Wednesday, December 17, 2008

update

I haven't posted in a while due mainly to the fact Julia has been doing so well health wize. We FINALLY got the ringworm fungus cleared up. She has started the orthodontist visits. She gets her appliance to widen her upper jaw on Dec 23rd. The doctor is placing two barbs on the end of it to stop Julia from her thumb sucking habit (one she had BEFORE she was born....we have ultrasound pics). I am hoping it doesn't mess up her tounge too much. That is all we need is for her to not eat due to her mouth hurting.
She is still taking her allergy meds and the Zithromax and Vemma as well. Those last two really do make a difference as when she doesn't take it after about 3 days she starts having breathing problems or comes down with a cold.
I heard reports for other parents at her school that 2 kids have scarlet fever and that there are 5 cases of RSV in the 4yr old program. OH MY!
Julia is still doing well with her mid morning snack. She eats "brunch" with the school secertary each morning. Julia says she is her "BBFF" meaning best brunch friend forever. She is such a hoot!
She is excited about Christmas. She plays an elf in her class's play. From Santa she wants Pixos and from us she wants a Tinkerbell doll and Incredible Hulk boxing gloves. What a combination!
Hope everyone has a safe, happy, and healthy holiday season.
Jenn
to learn more about Children's Interstitial Lung Disease please visit www.childfoundation.us

Sunday, October 12, 2008

NEHI: A Rare Diagnosis after Misdiagnosis

Below is a link to an article a friend of mine (whose son has the same lung disease as Julia) wrote. It is quite informative.

http://www.articles.complexchild.com/Oct2008/00078.html

Julia's health update


This school year got off to a rocky start as you could read in previous posts. The latest has been ring worms...lovely. We also had some strange blister looking marks on her. I thought they were bug bites even though she has never had anything like them before. After much research on the internet and talk with my school's nurse (doctor's office was closed). We concluded Julia MAY have had chicken pox. Yes she had the vaccine but that is not always 100% effective expecially in children with other issues like Julia. As I said I thought they were bug bites because there were so few of them, but even after staying indoors she had new ones coming up. So we are pretty sure that is what it was.
At Julia's teacher's request we have added a mid-morning snack. She has been doing much better eating every 3 hrs or so. She has breakfast at 7am, then snack at 10am. Lunch is at 12 and after school snack is at 3:30. Dinner is at 6pm and night time snack is at 8:30pm. She is maintaining her weight(even gained a pound), and has grown in height. So that is all good.
We did have to double her glasses strength this year. I am hoping this will not be a yearly occurance. Her sight in her left eye is pretty bad close up. No wonder the poor kid hated reading. Now that we have new glasses she is reading above her grade level rather than below. I did speak with the teacher about how much they read out loud in class. She said Julia doesn't seem to want to read as long as she things she is capable of. Uh lady....it takes a lot of air to read out loud for long periods of time. Once she remembered that she has let up on Julia.
Julia is looking forward to Halloween. She still hasn't made up her mind on her costume. She is either going as Cinderella again or going as a Lion.

Hike for Lung Health 2008


Julia did an amazing job with the help from friends, family, and even people we have never even met. She was able to raise over $2,000. The Children's Interstitial Lung Disease Foundation came in 3rd place with over all funds raised. This is great news.
We are so lucky to have people care about Julia the way they do. God Bless each of you.
Grant Hall from Norman who also has chILD, was able to make it to the Hike here in our hometown. Although we were unable to attend in Chicago, the same spirit was envoked. We want to help find a cause for this disease and a cure. Thank you all for the help!

Wednesday, August 13, 2008

my back hurts

Well I think we set a record for how many days we can go without
missing school. Only not the kind you would hope for. Julia made
it the first full day. BUT....apparently she fell back in her chair
and hit a desk that is behind her. She did not tell the teacher nor
did she go to the nurse. Yet at around 5pm on Monday she keeps
telling me her back hurts bad, her head hurts, her chest hurts. Ok
I am thinking she just doesn't want to go to school the next day. I
massage her back, put a hot pad on it, give her Moltrin, and she
still complained, I give her a hot stone massage (spoiled child yes
I know). She even asked me to take her to the doctor untill I
explained that after dinner time it would mean going to the
hospital. She wanted none of that. All the while I am asking her
all kinds of questions, did she fall?, did she get hit? She makes
up this very elaborate story about how one of the new girls got mad
at her for getting to see Cinderella and hit her in the back causing
her to fall back into the desk and hurt her back. HMM???? I asked
if she told the teacher, if the other girl got in trouble, if she
say the nurse....No, no and no. So I am thinking this is one fishy
story. I see no bruises or obvious signs of trauma. This child
doesn't want to go to school. I finally get her on to sleep ....in
our bed. She tosses and turns all night, breathing fast and heavy
despite her oxygen, and talks in her sleep. Yesterday morning comes
and she has a headache, stomach ache, and her back hurts really
bad. Again I am thinking she doesn't want to go to school. She has
no fever and again no signs of problems on the back. I talk her
into going on and let her bring her oxygen....more of a "safety
blanket" kind of thing. Well by 8:30 am her teacher is calling me
saying Julia is acting really sick saying her head hurts, her back
hurts and her stomach is hurting. She told me "I am all new to this
medical issue thing". Sigh! I send my mom to go get Julia. At
lunch I go check on her. Mom said she had a low grade fever and had
given her Moltrin and that Julia was sleeping with her oxygen on and
had been sleeping since 9 am. So at 1pm I call the doctor and take
her in. He can't find anything wrong with her back, despite her
telling him it hurt bad...."a 12 on 1 to 10 momma". He does however
say she has nice green snot in her sinuses. Lovely!
We leave with orders to start zithromax, mucinex, singular, flonase,
periactin, and lots of water. Still complaining of the back. So I
call my chiropractor who tells me to just bring her on in. He
examines her first as he says he didn't want to do an x-ray if it
wasn't necessary on a young kid. He feels along her back with her
saying ouch all the way. Finally he has her lay down on her tummy,
and again massages and pokes and prodes. Then POP! He popped her
back and she says "AWWWW that was it!". She was fine after that.
He said she had popped a rib up over the other one. WHAT!!!??? OMG
I felt horrible as I have done that and man oh man does that hurt.
I could hardly breath when it happened to me. Which would explain
the 89% o2 stat she had in the doctor's office. She was fine this
morning and was eager to go to class.
So this school year is off to a wonderful start. HA HA HA
Jenn

Tuesday, July 29, 2008

shopping with a lung disease...yuck

So I take Julia to shop for "back to school" clothes. Not a favorite of either one of us. Shopping is just not our thing. We left home at 9am. Drove 2hrs. Picked out 3 new outfits, tried on about 6 pairs of capri pants.......so frustrating having a child who is so skinny that the clothes that actually fit are not age appropriate. Sigh!
By noon we were hungry. After lunch Julia just became so tired out. I felt bad because I had thought of bringing the oxygen but decided against it. She has been doing so well this summer and well it is a pain in the arse to haul around, even though we have one of the battery portable oxygen concentrators (Inogen One ...it rocks!)
Poor kid slept the entire 2hrs home, ate very little for dinner and went to her room. She put her oxygen on herself and is watching a movie.
After all of this .....we still have to find some new shoes for P.E. class....crocs are great but not all the time.

Wednesday, July 23, 2008

Homecoming

It is official, Julia will be doing her Hike for Lung Health at 6pm on Friday, September 26, 2008. This is Sulphur High School's football homecoming game. We hope all of you can join us in Julia's quest to increase awareness of this rare lung disease. I have spoken with 5 other families whose children have varying severity of the same lung disease Julia has. They may possibly be joining us that night for the 1mile walk around the track. For more information feel free to contact me via e-mail or phone 405 615 8154. If you would love to help me out with this fund raising ordeal PLEASE call me. Julia and I are great at showing up to tell her story, smile and looking pretty, but organizing something of this nature takes talent and help. To learn more about the Hike for Lung Health go to
Hike For Lung Health

Jennifer Goodnight-Roberso(Mom to Julia age 7yrs with chILDren's Interstitial Lung Disease0

Tuesday, July 22, 2008

chILD Mystery Diagnosis iPodcast

Listen to the podcast version on the Discovery Health's Mystery Diagnosis show on chILD. "Lariah Palma"
Mystery Diagnosis Podcast

Monday, July 21, 2008

off to D. C.

Just wishing my friends Ann and Liz good luck as they hit D. C. to give a speach on child safe medical equipment. They are taking with them several stories and hundreds of pictures of small children tangled in oxygen tubing, children pulling out feeding tubes, children with huge oxygen tanks to lug around, and much more. May their voices and our childrens' pictures make way for some equipment changes.
Living to Breathe

Friday, July 18, 2008

Hike for Lung Health 2008

I just wanted to remind everyone about the Hike for Lung Health.
Julia will be participiting in this again this year. We will be doing the "virtural" walk meaning we will be walking here in our hometown and not in Chicago, but hey the money is all going to the same place for a great cause.
http://my.imisfriendraising.com/personalPage.aspx?registrationID=260181&LangPref=en-CA
That is the link to Julia's fund raising website.
Here is the link to the YouTube video from the Hike for Lung Health group.
http://www.youtube.com/watch?v=Ro6wmiPajLU

new oxygen tubing and cannulas

Hip Hip Hurray we got new cannulas and tubing today. And I finally (after 4yrs of Julia having Oxygen) , got swival clip connectors. Why on earth we were never given these to start with I will never know. Julia can now go 107 feet and not get caught on corners, furniture, toys, you name it. Of course it took me asking for a "water trap" to even get one of those way back when. Now we love our O2 man dearly, but you can tell that most patients who use oxygen are elderly adults who don't have to worry if the tubing will stretch from the house to the trampoline. I am so glad that two of the moms from the chILDren's Interstitial Lung Disease Parent Support group will be attending the medical device workshop in Washington D.C. soon. They are planning on having about 200 people from various groups that are interested in pediatric device development. They have expressed great interest in our stories and have asked us(chILD) to present in 2 different sessions and have asked Ann Gettys to be on a special panel at the end of the meeting. It is all very overwhelming, but it is a great venue for us to get our kids stories out there. I will post what she has to say when she gets back. Liz Jenkins will also be attending with Ann on behalf of chILD. For all you Oxygen dealers and RTs who read my posts try to remember not all of your patients are old farts. Some of them are snappy, sneaky, Houdini-like, little blonde hair girls who will put you through any test. Most worse than you will ever encounter in school

Thursday, July 17, 2008

oops on the slideshow

Well I did my best to transfer the slideshow from "Slide" that I used in Myspace to post it on over here in blogger. For some reason it didn't work quiet the way I had wished. All you seee is a bunch of http text and then the buttons to view the show. Only when you go to view it the music is not there. Grrr!
http://www.slide.com/r/AM-vma5Z2j_Hu9jw08-3WAY1lnom83TJ?previous_view=lt_embedded_url

Wednesday, July 16, 2008

A Rare Lung Disease journey begins

Julia was born a healthy full-term baby on June 26, 2001. Somewhere around her fifth month of life she started having trouble. We were in and out of the pediatrician’s office at least once a month with some sort of “cold” for almost two years. It was finally discussed that Julia’s chest was not growing properly and that could be a reason for all the illnesses. What started out as a simple check into Julia’s sunken chest, (Pectus Excavatum), in December 2003 developed into a much larger ordeal. The pectus, we were told, would have to wait; Julia had a very rare lung disease. We were in total shock and were very angry with that doctor. When we asked for information he simply said "there is not a lot of information known and what I do have is very scientific and you are going to be more interested in the emotional aspect of this disease"
We immediately sought a second opinion. I had to basically have an argument with our pediatrician over getting one. He wanted to send us to one of the other doctor's fellows. I did my research and discovered who was writing all the articles on this rare lung disease in children. We headed to Ft. Worth where we met with a doctor who had at least had seen a patient with chILD. Yes we still got the "hmm this is an interesting case", but at least we were meeting with someone who wasn't going to immediately schedule surgery on our 2yr old. She in fact told us if it came down to needing a lung biopsy she would send us to Texas Children's for the top chILD doctor to do it.
Doctors and other medical personnel did countless blood tests requiring painful needle sticks for Julia, numerous x-rays, two different CAT scans, swallowing tests, sleep studies, T & A removal, neurological testing, hearing testing, eyes tested, and 2 pH probes which revealed that Julia also has GERD, or acid reflux disease, upper GI and lower GI testing. Doctors said they “think” the acid has been silently aspirating into her lungs and caused her lung condition. Or, when she was around five months old, she caught a common cold virus, RSV. For some unknown reason, the virus caused a “lung injury”, meaning the lung tissue around the very small airways and the air sacs became inflamed, then scarred, and have stayed that way. Much like a deep cut with stitches on your skin does. Even after it has healed the scar remains. The latest research (June 2008) is now indicating that Julia’s form of chILD called NEHI which is short for Neuroendrocrine Hyperplasia of Infancy could be heredity. This scarring can cause decreased oxygen levels, a rapid breathing rate, exercise intolerance, heat intolerance, severe allergies to particles in the air; especially cigarette smoke or pollen; crackle or “Velcro” chest sounds, and poor appetite, which can all cause difficulty with growth and weight gain. Julia has for a long time been well below the normal growth charts.
Julia’s lung condition falls under an umbrella of a rare and complex category of lung disorders named Children’s Interstitial Lung Disease or “chILD”. There are a number of lung conditions associated with chILD. The severity of the disease has a wide range. We are extremely grateful Julia is alive and maintains a fairly normal childhood, because Julia has a mild form of chILD. Hers is manageable with medicines. Unfortunately, some children are not as lucky as Julia. Some children die of this disease within a few months of life. We have personally known three such children who have lost their battle with this lousy disease. Some long to play freely with their friends without being tethered to an oxygen tank. Some parents sit, wait, and hope for a new set of lungs through a transplant, and then pray their child’s fragile body will accept them. There are still others whose parents just want to know what lies ahead for their child as they live with a chronic lung disease. Will they make it to kindergarten? Will they make it through high school or college? Will they marry and have children? Will they even make it through the night? Will this breathe be their last.
As parents, the most frustrating aspect of this disease has been the lack of scientific data and studies on this type of condition in children. There are no standard medical evaluations, no proven or studied treatments, no patient registry, and no standards for caring for kids with these life threatening conditions. All too often parents faced with caring for a very sick child are given the answers of, “We just don’t know.” Children’s Interstitial Lung Disease is very rare, complex, diverse, frequently misdiagnosed and quite frankly has been neglected in the medical community.
The chILD foundation consists of families much like us. They are busy just like the rest of us. We have full-time jobs, as well as the added responsibility of caring for a chronically ill child, yet we still volunteer our time and energy to the foundation in order to do what we can to help our children. The mission of the foundation is to provide support, education, and hope to families affected with chILD, to advocate and to raise funds for more scientific research.
God willing, Julia will not be going to school with an oxygen tank attached to her face everyday. There will be days when she does not look or feel well though and will have her oxygen with her. We will ask that parents and teachers talk to the children about the importance of hand washing and covering their mouths with their shirt or a tissue when they sneeze or cough. A simple sniffle to you or your child can mean days out of school or possible hospitalization for children like Julia. For some it can even mean death.
As the age ranges and cases grow in the number of sufferers, there seems to be little growth in understanding of the illness and those who fight it. The biggest challenge, I've found, is not the strangers I meet each day who might ask questions, but those people who see my daughter everyday and seem forget she has a chronic lung issue. Someone mentioned being told, “They don’t look sick." Trying to explain the disease over and over again with what little knowledge we do have is like trying to explain astrophysics to a group of toddlers. This disease is as diverse as the selection of paint colors to choose from at the store is. Each case is so different yet the same in many ways. I feel helpless to assist those around me who are dealing with this. It is like being shot in the heart with a hole left. Yet, unlike Humpty Dumpy, there are no king’s horses to put it back together.
The doctors don’t know much either. There are only handful centers in the world that are truly qualified to treat our children. I have heard the dishearten news of many pediatricians reading an article, and considering themselves up-to-date on the illness. I know many parents who are just tired of their child being a guinea pig for all to observe. They grow tired of being told they are just overreacting. Yet, these same parents drive on, taking their child to ever medical person known because the previous doctors just “Didn’t know”.It is hard to have a lot of hope in the medical community that doesn’t understand your child or the hard road you travel. Doctors familiar with the disease still don't fully understand it. Research is a slim chance of hope with so little funds being sent for that research. The only way we have is to push ourselves further along at every pass, realizing our grace is in our strength and knowing we aren't alone in all of this. This disease put us all in a group we didn't want to belong to, but we can use it to make us strong. We can talk with anyone who will listen and we can put our energies into trying to be heard, instead of crying over no one listening. The choice, as with any illness, is the will you have within you, to either keep moving in life the best you can or sitting down and giving up. Yes, there will be times when all you can do is sit down and cry, but choose to get up again, too.
I encourage all of the families dealing with chronic illnesses to “keep on trucking”. You are all wonderful parents and are stronger than you realize. Many complications may arise and things might seem so terribly wrong and you may want to just give up. I have seen the spirit of determination in your will. All of us possess the unique and wonderful capability to see a challenge. Remember sometimes one plan moves slower than others. Sometimes they creep and crawl in small steps along the path of life. But so do caterpillars, and look what they become.
If you are interested in learning more about chILDren’s Interstitial Lung Disease feel free to ask me or even Julia. The only dumb question is the one that was never asked. We in fact perfer you ask questions rather than stare at us. You can also learn more by visiting The chILD Foundation’s website at www.childfoundation.us. Donations can be made via credit card there as well.
The best thing you can do for us is to help us spread the word about chILDren’s Interstitial Lung Disease. Networking is the key in today’s society. One person alone can not be heard when it comes to advocacy, it takes many voices to be heard in this vast world.