Easter!

Ben hunting for eggs on Easter weekend!

The usual scene of Ben following his big brother Ty.

Ben with his cousins ... getting ready for the egg hunt!

Ben's brother, Tymon, got a cold and passed it around to the family!  Ben came down with it this past Saturday.  Paul and Michelle tried to help him kick the virus with increased treatments, but he it wasn't working.  On Wednesday he was put on a two week oral antibiotic.  Please pray for Ben's family to maintain health after Ben's course of antibiotic. It would be a blessing for Ben to not get sick especially with the weather getting nicer!  

VX-809

The Cystic Fibrosis Foundation announced last week that they are beginning phase two trial for VX-809.  This drug has a potential to treat the basic defect in cystic fibrosis - a gene and its protein product, called CFTR.  

Here is apart of the article that is on the CF website:

"CF treatment involves the use of multiple drugs that address the symptoms of CF, however no therapy currently exists that targets the underlying cause of this disease,” said Robert J. Beall, Ph.D., president and CEO of the CF Foundation. “VX-809, which today entered Phase 2 clinical development, may have the potential to play a significant role in changing the future course of this disease for people with CF.”

 

"The advancement of VX-809 into Phase 2 development demonstrates our commitment to improve care for patients with CF," said Freda Lewis-Hall, M.D., executive vice president, medicines development, and chief medical officer of Vertex.  "This Phase 2a trial is designed primarily to provide a safety, tolerability and pharmacokinetic evaluation for VX-809.  Any additional signals observed in this trial, including changes in sweat chloride and nasal potential difference, that indicate VX-809 has an effect on measures of CFTR function may be highly informative and encouraging for planning future clinical trials with VX-809."

WHAT A BIG GOD we trust!!!!! Again we are reminded that Ben's every breath is in good hands!  This is exciting news about the advancements in medical technology.  We can only pray that God will use this medication for his glory to heal cystic fibrosis patients, like Ben!  

Matthew 9:27 - As Jesus went on from there, two blind men followed him, calling out, "Have mercy on us, Son of David!"  When he had gone indoors, the blind men came to him, and he asked him, "Do you believe that I am able to do this?"  "Yes, Lord,"  they replied.  Then he touched their eyes and said, "According to your faith it will it be done to you"; and their sight was restored.

YES LORD ... We believe that you are able to do this for Ben!  May a cure be found in Ben's lifetime!  This is our prayer!  According to our faith we will see it be done!  FAITH!

Water Park!

The whole family was given a gift to stay at Key Lime Cove Water Park in Gurnee, IL for a fun trip for the kids!  They adventured to the park this past week during Paul's spring break.  The boys were so excited to go!  They had a fun time playing in the water, going down the slides, and having a "sleepover" in the hotel room.  The pictures taken under the hot diggety dawg sign was dedicated to Caleb because that is his nickname!

Overall, Ben is doing great!  He is staying healthy and having fun with his brothers!  

Psalm 123 - I lift up my eyes to you, to you whose throne is in heaven.  As the eyes of slaves look to the hand of their master, as the eyes of a maid look to the hand of her mistress, so our eyes look to the Lord our God, till he shows us his mercy. 

Have a great day and thanks for checking up on Ben!  

Ben is 3!!!!!!!

We had a great time celebrating Ben's 3rd Birthday at Wheaton Academy's gym this past weekend (his official birthday is on March 17, St. Patrick's day).  A few of Ben's friends came to play games, run around, and eat cupcakes together.  It was a fun time and we are so blessed by Ben's life!

Children's Memorial Visit

Last week Michelle, Paul, and Ben went to Children's Memorial Hospital in Chicago for Ben's routine CF clinic visit.  The medical team tried to complete a Lung Function Test to see if Ben's lung capacity has reactive airways.  Ben was too young to sit through the test so there were no accurate readings.  Therefore, the test will have to be performed at an older age, but overall it was a positive experience to allow Ben to witness what he will have to do in the future.  Next, Paul and Michelle met with Dr. McColley and the Nurse Practitioner, Stacey VanderBranden.  They learned alot from them were grateful for their insight.

The big news was that Ben's BMI is up to 77%.  He gained a ton of weight over the past 2 months.  It is such a blessing to be over our goal of BMI at 50%.  In 8 months Ben has gone from the 5% to the 77%!!! Praise the Lord for His goodness and the gift of enzymes.

After the visit Paul and Michelle took Ben to see the Prayer Chapel that Paul and Ben went to every morning during this past summer.  Ben was so excited to see it and said a prayer of thanks for God's grace and blessings.  When they went to the Courtyard Ben let out a squeal of delight and said, "I love this place."  During the two week stay at Children's during the summer, Ben spent a lot of time in the courtyard running around because he could not go anywhere else.  

We are very grateful for God's faithful and goodness.  Ben came in to Children's Memorial Hospital as a very sick boy and left healthy and growing!

Psalm 34: 8 - Taste and see that the Lord is good; blessed is the man who takes refuge in him.

Special visitors!

Ben with Poppy

Ben enjoying his cousin Selah

Ben, Ty, Caleb, Zion, and Selah

Poppy and Lannie helping Ben with his vest treatment.

Grandpa and Grandma Ferguson (Poppy and Lannie) were in town last week and Ty, Ben, and Caleb were so excited!  They had so much fun with them.  The whole family traveled to downtown Chicago to see Missy and Hakeem (Paul's sister and brother-in-law), their cousin Zion, and new baby Selah.

Since Ben's last round of antibiotic, he has been doing so well!  He is healthy, energetic and playing constantly with Ty. 

We are so grateful for his health and pray it will continue through the end of winter.

 

Call for Prayer!

Two important things:

1.  Ben's new website is up and running ... VISIT  ben-ferguson.com!!!!!!!

2.  Yesterday Ben was prescribed a powerful antibiotic, Amoxicillin.  He was shown signs of either a sinus infection or a bacteria infection in his lungs.  He will be visiting the CF clinic tomorrow so they can obtain a culture to detect any possible bacteria growing in his lungs.    

Michelle has noticed for the past month that he was been more lethargic, not eating as well, and has a persistent cough. 

Please pray that the tests comes back negative!!  

We know Ben's life is in God's hands and we trust Him through every step!    

Ben and Ty like to drive their cars along the wall.

Ben loves to dump all the cars onto the couch and line them up.

Michelle and Paul have been debating if Ben needed to go on an antibiotic this week.  He has been doing pretty well but not his best.  The main symptoms were more irritable, less energy, coughing more, and harder to get him to eat.  Then Saturday night he woke up coughing around midnight and Michelle went to the Pharmacy around 12:30am to get Ben some antibiotics.  Sleepless night are never fun, but the antibiotic seems to be effective.  He is still not to his baseline but already Ben has more energy and is sleeping more soundly.  Please pray for wisdom for Paul and Michelle to know the when and when not to give Ben antibiotics.  They don't want to be too aggressive and give him antibiotics too much because of the risk of them becoming ineffective.  However, we want to make sure we prevent an exacerbation as it could lead to lung damage.

 

Ty and Ben love to play with their cars. They play with them everyday and for hours.  Ben can't handle it if the cars aren't near him at all times.  Ben has a bucket that he faithfully carries with him around the house. 

Getting Too Big!

Ben had his routine CF clinic visit earlier this week. Michelle and Ben met with Dr. Chung and the rest of the CF team.  According to the doctors Ben is looking good.  His lungs continue to sound clear and he is still gaining weight.  He gained a pound and a half and grew a little over an inch since Nov 21st.  It's hard for Michelle to keep up with his clothing sizes!  He is about to transition into his 3rd pants size in 6 months.  Crazy!  Ben's BMI (body mass index) lowered a little because his height increased more than his weight. So Michelle and Paul are continuing to work on his diet so he can gain weight and to get his BMI above 50%.  Ben also took a throat culture for a screening process and the results will come back in a week.

Within the next week Ben's official website (not just a blog) will be launched.  Looking back on all the pictures of when Ben was in the hospital will blow anyone away!  Within seven months of Ben's toddler years he looks like a completely different child!  It's amazing what the right medicines and treatments can do for his health.  

Deuteronomy 32: 3-4  -  I will proclaim the name of the Lord.  oh, praise the greatness of our God!  

He is the Rock, his works are perfect, and all his ways are just.  

A faithful God who does no wrong, upright and just is he.

For God's glory.

Merry Christmas and Happy New Year!!!

Looking back on 2008, we clearly see God has taken us through a year we will never forget.  Especially for Ben!  In June Ben was faced with a diagnosis that changed his life, and for the past 6 months of the year we have been adjusting to a new life style.    

For the past month Ben has been exceeding all expectations.  He is gaining weight, staying health (for the most part), and living an active, normal 2 year old life.  Ben has continued to do treatments twice a day.  He is also currently getting over a cold which was a concern for awhile.  We are grateful his cold has not got worse, especially since so many viruses are going around at this time of the year.  But thankfully Ben has not had to go back on antibiotics due to the decline in his cold symptoms.

Also, looking back on 2008, we clearly see the hand of God on Ben's life.  God has continued to strengthen our lives, our faith, and our hope for the future!  

Philippians 3:14  -  Forgetting what is behind and straining toward what is ahead, I press on toward the goal to win the prize for which God has called me heavenward in Christ Jesus.

And for YOU!  Thanks you for being interested in Ben's life.  Thank you for being a prayer partner and helping Michelle and Paul carry the burden.  Thank you for investing your time to be a part of Ben's life.  

And now as we look forward to the year 2009, we strain toward what is ahead; we press on toward the goal and to look heavenly bound.  Our eyes are on the Lord for the year 2009, therefore we know Ben's life is in good hands!  

Happy New Year!               

Cutting down the Ferguson Christmas tree was a fun adventure. The boys just wanted to chop trees down. They weren't really into my desire to find the perfect family tree like Michelle. Paul started his basketball season so the whole family has spend many hours in the Wheaton Academy gym. Ty, Ben and Caleb love it and can't get enough!  Also, recently Michelle rented the movie Kung Fu Panda and it's the new obsession in the house.  Everyone now karate chops each other, Caleb included.

 

Ben is doing well. His throat culture came back normal which is another answer to prayer. Please continue to pray for Ben's health this winter.

Exodus 15:2-3  -  The Lord is my strength and my song; he has become my salvation.  

He is my God, and I will praise him, my father's God, and I will exalt him.  

The Lord is a warrior; the Lord is his name.

Good news for which we are thankful!

Ben had a CF clinic visit this week.  He has grown more and his BMI had increased from 30% to 42%.  He has almost reached his goal of 50%.  Also, his lungs sounded clear which is a praise!  He has had a couple of colds over the previous 2 weeks, so Dr. Prestridge put Ben on a 3 week oral antibiotic. Patients with CF always have a some amount of bacteria in their lungs (non-CF people would not have any) so when Ben gets a virus/cold the bacteria levels in his lungs increase. So even if he doesn't have a lung infection, Dr. Prestridge wants to make sure the bacteria growth in his lungs is contained.

Michelle and Paul talked with Dr. Prestridge about getting a lung function test for Ben. They only can do toddler testing at Children's Memorial in Chicago which is called an IOS (impulse spirometor).  There are plans being made to do this test in January. It will give us a guideline on how Ben's lungs are doing as well as help us track his the health of his lungs as we move forward. Also, because of Ben's excellent growth over the past 2 months, the doctor increased his enzymes to 3 for a snack and 4 for meals.

 

Ben is doing really well. He is coorporating well with his treatments, enzymes, and medicine right now.  He is very active and plays non-stop with Ty.  They are best friends and it is such a blessing to watch.  Caleb tries to be involved but can't keep up with the older boys, even though he wants to!  One of their favorite activities is to go to the Wheaton Academy's gym.  The boys absolutely love to go see their Dad and run around the gym. 

Thank you for your prayers. The prayers of a righteous man are powerful and effective. We continue to feel your prayers in our life.

Psalm 18: 30-32  -  As for God, his way is perfect; the word of the Lord is flawless. 

 He is a shield for all who take refuge in him.  For who is God besides the Lord?  

And who is the Rock except our God? 

 It is God who arms me with strength and makes my way perfect.

THANK YOU!!! Cruisin' For The Cure was a success!

A little fun with the committee members while setting up!

Ben passing out gifts!

Ben picking the raffle tickets for the winners!

Christina, the famous babysitter, came to see Ben!

Ben with the Lowe family!  Thanks for coming!

THANK YOU TO SHANE'S DELI AND WHOLEFOODS for the food!

Of course Grandpa could not be out of sight!

Me and Ben!

Paul and Michelle share their story!

The family on a motorcycle!

Sister love!

The T-shirts, registration, silent auction, and pictures of Ben.

The man of the hour!

Yay!  The first annual Cruisin' for The Cure was a success!  The total amount raised is not yet finished being counted, but for the first annual event we are very thankful for the support!  About 50-75 people attending the event as we ate lots of food, tried on our new sweet T-shirts, raffles with great gifts, and listened to Ben's story!  We are excited to see where Cruisin' For The Cure will go in the future as we hope to expand our awareness and get more and more people involved.  

We would especially like to thank the committee: Karen Crumback (the CFF event director), Mike Morrison, Fred Gizzo, Rob and Rebecca Wolgemuth, and the other Bollier/Ferguson members! 

Haha, that sounded like a Grammy award!!  Anyway, THANK YOU AGAIN for anyone and everyone who supported the event!  Every penny is being put to use to help find ways to improve Ben's life.  It's something so precious and valuable!  Therefore, we are so grateful for your support!   

Ben walking in ... VERY excited!  Please notice his high pitched voice!  It's the best!

One day at a time!

Ben's fingers are healing from his little accident!  The doctors are thinking that he will not need skin grafts anymore ... we're hoping and praying the status stays that way! 

We're also very excited about Ben's first fundraiser! We are praying every detail will work out and that God's name will be glorified through the event!  

Thanks for you prayers!

Psalm 34: 8  -  Taste and see that the Lord is good; blessed is the man who takes refuge in him.

One Week Countdown!

One more week until CRUISIN' FOR THE CURE!

Mark it on your calendars, write it in ink!  

Come to Ben's first fundraiser for the Cystic Fibrosis Foundation to support research to find a cure for cystic fibrosis ... and show the Fergusons your support!

NOVEMBER 8, 2008

*Refer to the blog below for more information!

11 more days!

11 more days till Ben's first Cystic Fibrosis Fundraising event!  Come support the Cystic Fibrosis Foundation and the Ferguson family!  

NOVEMBER 8, 2008 @ Zylstra Harley-Davidson Dealership

131 S. Randall Rd, St. Charles, IL

*See invitation below!

Health Update

Last week Ben visited the dentist.  His teeth are healthy and he has no cavities.  This is good news because CF patients tend to have more problems with their teeth.  

Also, two weeks ago Ben got his fingers caught in the treadmill and he went to see the doctor again last week. Sadly, there is a change Ben will need skin grafts on his hand.  More decisions will be made this week regarding the possibility of this procedure.

We are praying the doctors will make the right decision.  We also pray that Ben's adventurous attitude will not get him in trouble any more than it has!

CRUISIN' FOR THE CURE 2008

The first Cystic Fibrosis Fundraising Event in honor of Benjamin Ferguson!

You're Invited!!

To a family event and motorcycle ride

Saturday, November 8, 2008

Zylstra Harley-Davidson Dealership

131 S. Randall Rd, St. Charles, IL

Ride registration: 1:00 pm

Bikes leave: 1:30 pm

Rally reception and Ben's story: 3:00 - 4:00 pm

Registration fee $25 (includes t-shirts)

Rider fee $10 (includes t-shirts)

General Admissions $5 - Come enjoy food and beverages!

Rev up your bikes and join us for the inaugural Cruisin’ For the Cure. This motorcycle ride and rally is to benefit the Cystic Fibrosis Foundation.  Enjoy riding through scenic St. Charles (weather permitting) or just join us at the dealership to meet Ben and hear his story.  There will be food, beverages and prizes…it will be a great day for a great cause!!  

For more information on donations and sponsorship, please contact

Karen Crumback @ 312.236.4491 ext 104 or kcrumback@cff.org

Or Email myself at megan.bollier@student.indwes.edu

Also:   TO REGISTER

Visit this link:  http://grillinois.cff.org/cruisin08

Getting Involved!

These are pictures of Michelle and my dad (aka the famous "Papa") two weeks ago when they attended the Cystic Fibrosis Foundation Fundraiser called The Breath of Life Gala in downtown Chicago.  It was a great experience for both Michelle and my dad to witness the passion they have to find a cure.  Four months ago Ben was diagnosis with cystic fibrosis, and already we are beginning to get involved with the foundation to raise money for the cure!  

*More information to come soon about an upcoming event to raise money for CF, in honor of little Ben!

A Little Accident

Today Ben had a little accident involving  his fingers and a treadmill which resulted in a three sliced fingers and a trip the emergency room.  Ben was playing in the basement while my mom was running and before she knew it, mischievous little Ben had his fingers stuck in the belt part of the treadmill.  My mom immediately stopped the machine, pulled his fingers out, and began assessing his condition.  After a half an hour we decided to take him to the emergency room because he seemed to be in a lot of pain.  At first when we told him he was going to the hospital, he said "No more poke, poke."  We kind of chuckled and said he didn't have to worry about that!  At the hospital we were in and out with antibiotic medication, pain killers, and advice for a follow up visit to check his condition.  He was a pro at the hospital though and did very well!  Guess it's just another thing to add to the list!  

We just have to keep praying.  I'm sure there are many more surprised to come and we have to trust God with every minute!

Finally!

Ben is back to his baseline and he rarely coughs anymore.  It took him 3 weeks but he is back! Thank you so much for your prayers!

Exodus 14:14  -  The Lord will fight for you; you need only to be still.

Dedicated Fans

Ben wakes up by 6am each morning and is quickly followed by Caleb. Either Paul or Michelle take them two downstairs for "vest and mask" time (Chest Therapy and Pulmozyme Nebulizer treatment). Ben wants to watch "Oh no You never let go," which is a DVD of Christian songs from Grandma Ferguson (Lannie). Ben has been watching this video 3 times a day for the past 2 weeks. Slightly obsessive?  I think so!  But it's a good obsession and the whole family enjoys it! Ben's favorite part of the song is, "Through the calm and through the storm. Oh no, you never let go. Lord, you never let go of me."  (When I go home this weekend, I'll get a video of it.)  What an amazing lesson for Ben to learn at a young age. We are so thankful that Ben is filling his soul with God's truth.  Please continue to pray for health for Ben's body as well as salvation for his soul. 

Ben seems to be doing well. Michelle and Paul are still continuing to do his vest treatments 3 times a day (which is increased from twice a day) and are closely watching him as he still has an increase of mucus. Michelle said she thinks it was less yesterday but they are still going to see how it is today and then talk with the Nurse Practitioner on Monday. If his mucus has not decreased, then they will take him to see Dr. Chung on Tuesday to make sure nothing more is going on. Ben doesn't seem to have anyother symptoms of lung infection, so we think it is just taking him a while to get over this cold.  Michelle also said she never expected him to struggle through a cold so much now that we have ways to help him.  But through it all we are reminded how important it is to protect Ben from exposure to illnesses and most importantly to bathe him in prayer. We are SO grateful for your prayers.  James 5:16 says, "The prayer of a righteous man is powerful and effective."

Last weekend my dad and Michelle went to a Cystic Fibrosis Foundation Fundraiser called the Breath of Life Gala. They gave me a full report, stating it was a very nice evening at the Ritz Carlton in Chicago. They met some wonderful people from the CFF as well as the Foundation's President Robert Beall.  Dr. Beall spoke about the great strides in the care and life of CF patients. He shared the exciting advances that have been made and are in the process of being made.  These include protein repair drugs that would address the root problem of CF.  It was exciting for my dad and Michelle to hear about all the work the CFF is doing for the impovement of CF patient's lives and the extremely confidence that a cure is in grasp. 

WOW!  How cool to think about the possibilities God has in store for Ben!  He could be one of the first to experience these life saving strides for a cure of cystic fibrosis!

"Not our will, but Yours be done."