Thursday, October 29, 2009

Some Blog Fun


1. You Can Only Use One Word.

2. Pass this along to 6 of your favorite bloggers.

3. Alert them that you have given them this award.

4. Have Fun!

The Fun Part:

1. Where is your cell phone? table

2. Your hair? shorter

3. Your mother? amazing

4. Your father? Determined

5. Your favorite food? Cake

6. Your dream last night? none

7. Your favorite drink? Dr. Pepper

8. Your dream/goal? amazing mom

9. What room are you in? living room

10. Your hobby? traveling

11. Your fear? critters

12. Where do you want to be in 6 years? Colorado

13. Where were you last night? Pictures

14. Something that you aren’t? Fearless

15. Muffins? Blueberry

16. Wish list item? Equinox

17. Where did you grow up? Dallas

18. Last thing you did? LP-Bed

19. What are you wearing? PJs

20. Your TV? huge

21. Your pets? Boomer

22. Friends? Amazing

23. Your life? Busy

24. Your mood? Tired/Sleepy

25. Missing someone? Family

26. Vehicle? Jetta

27. Something you’re not wearing? Shoes

28. Your favorite store? Coldwater Creek/Gymboree

29. Your favorite color? Purple

30. When was the last time you laughed? Tonight

31. Last time you cried? Sunday

32. Your best friend? Landon

33. One place that I go to over and over? Pediatrician

34. One person who emails me regularly? Scott

35. Favorite place to eat? Randy White's BBQ
I tag:

Wednesday, October 28, 2009

Doing the Two Step!

Landon took his first 2 steps tonight!! We were at his Great-Grandma's house after having his Halloween pictures taken professionally. He was playing and playing like normal, reaching from the coffee table to the couch, etc. Well I had Scott move the coffee table back a little bit to try and encourage him to maybe think about taking some steps...well about 30 minutes later, he lets go of the coffee table (he's been free standing for a few weeks now), and is free standing for about a minute. Well, then he looks at me and takes 2 steps to reach me!!! It was so neat to watch, and extra special because he had 5 people watching him! His Grandma (Scott's mom), Great-Grandma, Brother (Zach), Scott and I were all watching him, it was quite possibly the neatest thing I have seen :o) The cutest part I think of though was after he took the steps we were all saying "yay!!" and he started clapping and was so proud of himself! It won't be long before we are running after him :o)

Monday, October 19, 2009

9 months old!

My little guy is 9 months old today! I cannot believe that time is flying by so fast, and he is getting to be so big! His well check is not until the 28th so I will update will all of his stats then. He is doing very well and is getting to the point where he prefers table food, especially what Mommy & Daddy are eating, to baby food. He will still eat baby food but we have definately moved on to stage 3 foods and are quickly fasing those out! We go back to the Geneticists and the Metabolic Nutrisionist sometime soon. We had to cancel our original appointment because we had to come to Texas for some family things. I hope we get to meet with them soon so we can learn how to calculate fat % and what that means for his diet and what he can and can't eat depending on the fat %. It will definately be a learning curve, but I am looking forward to it because it means the whole family will be eating much healthier! Landon has accomplished a lot over the last month! He can now do the following:

~Pulling up on everything

~Standing for 1-2 minutes at a time w/o holding on to everything

~He is so close to walking, we expect it to happen any day!

~He can sign "more" and know the signs receptively for: no and finished

~ He is into everything!

~He can climb the stairs...and fast too! Don't worry we have gates up to stop him!

~He can clap, blow raspberries (aka stick his tongue out and spit), he takes his hands while he is babbling and puts them over his mouth and takes them off again to make (bababa) noise...kind of like the noise we made for "indians" as a child.

~Loves to take the dogs toys and them taunt them with's hillarious because they know they cannot take it from him.

~Loves to read the Elmo book "So, Big!"

~He loves to stand up on anything!

~Still loves to jump, especially while holding on to MaMa and standing on the's super bouncy.

~He babbles all the time...of course I am trying to teach him MaMa first :o)

Information on VLCAD

My Note on this: As it states below this is general info on all types of the disorder. I wanted to let you know how it effects other children and how lucky we really are that Landon has a very, very, mild case of this disorder. Landon does not have any of the heart disorders they will talk about, or for the most part any of the side effects or other issues covered in this reading. As I have stated before in the blog, Landon has the form of the disorder that presents like Hypoglycemia. He does have to be hospitalized if he gets really sick with a glucose IV, and he does take the LevoCarnitine they mention below to help him break down fats in his body. Landon however has the form of the disorder that he has the Carnitine enzyme, his body just does not produce enough of it. If you have any questions specific to Landon's case or not, feel free to ask me I would love to tell you more about our expereinces or the disorder in general.

Please note: This is a general description and information on the disorder. There are mild, moderate and severe forms of this disorder. In our case we are very lucky that Landon has an extremely mild case and his life will not be as effected as some of the stuff you will read below. Landon also has the "hypoglycemia" form of the disorder. He does not have any of the heart defects, liver, muscle, and kidney issues that go along with the more sever forms of the disorder. With Landon we just have to make sure that he does not get dehydrated, he is not allowed to fast at all, and if he does get the stomach flu or viruses like that he has to go into the hospital and have a glucose IV until he can keep food down for a number of hours. Landon's form of the disorder is not fatal unless he does get severly dehydrated and then he can slip into a coma, but it would take a lot for that to happen to him. We count our blessing everyday that he is so mild. With that being said, googling and reading all of this information when we were first facing the disorder scared us to death. Which is why I have started this foundation and blog to show other parents going through the same thing, that there is hope and these children can live normal, happy lives with just a few adjustment.

Without further rambling here is the article we were given by our Medabolic Nutritionist that adequately and fairly explains VLCAD and basic info on Fatty Acid Oxidation Disorders.

Fatty Acid Oxidation Disorders

Disorder Name: Very long chain acyl-CoA dehydrogenase

Acronym: VLCADD

•What is VLCADD?

•What causes VLCADD?

•If VLCADD is not treated, what problems occur?

•What is the treatment for VLCADD?

•What happens when VLCADD is treated?

•What causes the VLCAD enzyme to be absent or not working correctly?

•How is VLCADD inherited?

•Is genetic testing available?

•What other testing is available?

•Can you test during pregnancy?

•Can other members of the family have VLCADD or be carriers?

•Can other family members be tested?

•How many people have VLCADD?

•Does VLCADD happen more often in a certain ethnic group?

•Does VLCADD go by any other names?

•Where can I find more information?

This fact sheet has general information about VLCADD. Every child is different and some of this information may not apply to your child specifically. Certain treatments may be recommended for some children but not others. Children with VLCADD should be followed by a metabolic doctor in addition to their primary doctor.

What is VLCADD?

VLCADD stands for "very long chain acyl-CoA dehydrogenase deficiency". It is one type of fatty acid oxidation disorder. People with VLCADD have problems breaking down certain types of fat into energy for the body.

Fatty Acid Oxidation Disorders:

Fatty acid oxidation disorders (FAODs) are a group of rare inherited conditions. They are caused by enzymes that do not work properly.

A number of enzymes are needed to break down fats in the body (a process called fatty acid oxidation). Problems with any of these enzymes can cause a fatty acid oxidation disorder. People with FAODs cannot properly break down fat from either the food they eat or from fat stored in their bodies.

The symptoms and treatment vary between different FAODs. They can also vary from person to person with the same FAOD. See the fact sheets for each specific FAOD.

FAODs are inherited in an autosomal recessive manner and affect both males and females.

What causes VLCADD?

VLCADD occurs when an enzyme, called "very long chain acyl-CoA dehydrogenase" (VLCAD) is either missing or not working properly. This enzyme's job is to break down certain fats from the food we eat into energy. It also breaks down fat already stored in the body.

Energy from fat keeps us going whenever our bodies run low of their main source of energy, a type of sugar called glucose. Our bodies rely on fat when we don’t eat for a stretch of time – like when we miss a meal or when we sleep.

When the VLCADD enzyme is missing or not working, the body cannot break down fat for energy and must rely solely on glucose. Although glucose is a good source of energy, there is a limited amount available. Once the glucose has been used up, the body tries to use fat without success. This leads to low blood sugar, called hypoglycemia, and to the build up of harmful substances in the blood.

If VLCADD is not treated, what problems occur?

VLCADD is variable and can cause mild effects in some people and more serious health problems in others. Symptoms may start in infancy or not until adulthood. There are three forms of VLCADD: “Early”, “Childhood” and “Adult”.

It is common for babies and children with the early and childhood types of VLCADD to have episodes of illness called metabolic crises. Some of the first symptoms of a metabolic crisis are:

•extreme sleepiness

•behavior changes

•irritable mood

•poor appetite

Some of these other symptoms may also follow:






If a metabolic crisis is not treated, a child with VLCADD can develop:

•breathing problems

•seizures•coma, sometimes leading to death

Periods of hypoglycemia can happen with or without the other symptoms. Hypoglycemia can cause a child to feel weak, shaky or dizzy with clammy, cold skin. If not treated, it can lead to coma, and possibly death.

Either hypoglycemia or a full metabolic crisis can occur:

•after going too long without food

•during illness or infection

•after heavy exercise

Symptoms of early and childhood VLCADD often happen after a period of having nothing to eat for more than a few hours. Symptoms are also more likely when a child with VLCADD gets sick or has an infection.


About half of babies diagnosed with VLCADD have the “early” type. They usually start to show effects between birth and 4 months. In addition to metabolic crises, babies can also have:

•enlarged heart, irregular heartbeat and other heart problems

•enlarged liver and other liver problems

•muscle problems

If not treated, babies with early VLCADD usually die young.

Childhood VLCADD

About one third of people with VLCADD have the childhood type. They usually show symptoms in late infancy or early childhood. Episodes of hypoglycemia or full metabolic crisis happen during illness or after long periods of not eating. Other effects can include:

•enlarged liver

•other liver problems

•muscle weakness, especially after exercise

Heart problems are usually not seen in childhood VLCADD.

Some children with VLCADD have never had symptoms and are only found to be affected after a brother or sister has been diagnosed.


About one fifth of people with VLCADD have the adult type. They usually show symptoms starting in the teen years or in adulthood. Periods of muscle weakness are common. Breakdown of muscle fibers can occur. This usually happens during heavy exercise or after going without food for a long period of time.

Signs of muscle breakdown are:

•muscle aches



•reddish-brown color to the urine.

Adults with muscle symptoms who do not get treatment can develop kidney failure.

People with the adult form of VLCADD usually do not have heart problems, hypoglycemia or metabolic crises.

What is the treatment for VLCADD?

Your baby's primary doctor will work with a metabolic doctor to care for your child. Your doctor may also suggest that you meet with a dietician familiar with VLCADD.

Certain treatments may be advised for some children but not others. When necessary, treatment is usually needed throughout life. The following are treatments often recommended for children with VLCADD:

1. Avoid going a long time without food

Infants and young children with VLCADD need to eat frequently to prevent a metabolic crisis. Your metabolic doctor will tell you how often your child needs to be fed. In general, it is often suggested that infants be fed every four to six hours. Some babies need to eat even more frequently than this. It is important that infants be fed during the night. They may need to be woken up to eat if they do not wake up on their own. Your metabolic doctor and dietician will give you an appropriate feeding plan for your infant. Your doctor will also give you a ‘sick day’ plan tailored to your child’s needs for you to follow during illnesses or other times when your child will not eat.

Your metabolic doctor will continue to advise you on how often your child should eat as he or she gets older. When they are well, many teens and adults with VLCADD can go without food for up to 12 hours without problems. The other treatments usually need to be continued throughout life.

2. Diet

Sometimes a low fat, high carbohydrate diet is recommended. food plan is recommended. Carbohydrates give the body may types of sugar that can be used as energy. In fact, for children needing this treatment, most food in the diet should be carbohydrates (bread, pasta, fruit, etc.) and protein (lean meat and low-fat dairy foods). Any diet changes should be made under the guidance of an experienced dietician.

People with VLCADD cannot use certain building blocks of fat called “long chain fatty acids”. Your dietician can help create a food plan low in these fats. Much of the rest of fat in the diet may be in the form of medium chain fatty acids.

Ask your doctor whether your child needs to have any changes in his or her diet.

3. MCT oil and L-carnitine

Medium Chain Triglyceride oil (MCT oil) is often used as part of the food plan for people with VLCADD. This special oil has medium chain fatty acids that can be used in small amounts for energy. Your metabolic doctor or dietician can guide you in how to use this supplement. You will need to get a prescription from your doctor to get MCT oil.

Some children may be helped by taking L-carnitine. This is a safe and natural substance that helps the body make energy. It also helps the body get rid of harmful wastes. Your doctor will decide whether your child needs L-carnitine. Unless you are advised otherwise, use only L-carnitine prescribed by your doctor.

Do not use any medication or supplement without checking with your doctor.

4. Call your doctor at the start of any illness

Always call your health care provider when your child has any of the following:

•poor appetite

•low energy or excessive sleepiness



•an infection

•a fever

•persistent muscle pain, weakness, or reddish-brown color to the urine

Children with VLCADD need to eat extra starchy food and drink more fluids during any illness - even if they may not feel hungry – or they could develop hypoglycemia or a metabolic crisis. When they become sick, children with VLCADD often need to be treated in the hospital to prevent serious health problems.

Ask your metabolic doctor if you should carry a special travel letter with medical instructions for your child’s care.

5. Avoid prolonged exercise or exertion.

Long periods of exercise can also trigger symptoms. Problems occurring during or after exercise can include:

•muscle aches



•reddish-brown color to the urine.

If muscle symptoms happen, prompt treatment is needed to prevent kidney damage. Children and adults with muscle symptoms should:

•drink fluids right away

•eat something starchy or sugary

•get to a hospital for treatment

To help prevent muscle symptoms:

•avoid prolonged or heavy exercise

•keep the body warm

•eat carbohydrates before and during periods of moderate exercise

What happens when VLCADD is treated?

With prompt and careful treatment, people with the childhood and adult forms of VLCADD can often live healthy lives with typical growth and development. Before diagnosis through newborn screening was available, the early form of VLCADD was fatal. Now, with immediate and ongoing treatment, many infants with VLCADD are surviving.

What causes the VLCAD enzyme to be absent or not working correctly?

Genes tell the body to make various enzymes. People with VLCADD have a pair of genes that do not work correctly. Because of the changes in this pair of genes, the VLCAD enzyme either does not work properly or is not made at all.

How is VLCADD inherited?

VLCADD is inherited in an autosomal recessive manner. It affects both boys and girls equally.

Everyone has a pair of genes that make the VLCAD enzyme. In children with VLCADD, neither of these genes works correctly. These children inherit one non-working gene for the condition from each parent.

Parents of children with VLCADD are rarely affected with the disorder. Instead, each parent has a single non-working gene for VLCADD. They are called carriers. Carriers do not have VLCADD because the other gene of this pair is working correctly.

When both parents are carriers, there is a 25% chance in each pregnancy for the child to have VLCADD. There is a 50% chance for the child to be a carrier, just like the parents. And, there is a 25% chance for the child to have two working genes.

Genetic counseling is available to families who have children with VLCADD. Genetic counselors can answer your questions about how VLCADD is inherited, options during future pregnancies, and how to test other family members. Ask your doctor about a referral to a genetic counselor.

Is there genetic testing available?

Genetic testing for VLCADD can be done on a blood sample. Genetic testing, also called DNA testing, looks for changes in the pair of genes that causes VLCADD. Talk with your metabolic doctor or genetic counselor about whether DNA testing for VLCADD would be helpful to you.

DNA testing is usually not necessary to diagnose your child. It can be helpful for carrier testing or prenatal diagnosis, discussed below.

What other testing is available?

VLCADD can be confirmed by a special test called a "fatty acid oxidation probe"using a skin sample. Talk to your doctor or genetic counselor if you have questions about testing for VLCADD.

Can you test during pregnancy?

Yes, it is possible to test for VLCADD during pregnancy. The sample needed for this test is obtained by either CVS or amniocentesis.

Parents may either choose to have testing during pregnancy or wait until birth to have the baby tested. A genetic counselor can talk to you about your choices and answer other questions you may have about prenatal testing or testing your baby after birth.

Can other members of the family have VLCADD or be carriers?


The brothers and sisters of a baby with VLCADD have a chance of being affected, even if they haven’t had symptoms. Finding out whether other children in the family have VLCADD is important because early treatment may prevent serious health problems. Talk to your doctor or genetic counselor about testing your other children for VLCADD.

VLCADD Carriers

Brothers and sisters who do not have VLCADD still have a chance to be carriers like their parents. Except in special cases, carrier testing should only be done in people over 18 years of age.

Each of the parents’ brothers and sisters has a 50% chance to be a VLCADD carrier. It is important for other family members to be told that they could be carriers. There is a small chance they are also at risk to have children with VLCADD.

Some states do not provide newborn screening for VLCADD. However, expanded newborn screening through private labs is available for babies born in states that do not screen for this condition. To learn more about expanded newborn screening, see How to obtain MS/MS.

When both parents are carriers, newborn screening results are not sufficient to rule out VLCADD in a newborn baby. In this case, special diagnostic testing should be done in addition to newborn screening.

During pregnancy, women carrying fetuses with VLCADD may be at increased risk to develop serious medical problems. A small number of women are known to have developed:

•excessive vomiting

•abdominal pain

•high blood pressure


•abnormal fat storage in the liver

•severe bleeding

All women with a family history of VLCADD should share this information with their obstetricians and other health care providers before and during any future pregnancies. Knowing about these risks allows early treatment.

Can other family members be tested?

Diagnostic testing

Brothers and sisters of a child with VLCADD can have special testing to check for this disorder. Ask you metabolic doctor whether your other children should be tested for VLCADD.

Carrier testing

Carrier testing may be available to other family members. Your metabolic doctor or genetic counselor can advise you about carrier testing. .

How many people have VLCADD?

VLCADD is thought to be a rare disorder. The actual incidence is unknown.

Does VLCADD happen more frequently in a certain ethnic group?

No, VLCADD does not happen more often in any specific race, ethnic group, geographical area or country.

Does VLCADD go by any other names?

VLCADD is sometimes also called:

•VLCAD deficiency

•ACADVL deficiency

Wednesday, October 14, 2009


Thanks for stopping by our new blog! I have set up this blog as part of a foundation I am starting called Landon's Place. I hope to provide information on VLCAD (Very Long Chain Acyl Dehydrogenaise Disorder) and other Fatty Acid Oxidation Disorders, show that it is possible for children and families who have children with these disorders can live normal lives through my son, Landon and his adventures. I am also aiming to raise awareness of these disorders so other families will not be blind sided with the diagnosis like we were. My goal is for this foundation to be nationally recognized and well known, so there is awareness and knowledge of FAO disorders among everyone. I want to help fund research, provide scholarships for students to go into the Metabolic Genetics field, and for doctor every where to have knowledge and understanding of FAO (Fatty Acid Oxidation) Disorders. I also want every state to include FAO disorders in their newborn screenings...It could save so many lives and increase the quality lives in many others. I hope you will join in our cause and help make our foundation and our goals a success. I promise this blog will not be all medical will hopefully also include stories about Landon and other children who are living with this disorder daily and show their successes, joys in their daily lives, and adventures along the way. If you are a family with a child who has VLCAD or any FAO please contact me so I can share your story.

Tuesday, October 13, 2009

Dallas Arboretum

My mom and I took Landon to visit "Autumn at the Dallas Arboretum." We decided to go on a whim, since we were already here and it was a relatively nice day outside. We had a blast walking around and looking at all of the flowers and fall decorations. Landon also really enjoyed playing in the pumpkin patch! I am really glad we were able to go, and Landon came out with a super neat Bib that has the State flag of Texas on it! I just couldn't resist getting it for him, since after all his mom is a Texan!

Here are some pictures from our trip to the Arboretum!

Landon playing in the pumpkins at the Pumpkin patch!

Landon and Mommy with a Landon sized Pumpkin!

Landon and Mommy in standing in the Pumpkin House.

One of my favorites, he looks like being in the Pumpkin Patch is serious business.

I Love that he is smiling and so happy to be playing in the pumpkins!

Tuesday, October 6, 2009

Thanks Grandma!

My mom came to visit us here in Arizona, and while she was here she taught landon how to stick his tongue out (kinda) and spit. So what is Landon's new favorite thing to do...yeup that's right, spit, it's really cute until he does it in your face, or in when you are riding the bus at the Grand Canyon and he is spitting at everyone around you. Thankfully they all thought it was cute too.

Other than spitting we are doing well. We tried a new formula out that had a corn carbohydrate in it, not corn syrup but something different. Well Landon now has a rash all over his chest, upper arms, upper legs, and his neck. So I am going to take him to the Pedi tomorrow just to make sure it is only an allergy rash and not something more. This rash looks different than the original allergy rash that we had way back when.

Unfortunately Landon and I will be heading back to Dallas in the next week or so. My Aunt (dad's sister) is quickly losing her battle with rheumatiod arthritis. She is in Renal Failure and will fall asleep, go into a coma, and that will be it. I am really sad about it, and really wish she would have been able to meet Landon, but he wasn't allowed to visit her in the hospital due to his disorder and she wasn't released to hospice at home until after we had already left town. Please put her and our entire family in your prayers. Also please pray for safe travel for Landon and I flying to Dallas and then the majority of our family driving to and fromt he services when the do occur.