Welcome to Team BAM!!
Team BAM
Team BAM
Welcome to Team BAM!! Since 2013, our team has raised about $126,400 for the Cystic Fibrosis Foundation! Our 2025 goal is to raise $10,000! Will you help us by donating, walking and/or fundraising?
Our backstory and a 2025 update...
Bryce (BAM) was born in the summer of 2012 and diagnosed with cystic fibrosis at only 5 weeks old. He is now a happy, intelligent, and energetic 12 ½ year old who is crushing it in middle school! When he first visited the Cystic Fibrosis Clinic in 2012, his BMI (body mass index) wasn’t even on the growth chart! Now he typically falls between the 30th and 40th percentile which is actually a little low for those with CF but he is working hard to maintain and gain some weight! Bryce loves to run, watch and play sports (especially soccer), play with his younger brother (Paxton), and play video games!
Cystic fibrosis (CF) is an inherited chronic disease that affects the lungs and digestive system of about 40K children and adults in the US (105K worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that clogs the lungs, potentially leading to life-threatening lung infections, and obstructs the pancreas, stopping natural enzymes from helping the body break down and absorb food. There are many treatments available for those with CF as each case is slightly different. In addition, real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease.
Currently, Bryce uses airway clearance, multiple breathing treatments, pancreatic enzymes, high calorie drinks and high fat meals, CF vitamins and multi-vitamins, a laxative, and a CFTR modulator to maintain his health and function “normally” each day. Airway clearance is typically performed using a vibrating vest that pumps air through hoses and into a vest that vibrates/shakes to help break up the sticky mucus and remove it from his lungs in an attempt to keep bacteria from causing infections. When healthy, Bryce sits for 30 minutes twice a day while using this vest. When he is ill, he will do additional vest treatments, manual chest percussion therapy (CPT), and/or use an oscillating positive expiratory pressure device called Aerobika. Prior to the vest, we did manual CPT at least twice a day as he was too small for the vest.
In addition to airway clearance, Bryce also takes pancreatic enzymes each time he eats food with fat and/or protein, which is most of the time as CFers require those nutrients (and many extra calories!) to maintain a healthy weight. He’s been taking enzymes and doing airway clearance since he was 5 weeks old! In an effort to keep the weight on our energizer bunny, we are always encouraging him to eat more and try new things! Bryce used to take an appetite stimulant twice a day but since starting a new modulator (Trikafta), his appetite has improved and his weight seems to be stable, so we were able to eliminate that medication. Bryce mastered the art of taking pills at a young age and can take several at a time – I think the most I’ve seen is 10 at once!
CF can also complicate things in the GI tract, causing constipation and blockages from the thick mucus. This is where the daily laxative comes into play.
At the moment, Bryce uses a nebulizer at least twice per day. One medication is Sodium Chloride (also called Hypertonic Saline) that helps to loosen and move the mucus in his lungs. The other is a mucus-thinning medication called Pulmozyme. He also uses an inhaler prior to Sodium Chloride to reduce the risk of bronchial spasms.
When ill, he will use an inhaler or nebulizer every 4 to 6 hours for delivery of albuterol. This will help keep his airways open, alleviate wheezing, and help minimize coughing. In this case he would also increase the Sodium Chloride to twice per day along with the other airway clearance (vest and/or Aerobika).
Prior to this past summer, we did not use Sodium Chloride as part of his regimen – whether healthy or ill. However, he was pretty sick over the summer and in an attempt to avoid hospitalization, we added in Sodium Chloride as well as increasing treatments to at least 4x/day. Thankfully we were able to get him over the rough patch and even better than his normal by improving on his lung function test and gaining a good bit of weight!
If his respiratory culture (a test done at each visit to the CF clinic that resembles a strep culture/swab) comes back positive for risky bacteria, he may also use the nebulizer for that medication or he could be placed on oral antibiotics to try to avoid a lung infection.
As mentioned above, we added in a CFTR modulator/corrected called Trikafta in July of 2021. This medication has been proven to not only minimize the symptoms of CF but also to slow down the progress of the disease! This drug works by helping the salt to move correctly throughout his body, thereby decreasing the thick, sticky mucus and minimizing some of the problems! This is the best treatment yet as it can treat as many as 90% of the CF population! It has been shown to improve lung function, lower sweat chloride levels (the amount of salt lost from the body that is detected with a test used to diagnose CF), reduce exacerbations and hospitalizations, improve appetite and weight gain, and improve overall quality of life!
So far, we are pleased with the GI results of Trikafta – better appetite, weight maintenance/gain, and no appetite stimulant! His lung function has remained steady but that was expected since he typically has great results on his PFTs (Pulmonary Function Tests). He still needs to continue his daily therapies for the time being but his overall health should be maintained, if not improve!
There is another new medication similar to Trikafta that has been approved for use as of this January – Alyftrek. As you may or may not know, Trikafta has been known to cause some harsh mental and/or physical side effects for many with CF which often causes them to have to stop taking the medication. This new medication is said not to have as many side effects but be a little harder on the liver. In addition, it appears that several new mutations will be able to take Alyftrek. We have no plans to take Bryce off of Trikafta at this point as he is doing well on it but the fact that yet another new medication is available shows that YOUR DONATIONS are hard at work!!
Although we do our best to not to let CF control our lives, we still need to take precautions above and beyond the "typical family"…especially with COVID so prevalent over the past couple of years. But we also feel like CF prepared us for the pandemic (and beyond) as we have always had some limitations... missing out or delaying events and gatherings, utilizing more soap and sanitizer than you can ever imagine, and wearing masks to doctor’s visits and frequently in public during cold and flu season.
We are very excited and so thankful to all involved! And even though the CF Foundation and the pharmaceutical companies have done GREAT things, we can't stop now!! There is still a long way to go before those with ALL CF mutations are given a chance to breathe easy as the modulators cannot treat all patients with CF and they are NOT a cure!
By donating to Great Strides, you will help fund research to continue monitoring of those on the newer medications, development of additional medications and treatments, research toward finding a drug that will eliminate not only the root cause but also the need to do hours of daily treatments, and to finding a CURE for not only those with a few mutations but ALL CFers! The CF Foundation also helps patients and their families find the best insurance coverage and co-pay assistance programs, helps cover the cost of medications and treatments for those that qualify, as well as many other programs so that everyone with/affect by CF can live a full life! Without the CF Foundation and the co-pay assistance programs, we would not be able to afford Bryce’s medications as his enzymes, inhaled treatments, and Trikafta alone would be more than $30,000 per month... and that’s with decent insurance!
By participating in and/or donating to the Great Strides walk, we are helping to add tomorrows for not only Bryce but for everyone living with CF by funding life-saving research and medical progress. CF research is not funded by the federal government; therefore, we need every single penny. The CF Foundation has been recognized by publications such as SmartMoney as one of the most efficient organizations of its kind. Nearly 90% of every dollar of revenue raised is available for investment in vital CF programs to support research, care, and education. And don’t forget... your gift is 100% tax deductible!
Will you join us? Support Team BAM and the CF Foundation by making a donation to our Great Strides fundraising campaign! For more information about CF or Great Strides, please visit www.cff.org or feel free to contact us!
Thank you!
Amy & Josh
Our backstory and a 2025 update...
Bryce (BAM) was born in the summer of 2012 and diagnosed with cystic fibrosis at only 5 weeks old. He is now a happy, intelligent, and energetic 12 ½ year old who is crushing it in middle school! When he first visited the Cystic Fibrosis Clinic in 2012, his BMI (body mass index) wasn’t even on the growth chart! Now he typically falls between the 30th and 40th percentile which is actually a little low for those with CF but he is working hard to maintain and gain some weight! Bryce loves to run, watch and play sports (especially soccer), play with his younger brother (Paxton), and play video games!
Cystic fibrosis (CF) is an inherited chronic disease that affects the lungs and digestive system of about 40K children and adults in the US (105K worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that clogs the lungs, potentially leading to life-threatening lung infections, and obstructs the pancreas, stopping natural enzymes from helping the body break down and absorb food. There are many treatments available for those with CF as each case is slightly different. In addition, real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease.
Currently, Bryce uses airway clearance, multiple breathing treatments, pancreatic enzymes, high calorie drinks and high fat meals, CF vitamins and multi-vitamins, a laxative, and a CFTR modulator to maintain his health and function “normally” each day. Airway clearance is typically performed using a vibrating vest that pumps air through hoses and into a vest that vibrates/shakes to help break up the sticky mucus and remove it from his lungs in an attempt to keep bacteria from causing infections. When healthy, Bryce sits for 30 minutes twice a day while using this vest. When he is ill, he will do additional vest treatments, manual chest percussion therapy (CPT), and/or use an oscillating positive expiratory pressure device called Aerobika. Prior to the vest, we did manual CPT at least twice a day as he was too small for the vest.
In addition to airway clearance, Bryce also takes pancreatic enzymes each time he eats food with fat and/or protein, which is most of the time as CFers require those nutrients (and many extra calories!) to maintain a healthy weight. He’s been taking enzymes and doing airway clearance since he was 5 weeks old! In an effort to keep the weight on our energizer bunny, we are always encouraging him to eat more and try new things! Bryce used to take an appetite stimulant twice a day but since starting a new modulator (Trikafta), his appetite has improved and his weight seems to be stable, so we were able to eliminate that medication. Bryce mastered the art of taking pills at a young age and can take several at a time – I think the most I’ve seen is 10 at once!
CF can also complicate things in the GI tract, causing constipation and blockages from the thick mucus. This is where the daily laxative comes into play.
At the moment, Bryce uses a nebulizer at least twice per day. One medication is Sodium Chloride (also called Hypertonic Saline) that helps to loosen and move the mucus in his lungs. The other is a mucus-thinning medication called Pulmozyme. He also uses an inhaler prior to Sodium Chloride to reduce the risk of bronchial spasms.
When ill, he will use an inhaler or nebulizer every 4 to 6 hours for delivery of albuterol. This will help keep his airways open, alleviate wheezing, and help minimize coughing. In this case he would also increase the Sodium Chloride to twice per day along with the other airway clearance (vest and/or Aerobika).
Prior to this past summer, we did not use Sodium Chloride as part of his regimen – whether healthy or ill. However, he was pretty sick over the summer and in an attempt to avoid hospitalization, we added in Sodium Chloride as well as increasing treatments to at least 4x/day. Thankfully we were able to get him over the rough patch and even better than his normal by improving on his lung function test and gaining a good bit of weight!
If his respiratory culture (a test done at each visit to the CF clinic that resembles a strep culture/swab) comes back positive for risky bacteria, he may also use the nebulizer for that medication or he could be placed on oral antibiotics to try to avoid a lung infection.
As mentioned above, we added in a CFTR modulator/corrected called Trikafta in July of 2021. This medication has been proven to not only minimize the symptoms of CF but also to slow down the progress of the disease! This drug works by helping the salt to move correctly throughout his body, thereby decreasing the thick, sticky mucus and minimizing some of the problems! This is the best treatment yet as it can treat as many as 90% of the CF population! It has been shown to improve lung function, lower sweat chloride levels (the amount of salt lost from the body that is detected with a test used to diagnose CF), reduce exacerbations and hospitalizations, improve appetite and weight gain, and improve overall quality of life!
So far, we are pleased with the GI results of Trikafta – better appetite, weight maintenance/gain, and no appetite stimulant! His lung function has remained steady but that was expected since he typically has great results on his PFTs (Pulmonary Function Tests). He still needs to continue his daily therapies for the time being but his overall health should be maintained, if not improve!
There is another new medication similar to Trikafta that has been approved for use as of this January – Alyftrek. As you may or may not know, Trikafta has been known to cause some harsh mental and/or physical side effects for many with CF which often causes them to have to stop taking the medication. This new medication is said not to have as many side effects but be a little harder on the liver. In addition, it appears that several new mutations will be able to take Alyftrek. We have no plans to take Bryce off of Trikafta at this point as he is doing well on it but the fact that yet another new medication is available shows that YOUR DONATIONS are hard at work!!
Although we do our best to not to let CF control our lives, we still need to take precautions above and beyond the "typical family"…especially with COVID so prevalent over the past couple of years. But we also feel like CF prepared us for the pandemic (and beyond) as we have always had some limitations... missing out or delaying events and gatherings, utilizing more soap and sanitizer than you can ever imagine, and wearing masks to doctor’s visits and frequently in public during cold and flu season.
We are very excited and so thankful to all involved! And even though the CF Foundation and the pharmaceutical companies have done GREAT things, we can't stop now!! There is still a long way to go before those with ALL CF mutations are given a chance to breathe easy as the modulators cannot treat all patients with CF and they are NOT a cure!
By donating to Great Strides, you will help fund research to continue monitoring of those on the newer medications, development of additional medications and treatments, research toward finding a drug that will eliminate not only the root cause but also the need to do hours of daily treatments, and to finding a CURE for not only those with a few mutations but ALL CFers! The CF Foundation also helps patients and their families find the best insurance coverage and co-pay assistance programs, helps cover the cost of medications and treatments for those that qualify, as well as many other programs so that everyone with/affect by CF can live a full life! Without the CF Foundation and the co-pay assistance programs, we would not be able to afford Bryce’s medications as his enzymes, inhaled treatments, and Trikafta alone would be more than $30,000 per month... and that’s with decent insurance!
By participating in and/or donating to the Great Strides walk, we are helping to add tomorrows for not only Bryce but for everyone living with CF by funding life-saving research and medical progress. CF research is not funded by the federal government; therefore, we need every single penny. The CF Foundation has been recognized by publications such as SmartMoney as one of the most efficient organizations of its kind. Nearly 90% of every dollar of revenue raised is available for investment in vital CF programs to support research, care, and education. And don’t forget... your gift is 100% tax deductible!
Will you join us? Support Team BAM and the CF Foundation by making a donation to our Great Strides fundraising campaign! For more information about CF or Great Strides, please visit www.cff.org or feel free to contact us!
Thank you!
Amy & Josh
Comments