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Feedback June 21, 2011

Posted by Not Just Rockets in Site News.
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Serve. Give. Just Do It. May 7, 2012

Posted by Not Just Rockets in Local Charities, Special Interest, Uncategorized.
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None of us can do anything great on our own, but we can all do a small thing with great love – Mother Teresa

Almost two years ago, I walked into a local hospital for the first time as a Now I Lay Me Down to Sleep (NILMDTS) volunteer photographers’ assistant. It was at a time in my life that things were about as difficult on a personal level as they had ever been. The American economic crash had drastically changed my life. We had to close what had been, before the downturn, a wildly successful family business and I really do mean “family”. Unfortunately, the business was tied directly to the housing and construction industry and that was the area of the economy hit the hardest.

We were fortunate to have our children working with us, but it also meant that when the business closed, they would also be out of work. We lived in one of the most beautiful places you can imagine. Being at home was like being on vacation. Closing the business would mean that we could no longer afford to live there and would have to move. We had no idea what the future would hold for any of us. The weight of it all was almost crushing. I walked in to the hospital two years ago, on my first NILMDTS call, a woman full of worry, weighed down heavily with burdens. By the time I walked out of the hospital two hours later, after multiple sessions, I realized I had very few, if any real problems. I had just experienced, over the course of those two hours, profound examples of real pain, real tragedy and my perception had shifted.

Today, two years later, when I walked into the same hospital to serve two families needing NILMDTS services, it hit me that I was as different from the woman that walked in two years ago as I could possibly be. My circumstances have changed, but the real change has been in me. Service to someone with a greater need than my own, at a time when I was stuck mentally, emotionally and spiritually in a very unhappy place, saved me.

You hear that a lot. It seems as if every TV psychiatrist, self-help author, minister and great philosophical thinker generally puts forward the notion that if you reach out to help others, even in your darkest moments, the gift that you ultimately give is to yourself. It doesn’t always make a lot of sense when your life has been turned upside down. You hear what they are saying, but you don’t always feel it. You are doing great to get out of bed in the morning. Doing something for someone else would require mental, emotional and spiritual energy. Your tank is empty of all three. All you are trying to do is to make it through the day.

I can tell you from experience two years later, they are right. Simply being of service to someone in need without any thought of receiving something in return will change you in ways that are beyond your understanding in that moment. I have received more than I have given and in such abundance that I am in debt to these families to an extent that I could never repay. I walked in burdened and with the weight of the world on my shoulders two years ago, and today I walked with no burdens, no weight. Just peace. My personal circumstances have changed, but my perception of them has changed more.

Serving expanded my view of the world and of myself. In hard times your world seems to get smaller and smaller. Giving of yourself opens your spirit not only to where you were before, but to a level that was beyond your imagination at the time. I don’t think it matters what you do to serve someone other than yourself or what you have to give them. It only matters that you do. Serve. Give. That’s what’s important. The actual act of love that you extend is what is important. You don’t have to understand it right now. You don’t have to believe it. I probably wouldn’t have at the time. Just do it. You don’t need money or any particular talents. She was right. Do small things with great love. It will change your life.

Information on Now I Lay Me Down to Sleep

Previous NJR NILMDTS articles

Women’s Conference with Kelly Minter April 20-21 April 17, 2012

Posted by Not Just Rockets in April 2012, Book Reviews, Churches, special events, Special Interest.
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Women’s Conference with Kelly Minter (Live)

at Asbury Church in Madison

Nehemiah: Be the Hands and Feet of Jesus

April 20 6:30pm – 8:30pm (doors open at 6pm)  April 21  10am-1:30pm (doors open at 9:30am) – Lunch is provided. Tickets $15.00 advanced (click here) and $20 at the door. Contact Lisa Murray @ Asbury Church for more information. 256-783-4260

Kelly Minter is a Christian worship leader, author, speaker, songwriter, and musician. Kelly brings her unique talents for teaching through scripture and music to women’s events all across the country. Her passion is sharing with women in the hopes that women will make the connection between the pages of Scripture and their everyday lives.

Kelly is the author of several books for women. (Amazon.com links below) Fitting Room is free at Amazon.com in the Kindle version for a limited time.  I am currently reading this book and have found it hard to put down. I am about halfway done. So far, it’s great. Be sure and grab the free kindle copy while it is available. Each of these books has an Amazon Readers Rating of at least 4.5 out of 5 stars.

Fitting Room: Putting On the Character of Christ (free right now on Amazon Kindle Version)

No Other Gods: Confronting Our Modern Day Idols

Ruth: Love, Loss and Legacy

Water Into Wine: Hope for the Miraculous in the Struggle of the Mundane

Hannah’s One Wish: A Bible Study for Teens

Follow Kelly on Facebook , Twitter or Visit Her Website and Blog:

Prayers for Logan’s Family March 3, 2012

Posted by Not Just Rockets in 2012, Special Interest.
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Update: Logan passed away this evening. Our prayers go out to his family. This brave little boy his family and his community fought so hard. Below is our previous posting. His community raised the money for Logan’s treatments and much more than was needed. Logan’s was able to travel to New Jersey for treatments that did seem to do him a great deal of good. His little body had just been through too much.

You would think the day a doctor walked in the room and told you that your child had leukemia would probably be the worst day of your life. Until it wasn’t.

For 11 year old Logan Baugher’s mom, that day wasn’t even close to the worst day of her life. They were given the diagnosis, last year on January 19, 2011, and last week the doctors at St. Jude Children’s Research Hospital told her there was nothing else they could do for Logan. He has Stage 5 AML Leukemia and has been given approximately 5 weeks to live. He is not strong enough for more treatments at this time. There is one program in New Jersey that offers Logan hope to get strong enough for more treatments, but it is expensive and the family’s insurance doesn’t pay for it. It is Logan’s only hope.

Logan Baugher was a normal boy, leading the life of a very loved child, attending Owens Elementary School in Limestone County. He began complaining of headaches and stomach aches off and on over a 3 month period. He was diagnosed with strep throat and a stomach virus during this time, but then also began complaining of pain in his groin.

Lab work revealed that something was wrong, but it was possible that it was some type of virus, possibly mono. Logan was admitted overnight to Huntsville Hospital and underwent many tests. The next morning, Dr. Carolyn Russo, a pediatric oncologist/hematologist, broke the news that Logan had leukemia and that he was being transferred to St.Jude Hospital that day. Once at St. Jude, Logan was diagnosed with AML (acute myelocytic leukemia). Logan and his family have battled ever since to win this fight against his cancer.

After a year of treatment at St. Jude, the only avenue available to Logan now is the program in New Jersey that is having good success helping cancer patients regain enough strength to endure more chemotherapy and another bone marrow transplant. They are willing to take him into the program, but the costs would be $7000-$8000.

Ever since word got out, Logan’s community has come together in an amazing show of support with fundraisers and donations, to help pay for the treatments and expenses. Last night the Pizza Hut Express on Hwy 72, donated a portion of their profits to help Logan get the treatments he needs. At one point the wait for pizza was 3.5 hours and they finally had to close, because they had run out of food. Several local individuals and businesses including several local Papa John’s and God and Me Photography are holding fundraisers for Logan. Papa John’s will be donating 25% of orders from Jan. 18-29, 2012 to Logan’s fund. This printable form from Papa John’s includes instructions on how to designate your order as an order for Logan and the locations of the participating Papa John’s.

Donations to Logan’s fund can be mailed to Compass Bank 105 West Green Street, Athens, AL 35611. For information on other ways you can help, please click here for a complete list (as of today) on all fundraising activity for Logan and check out God and Me Photography’s Facebook Page (under the MY SITE tab, click on Contest for Logan) or the Fundraisers and Events for Logan Facebook Page. There is also a Pray for Logan page on Facebook and Logan’s mom has a blog on Caring Bridge.

(For those of you that have read my earlier posts on Luke Baugher, Logan is his cousin. Update on Luke: He is home from St. Jude and is doing great. So far, tumor free.)

Weather Safety and Emergency Preparedness February 29, 2012

Posted by Not Just Rockets in 2012.
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God & Me Photography 2011 East Limestone, Alabama

Today’s weather reminds us all that we really can’t be too prepared for bad weather emergencies. Some of the most important new information from safety officials concerns new recommendations for keeping young children safe. It is now recommended that in addition to going to the designated safe area of your home, if you have small children, babies should be in their car seats strapped in just as they are in the car and small children should have their bicycle helmets on and strapped down. The most traumatic tornado injuries tend to be head injuries, so bicycle helmets if you have them might not be a bad idea for the entire family. You might feel slightly silly, but if you have them, why not use them?

Due to the week we spent last year with no electricity after tornadoes hit our area, we already have a tab on our blog on weather preparedness and links to the Ready.gov website. http://notjustrockets.com/emergency-preparedness-2 This site has great information about all types of emergency situations and is a good resource for getting your family emergency plan together. This page gives specific information about what to do before/after and after a tornado.  http://www.ready.gov/tornadoes

Below are a few links you might find useful in the Huntsville Area:

Madison County EMA: http://madisoncountyema.com

Huntsville: http://www.weather.com/weather/today/Huntsville+AL+35801

Madison: http://www.weather.com/weather/today/Madison+AL+35757

Fayetteville, Tn: http://www.weather.com/weather/today/USTN0178

Channel 19: http://www.whnt.com

Channel 48: http://www.waff.com

Channel 31: http://www.waaytv.com

Red Cross North Alabama: http://redcrossrelief.org

How You Can Help Logan Baugher January 19, 2012

Posted by Not Just Rockets in 2012, Local Charities, special events, Special Interest.
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You would think the day a doctor walked in the room and told you that your child had leukemia would probably be the worst day of your life. Until it wasn’t.

For 11 year old Logan Baugher’s mom, that day wasn’t even close to the worst day of her life. They were given the diagnosis, last year on January 19, 2011, and last week the doctors at St. Jude Children’s Research Hospital told her there was nothing else they could do for Logan. He has Stage 5 AML Leukemia and has been given approximately 5 weeks to live. He is not strong enough for more treatments at this time. There is one program in New Jersey that offers Logan hope to get strong enough for more treatments, but it is expensive and the family’s insurance doesn’t pay for it. It is Logan’s only hope.

Logan Baugher was a normal boy, leading the life of a very loved child, attending Owens Elementary School in Limestone County. He began complaining of headaches and stomach aches off and on over a 3 month period. He was diagnosed with strep throat and a stomach virus during this time, but then also began complaining of pain in his groin.

Lab work revealed that something was wrong, but it was possible that it was some type of virus, possibly mono. Logan was admitted overnight to Huntsville Hospital and underwent many tests. The next morning, Dr. Carolyn Russo, a pediatric oncologist/hematologist, broke the news that Logan had leukemia and that he was being transferred to St.Jude Hospital that day. Once at St. Jude, Logan was diagnosed with AML (acute myelocytic leukemia). Logan and his family have battled ever since to win this fight against his cancer.

After a year of treatment at St. Jude, the only avenue available to Logan now is the program in New Jersey that is having good success helping cancer patients regain enough strength to endure more chemotherapy and another bone marrow transplant.   They are willing to take him into the program, but the costs would be $7000-$8000.

Ever since word got out, Logan’s community has come together in an amazing show of support with fundraisers and donations, to help pay for the treatments and expenses. Last night the Pizza Hut Express on Hwy 72, donated a portion of their profits to help Logan get the treatments he needs. At one point the wait for pizza was 3.5 hours and they finally had to close, because they had run out of food. Several local individuals and businesses including several local Papa John’s  and God and Me Photography are holding fundraisers for Logan. Papa John’s will be donating 25% of orders from Jan. 18-29, 2012 to Logan’s fund. This printable form from Papa John’s  includes instructions on how to designate your order as an order for Logan and the locations of the participating Papa John’s.

Donations to Logan’s fund can be mailed to Compass Bank 105 West Green Street, Athens, AL 35611. For information on other ways you can help, please click here for a complete list (as of today) on all fundraising activity for Logan  and check out  God and Me Photography’s Facebook Page (under the MY SITE tab, click on Contest for Logan) or the Fundraisers and Events for Logan Facebook Page.  There is also a Pray for Logan page on Facebook and Logan’s mom has a blog on Caring Bridge.

(For those of you that have read my earlier posts on Luke Baugher, Logan is his cousin. Update on Luke: He is home from St. Jude and is doing great. So far, tumor free.)

Texting and Driving…Please Don’t December 17, 2011

Posted by Not Just Rockets in December 2011, Random Thoughts.
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20111217-010736.jpg

We hear it everyday, don’t text and drive, don’t text and drive, don’t text and drive. Eventually, it sounds like yada, yada, yada…we hear it so much that it just becomes noise at some point. The NTSB has recommended a ban on texting while driving and possibly even a ban on talking on the phone while driving even hands free. Here is why I think they may just be right.

My youngest child graduates from college today. It’s amazing in so many ways. I can not begin to tell you how proud I am of her. Not just because she is graduating, but because she managed to do it after she was in a car accident that left her with what most likely, at this point, is permanent trauma to her brain. She was hit by a someone who was texting and driving. He admitted at the scene of the accident that he got a text and looked down to read it and never saw the light turn red. He never even slowed down.

I received a call from the emergency room at the local hospital in her college town which is 6 hours away from home. A terrible phone call when you can’t get to your child. The ER doctor said he thought she had a case of whiplash, but was otherwise ok. When I spoke to her, she said “Mom, I hit my head, it hurts”. The ER doctor assured me her CT scan was good. The EMTs had to pull her from the passenger seat through the drivers side door because her door was too badly damaged to open without cutting her out. The doctor sent her off with a prescription of pain meds and I spoke with her again while she was at the pharmacy. She seemed to be in good spirits and I went to bed feeling like a pretty lucky momma.

And then, she called at 2:00 am, screaming. She tried to lay down in bed and the pain was too much to bear. That was the beginning of what has been a nightmare for her. The second diagnosis was concussion. My husband ended up going to get her and bringing her home a week early before Thanksgiving break, because something did not seem quite right and we wanted her to see our doctor, because we trust him so much.

The real diagnosis in the end has been Post Concussion Syndrome. It is the same thing that NFL players often suffer from after being hit in the head too many times. We all felt like it was just too much for her to handle school and this new reality of dealing with her life after the injury and tried to talk her in to taking time off from school or maybe not going back at all.

She is a hard headed little thing and when she said she was going back and finishing school, I told our doctor, she might be just hard headed enough to pull it off and she has. It’s been a struggle everyday for her. Days when her head hurt so badly, she couldn’t move. Nights when she couldn’t sleep at all because it hurt too much to lay down. Classes that she had to retake, because she just couldn’t make it to class too many days. So many times, I just wanted to drive there and pick her up and make her come home.

But, I have always believed that our children belong to themselves and to God. I was just blessed that he allowed me to be their mom. So, I didn’t make her come home and she finished. It took her two extra years, but she finished. Today she will graduate from college. She made it.

While she is finished with school, she will probably never be finished with the migraines, the enormous amount of medication it takes to keep her functional and that give her the ability to lay down and sleep. Even on the medications, being any place loud, like a movie theater sets off her headaches every time. There are questions about how she will get through pregnancy when she is ready to have children, because you are not able to stay on these medications while you are pregnant.

The bad thing about all of this? I was a lucky momma to get that phone call. I am so thankful that she is still here. Many, many other moms are not so lucky. Recent research has found that texting and driving is more dangerous than driving drunk. Studies have shown you are 6% more likely to have a car accident if you are texting and driving than if you are driving intoxicated. The statistics for teenagers that are distracted while driving are even worse.

The Virginia Tech Transportation Institute conducted a study on truck drivers that text while driving and found that they were 23 times more likely to be involved in an accident. The average time that a driver was distracted by texting and driving was 4.6 seconds. That doesn’t sound like a big deal right? Wrong. At 55mph, the same study shows, that your car travels the length of a football field in those 4.6 seconds.

Next time you are at a football game, take a good look at how far that really is to basically be driving blind. Imagine that it has people standing on it. Someone’s children, someone’s parents, grandparents. Now, how about I put you in a car at one end of the field and blindfold you and tell you to drive to the other end. Oh, and by the way, the people on the field are not allowed to move even if you are coming towards them. What if they were all people you love? Would you drive that field? That is the position you put yourself in every day if you text and drive. The people around you don’t know you are texting and driving. They don’t know you are distracted. Many times they don’t have the luxury of getting out of your way. My daughter didn’t.

Like I said we are lucky. Some parents will never get the chance that I get today. To see someone you absolutely adore accomplish her goals, even if she had to drag herself all the way and it took every ounce of restraint I had as a mother to stand back and let her do it. Don’t text and drive. You don’t want what happened to my daughter, or something much worse, to happen to you or someone you love, but you know what you really don’t want? You don’t want to be the person that did it to someone else, either.

So, for at least today, in honor of Laura Lee, for me…no texting and driving. I would love to believe that while I am sitting there watching this beautiful, strong willed, determined child walk down the aisle and get her diploma, someone is listening to more than just noise.

Now I Lay Me Down to Sleep and the Duggar Family Photos December 15, 2011

Posted by Not Just Rockets in December 2011, Random Thoughts, Site News, TV Reviews.
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It is so very hard to sit back and read the comments posted on various websites regarding the Duggar family’s recent miscarriage and the uproar over private photos taken by a volunteer photographer for Now I Lay Me Down to Sleep (NILMDTS). I read a few today. I don’t think I will read anymore. First of all, this is really only the business of the Duggar family, but I do want to say something about NILMDTS.

These photos were taken by a photographer that is part of a network of over 7000 volunteers worldwide who donate their time, money and countless hours, to make sure that parents who have a baby born still or with a terminal diagnosis have the same opportunity that those of us with healthy children get everyday. This service is only provided at the request of the family. No photographs are taken by NILMDTS volunteers without first being called by the hospital (on the family’s behalf) or by the family directly and with written consent from the parents. NILMDTS provides the family with portrait quality photographs of their child whether the baby has already passed or is still alive, but is not expected to survive.

For those of us blessed enough to have healthy, happy children, how many photos do we have of our kids ? Hundreds, maybe for some of us thousands over their lifetime. Why so many? Because our children are precious to us at every age. We know they are going to grow up and change and we cherish our photographs of them because they are the only way to remember all those tiny little details that would otherwise be lost to us over time as memories fade.

Photos from the moment they were born, their first day of school, birthdays, Christmas, graduations, weddings,  all those moments we want to capture forever or share with family and friends and are precious to us. For most people I know, their family photos are one of the first things they think of saving in a disaster or are the most heartbroken over if they are lost or destroyed. For those of us lucky enough to a lifetime of photos for each of our children, can you imagine not having one photo of your child ever? What if  something happened to your child and you did not have one single photo of them? For the families that NILMDTS serves these photos are the only portrait photography they will ever have of their children. For some families they are the only photos they will have at all of their precious child.

Memorial photography is not new. Hundreds of years ago it was the norm. So many children did not survive early childhood due to the lack of medical technology that we take for granted today. Early childhood and infant mortality rates were very high. Many times, especially if the family could not afford a photographer under normal circumstances, the memorial photos were the only photo of their child that existed. Ever. This practice was very common in the United States and Western Europe for centuries.

One of the comments I read today on one site said, “Photographs are for living, not the dead. For celebrating, not mourning”. It struck me that this comment can only be made by someone who has been lucky enough to never have to be in the situation the Duggar family finds themselves in today. Someone who has never had to make the decision to have memorial portraits made of a baby that was gone too soon or to let them go with no photographs. The photograph of Michelle Duggar holding her daughter’s tiny hand is precious. It is tangible proof that her baby was here and she mattered to her family. For some families that is very important. Every family makes their own choices and grieves in their own way. How they do it is really, as I said in the beginning, no one’s business but theirs. Those photos were meant to be private and shared only with those people that the parents chose to share them with. Not plastered all over the internet. I hope the intent of the person that shared them originally on Twitter was not malicious, I hope they just didn’t think and weren’t intentionally trying to be hurtful to this family, but TMZ and other websites who chose to post them need to take them down and take them down now. As a NILMDTS volunteer, I don’t find the photos offensive in anyway. They are just really, really no one’s business.

It doesn’t matter how many children these people have. They will still mourn this baby every bit as much as anyone that has ever lost a baby and they deserve to do it with the same respect and dignity the rest of the world is allowed in this situation. For more information on Now I Lay Me Down to Sleep…go to www.nilmdts.org or see my previous post on NILMDTS.

Related article: LA Times Blog Post

 

Operation Christmas Bear 2011 December 6, 2011

Posted by Not Just Rockets in Army Family and MWR, December 2011, Holidays, Local Charities, special events.
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Military deployments can be especially tough on children of military personnel with a parent deployed during the holidays.  This weekend an extra special visit from Santa will help lift the spirits of these very special children of active military, National Guard and Reserve.

The Cahaba Shrine Temple annual Christmas Party is this Saturday, held in honor of military families with a family member deployed overseas for the holidays. This is the 8th annual party.The 2010 Christmas party served approximately 110 families for a total of  about 212 children

Activities include storytelling by Mrs. Claus, music, crafts and games for the children along with a magician, rock wall and inflatables. Santa arrives at 1:00 p.m.  A professional photographer will be on hand to take pictures of the children with Santa.

The Veterans Coalition is an all-volunteer group of more than 40 veteran and civic support groups dedicated to community service. Families who want to participate in the Christmas party can register by contacting Breeden at 256-876-5397 or at mary.breeden@conus.army.mil. The festivities are sponsored by the North Alabama Veterans and Fraternal Organizations Coalition.

Papa John’s Will Donate $1 Per Order on 11/11/11 to USO November 11, 2011

Posted by Not Just Rockets in Army Family and MWR, Local Charities, November 2011, Special Interest.
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Logan’s Donating 25% of Nov 11th Proceeds to Military Families November 10, 2011

Posted by Not Just Rockets in Army Family and MWR, special events, Special Interest, ThingS to Do.
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Logan's Donating 25% of Nov 11th Proceeds to Military Families

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