise for March for Babies will help:
...support all-important research offering preventions and solutions for babies born too soon or with birth defects
...educate women on things they can do to increase their chances of having a healthy baby
...provide comfort and information to families with a newborn in intensive care
...push for newborn screening and health insurance for all pregnant women and children.
Please help our team help babies— click JOIN THIS TEAM at the top of the page and get started!

The mission of March of Dimes is to improve the health of babies by preventing birth defects, premature birth and infant mortality..
Snowy Day!

Today it is snowing outside, a lot! I don't think I have seen this much since we lived in Germany.

Carter has had a good few weeks. His lungs are still very sick but he is growing, which is good. Still no feeds but with any luck, today is the day! He is 1285 grams today. Who would have thought that my college math classes would come into play in my lifetime :) Carter is 59 days old today!

Heather Ablondi came to visit Carter and I last week. She had two premature deliveries herself so it was wonderful to have someone who has been there to come visit. She has done remarkable work with the March of Dimes. I have come to use them as a source of information. You can feel very alone in the NICU sometimes but I have come to realize that there are many babies born prematurely. I am going to walk for Carter in April for the March of Dimes. Once I have all the information, I will post it...hopefully you can share in my journey and help to make a difference.

Each day I find us getting stronger, ALL OF US. They always say God does not give you anything you cannot handle. For him, my son and my husband...I am choosing to be the best I can be everyday and do the best I can. As I have said, laying down is not an option.

Tuesday, February 24, 2009








Things have been quiet with Carter for the last week! Yes, this is good news! Is Carter getting "better"...No but he is getting bigger which is what we need for his lungs. We have been very lucky that his NEC has not progressed. Hopefully on Friday he can start feeds, very small, but still the nutrition he needs. It has been almost three weeks for him.

I firmly believe in the power of prayer and in little miracles. I cannot thank everyone enough for all the love and support that has come our way.

This week was also Halo's birthday. As some may know, Halo was given to me by my Mother and was the last gift I recieved from my parents so she is a very special little girl to us. She celebrated her birthday with Jack & Josie and cannot wait to meet our little Carter.

I also want to thank "The Stars" @ The Bridge Community Church and Rebecca Crosen for their beautiful get well cards for Carter.

Carter is 53 days old today. He is 2 lbs and 11 oz. A friend of mine called him "ROCKY" and the name sticks. He is our fighter, our blessing, and a gift to remind me daily that God is with us and to believe we are never alone.

Some have wondered how I am getting through things. I feel like I am channeling my Father when I say we have choices in life. God gives us lessons and fills us with love. If I lay down now, what good am I for my son.

With much love and many, many blessings...Deanna, Andy, Carter, Halo, Josie and Jack.

Thursday, February 19, 2009

Wanted to give an update on Carter. I included definitions as far as what some things are. Thank goodness for Google! This explains things better than I can.



Carter has had a few quiet days, thank goodness after Saturday. Nothing really has changed except minor changes to his vent. We spoke with the third year fellow last night and he did say to us that in his three years as a fellow he has never seen lungs as sick as Carter. I also blatantly asked him if this can be resolved and he did say yes but he will need to get the advice of others. I am taking this as positive but we know that Carter has really sick lungs. Pulmonary Blebs are uncommon in preemies and being on a vent for 47 days is also damaging to the lungs. They try to be informative and keep us in the reality of it all at the same time. At least they are not giving up hope.



The also spoke with us that there is a POSIBILITY and I say that is more of a … “hey we will keep an eye on it”….that Carter may have NEC.



What Is Necrotizing Enterocolitis?

A gastrointestinal disease that mostly affects premature infants, NEC involves infection and inflammation that causes destruction of the bowel (intestine) or part of the bowel. Although it affects only one in 2,000 to 4,000 births, or between 1% and 5% of neonatal intensive care unit (NICU) admissions, NEC is the most common and serious gastrointestinal disorder among hospitalized preterm infants.

Today he is having a head Ultrasound. His platelets are low and have been consistently so they are checking for where they may be going or if he is just not producing enough of them. He has had multiple transfusions. Because he has IVH, they are just doing the ultrasound to rule out possibilities so at this time there is a not a point of concern. We will get results today.



(INTRAVENTRICULAR HEMORRHAGE Intraventricular hemorrhage (IVH) is a generic term that refers to bleeding that begins in the germinal matrix of the brain’s ventricles. This condition most commonly affects premature babies. IVH is graded into four categories from mildest to most severe: subependymal haemorrhage or Grade I IVH, intraventricular hemorrhage or Grade II IVH, ventricular dilatation also called ventriculomegaly or Grade III IVH, and intraparenchymal hemorrhage due to rupture of the blood into the brain from within the ventricles or Grade IV IVH.)



They did an x-ray this morning but the doctors have not reviewed them yet. They had a new admit and rounds. By noon, we should know if there are any changes and if anything will change from a medical perspective today. I am just waiting.



It does feel like everyday there is something and Carter is our little “Rocky” as far as continuing to push through. We are very proud of our little man.



Weight 2 pounds, 5 oz and 14 inches

Sunday, February 15, 2009


As a Mother in the NICU, I feel incredibly helpless and alone. Carter's last 24 hours have been very rough. We were called at 2am because Carter was have respiratory issues. We arrived at the hospital to find him on 100% oxygen and saturating at 48-60. It was once again the feeling of watching the monitors and praying to God to give Carter strength. His color was a blue grey and he was not his fiesty self. Many hours later Carter was showing improvement due to the great care and the power of God. We then found out upon xray that it appeared that one of his pulmonary blebs (yes, that is actually the technical term)ruptered.The room began to spin and I fought ever urge to scream that Carter needed a break...enough. We waiting as if it did not self resolve we would need to have a procedure where they stick a needed around his heart to release to air. This procedure is very dangerous. Again, we sat, watched the monitors and prayed....as of right now, at this moment our little Carter is stable. I can only judge everything on a moment to moment basis.

As I sit in the NICU I think a lot. Not always good if you live in my head. I am terrified 100% of the time and blame myself for the struggle of my child. I know I have been told it is nothing "I" did but the feeling is always there.

Andy and I feel so blessed for the love of family, friends and prayers. This is truly what gets us through each day and gives strength to our little miracle.

Today we are exhausted....but Carter continue to do all the hard work.

Lois is here this weekend.

Much love-

Deanna, Andy & Carter

Thursday, February 12, 2009

What to NOT expect when expecting....

Carter is 41 days old today and 2 pounds. He has not been on feeds for about two weeks so has actually lost weight.

What they never tell you or you never read about (or atleast you don't look for it) is what happens that is not expected.

Carter has been bradying a lot or 22 times by documentation. That and d-satting. One may ask, "what does that mean" and the answer is , " I don't know". This is the same answer you get from the doctors that have had to "bag" him in the last 24 hours. SCARED, yes, NUMB, yes....

I am SOOOO proud of my little Carter. He is a wiggle worm and what I also like to call my little monkey.

Love to all- Deanna, Andy & Carter

PS- Good luck to all competing in VA INT'l this weekend. Deshawn is amazing and it will be an amazing year for you!

Sunday, February 08, 2009

Hello-

This past week has been the worst week of my life. I spoke to friends on Friday night and there was probably no doubt I was losing it.(that and Reglan which causes depression) We were told twice that Carter would not make it through the night. I am not sure how one is suppose to deal with that so I think I went into automation mode. I have lost both my parents after surgeries for heart disease and I think I just started to shut off. Carter proved them wrong and I think it is because he knew Mommy and Daddy were with him and weren't letting go.

They found a source of his infection which is a staph infection in the MRSA family but not drug resistant. He is on new antibiotics and seems to be responding. He still has very sick lungs which is not related but is making impressive strides I think by clinical standards. (proud Mommy talking)

I have often talked about perspective but this week I had a good dose of it. I believe so much in little miracles and the power of prayer. The love of family and good friends continues to see us all through and the love of God. Sometimes when you lose those in life you lose faith in life, in people and in God. I was lost, but now found and God is with us daily and with Carter each second.

Carter is stable, good no, but doing better. He is my living angel and continues to remind me that life is about love, family and faith. For that we are so blessed....Carter is 37 days old today.....2 pounds, 2 ounces.

Much love-

Deanna, Andy, Carter, Halo, Josie & Jack

Wednesday, February 04, 2009









Carter has had a rough few days. A few words I have come to hate in the NICU are this is, "something expected in a preemie born at his gestational age", this is "common" or "he is in a better place than he was"....He is getting great care but to Andy, Carter and I nothing about this situation is expected and it certainly is not common.

Carter suffered from an infection last Friday and since then his lungs collapsed. As of right now, at this moment....he is better. I have learn to gage things on a moment to moment basis as they change so quickly. I live in an anxiety of the phone ringing if we aren't there and that the alarms will go off if we are.

Carter is beautiful and opened his eyes yesterday which excited Andy and I. He had been so endemic that we have not seen his beautiful eyes since last Friday.

It is day by day, moment by moment so thank you for all the prayers. He is our strong little man and much like his Daddy, very happy the Steelers won the Superbowl.

Much love-
Deanna, Andy, Carter, Halo, Josie & Jack

Saturday, January 31, 2009

Yesterday afternoon, we were told Carter would not make it through the night. The next 12 hours were critical. Carter was septic and has chronic lung disease. Common in preemies, a statement I have come to hate.My Mother and Father in law came down. Carter made it through the night and today. We did nitrate Oxide treatment today but is still have lung issues. He is our miracle. I love our little Carter. He continues to prove them wrong....

Wednesday, January 28, 2009




Carter was born on 1/2/09 at 318am. He was a miracle as many told us he would not make it. Each day continues to be a journey. He had heart surgery last Friday and his lungs continue to be a period of up and down's. He was born at 1 lb and today was 920 grams...roughly two pounds. Before he was born the doctors told us he would not be alive and we had to make the decision whether he should be recessitated. Carter came out breathing and fighting. He does need help but initially he made the choice for himself.

Our little miracle......

Carter looks like Andy and was named after both of our Father's. "Thomas" is Andy and my Father's name. Carter is his Mom's maiden name. I think my Dad would have been proud.
The last few months have been challenging for Andy and I and have held a few surprises. Andy and I have been trying for five years to have a child and have had a few loses. We found out we were pregnant at the same time we found out about a few other female issues. We were told that our little Carter would not make it and at 23 weeks...he came out fighting. He had heart surgery last Friday and everyday is another blessed day.


I will write more later but since this made it to facebook, I thought I would share.

Much love and photos to follow....

Andy, Deanna & Carter (halo, josie and jack)

Friday, January 09, 2009

Heart Health:
National Wear Red Day is February 6.

Sunday, December 21, 2008






Being stationed in Iraq or Afghanistan isn't much of a way to spend the holidays. It's a time when a soldier can't help but think of the comforts of home — a warm fireplace, ribbon-bound packages with loved ones gathered around — all of the things that we take for granted this time of year.

They have a job to do, and they're willing to do it — for the sake of their families and your family, too. And we can do something in return. We can help bring a genuine taste of holiday spirit to them, however far away they may be.

There's no time of year when the USO means so much to our soldiers. Faced with a ruthless enemy, bearing up under stifling desert heat or terrible mountain cold, they look to us — and to you — for any taste they can get of a back-home holiday season.

Won't you help us help them? It's everything from a concert ringing with joyful music by a top entertainer — to something as simple and personal as a prepaid phone card that brings the voice of a loved one. Please find it in your heart to be generous to the people who are fighting for our freedom in distant and dangerous places — and who ask nothing more than knowing that, in this special time of year, we appreciate their sacrifices, we remember, we care. And we do a little something to help.



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Friday, December 19, 2008

News Releases
Women are more likely than men to die in hospital from severe heart attack
Study highlights:
• Women and men have about the same overall in-hospital death rate after heart attack.
• However, women are twice as likely as men to die if hospitalized for a type of heart attack known as ST-elevation myocardial infarction (STEMI).
• Women are also less likely to receive appropriate and timely treatment for heart attack.


DALLAS, Dec. 9, 2008 — Men and women have about the same adjusted in-hospital death rate for heart attack — but women are more likely to die if hospitalized for a more severe type of heart attack, according to a report in Circulation: Journal of the American Heart Association.

Among patients with ST elevation myocardial infarction (STEMI) in a recent study, the death rate was 10.2 for women compared to 5.5 for men. Researchers said the women were older and had higher overall baseline risk profiles than men. After adjustment for these and other differences, women with STEMI had a 12 percent higher relative risk for in-hospital death compared to men.

The study also found that some recommended treatments are delayed and underused in women.
Researchers analyzed data from the American Heart Association’s Get With The Guidelines (GWTG) program to determine if recent efforts to improve heart attack care at hospitals had closed the gender disparity gap. They reviewed the clinical characteristics, treatments and outcomes of more than 78,000 patients diagnosed with myocardial infarction admitted to 420 hospitals between 2001 and 2006.

“The finding that bears the most emphasis is that among both men and women presenting to Get With The Guidelines participating hospitals, there were no clinically meaningful differences in in-hospital survival after heart attack, once we factored in differences, such as age and other existing illnesses,” said Hani Jneid, M.D., lead author of the study and assistant professor of Cardiovascular Medicine at Baylor College of Medicine in Houston, Texas.

A decade ago, women had an overall higher death rate after heart attack compared with men. This suggests that these hospitals are now using high rates of evidence-based therapies shown to increase survival after heart attack.

“However, the finding of persistently higher death rates among women experiencing the more severe type of heart attack (STEMI) and the persistent gender gap in certain aspects of care underscore the existing opportunities to enhance post-heart attack care among women,” Jneid said.

In the study, Jneid and colleagues found that, compared to men, women were:
• 14 percent less likely to receive early aspirin;
• 10 percent less likely to receive beta blockers;
• 25 percent less likely to receive reperfusion therapy (to restore blood flow);
• 22 percent less likely to receive reperfusion therapy within 30 minutes of hospital arrival; and
• 13 percent less likely to receive angioplasty within 90 minutes of hospital arrival.

“We could not determine in this study to which extent these differences were due to physicians’ failures to administer optimal therapies to women vs. appropriate decision-making based on biological and other differences between men and women,” Jneid said.

Furthermore, researchers found that women admitted with a STEMI were about twice as likely to die in the first 24 hours of hospitalization as men.

“Although STEMI is not as common among women as it is among men, it is a concern that there is still this gap in mortality between men and women after the more severe heart attack,” said Laura Wexler, M.D., co-author of the study and senior associate dean at the University of Cincinnati College of Medicine.

Get With The Guidelines helps improve physicians’ awareness of proven post-heart attack therapies, said Gregg C. Fonarow, M.D., chairman of the Get With The Guidelines steering committee.

“As part of this effort, the American Heart Association has been collecting data from a large number of hospitals about the treatments and outcomes of therapy for heart attack victims,” said Fonarow, a professor of cardiovascular medicine at UCLA. Thus, GWTG “has not only helped improve care but also created a powerful research tool,” Fonarow said.

Study authors with Jneid, Fonarow and Wexler are: Christopher P. Cannon, M.D.; Adrian F. Hernandez, M.D.; Igor F. Palacios, M.D.; Andrew O. Maree, M.D.; Quinn Wells, M.D.; Biykem Bozkurt, M.D.; Kenneth LaBresh, M.D.; Li Liang, Ph.D.; L. Yuling Hong, M.D., Ph.D.; L. Kristin Newby, M.D., M.H.S.; Gerald Fletcher, M.D.; and Eric Peterson, M.D. Individual author disclosures are available on the manuscript.
The American Heart Association’s Council on Clinical Cardiology funded the study. Get With The Guidelines is funded in part by the Merck/Schering Plough Partnership.

Editor’s Note: The American Heart Association’s Get With The GuidelinesSM quality improvement program is designed to help hospitals treat patients with evidenced-based medicine known to improve health outcomes. For more information, visit www.americanheart.org/getwiththeguidelines. In addition, the association’s Go Red For Women program offers valuable tools to help women learn healthy lifestyles to decrease their risk of STEMI at www.GoRedForWomen.org.

###

Statements and conclusions of study authors published in American Heart Association scientific journals are solely those of the study authors and do not necessarily reflect the association’s policy or position. The association makes no representation or guarantee as to their accuracy or reliability. The association receives funding primarily from individuals; foundations and corporations (including pharmaceutical, device manufacturers and other companies) also make donations and fund specific association programs and events. The association has strict policies to prevent these relationships from influencing the science content. Revenues from pharmaceutical and device corporations are available at www.americanheart.org/corporatefunding.

NR08 – 1172 (Circ/Jneid)

Wednesday, September 17, 2008



Last night, I had the honor of speaking at the Go Red and Jafra Cosmetics conference. Thank you to Jafra Cosmetics for making me feel so welcomed and for having Go Red be a part of the event.

Friday, September 12, 2008




Side note...while going through my camera, I came across photos of the Renaissance Festival with the Linz clan....yes, I rode an elephant! I could camp if they only had plugs in trees!






Homes for OUR TROOPS in Honor of CPL. Joshua Hoffman


The evening was a wonderful one with an attendance of over 200. Josh and Heather looked wonderful and Jan Taylor did an amazing job with the benefit. There were many speakers including Senator Valde Garcia, Dr. Joseph E Thomas Jr and CPL Todd Caccamo, USMC. Surely there was a VP in the bunch! Dr Thomas held atleast 4 degrees and multiple certificates alone!

No doubt an emotional night and I was also honored to have Cay Stout there who read a letter from George W Bush...THANK YOU CAY FOR BEING SO AMAZING AND SO UNSELFISHLY INVOLVED. Beautiful soul....

So a few bits from the evening, I did have a lady tap me on the shoulder and asked me if I took credit...she looked JUST LIKE SARA PALIN....after my initial , "excuse me" and , " I do declare"...it was for the silent auction :))))

Andy emceed with me and was my usual hero. Baritone meets high squeeky voice...we are the perfect couple! Baritone me of course:)

Josh, Heather...we love you both! What a journey and what a love story. Jan, YOU MAKE A DIFFERENCE EVERYDAY AND ARE PROOF TO WHAT ONE HEART CAN DO!

God bless...good night....

Deanna & Andy

PS- Along with the ever pondering question as to why yawns are contagious is the one...why is my face always FIVE shades lighter than my body...must just be my internal glow....:)))

Thursday, August 14, 2008

Hello~

I know everyone is busy and times are tough but I was hoping for some help. Below is an event being held in Brighton, Michigan.

HOME FOR OUR TROOPS has built a house and they are giving it to Josh & Heather. If you have followed my blog, Andy & I met Josh and Heather over a year ago. He was severely injured in Iraq after an IED attack. Josh cannot move from his neck down due to a spinal cord injury. Their story is one of true hero's and love. Heather has stayed by him as his fiance. The military awards NOTHING to a fiancee to cover the fees she occurred while staying with Josh in VA. She is only 21 and their life will be one of many trials but I have confidence they will get through it all. This event is to raise money for Josh & Heather and HOME FOR OUR TROOPS to help start their new life together.

If you know anyone in Michigan (or any state) that may be able to attend or provide financial assistance, (sports figures, pageant sisters or anyone who just wants to say thank you for serving), please pass along this information. They are also registered at Target if you are able to provide a house warming gift.


Lots of love to all and thank you for any help or guidance you may provide.

Deanna

www.deannamlinz.blogspot.com
www.homeforourtroops.com


About Josh courtesy of Home For Our Troops:
Cpl Joshua Hoffman

Freeport, MI


January 6th, 2007 Cpl Joshua Hoffman was on patrol in the streets of Fallujah, Iraq when a man with a rocket propelled grenade appeared in his line of sight. The insurgent ran off, forcing Josh's group of Marines to follow and capture him. It was a standard, by the book procedure that they followed effortlessly. Josh was assigned to lead the group of men on foot. One shot rang-out, the men yelled "take cover!", and everyone dove to the ground. His men got up to make sure everyone was okay - but one man did not. Josh lay face-down in the filthy Iraq soil, unable to move, until his Navy Corpsmen came to his aid. His men frantically did everything they could to keep everyone safe while trying to save his life, and it worked. Every other person that day walked out of there untouched, but emotionally distraught over the happenings of that day.
Josh has spent the last 20 months away from his home, his friends, and his family. Fourteen of those months have been spent inside the four walls of his hospital room, 800 miles away from home. Fourteen months he lay in the same bed, staring at the same ceiling, praying to wake up and be back in Iraq, having all this be a bad nightmare. Fourteen months straight he has awakened to the crude reality of what has happened to him, to his body, to his life, and yet he is more optimistic than 95% of the other men here who have so much more use of their bodies. He tells me he's lucky - lucky to be alive, and lucky it's not worse. A man who had everything, a life many dream of, and now can hardly speak, barely see, and cannot move even a finger to itch his nose. Yet, he still says he is lucky.
Josh has had pneumonia 5 times, a urinary tract infection more than 10 times, fears of meningitis, complete kidney failure resulting in his body ballooning to 3 times his normal body size (his eyes were swollen shut, his bottom lip so big it touched his nose, and blisters that covered his entire body), and currently deals with multiple kidney stones too large to pass. He was dependent on a ventilator to breathe for him for 6 months, and still relies on a tracheotomy and oxygen. He fights everyday to relearn his speech, regain abilities to move, and hope that maybe soon he'll be able to return home. It's been a long road to recovery, but he's fighting on and he will indeed make it. After all, he is a US Marine!
Please help Homes for Our Troops build this young Marine the home he needs to aid in his recovery. He has fought for us now it is our turn to fight for him.



Fundraiser for HFOT @ the Genoa Woods Conf. Center
Brighton, MI
Please join us by showing your support as we move toward building a specially adapted home for a young, seriously injured Iraq war Veteran.
Event Date: Friday, Sept. 12, 2008 @ 730pm
Location: Genoa Woods Conf. Center, 7707 Conference Center Dr, Brighton MI
Highlights of the Evening Include:
Keynote Speakers and Dignitaries
Strolling Hors D'oeuvres
Musical and Dance Ensemble Entertainment
Martini/Cash Bar, Desserts
Silent Auction - local & national merchant/restaurant gift certificates, sports items and events tickets, show tickets and fun, exciting gift items for all!
Tickets: $60/each (donations appreciated in any amount). Adult-only Evening, please
Paypal: michHFOT@yahoo.com, Indicate name of attendee(s) in Remarks section; if you are unable to attend, indicate "donation".
Checks must be made Payable to: "Homes for Our Troops" (Tax ID# 54-2143612) and mailed to: Jan Denise Taylor, 3464 Hunter Road, Brighton MI 48114. Names/tickets will be at will-call at the door on September 12th.
Cocktail attire - Service Members and First Responders are respectfully requested to wear Dress Uniform
Gold Star Families are our Honored Guests
Questions - Jan Taylor at 810.299.2915, 810.923.9083 or jandenisetaylor@comcast.net

Date: Friday, September 12, 2008
Time: 7:30 PM
Please make a Difference in the Lives of
Seriously Wounded Michigan Heroes

Event Date: Friday, Sept. 12, 2008 @ 730pm Location: Genoa Woods Conf. Center, 7707 Conference Center Dr, Brighton MI

Highlights of this Patriotic Evening Include:
• Speakers and Dignitaries - Sen. Valde Garcia, Sgt. Todd Caccamo, USMC
• Emcee - Deanna Linz, Mrs. Washington DC International 2008
• Strolling Hors D'oeuvres
• GIGband musical entertainment, Michelle’s Academy of Dance ensemble, Dance floor
• Martini/Cash Bar, Desserts Adult-only Evening, please
• Silent Auction
Homes for Our Troops (HFOT), a national non-profit 501(c)3 Corporation, builds specially adapted homes for seriously injured Veterans through donations and at no cost to the Veteran. Cpl Joshua Hoffman, USMC 1st BN 24th Marine Regiment-Michigan, was hit by sniper fire in Iraq in 2007 on his 3rd tour of duty.

Space is Limited - Please Reserve Now
Tickets: $60/each (Donations appreciated in any Amount)
Mail Check: Payable to “Homes for Our Troops" (Tax ID# 54-2143612) to:
Jan Denise Taylor, 3464 Hunter Road, Brighton MI 48114 (810)229.2915, (810)923.9083
jandenisetaylor@comcast.net
All Names will be at will-call at the door on September 12th
Cocktail attire - Service Members and First Responders are respectfully requested to wear dress uniform
Gold Star Families are our Honored Guests

Tuesday, August 05, 2008

Todd & I
Lois & Benjamin

Busch Gardens Adventures

Go Devil Rays!!!!
My wonderful and brilliant nephew and I
Andy and I
Todd and Lois Lane
With family in Florida


Hello-

Things have been a little crazy and emotional. We did spend a week in Florida with the family after the pageant. Sleeping in until 10:30am can really spoil someone!Lois is doing well and I had said it before but her hair is REALLY curly! One of the medications she is on is Tamoxifen. Unfortunately, a side effect of the drug is the possibility of uterine cancer. Please keep her in your prayers. She was biopsied and we are awaiting the results.

Andy had PRK surgery through the US Army. Andy is (was we hope:))) legally blind so this was a great thing for us. Unfortunately the recovery is long. At the hospital this morning we were informed it would take up to 6 weeks for him to gain clarity in his vision....

On a few different notes, Josh & Heather are doing great. We are excited to be a part of their ceremonies!!! Josh & Heather are registered at Target if you are interested in providing a house warming gift!!!

Our thoughts are prayers also go out to the Devine's. Shannon & Jason are not able to bring Halle Grace home yet. Log onto http://ourdevinemiracle.blogspot.com/ to follow their journey. They are incredible people and will be incredible parents. Thank you to AJ for making strides on their behalf!

Lots of love to all-

Deanna