What's Up Doc?

This has been a week of doctor visits for Logan, Lainey, Papa, and Gigi. Some reports were better than others. Some things we heard from the doctors we questioned and are still questioning. Hopefully now we will have a break from going to the doctor....at least for a couple of weeks!

Logan had his 5 year old checkup at the pediatrician's office on Thursday. He was above the 90th percentile for his height and weight! Although he is a big boy, weighing in at 64 pounds, the doctor was not concerned. He is also 45 1/2 inches tall, thus balancing his weight. Keeping him active and teaching him healthy eating habits is our main goal. Logan loves to eat, but he is also all boy ~ meaning he is always on the go! In addition to a full exam, Logan was the lucky recipient of 4 shots in the thigh! Needless to say this meant cornering him, carrying him to the table, and holding him down. He is still complaining about the pain in his legs from the shots! I am sure we will still hear about it for at least two more weeks! Other than yearly flu shots, he is finished with vaccinations until he is ten! Yeah....except I am not sure I will be able to wrestle him when he is ten if it is this difficult when he is five!

Lainey also had her checkup at the pediatrician's office on Thursday, as well as her monthly clinic visit at the Cystic Fibrosis Center on Friday. Dr. Onal, the pediatrician, is extremely thorough and is in complete awe of Lainey and her accomplishments ~ developmentally and with her health. Lainey hated his assessment of her ears, mouth, and stomach. She cried like I have never heard her cry before and continue to whimper even after his exam. Everything with exception of her eyes and a possible ear infection, checked out to be great. Dr. Onal has prescribed eye drops for Lainey's eyes and has referred her to a pediatric opthamologist. He suspects clogged tear ducts, but isn't convinced that what her eyes are producing isn't mucus related to the Cystic Fibrosis. Lainey didn't have to have any shots for her 9 month visit! YEAH!

Our visit to the Cystic Fibrosis Center was the best visit we have ever had. Lainey gained 2 lbs. 5.3 oz since her last visit in January, bringing her up to 18 lbs. 6.8 oz! Woo Hoo! 30 calorie Alimentum with Polycose Powder is our new BEST friend. She also grew another inch and is now measuring 28 1/4 inches long! Although she is still in the YELLOW ~ at risk, monitor carefully range, we are so close to seeing the GREEN! Dr. Caplan and Liz (the dietitian) were completely thrilled with her progress. From his examination, Dr. Caplan didn't think Lainey had an ear infection as suspected by Dr. Onal. He also acted as if it was completely normal that Lainey's eyes were draining and was somewhat confused about her going to the pediatric opthamologist. I am not sure if she should go or not.....Is it a CF thing ~ clumpy, yellowish-green junk in the corners of her eyes, and tears falling from the outside corners of her eyes? Is it necessary for her to go the pediatric opthamologist? Should she try the drops, then decide if the pediatric opthamologist is the next step? Ahhhhh.....Questions, but no answers.......yet! Not one thing about Lainey's medications or diet changed as a result of her visit today! The dietitian said she was fine with Lainey eating more high calorie table foods and drinking less formula. This was great news since Lainey is only consuming about 20 oz of formula from her bottle. We usually sneak formula into other meals through rice cereal, just to pack on the calories! The doctors have a goal of Lainey gaining 1 lb. 5 oz. by her next clinic visit on March 20th, bringing her to 20lbs!!! We are up for the challenge....now we have to get Lainey on board!

To kill several birds with one stone, Gigi and Papa scheduled their appointments for the same time as Lainey's. On Friday morning we left Gainesville at 8:30 am to head to Egleston and Emory. Papa dropped Lainey and I off at the CF Center at 9:50 and they headed over to Emory for their echocardiograms. *** My dad, Papa, had his aorta replaced in February of 2000 due to a tear in the mitral valve causing the blood to go around the aorta rather than through it to the heart. After his surgery, one of his lungs collapsed. Although the surgery and several days afterwards were emotionally and physically draining for all of us, he recovered remarkably well after being release from the hospital. *** The doctors continue to check on my dad's valve and high blood pressure. He went back to work shortly after his heart surgery and worked ridiculous hours. He was stressed out and it the stress showed it's ugly face by causing problems with his new valve. During that time he was diagnosed with stage 1 rectal cancer. He underwent surgery in October 2005 and now has a permanent colostomy. He caught the cancer early enough that he did not need chemotherapy. With the cancer added more stress to his new valve. The doctors now perform yearly echocardiograms to keep a check on the valve.

Lainey's CF clinic was over around 12:00, but Papa and Gigi had finished their echos, and were waiting to see their doctor in the Adult Cardiac Clinic at Emory. Finally my dad decided he had made me wait long enough and he came to pick Lainey and I up at the CF Center at 1:00. I would have walked to Emory, but it was pouring and we were under a flood watch! In the meantime, mom and dad's doctor was busy and she sent mom to the lab for several tests. After parking and traveling to the lab, she was still waiting. After the lab my mom was scheduled for a chest x-ray in the radiology building! Needless to say, this was nowhere close to her clinic. We waited for 30 minutes only to get a call from her doctor saying she was ready to see both her and dad! Without the x-ray we went back to the cardiac clinic! I am not sure exactly how long their appointment took because Lainey and I took a nap in the waiting room! We went back to radiology after mom and dad's clinic, only to wait an hour before my dad went to find out what was taking so long. They didn't have mom's paperwork because they had filed it after she left the first time! Amazingly enough it only took 10 minutes until they called mom back for her x-ray after speaking with my dad! We were finally finished with all of our appointments by 4:30! By the time we sat in rush hour traffic, picked Liam up at Aunt Dayna's house, and picked Logan up at Chick-fil-A where he was hanging out with his friend, it was 6:30 when we got to my parent's house!

Papa got a good report...well, according to what he is telling us! Gigi.....well, hers was not what we would have liked to hear. Her disease is progressing (read more about it here). The doctors are unsure if it is her heart that is causing her problems or if it is the secondary pulmonary hypertension. She is now on Lasix to assist in lowering the amount of fluid in her body. The amount of fluid in her body causes more pressure on her heart, thus making it work harder. If the Lasix works, then mom should feel better (less fatigued and less out of breath) by Monday. This means that her heart is the causing the majority of her problems. In saying this, there isn't much the doctors can do. The harder her heart works, the harder her heart gets, thus not working properly. IF the Lasix don't make her feel better, then it is the secondary pulmonary hypertension that is causing her to feel as she does. The doctors can do a few things for this, such as changing some of her medications and introducing some intense medications like Flolan. There are very few options left for my mom. We know she is a strong woman and will fight until the end. As anyone would, I hate hearing that there are few options left for my mom. She and I are best friends. We call each other at least 5 times a day and unless my parents are out of town, I usually see her everyday. Several years ago I vowed to myself to do for her what ever she needed. I also decided that I would spend as much time with her as possible. She and I have grown so close. We are always finishing each other's sentences, we have the same mannerisms, and we often say the same exact thing at the same exact time.

At times I am glad my husband is in the medical field, but at other times I absolutely hate what he knows. He tries very hard to cover up his feelings and answer my questions honestly. After shedding many tears last night, I have decided to look at some of my vows from several years ago. My vows will continue to stay the same, but I will be adding a few new ones. One vow is to come home on time from work 3 days a week (I often work until 5:00 when I am finished at 3:30). In doing this, mom and I will be able to go shopping. It will also provide her with a break from watching Logan and Lainey for an additional hour and a half. Another vow is to do even more to help her...whether it be to pick up groceries, pick up her medications, take her out to places she needs or wants to go, wash her dogs, vacuum, etc. I want her to be less stressed, less worn out, less out of breath....so she can be here for more years to come. I also vow to not dwell on "what mights" and "what ifs". I will enjoy the time we have together....and try not to focus on what I will do with myself when the time comes.

With all of the news we received at the numerous doctor appointments over the past few days, I can say that we are overall thankful for what God has given us. We still have each other and we are still hanging in there! Thank you for all of your prayers for our family. Please continue to pray for Lainey and my mom, Gigi! We feel all of your prayers daily!

With Love,

DeAnn

Counting Calories and Having Fun!

So......Just how many calories are there in a plastic spoon?

Lainey's new favorite thing ~ eating her spoon when she is tired of drinking formula or eating baby food!

This weekend the boys, Lainey, and I went to the local Home Show with my parents. Our home is fairly new, so I don't really know why I went other than it was an escape from the house! In addition to the escape, it meant that I had two other people helping me with my children for at least a couple of hours. Although one would think the home show would be boring to a 5 year old, almost 3 year old, and a 9 month old, the kids had a blast! They were some of the only, if not the only, kids at the home show. They racked up gathering free "goodies" from each booth! We now have mini flashlights, foam baseballs, potted flowers, notepads, pens, crayons, bandaids, coloring books, candy, and much more! I went to the Home Show several years ago and won a patio table and chairs, so that is always incentive for me. No such luck this year! I didn't win anything, but having a day of entertainment made me feel like a winner! Thanks mom and dad for getting all 4 of us out of the house! We had fun at the Home Show and enjoyed some yummy food at Brad's Grill (compliments of Gigi and Papa)!

The Bug!

Logan and the frog at the Home Show!

Liam did not want his picture taken....but here he is with the frog!

This week brings several appointments. We were suppose to go to the pediatrician's office and the CF Center last week, but our plans changed. The pediatrician was sick on Thursday, therefore Logan's 5 year checkup and Lainey's 9 month check up were cancelled. We are now scheduled to go this Thursday morning. I rescheduled Lainey's CF appointment because the boys were still under the weather from having Strep Throat. We will be going this Friday for her appointment at the CF Center, while Gigi and Papa go for their checkup at the cardiac clinic at Emory. This works out perfect because we can take one vehicle to Atlanta since the CF Center and Emory are next door to each other. I am also happy we are going the same day as my parents because now I do not have to find a babysitter for Lainey! Since my parents take care of Lainey, when they are traveling, at the doctor, or are sick, I must find another place for Lainey...or take a day off of work. I like being home with Lainey, but I am trying to save my days for our Disney Cruise in October and incase Lainey were to get sick. Thanks to Josie's mom, Kay, Lainey usually has a place to stay when Gigi and Papa are not available!

Please pray for good visits at both the pediatrician's office and at Lainey's CF clinic. We are hoping that Lainey has met our goal of 18 lbs! Check back later this week for updates on our visits! :)

BYE!

The Smithsons

A Buggy Kind of Day

Lainey and I enjoyed playing today while the boys were taking a nap! We needed some girl time since I went to the CF Family Day at Emory in Atlanta Friday night and got home Saturday evening. Sid had to work all weekend and the CF Family Day began at 8:00 am on Saturday, therefore I had to find places for the kids to hang out! Lainey went with Gigi and Papa to Warner Robins, Georgia on Friday and came back Saturday night. Lainey got to go see her Great Grandpa Bob, Great Grandma Lil, Great Pop, and Great Grandma Dorothy while she was visiting in Warner Robins. Liam and Logan went to hang at their Papa Dan's house Friday night until I picked them up on Saturday evening. Liam and Logan got to visit with their Great Grandma Barbara. Although I was told that each kid was very well behaved, each grandparent looked worn out!





Friday night, Jenn and I went to Atlanta to eat (without kids and husbands) and spent the night at Grandmomma's house (Jenn's Grandmother-in-law). Grandmomma lives on the same road as the Cystic Fibrosis Center at Egleston! We had a great time eating at Chili's without someone throwing a fit, someone needing more juice, someone tying to get out of the highchair, and someone having to go to the bathroom! It was nice to have an adult conversation and actually enjoy a meal! Staying at Grandmomma's was also great because we left her house at 7:50 am for the CF Family Day, which began at 8:00 am! This was way better than driving an hour from Gainesville and hoping we got their on time. Thank you for letting us stay at you house Grandmomma!

When we finally found our way to the CF Family Day activities, there was a wonderful spread of breakfast foods. While we ate we walked around to all of the CF related vendors. There were so many vendors with things I had never seen before. Jenn and I had a great time walking around to each vendor. We learned and saw a lot of cool things...we also picked up a lot of FREE goodies! If anyone uses Ultrase, the rep informed me that there will be some new and exciting things the company will be starting soon...but she couldn't tell me about it yet! She said the people using Ultrase, Scandi Shakes, etc. will receive something in the mail around February 16th! I can't wait to find out what is new!

The CF Family Day also included several speakers sharing information about current CF research, nutrition, phase 3 drugs, and the importance of airway clearance. I learned soooo much! To answer Reilly's mom, Cindy's question she once asked, Do CF carriers have symptoms?, YES! The doctors said that many carriers of CF may also have sinus issues, asthma, frequent upper respiratory infections, digestive issues, anemia, vitamin D deficiencies, and more!! Hearing this bit of information gave me some understanding behind many of my personal health issues. I am constantly battling a sinus infection, I have had sinus surgery, each winter/spring I get chronic bronchitis, I have always had digestive issues, I am anemic and vitamin D deficient! Wow....one could think I had a mild case of CF...but my blood work says I am just a carrier of Delta F508!

I learned that 90% of people with CF or people who are carriers of CF, have the gene mutation DF508. Researchers are working on ways to correct the DF508 mutation. It is believed that if at least one of the mutations causing CF can be corrected, then it would be as if the person who once had CF was now just a carrier! Since carriers are typically healthy people, the hope is that would also be the case for those with the repaired mutation. The data and research findings were incredible. A CURE is within reaching distance....I am sure! It was noted that they are having difficulty funding the much needed research due to the economy, so it is up to the people who are affected by CF to spread awareness. It is vital to Lainey's life as well as others affected by CF for the CF Foundation to continue receiving funding for their research. Please donate if you can...you will be saving lives sooner rather than later! Here is the link to Lainey's donation page ~ http://www.cff.org/GiftReg/DeAnnSmithson

There was so much more I learned, but I could never post all of it...not because I can't remember or don't have the energy to talk about it...but because I don't have the time to type it all! Talking is my favorite thing to do....as if most people didn't already know that....so ask me some questions the next time you see me!

Please continue to pray for our family! I think we are all over the stomach virus, but we all still have stuffy and runny noses! We are hoping that Lainey's runny nose goes away or at least continues to stay clear! This week brings many things...inquiring about putting our house on the market, Logan's 5th birthday, doctor appointments, a WIC appointment, Valentine parties, Synagis shots, and I am sure there will be more! Good health and sanity continues to be in my hourly prayers!

Have a blessed week,
DeAnn

PS ~ Lainey is sitting up on her own now!! YEA Lainey! She loves seeing everything from her new view!

We've Caught the Christmas Bug!

Lainey at the Cystic Fibrosis Center for an appointment.

Today my mom had an appointment at the Adult Cardiac Clinic at Emory and Lainey had her monthly check up at the Cystic Fibrosis Center. This was a long day, but not too much change ~ this is good for some areas of both mom's and Lainey's check up, but not so good for other areas!

Mom's numerous doctors think she doing well, but will be doing better when she gets over her cold. Last week she went to her local doctor only to find out she was about a day away from developing pneumonia! After a week of medications, she sounds and feels much better. Her doctors at Emory want her to begin her breathing treatments again when she is completely over her cold. The breathing treatments were working well for mom for a long time, but her body quit responding as well after several years. In July the doctors took her off of the treatments and put her on another medication given through a needle in the stomach! After a week in the hospital and a week at home, mom was in so much pain that she never left the house. Her quality of life was effected by the medication, not to mention the pain was horrible. When the doctors took her off the medication, they decided to wait on starting her treatments again. Since August, mom has been able to feel a huge difference in her energy level without the breathing treatments. Hopefully when she begins the treatments again in the next few weeks, she will feel better. The biggest downside to the treatments is the strict regimen it requires. Every three hours she must use a nebulizer to complete her 10 minute treatment. This is quite difficult when you try to go out shopping or when you are driving somewhere. Although it can be inconvenient, anything to keep mom happy and healthy is something we can deal with!

Lainey also had some good and some not so good reports at the doctor today! Her height was 26 .75 inches and her head was 17.5 inches ~ both of which were the same as when she went to her regular pediatrician two weeks ago. Her weight was 15 lbs. 3.8 oz. This is where the issue lies! She has only gained 4 oz since her appointment at the CF Center 1 month ago! She weighed less that she did at her pediatrician's office two weeks ago! Our new plan for weight gain is to begin feeding her every 3 hours, only formula. If she finishes 5 oz. of formula, she can have baby food. Her dietitian wants her to take at least 30 oz of formula per day. Currently she is only consuming about 20 oz. If she doesn't gain weight or drink the 30 oz. per day within the next couple of weeks, then we will need to make her formula higher in calories. Hopefully that will work or they may need to start a feeding tube! Blah!

Other than her very little weight gain, Lainey checked out well. Her lungs sound clear, she was at 100% oxygen level, and she is developing appropriately. We are so thankful for her good health. Please pray that she gains weight. We are sure she will be her goal weight by our next visit on January 16th.

Please continue to check back for more pictures during the holiday season. Below are pictures from Lainey's visit to the CF Center. Enjoy!

Merry Christmas and Happy New Year!

Love Always,

The Smithsons

Sleepy Bug ~ Her 2 to 3 hour visit at the CF Center always wears her out!


Night Night Buggy!

Lainey and "Yellow" ~ "Yellow" was a Christmas gift from the doctors, nurses, and staff at the CF Center.

Lainey and her new friend, "Yellow."

Now is a great time to donate to the Cystic Fibrosis Foundation! Any amount will help find a cure for Cystic Fibrosis! Thank you. To donate directly in Lainey's honor, please click on the link http://www.cff.org/GiftReg/DeAnnSmithson .

Good Times

1998 ~ 10 year class reunion, November 22, 2008.

Sid and I with one of my 8th grade boyfriends, Skipper Brown, and his wife Karley.

This weekend Sid and I attended my 10 year high school reunion. After months of planning the reunion with several of my classmates, it finally all came together! It was great seeing some of my classmates that I haven't seen in 10 years! Many still looked the same, while others had changed dramatically!

Our D.J. was awesome, bearing lottery tickets as prizes for the categories game. Sid and I happened to win 2 categories! We have been married the longest (6 1/2 years) and we have the most children! These are not exactly what I thought my winning categories would be as I graduated 10 years ago, but I am proud of these accomplishments.

Sid was especially excited to meet several of my past boyfriends! While adorning my picture on his name tag, Sid was approached by two of my eighth grade boyfriends. Wow, talk about awkward...especially since Sid works with one of them at the hospital and neither of them knew they had me as a connection!

We thoroughly enjoyed our child-free evening at the reunion. At this point, our ideal child-free evening would be getting in bed by 9:00 and sleeping in until 8:00! This MAY happen in about 18 years! As for my parents, AKA the babysitters, they were glad to offer their services. Next time they would prefer their hot water heater was working! They had to bring the kids to our house so they could all have a warm bath. In addition, they would probably prefer the kids' bedtime to be before we left for the evening! Watching the three of them is not an easy task!

As for mom, her visit to Emory on Wednesday went well. She will begin her breathing treatments again soon. She has been instructed to begin slowly and work her way back up to a comfortable dosage. Although the doctors do no think this is the solution to mom's problems, this is what she will need to do until science has more to offer. The pains in her arms and chest are just occurrences due to pulmonary hypertension. They have also prescribed an inhaler to assist in her breathing. She will go back again next month for a follow up.

Dayna, Brad, and Lilly Anne were discharged from the hospital on Thursday. On Friday Lilly Anne went to the doctor for a checkup only to find out that her bilirubin was elevated. She had a bili bed in front of the window for the weekend. This allowed her to microwave enough to lower her levels dramatically. With a little supplementing of formula mixed with some breast milk, she is well on her way to sleeping in her own bed (rather than the bili bed.)

As many already know, I love teaching. The love for kids and teaching them skills for life runs in our family. Today I was nominated for teacher of the year along with 2 other teachers. This is a great honor. This is only my 3rd year at Fair Street, 7th year of teaching, and to know others are aware of my love for the children at our school humbles me. Although I was not ultimately chosen as our teacher of the year, I feel as though I am one step closer to my personal goal. Sharing my love for teaching through my actions toward the students as well as my coworkers is truly my calling. One day I hope to follow in my mother's footsteps, becoming teacher of the year for my school and possibly for the entire system. My mom has always been an inspiration. I have big shoes to fill and many footsteps to catch up with, but I look forward to the day I can walk along with my mom. She is an amazing woman!

I received a letter from my endocrinologist, only to find out that my Prolacin levels (lactating when I am no longer nursing) are still elevated! I am instructed to continue taking the medications I have been taking for a month and a half. No other test results have been presented, therefore either of two things could have happened. One, she may not have had the blood run for anything other than my prolactin levels, or she has not had the time to look at the other results in order to let me know what to continue or discontinue. I see a second opinion in my near future!

For Thanksgiving our family will be at Stone Mountain. We are taking our camper and meeting up with mom and dad, grandpa Bob and grandma Lil, Uncle Donn and Aunt Jenny and their 4 kids. Mom and dad left on Sunday and took Lainey Bug along! When the babysitters leave, you have no choice but to send the baby with them! I am not sure dad was prepared for the amount of things I packed for Lainey, but he grinned and loaded them up! It is amazing how the smallest person in the house requires the most stuff! We love camping and this will give Sid and I some much needed rest from our everyday hustle and bustle. The kids think the "Big Mountain" is awesome and have been ready to go since we mentioned it last week. On Thursday, Dayna, Brad, and Lilly Anne will join us for our Thanksgiving meal at our campsite. Mom and dad will be leaving Stone Mountain on Friday to go to Athens for the UGA vs. Georgia Tech game!

This year we have so much to be Thankful for. We are thankful for all of our friends, family, and people who follow our story with loving hearts and prayerful minds. We are thankful for our health. We are thankful for our two amazing little boys! We are thankful for the arrival of our little girl and to have her in our lives and our hearts. We are thankful for the numerous nurses and doctors that took care of Lainey in her most critical times. We are continuously thankful for the doctors who take care of Lainey on a regular basis. We are thankful for an overall healthy year for mom and dad. We are thankful to have parents that are able to care for our baby while we work and attend school. We are thankful for the safe arrival of many new babies in our lives, especially Lilly Anne! We are thankful for stability in our jobs and the ability to make it through the financially difficult time in our lives and in the country. Most of all we are Thankful to have God in our lives, for He is the reason we have everything else to be thankful for! Have a blessed Thanksgiving.

Love Always,

The Smithsons

CF Kisses

Today was a packed day. Mom, Lainey, and I headed down to Atlanta around 9:00 for several appointments. Mom went to the adult cardiac clinic this morning to meet with her doctors. Everything seems to be the same with her health, just a little adjustments to her medications. She was doing well enough that she is not going back until November. Although the appointment was for Gigi, Lainey took a lot of the doctor's time! Dr. Book was ready to take Lainey home with her! It was really cool that after mentioning a heart murmur Lainey's pediatrician noticed, a pediatric cardiologist came to check her out at Dr. Book's request. All sounds fine, just a murmur she should outgrow. After a trip to the lab with Gigi, we were finished at Emory.

Following a quick lunch, we went to Lainey's appointment at the Cystic Fibrosis Center. Every time I step foot in the door of the center, I get an overwhelming sense of comfort and relief. Every person in the center is so caring and personally invested in your child's health. They are an awesome addition to our family and friends support group! Several members of her care team are no longer at the CF Center due to a few changes with Egleston and Emory. The two hospitals at one time worked hand in hand, but have slowly parted. Now that the hospital has moved some of the patients from the CF Center, which is part of Emory more so than Egleston, many of the team moved as well. With their seniority, leaving Egleston would mean starting over in their career. The new people are just as caring as the ones we have become to know and like so well. Our favorite, Dr. Caplan, will probably die doing what he loves best ~ taking care of his delicate patients. We love him so much, we have decided to adopt Dr. Caplan as another great grandpa for Lainey!

Lainey and Doctor Caplan

Lainey weighed in at 12 lbs. 2.5 oz. This is a little over a pound since our visit one month ago. Although I was hoping for 13 lbs., her CF care team assured me that I should be happy with any weight gain! As she gets older, her growth rate will slow down making her weight gain less each visit. In addition to the weight gain....she grew in length! She is now 24 inches long! I am not sure where she got the traits of being tall and skinny. If she didn't look like me, I'd think she was adopted! Everything with her lungs sounded good and clear. This is awesome since we are quickly approaching the season of germs! The dietitian and Dr. Caplan want us to continue using the pancreatic enzymes, Ultrase. Lainey is now on a program offered by the drug company that supplies her vitamins and enzymes at no charge until she is 2 years old. We are so very blessed to have the opportunity to participate in these programs. We are also going to begin introducing rice cereal. It is our hope that the rice cereal will encourage and produce significant weight gain. Overall, nothing has changed with Lainey and the effects of Cystic Fibrosis on her health and body. Dr. Caplan was completely in awe of Lainey's growth and early reached milestones. Lainey spent most of her visit cooing and "talking" to Dr. Caplan as he snuck in a few kisses here and there! Seeing his amazement of her, takes a major weight off my shoulders. It allows me to stop worrying for a moment, something my body and mind greatly appreciates.

We received frustrating news on Monday from the kids' pediatrician. Supposedly the tubes used to collect Logan and Liam's blood sample for the CF test were not the correct tubes. The cap on the tubes were a different color yellow than what they typically use when testing for genetic diseases. All in all, the blood samples are no good. They must be drawn again! I am refusing to go through that torture again...It is Sid's turn! Most of all, I hate it for the boys. They should not have to go through the pain again because somebody used the wrong colored tube lid when collecting their blood! For those of you that know what I am like when I am mad, be assured the pediatrician will know as well! I am waiting for a phone call back from him! When we have more news on the boys' tests, I'll let you know.

Reminder ~ Lainey will be baptised at 10:55 on Sunday at Gainesville First United Methodist Church! Please join us if you would like. Thank you for all of your support! Prayers are always needed and greatly appreciated! Please continue to pray for good health, weight gain, working enzymes, and correctly gathered blood samples!

Much Love from our family to yours,

The Smithsons