Showing posts with label medical. Show all posts
Showing posts with label medical. Show all posts

31 October 2013

Herd Immunity and What To Do About It

I haven't written an update on Caleb in awhile.  He is really doing awesome overall.  We are still going to the doctor every month for blood work, but everything always checks out really good.

In August, the doctor ordered several blood tests to see if any of the antibodies from his childhood vaccinations were still present in his system.  All of the tests came back negative, so technically he is no longer immune to the childhood diseases that the vaccines prevent.  I was a little concerned, but the doctor said the reason he was fine and not getting sick was because of something called "Herd (or Community) Immunity".

Here is a blurb about what Herd Immunity is from the web:
 "Herd immunity (or community immunity) describes a form of immunity that occurs when the vaccination of a significant portion of a population (or herd) provides a measure of protection for individuals who have not developed immunity. Herd immunity theory proposes that, in contagious diseases that are transmitted from individual to individual, chains of infection are likely to be disrupted when large numbers of a population are immune or less susceptible to the disease. The greater the proportion of individuals who are resistant, the smaller the probability that a susceptible individual will come into contact with an infectious individual. Vaccination acts as a sort of firebreak or firewall in the spread of the disease, slowing or preventing further transmission of the disease to others. Unvaccinated individuals are indirectly protected by vaccinated individuals, as the latter are less likely to contract and transmit the disease between infected and susceptible individuals. Hence, a public health policy of herd immunity may be used to reduce spread of an illness and provide a level of protection to a vulnerable, unvaccinated subgroup. Since only a small fraction of the population (or herd) can be left unvaccinated for this method to be effective, it is considered best left for those who cannot safely receive vaccines because of a medical condition such as an immune disorder, organ transplant recipients, or people with egg allergies. "
Because this isn't a fail safe method of avoiding these diseases, Caleb is now on a schedule to receive most of his original shots over again!  As of today, he's had nine of his childhood immunizations re-administered. Some of the vaccines (live virus types) cannot be given to him at all until he is at least 24 months past his transplant date... in fact, we have had to defer three live vaccines for Kalia until that time as well.

So that's about it for an update.  Like I said, he is doing really well, but he still has some hurdles to overcome.  Good thing he has Brooklin's blood...she is a state champion hurdler! ;)

and did you notice they are all wearing Star Wars shirts?? =)

14 August 2013

One Year Anniversary!

Last year, on August 14, 2012, Caleb endured a bone marrow transplant and Brooklin endured a three hour bone marrow harvest.  I am so proud of them both.  Caleb for being so courageous and brave during his month long stay in the hospital and Brooklin for her immediate willingness to be his donor.  A lot has happened this past year; some hard things, some amazing things, but the things that stand out the most are the numerous miracles we have experienced.  God gave us the hardest things we have ever had to go through, but he also surrounded us with angels...literally.  I am grateful for this experience.  We are unable to fully comprehend the sweetness in life without having the experience of tasting the bitter.

Top: Transplant day  Bottom: One year later

13 February 2013

Pilot For a Day: Caleb Jensen

Pilot For a Day: Caleb Jensen

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Pilot For a Day
Caleb Jensen, Pilot For a Day participant, operates a bomb robot as part of the Pilot for a Day program at Joint Base Pearl Harbor-Hickam, Hawaii, Feb. 8, 2013. After being diagnosed with aplastic anemia, a condition which causes the body to stop producing new blood cells, Caleb was recommended for the program which aims to benefit children in the local community suffering from serious or chronic illnesses. (U.S. Air Force photo/Tech. Sgt. Jerome S. Tayborn)
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Pilot For a Day: Caleb Jensen

Posted 2/13/2013   Updated 2/13/2013  Email story   Print story


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by Staff Sgt. Terri Barriere
15th Wing Public Affairs


2/13/2013 - JOINT BASE PEARL HARBOR-HICKAM, Hawaii  -- Caleb Jensen has dreamed of becoming a pilot for as long as he can remember. He thought about it, talked about it and on Feb. 8 his dream came true.

Caleb, 15, was selected for the Pilot For a Day program after undergoing an intense battle with aplastic anemia, a condition which causes the body to stop producing new blood cells. After being admitted to Kapi'olani Medical Center for Women and Children for treatment, he was identified by the hospital's child life specialist and nurses as a good candidate for the private organization, Pilot For a Day, and an experience with the 15th Wing, focused on children with serious or chronic medical conditions.

Capt. Todd Walker, said Pilot For a Day invites children of all ages, military or civilian, to be guests of the wing and one of its flying squadrons for an entire day. In so doing, the mission is to give each child a special day and a break from whatever challenges they are facing.

"Pilot For a Day came at the perfect time," said Melissa Jensen, Caleb's mom. "It came at the end of his treatment and was really a good way for us to celebrate things getting back to normal."

Melissa said after finding out Caleb's diagnosis in June, setting up a bone marrow transplant between him and his sister in August, and home-schooling him while nursing him back to health for the remainder of last year; she knew Pilot for a Day would be perfect for him.

"I agreed to let him participate, because I knew he'd love it," she said. "He's done nothing but talk about being a pilot and his love for flying for a while now. This was perfect for him."

After receiving a clean bill of health at his most recent medical appointment, Caleb was more than ready to leave the doctors and hospitals in the past and engage in a little fun.

Caleb, who said he's not sure of anything else he'd like to accomplish other than becoming a pilot of "something big," is now considering the military as a possible avenue to fulfilling his life-long dream.

"This was really good timing, I'm feeling tons better," he said. "My favorite part of the day was definitely the KC-135 simulator. It's as close to flying as I can get right now and it was really a lot of fun. I can't wait to tell my friends I got to fly a plane while they were at school."

To make the moment even sweeter for Caleb, his parents, brother and three sisters were able to share the experience. And just as his family rallied around him in support as he underwent his treatments, they were there to share the moment he notably marks as one of the best days of his life.

"We've been through a really hard time together, so it's good to be able to experience the really good ones together as well," Melissa said of her family's participation in Pilot For a Day. "This will be a lasting memory my whole family shares and it was a lot of fun."
The mother said that after the ups and downs of the past several months, it was refreshing to see her children having so much fun.

"Just watching their faces light up ...everyone had these great big smiles on their face," she said.

Col. Terry Scott, 15th Wing vice commander, said those smiles, in essence, are what the Pilot For a Day program is all about.

"I feel lucky, privileged, honored and very fortunate to participate in Pilot For a Day," he said. "It's great to meet such good people who have overcome such obstacles. They've earned my respect and it doesn't matter how old they are, it's respectable to see someone not giving up, not quitting, taking life by the horns and going out there and living - seizing life."

Scott said supporting programs like Pilot For a Day show the compassionate side of the U.S. military, a point not lost on the Jensen family.

"Thank you so much for your generosity," said Caleb. "This was so much fun. I really would enjoy coming back to do it again. This was definitely the best Friday ever!"

16 September 2012

Another bald baby!

Facebook post from 09/16/2012


Now we have three baldies! (Isaiah wanted to wait until after his school pictures.)



13 September 2012

PICC line removal

Facebook post from 09/13/12

Caleb had his PICC line removed today. The MRI showed that his body was trying to form another clot...but there is not a significant one there now. They took the PICC line out as a precautionary measure. The up side is he no longer has a direct line into his body, which cuts down on infection risks. The down side is he will have to be stuck twice a week for blood tests.








05 September 2012

HE IS HOME!

Facebook posts from 09/05/2012

CALEB IS HOME FROM THE HOSPITAL!!!!


All home!! I'm so happy!! Not out of the woods for awhile...but so glad he is home!!!!!






Facebook comments:

Wendy Burns Dalton Yeah!!! Amen!
September 5, 2012 at 8:45pm · Like

Jp Dalton Awesome!!!! Yea for all.
September 5, 2012 at 8:47pm · Like

H Jensen Graham wooooooohoooooooooooo!!!!!!!!!!!!!!!!!!!!
September 5, 2012 at 8:48pm · Like

Kathleen Houtz Benner :)
September 5, 2012 at 8:51pm · Like

Brooklin Jensen :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D :D !!!!!!!!!!!!!!!!!!!!!!
September 5, 2012 at 8:51pm · Like · 1

Tamara Bird Olson Yay!!! We've been praying so hard for him and you all. Have a awesome night with your whole family at home.
September 5, 2012 at 8:53pm · Like

Mindy Patterson Andrew Yay! I was just wondering earlier today how much longer he would be there.
September 5, 2012 at 8:56pm · Like

Emily Y Scott AK yayayayay!!
September 5, 2012 at 9:01pm · Like

Steph Alaska Yes!
September 5, 2012 at 9:08pm · Like

P Nichole Caldwell Awesome! So happy for you all!
September 5, 2012 at 9:09pm · Like

Calista Strasser Laney Wahoo.
September 5, 2012 at 9:10pm · Like

Estrella Strasser BEST :) DAY :) EVER :) !!!!!
September 5, 2012 at 9:15pm · Unlike · 1

Anelalani Livingston-Sturge Amen!!!!
September 5, 2012 at 9:24pm · Like

Ketra Kennedy Arcas Great news!!
September 5, 2012 at 10:06pm · Like

Sarah Portmann *jump for joy*
September 5, 2012 at 10:19pm · Like

Gma Pita How wonderful for him and all of you! <3 span="">
September 5, 2012 at 11:10pm · Like

Angeline Morrill-Quiner extra snuggles with the family tonight!
September 6, 2012 at 12:33am · Like

Matthew Strasser SAH-WEEEEEEEEEEEEEEEEEEEETT!!!!!!!!!!!!!!!
September 6, 2012 at 10:38am · Like

Tricia Robinette Loder So happy for you all!!!!
September 6, 2012 at 4:47pm · Like

Christy Tenney Strikwerda Yahooo.....
September 6, 2012 at 6:04pm · Like

Angelica Strasser McDonald SO HAPPY!!
September 7, 2012 at 8:35am · Like

Tannis Bingham Kearns yeah! Was that an early relaease?
September 9, 2012 at 11:44pm · Like

Pamela Whillock-Olliff That is great!
September 9, 2012 at 11:48pm · Like



Elena Bechert Cabatu So happy for you guys!
September 5, 2012 at 9:56pm · Like

Marnie Siebach YAY!!!!!!! Holding his Buddy! This is the happiest picture I have ever seen!
September 5, 2012 at 9:56pm · Like

Jana Krout Pierce Yippee! So happy for you!
September 5, 2012 at 9:58pm · Like

Ian League · Friends with Caleb Jensen and 8 others
:)
September 5, 2012 at 10:01pm · Like

Lori Strikwerda Shepherd Party time!!!
September 5, 2012 at 10:11pm · Like

Kylee Kim Awesome!
September 5, 2012 at 10:39pm · Like

Mia Wolfe League Yay! Please continue to get well.  =)
September 5, 2012 at 11:31pm · Like

Emily Y Scott AK So so so wonderful :) Thanks for posting this amazing photo  :) We are so happy for you guys, we are still praying for a good full recovery!
September 5, 2012 at 11:50pm · Like

Dulcie Larsen yeah!!!!! what a relief!!!! Now the sleeping fairy will have someone else to work her magic on!!!
September 6, 2012 at 12:18am · Unlike · 2

Renee LeAnn Johnson Great news!
September 6, 2012 at 8:22am · Like

Patricia Franceschine Yeah! You all look so happy. I am so happy for you all. Praise God!
September 6, 2012 at 10:37am · Like

Tricia Robinette Loder I bet he is so happy to be home. Love you guys!
September 6, 2012 at 4:48pm · Like

Sally Lee Wahoooo!!!!! Welcome home, Caleb!!!!!!

September 7, 2012 at 11:22am · Like



Day 29 - ...and day last in the hospital we hope!

Facebook post from 09/05/2012

Caleb's last day (we hope) in the hospital!! 29 days!! His nurses made him this little version of "Elder Tree" (what he calls his IV stand) because they were SURE he was going to miss all the beeping it did and having to take it everywhere with him...lol!! They also signed a card for him! So sweet and thoughtful!



Facebook comments:

M S YAY!!!!! This makes me so happy!!! Almost done Caleb! You did it!!!
September 5, 2012 at 4:20pm · Like

T A Woooooohooooooo!!!! Go Caleb!
September 5, 2012 at 4:44pm · Like

P F Woo Hooo! I am so happy for Caleb and the whole family. There will be happy times in the Jensen house when he arrives home.  =)
September 5, 2012 at 4:55pm · Like

A B Yay Caleb!!! You are awesome!!!
September 5, 2012 at 4:58pm · Like

K G so happy he can be home soon!
September 5, 2012 at 7:22pm · Like · 1

S L God bless you with a strong immune system, Caleb!!!

September 5, 2012 at 8:37pm · Like

02 September 2012

Day 26 - Another bald baby



Darwin decided to shave his head, so Caleb wouldn't be the only bald baby in the house. =)

31 August 2012

Day 24 - First time out of his room

Facebook posts from 08/31/2012


Caleb gets to be unhooked from his IV stand (we call it Elder Tree) for an hour today so he can have an MRI. (He is pretty excited about that!) They docs are still trying to figure out what is causing his shoulder and neck pain...












Well, we just found out why Caleb has been having shoulder/neck pain. He has an infection/clot in his jugular vein. The good news is the docs know how to fix it! He will be having his Hickman (chest catheter) removed this afternoon and will have a PICC line placed in his arm instead. They will also adjust his antibiotics to get rid of the infection.
The doc came in 20 min. ago to tell us the news and the only thing Caleb said was, "But mom! It's two o'clock! The BSU game is starting!" 









Facebook comments:


CNT: the picc line will be able to stay in longer with less risk of infection. Still praying for him and your family!
August 31, 2012 at 5:24pm · Like

HG: Poor kid! At least the docs can fix it. And like always, he seems to be pretty up beat. Go BSU!!!!
August 31, 2012 at 5:31pm · Like

AUU: PICC lines are the best!
August 31, 2012 at 6:02pm · Like

CKC: Groan...then yay! Always amazed when the realization of how great the blessings are by how much worse things could have been! My prayers are with your family! <3 span="">
August 31, 2012 at 6:08pm · Like

DL: glad he stuck by saying that it hurt and didn't discount it!!! even better they figured it out!!! whew!!!
August 31, 2012 at 6:19pm · Like

GL: So happy they figured it out. And that Caleb can watch the game, go BSU!!!
August 31, 2012 at 6:26pm · Like · 1

JAT: i love caleb..
August 31, 2012 at 8:00pm · Like

MWL: Do they have to put him under to do this? When my kids had the PICC lines in they were awake (not fun to watch) I am happy he wants to watch the game! We are still praying for all of you guys.  =)

August 31, 2012 at 10:22pm · Like

Day 24 - ANC of 2000

Facebook posts from 08/31/2012

Caleb's ANC is 2000!! (1500+ is normal range). He hasn't been above about 300 since before he was diagnosed! (google ANC for what that means...I'm on my phone and don't want to type it all out with one finger...lol)


Facebook comments:

WBD: Yeah!!!
August 31, 2012 at 12:53pm · Like

PF: Praise God! That is awesome!
August 31, 2012 at 1:04pm · Like

SK: Yay! We're root'n for ya, Caleb!
August 31, 2012 at 1:38pm · Like

AH: That is wonderful! :o)
August 31, 2012 at 2:44pm · Like

KR: Awesome news!!!
August 31, 2012 at 3:33pm · Like · 1

DL: yeah baby!!! time to come home!!!!
August 31, 2012 at 5:13pm · Like

SJ: EXCELLENT news!!!
August 31, 2012 at 5:41pm · Like

MWL: Yay! I know what that means and I am doing the "happy dance" over here!
August 31, 2012 at 10:23pm · Unlike · 1

TRL: Soooooo happy to hear this!!!!!!!!
September 1, 2012 at 9:13am · Like

TBK: su--------weeeettttt.
September 1, 2012 at 11:20am · Like

KB: Yeah!!! That is great news!!
September 1, 2012 at 7:00pm · Like

RRS: African National Congress??????????
September 1, 2012 at 10:58pm · Like

RRS: Arkansas Northeastern Conference?????
September 1, 2012 at 10:59pm · Like

RRS: Advisory Neighborhoods Commissions??????
September 1, 2012 at 11:00pm · Like

MJ: Absolute neutrophil count
September 2, 2012 at 12:06am · Like

HT: That is great news!!!

September 4, 2012 at 10:22am · Like


29 August 2012

Day 22 - Almost completely bald

Facebook post from 08/29/2012

All that's left of Caleb's hair! Does it look like Hawaii to anyone else??






Facebook comments:

ATG:I miss Hawaii...hahaha
August 29, 2012 at 8:05pm · Like

DC: Hawaii was petty awesome!
August 29, 2012 at 8:35pm · Like

APD: it sure does......
August 29, 2012 at 8:48pm · Like

ALS: love the island chain :) thats cool!!
August 29, 2012 at 9:18pm · Like

GL: And he's even a handsome dude from the back! Love bald, and Caleb, you've got style too!
August 29, 2012 at 10:30pm · Like · 1

MT: Haha it does look like Hawaii!
August 29, 2012 at 10:32pm · Like

MWL: Hahaha....that's very funny.
August 29, 2012 at 11:09pm · Like

LPS: well at least we can be KIND of sure he wont have a bald spot on the back of his head when he is older... looks like that hair is pretty strong. haha
August 30, 2012 at 9:10am · Unlike · 2

TBK: bless his little heart......

August 30, 2012 at 4:36pm · Like

27 August 2012

Day 20 - Rest and pain

Facebook post from 08/27/2012

Day 20 - He has had a lot of pain in his shoulder and arm the past few days, so later tonight he is going in for a CT scan...and possibly an MRI. He didn't sleep very well last night, but he just ate lunch and conked out, so I'm headed home now.
Sweet dreams Brother! 
xoxo, Mom




Facebook comments:

SA: Poor thing! Praying here for him
August 27, 2012 at 4:39pm · Like · 2

RRS: Snug as a bug in a rug!
August 27, 2012 at 10:49pm · Like

PF: Such a handsome young man. Praying for him and you and your family.

August 28, 2012 at 9:17am · Like

26 August 2012

Day 19 - Loosing more hair, gaining more faith





I heard this song while driving home from visiting Caleb at the hospital tonight...and it reminded me of how much God loves me, and that he is helping us get through the ugly stuff and helping us see all the blessings he has given us.
The Lord has blessed me with simple faith.
If I pray for help, He will give me strength.
I will do His work. I will gladly serve.
I'll follow Him in faith.
The Lord has blessed me to feel His love.
I have felt His promptings and learned to trust.
So in all I do, I'll be faithful to
The things I know are true.
The Lord has blessed me in many ways.
With a thankful heart I will sing His praise.
I will raise my voice and proclaim my choice
To follow Him in faith.

25 August 2012

Day 18 - Facetime is the best!

Facebook post from 08/25/2012

I LOVE FACETIME!! We can have family prayer and scriptures with Caleb while he is in the hospital! He has also been able to attend seminary and some of church using FaceTime! So grateful for technology!!




Facebook comments:

MWL: Wow...I didn't know you could do seminary online..so cool.
August 25, 2012 at 11:29pm · Like

KK: Seriously! That's awesome!
August 25, 2012 at 11:48pm · Like

MJ: His sister takes the iPod to seminary, and then he just facetimes her and listens and participates that way!
August 25, 2012 at 11:49pm · Like · 2

ZZ: Seminarys started down there already!?!
August 25, 2012 at 11:57pm · Like

24 August 2012

Day 17 - Going bald

Facebook post from 08/24/2012

Today was hard. Chemo finally caught up with Caleb and he asked me to shave his head so he would have less hair on his pillow and sheets. He was pretty upbeat this morning, but around noon he just got so tired that he fell asleep sitting up and he also had great pain in his left shoulder that brought him to tears. It is so hard to watch my boy endure this...but he is being really strong and he has a lot of supporters! I know that some of his cousins and uncles have already (or are going to) shaved their heads to show support for him. It is comforting to know that so many of you are praying for him and our family! Thank you doesn't seem to be a big enough word...



Facebook comments on this post:

KHB: Is all of this expected? My heart hurts for him. Praying for this to be over soon.
August 24, 2012 at 11:21pm · Like · 1

MJ: Yes...all expected, just harder when it's real.
August 24, 2012 at 11:37pm · Like

HMM Ur in our prayers in Alaska sweet Caleb I'm so sorry ur having this great trial and mom and dad hang tough we r sure praying! Never met u personally but love Lila and Jo Jo like our own :)
August 25, 2012 at 12:40am · Like

MWL: I am sorry Caleb is feeling so yucky tonight =( We will pray extra hard tonight....for a good night sleep.
August 25, 2012 at 1:09am · Like

GP: Praying always <3 div="">
August 25, 2012 at 1:33am · Like

ESL: This is so sad to hear. What the pain in his shoulder from is PICC line??? I used to get some pretty bad pains in my should area from my PICC line, I put a heating pad on and it helped take away the pain. You guys are amazing stay so faithful as you go through these trials.
August 25, 2012 at 1:45am · Like

SA: More prayers here, he is such a trooper. I just keep seeing that sweet little guy when he was little. What a tough, strong young man he is today
August 25, 2012 at 7:32am · Like

SJ: Sad day! For what it's worth though . . . he has a really nice shaped head for being bald :)
August 25, 2012 at 8:31am · Unlike · 2

AMHS: Keep fighting the fight Caleb...we're all behind you! Brother Savage says "He's in"....and shaved his head today too!
August 25, 2012 at 10:49pm · Like