March 2018: Mermaid Tails and The Luck of The Irish

March 9, 2018

The Luck of the Irish has reached Primary Children’s and Susie did just fine (Avastin).

We made it home before the nausea started.
Home-sweet-home. 🙂

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March 10, 2018

Sweet family and friends ran in honor of Susie today at the Rex Lee Run.

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March 22, 2018

My friend, Keri, stopped by Monday with a gift in tow.
A darling Mermaid Tail Blanket, donated by www.whimsytails.com for Susie, along with hand crafted cards from her darling daughters And a testimony from her!
So thankful for beautiful friends who remind us of God’s love. 💕

March 23, 2018

Rainy highways. Thankful for Hannah’s friends, Sam and Emily, for filling in with younger children today. Liam loved playing with cousin Indy—Thanks, Amy.
Heart torn: thankful, grateful, homesick, missing family and time with them, too. Saudade. 💕

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February 2018: Oxygen and a Train Ride

February 2, 2018

Friday. Another Pediatric Cancer Clinic day.

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Exercises with Dr. Whipple—checking weakness/side effects of Chemo.

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February 3, 2018

Thank you for your prayers for Susannah. 🙂

February 4, 2018

Oxygen desaturation and fever began as usual this morning (post-Chemo).

Good thing Uncle Matt (Pediatrician) makes house calls. Gray paler. Low oxygen. Fast heart rate. Body aches and pains. Nausea.
“She needs an ambulance to get to Primary Children’s ER or (portable) oxygen..”
Double checked oxygen at his office.
Admitted to Utah Valley to observe overnight.
Rocky day.

Chest X-rays. Hard work. Nurses Hailey and Madi.

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Port access ROUGH.
Third times a charm.
Brave princess.
Every times she falls asleep her oxygen desaturates. No one knows what is going on.
Atypical Chemo reactions. LONG, painful day.
Canceled Make-A-Wish declaration.
Just want a peaceful weekend. No such luck.

Changing of the guard. Heart beat too fast for sleeping (over 120–tachycardia). Oxygen too low for already being on oxygen (half, turned up from a quarter liter.)

Went to pick up Susie and Joe.
Rechecked oxygen saturation.
Anything below 88, during the day, needs oxygen. Color a bit better today. No fever currently.
(No known cause yet for increased heart beats, fever of unknown origin, and low oxygen saturation except that this has been her pattern after her second dose of her third Chemo.☹️) Still no answers.

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During this Winter season, I appreciate the Hospital staff for wearing gowns, masks, and gloves.
Thanks for keeping your sick little ones home to prevent the spread of illnesses! 👍🏼😊

Home!
We got more Super-girl accessories.
Oxygen makes for smarter breathing.
(Heart rate looks great!)

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February 7, 2018

I hate feeling helpless and vulnerable.
Raw motherhood emotions tonight.
Susannah has a bad headache and eye-ache early this evening.
Desaturation. Oxygen. Hungry. Grumpy.
Ate three carrots and a sip of berry smoothie.
Cancer. Bah!

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February 9, 2018

5:00 a.m. for 7:30 port access.
Susie’s yawn says it all.
Oxygen accessory.
Low oxygen. Fast heart.

Weigh-in and a tearful anticipation of a smooth port access. (Thank you, Cami with great hair. Only one poke).

Image may contain: one or more people, people sitting and closeupLife’s better when gaming with Dad. Terraria!

Checking out yet more side effects. Palms for elevated bilirubin. Signs of oxygen.
Thankful Doctor Whipple picked up side effect of antibiotic, Dapsone.
Methhemoglobinemia—her blood holds onto the oxygen and doesn’t want to release it to her body. Oxygen levels are difficult to raise even while ON oxygen.
“Dusky” episodes—of blue green skin.
“The gray lady.”

Another Avastin (vasoconstrictor) dose. No Vinblastine (Chemo) today.
Hopefully with no Dapsone her oxygen levels will rise over the next few weeks.

No Brown recluse bite. No well water. Uncommon drug side effect.

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Infusion clinic.

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Going HOME! ❤️

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February 23, 2018

Tricky Snow Day going to Primary Children’s.
Dropped Liam off in Springville and decided to take Frontrunner up.
Met Iris and Vi’cente from Peru who traveled up with us.

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February 24, 2018

Port access tricky. Two “pokes.”
(Guess I should photograph needle-port needle looks like a venomous snake fang but almost an inch and a half long. Nurse brings it up to Susie’s chest lvl, right under her eyes, about seven inches. Scary!)

So glad we could meet Dad in Murray and travel up with him. Whew.
Springville roads this morning about the worst I’ve ever driven on—icy, trucks “fish tailing” at 5-10 mph

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January 2018: Cancer Birthday

January 3, 2018

Pensive. Challenging trip up to Primary Children’s today for Susannah.
Susie’s tumor has grown on four months of Chemo.

Joseph joined me to discuss future treatment with our Oncologist.
Suggested switch to weekly Chemo (Vinblastine/Velban) and a Medicine from Huntsman, Avastin (Bevacizumab).

Susie checked for nerve damage and weakness.
Doctor, Care Cordinator, RN, Dad leaves.
Susie begins to talk.
Nurse comes back and informs us that Susie’s blood work will not support Chemo today.
(ANC too low. High Bilirubin).
Port unaccessed. Hooray! 🎉

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Lunch at the Ronald McDonald House.
Haven’t seen this beautiful, cheerfully smile in awhile. 😊

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January 5, 2018

Susannah and I listened to this and spoke of how this applies to us in our life today, just as much as to Nephi, in the Middles East many years ago, on our way up to Primary’s on Wednesday. I listened again last night and felt His comfort bring peace.

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January 12, 2018

Thankful for friends Stephanie, Becky, and Kristen, and many more for helping with rides and entertainment for my two youngest. 💕

(Liam “helped” with taking down Christmas lights.)

Always feel torn when with Susannah up at her appointments. Grateful for the time, one on one, to be with her. At the same time, I’m worried, about the children who are apart from me at home and missing them. ❤️💔

This is the bittersweet part of this amazing journey of life.
So thankful for it.

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Meet “Rapunzel!”
Susie confessed she has always wanted to be a blonde.
(Volunteers make and donate these darling hair pieces. No sooner than we had sat down, then a darling little lady, 3 years old(?), found a red haired Mermaid hat with sea flowers and sewn shell and put it promptly on her beautiful Round shiny head.)

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Susannah was very brave today during port access. (It was tipped and so off the skin and painful today.)
She was in great spirits and playfully interacted with her Dr., Nurse Paul and Care Coordinator Gina.

She starts Avastin today (an expensive, new vasoconstrictor medication being tried for children from Huntsman Institute) but none of the new weekly Chemo (Vinblastine) because yet again, she is Immunosuppressed with ANC lvls too low.

Thai Massaman Curry for lunch with Dad! (He really delivers! 😊)

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Willow, the Service Dog shares smiles and love.

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Employees are encouraged to play. Patrons can play also.
One of our first visits, a resident was playing a Cello.

It is so soothing and magical to hear uplifting, beautiful music in a place that can bring to mind fear, tears, and pain.

What a cloud of peace this little walk past here was for me today. (Stalker video. Short clips for Joe.)

(Video of beautiful music accessible on Facebook.)

January 19, 2018

Susannah’s appointment at Primary Children’s today was to start a different Chemo drug (Vinblastine/Velban).
This is her first Chemo since Dec. 1.
Susie shows me how to take a “normal” Selfie.
This keeps her VERY entertained.

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Darling Girl “Brookie” in Oncology Clinic gave HUGS before her appointment.
(I got to walk her back to her mom/room. Such an open, loving gal.)💕
She gravitated to Susie.

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Susie brave when Chemo finally came.
“Push” dose today.

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HOME!

Ready to cry.
Long day.
So blessed with wonderful friends.
Lisa brought warm soup, GF corn bread, salad, and honey butter.

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January 20, 2018

And we are back…we haven’t toured the ER for a month or so. 🤪

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Can’t figure out Susie’s elevated heart and respiratory rates?! Docs said they wouldn’t release us until she was below 110. She never got there. Consistently 120s though. (These shots were taken a couple of seconds apart.) Released!

Home at last!
🎉👑Happy Birthday to my “Graceful Lilly” Girl.🎍🎂
So glad we got to celebrate at home in our own beds. 🛌🎁

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January 21, 2018

Susannah is feeling much better. Thank you for your prayers. 💕

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January 26, 2018

I.V. today because of Holter. (Most kids wouldn’t like this. Susie does! No port access. Hooray.)

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Cell phones, tweens, questions—“every week”! Repeat. Every week.
Thankfully it’s Friday. 😉

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She’s wired! (All hooked up. Cancer meds and heart monitor this week.) Susie’s attitude rocks. ❤️

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December 2017: Secret Santa and Chemo Clinic

December 1, 2017

Another Friday. Another Chemo Infusion Clinic
Susie shows Courage amidst fear from past port access struggles. Smooth port access. (Blood clots block line and delay treatment a couple of hours.)

2 Timothy 1:7 For God hath not given us the spirit of fear; but of power, and of love, and of a sound mind.

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Crafts make life bearable!
(Silly face for Dad!)

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Susie asked about getting a puppy pal.
Told “not during treatment.”
Interacting with nine year old furry friend, Willow.

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December 2, 2017

Friends and Family,
Please pray for Susannah—that her nausea and low grade fever will subside. Thanks. 💕

December 3, 2017

Back at Primary Children’s.
Susie has a fever following Chemo.
Rocky Time recently.
Everyone short on sleep.

Image may contain: one or more people, people sitting and indoorI.V. Fluids, Rocephin, and Zofran and Susie is good to go! Fever below 100. The Magic Bullet.
Discharged and soon we will be headed home!
Thanks for your kind thoughts and prayers.💕
(We sat across from a Christmas tree decorated with miniature, beautifully painted and framed pictures from local artists—in front of an Auditorium door at 8:50 a.m.
people were gathering, dressed up.
It only hit me at 10:00 a.m. as we were headed to the car that this may have been a Church Service! 😞 Sad to have missed the Spirit brought by talking about and rejoicing together in Jesus Christ, the Light of the World. )

Image may contain: one or more people and people sittingNew motto: TOGETHER IS A WONDERFUL PLACE TO BE! ❤️

Image may contain: one or more people, people sitting and indoorHome. Restful daughter.
(Noise canceling earphones protect hearing from Freeway deafness—we learned from Audiologists. Chemo increases her risk for irreversible deafness from loud noises. 😬🧐🤨😞).

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December 16, 2017

And we are back for platelets!

(And mom is so tired, that I’m more interested in sleeping than Hallmark movies or toe painting. 😴)

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I know some of you are wondering…there’s a bidet!
Did Susie’s nails festive.
She succumbed to IV Benedryl (which was good since she can sleep thru the beeping. I can’t.)

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Image may contain: 2 people, including Julie Clayton Campbell, people sleeping, child, closeup and indoorWe began things cheerfully.
Things got rocky and emotional after the IV Benedryl sleep wore off. A small fever arose and horrible headache. (This seems to be a trend with her and platelets. AB- this time.)
Home now.
Grateful for hospitals, nurses, assistants, Pathologists, and techs. 💕
Hoping for a peaceful, fever free night.

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December 20, 2017

Sometimes when one child has cancer, it’s easy to forget your healthy children.

Thank you, Princess and Wild Man, for your original Play,”Who Stole the Cookies from the Cookie Jar!?” (Sunday evening) complete with refreshments and barstool seating!

So thankful for ALL of my children!

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Secret Santas…you bring us JOY!

Image may contain: 1 person, smiling, indoorSecret Santa’s, Day 2!

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What an amazing day and age we live in when so much I formation is available to learn and study.
Boswellia Serrata (India) is the oil made from Frankinsence Resin.
“A glioma is a type of tumor that starts in the glial cells of the brain or the spine. Gliomas comprise about 30 per cent of all brain tumors and central nervous system tumors, and 80 per cent of all malignant brain tumors.”
Wikipedia

No wonder Frankincense is dubbed the “king of oils.” Used to treat childhood seizures and systemic inflammation, Frankincense has a promising future in treating cancer.

(One trick with brain cancer is finding something that passes the blood brain barrier…elligic acid does. Eat your raspberries! So does Pomegranate juice—which shrink all types of tumors, including prostate.)

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December 21, 2017

Susie’s Secret Santas Day 3:
A work in progress!

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December 22, 2017

Secret Santas strike again!

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Clean, friendly, windy, and decorated.
Christmas is coming…

Can you tell who is “done” and ready to go home?

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December 25, 2017

More Secret Santa Gifts for Susie—Spaaaaa…

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Image may contain: 1 person, smilingMoran Appointment and Tests (Spiritual), Tests (Physical), and more Tests (Emotional)!
A very real “Sacred Grove” complete with darkness and light.
Your faith and prayers carried us today.

Doctors evaluate and mediate.
New thoughts and a new medication to try.
Hope.
Holiday.

Good will towards all. 🎄

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More Secret Good Will! 😁

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Susie’s Secret Santas revealed—friends Abbie (Emily Russ) and Nielie (Tricia Biggs). 💕
Thank you for hope, anticipation, sweet memories and love.

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December 31, 2017

“Mom, I don’t need any more doctors.
I can heal on my own—here at home!”

Cuddles and words of affirmation, love, forgiveness, and wholeness.

Journey of healing, hope, faith, and miracles continues. ❤️

November 2017: Unexpected Hospital Visits

November 3, 2017

So…this is happening. Chemo caused Susie’s blood levels to drop. At Utah Valley getting blood transfusion and platelets. (Thank you to ALL the friends who have rearranged schedules today to help with carpools and childcare.)
Susie has been courageous with her pic line. (Port still traumatizing.)

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Meanwhile, Susie has had a reaction to the platelets and so necessary reports filed, Benedryl and Tylenol given and more time passes.
Nurse April goes to get the blood transfusion.
Half way done. Eight hours in!

Lots of blessings:
Susie receives: Sprite Zero, Salmon dinner, and PB and apple slices and fresh pineapple for late lunch. Big hit.

We watch Disney Descendants 2 together during Platelets and lunch.

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Joe comes and brings me delicious Curry over brown rice from friend! (Thanks Lisa West Fielding.)

Susie gets dinner while she waits for reaction to clear, tests taken, and we wait for blood transfusion.

(Coke was ordered for parent driving in the middle of the night or encouraging “outpatient Susie” on high amounts of Benadryl, to walk to car.)

Love the orchid tropical feel! He he.
(It’s not a vacation but you might as well feel like it is one, it’s gonna cost as much! 🤣)

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Hannah gives me a ride home, and Joe stays with Susie.

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Joe texts:
11:21 p.m.
Blood started. Filter on iv caused problems. Constant beeping. Now fixed. Just 3 more hours. I’m way tired.

(Just keep swimming, just keep swimming. 😉)

November 17, 2017

Prayers appreciated for Susannah this morning.

Thank you for your prayers! They worked.

Susie wasn’t feeling well and was very worried about port access this morning for Chemo.
We got a call from Primary’s after 8:00 a.m. that her ANC lvls (Immune System) was too low and that they would delay Chemo until Wednesday or possibly the week after Thanksgiving. 😊
An answer to prayers, really.
She will have a higher immune system for Thanksgiving and Christmas, hopefully.
Change of plans—
She’s now in school but very yellow. 😕

(Her hand is saying, “oh, mom!”)

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October 2017: Cancer Clinic

October 6, 2017

Third Cancer Clinic Day.
Somber mood.

Many sick children today, wait with masked faces in waiting room. No laughter here. Voices muted.

A young teen amputee (lower right foot), masked, bald with hat, sits to the side of us. Crutches propped on the wall.
What is her story?
What does she think of?
No magazine in her hand.

My tween worries of fashion, shoes, fitting in, friends.

Life can be so fragile.

Susie has a reaction to the numbing cream and cleansing agent.
Redness, swelling, prickly rash.
Nurses consulted. Doctor checks.
No one has seen this before.
(itching 2% and rash, less than 1%.)

Doctor delayed.
Third Chemo Treatment and Flu shot given.
“Long needles!” Susie’s eyes wide.
Bravery indeed.

Grateful to friends who care for my younger children.

Long days.
Grateful for home.

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October 18, 2017

Second ER visit with second child since Sunday morning. I think I should rent a room here—I would definitely get more sleep! He he.
(Susie spiked a fever on Chemo. ☹️)

October 19, 2017

Some darling angels brought Susie a quilt while we were at the hospital. 💕

Now home and she is surrounded by these girls beautiful gift.

ThAnK yOu! 😘❤️

October 20, 2017

“Courage is found in unlikely places”
Fourth Chemo Clinic—Primary Children’s

Susannah has been a trooper today.
Port access difficulty following failed port access trauma at Utah Valley’s ER two nights ago.
Courage shirt needed! (Thanks, Cassy).

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Infusion Clinic went smoothly—
Crafts make everything more fun!

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Image may contain: 1 person, smiling, sittingWhat a warm and wonderful quilt for Susannah. I felt it deserved a post to show case just how beautiful and creative it is!
Thank you Gwen, Audrey, Addy, and Margot (and loving leaders and parents like Katharine and Holly LeSue!)

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So slow at writing Thank Yous but feel such gratitude for all the help we have received. THANK YOU friends and loved ones. You help us to keep going. 💕

September 2017: The Longest Day

September 14, 2017

My heart touch beyond words. Fourteen year old son fasting for his sisters, midweek, because he cares. 💕

September 23, 2017

Everyone has a story.
Here is a part of ours:

Susie had a “port” (central nervous system line) surgically inserted underneath her skin for easy I.V. access for Chemotherapy yesterday.

It is hard to see your “baby” suffer from anesthesia’s after effects. (Your baby is still your baby, even at ten years old.)

Susannah had a reaction to medication put in her eye and trouble with nausea.
Good thing the Anesthesiologist is not a close friend. She kept saying, “I do not like that man! I do not like him!” (There was no reasoning with her that it was the medicines, not the man, that she struggled with.)

One side effect of a Chemo drug is hearing loss. Permanent hearing loss.
Susie was barely Post-Op when she was wheeled to Auditory for hearing screenings.

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Fighting childhood cancer. Go GOLD!
Joe and I trail a small bald child pushing her own IV stand. Here is courage.

We are NOT winning the “war on cancer.”
Spread awareness.

This war will visit your family or loved ones.

Have hope. Learn more. Fight!

Who knew that having a child with (brain) cancer would mean getting to know so many wonderful people: Oncologists, surgeons, Anesthesiologist, nurses, techs, nutritionists, case workers, social workers, care coordinators, specialists.

The Ronald McDonald House rooms located inside the hospital are a haven for families and parents.

Here is a place to get a warm meal, a snack, a place to charge phones, shower, nap, use a computer, entertain other children, or take a brief break from discouraging reality to have a good cry (red nose results) and then put on a “good face” before returning to your in pain/nauseated daughter’s room.

Joe and I slipped out to get a quick dinner last night. Taco Salad.

“Togetherness Heals.” ❤️

So many parents and families fighting through their own childs’ battles.

Warriors.

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Love is here.
My heart is so full.

A mother is on a cell phone, sobbing.
I wonder if I should stop to hear her story or offer a hug. Feels like an intrusion into her own personal grief.
I say a silent prayer for her instead and hurry on.

I leave into the dark, cold night and drive home to children with the assistance of a “medicine soda” and Excedrine.

Long day. Very short night.

Hot then cold. Shaky and quaky.

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Children at home miss sister Susie.
Eva cries. Liam just puts on a “neck beard” (a rice bag) to make her stop and laugh.

Sister Eva worked in her room this morning tidying up for Susie to (hopefully) come home!
“Mom, Liam helped too. He helped with the lights, and that was the tricky part.”

Someone said something silly to make Liam smile. Eva slightly disgusted.

Susie went into anaphylaxis with IV antibiotics and so Benedryl made her sleepy. Breathing back to normal, thankfully.
Just set us back a few hours, but we should be home by tonight.

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For lunch we headed to the Ronald McDonald House Rooms.
Earthly Angela from a Relief Society brought in hoagie fixings, salads, chips, and pink lemonade.

Favorite quote was from Liam:
“Mom, look. Look! An ice cream truck.”
“Yes, that looks very colorful. Like an ice cream truck. It’s a city bus.”

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And Susie is HOME!

September 27, 2017

Saturday evening at Primary Children’s, discharge papers finally charged and Nurse Dave just must pull out the needle (deport) and we can leave.
Susie motions me down to her level. She pulls my ear closer.
“(Mom) I don’t want to do this!”
“I don’t want to do this either, Baby.”
My voice breaks. We have a silent cry together.

Childhood Brain Cancer sucks.

September 29, 2017

Cute new hairdo for Chemo clinic easy care.
(Susie is not enthusiastic about the poofiness of this cut.)

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September 29, 2017

Susannah’s First Chemo Clinic Visit done.
(Second dose of Chemo–first round in hospital last week).

We are touched by the love, care, and service that goes in to serving these beautiful bald children (and their parents/family) from so many unseen angels.

Cancer. A battle to wage, a war to win, hearts softened, Heaven petitioned.

Susie was cold and so she was brought a quilt. Nurses encouraged her to take it home (because washing it at the hospital would ruin all the work that went into this work of art).

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August 2017: Fast and Gratitude

August 20, 2017

Went all Summer with no sugar to support Joe on Keto Diet and Susie with her brain tumor.
Told the kids once school started we could roast marshmallows and make Smore’s.
Eva is SO excited tonight!

August 26, 2017

Friends,
In your Fast this weekend, please remember Susannah and her brain tumor. I have faith in God and where He will lead us but also know the strength of your faith.

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August 26, 2017

“Find that gratitude(!)…”

Dear Ones,
What if you were told that someone you cared deeply for may someday soon loose sight AND that on an unspecified day in the future would also wake up with irreversible deafness?

Life has been SO beautiful and sweet, when I comprehend the incredible clouds in the blue, blue heavens or hear my children laugh at the small chipmunk at the very top of the huge pine tree that delights them by picking pine cones and chucking them down below like a computer generated Donkey King with unlimited wooden barrels.

Sure there are feelings hurt when children try to navigate voice tone, anxiety, worry, and love for one another in the imperfect way we as humans interact.
Love can be sweet even in the imperfect way that is humanity.

Please gaze around you with new eyes and appreciate the beautiful world God has given you today!

Listen with all of you to music so sweet it brings you to tears and the voices of those you love.

Live in the moment.
Live in faith.
Let Go and Let God.

(Shared from Facebook–see video link below.)

July 2017: Broken Arm, but not a Broken Heart!

July 8, 2017

Had this song running through my head all day today.
Jesus IS a God of Miracles! ❤️

July 26, 2017

Tender mercies today:
Thank you blond curly haired stranger “Julie” from down around the corner for driving my broken child home with her bent bicycle after her wipeout.

Thank you Doctor Johnson for setting her splint on her buckle fracture.

Thank you Rebekah for staying home with the little ones and encouraging them to write darling cards to a sad sister.

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July 27, 2017

Prayers for Susannah appreciated.
She is struggling tonight to get pain from a fracture under control.
Thank you!

July 30, 2017

Susie is feeling much better!
Thank you for your thoughts and prayers.
(Thank you, sweet neighbors, Kristin and Ava, for the darling bracelets and balloon!)

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May 2017: Walking by Faith…and Walking by an Apostle, Coincidentally.

May 7, 2017

Our sweet Susie was very touched by Anna’s story (Anna Ortega, AZ). They share many similarities, both being ten and having glial (Glioma) tumor’s. Anna’s is on her brain stem and considered fatal.

Susie wanted so badly to bear her testimony today. She saw her NeuroOpthamologist up at the Moran Eye Center on Friday. We were scolded (and strongly encouraged to still meet with Oncologists) but informed that Susie’s brain tumor was markedly better with less swelling and inflammation.

She was tested for eye correction so that she might wear glasses again but the vision is SO different, that it will not be easy. “The fact that her eyes don’t register the double vision as profoundly as it is suggests that she has had this tumor for much longer than originally suspected.”

Joe and I wish to thank you for your faith and prayers in Susie’s behalf.

(Picture of Anna Ortega, AZ, below)
https://www.gofundme.com/annaishope?pc=fb_dn_cpgntopstickysmall_r&rcid=db81e00000e64b1f82699863def80719&fbclid=IwAR1AXJnakboIL8S0_2ZLZQt3ojMfnYeZDRxP5dU2tlmLEibW8JWyWm18jXc

May 13, 2017

Remember that time that (Lupus and) migraines were getting the best of you, and so your sweetheart bundled the kids in the car to take them on an early morning hike, so you could rest, and they just happened to run into someone you would love to meet…oh wait,
that was this morning!

Happy Mother’s Day to Harriet, from a distance.
(Thankful to Susie who wanted a picture with Elder Dieter Uchtdorf and his wife, Harriet).

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May 31, 2017

🌸Friends,
THANK YOU for your prayers today.
All went well. 💕

The Oncologist pointed out the unusually large size and place (contained in the right eye orbit) of Susannah’s tumor.
Inoperable and unbiopsiable.

MRIs spaced over three months show the tumor to have not grown in size and this is good news, as it allows us time to study treatment options.

Thank you again for your prayers. We are walking in faith and feel your support.

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May 31, 2017

Our family is making choices towards health and to support Susie (with her brain tumor), we are going for periods of time without sugar (candies, sweets, sodas, etc.)…appetite is suppressed, emotions peaceful, and sleep better.
Will you join us?
Go sugar free.