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McLaren Clan Comes to Texas

They drove all night and came from Alabama, Louisiana and Mississippi.  They descended upon our home in the form of a set of grandparents, two aunts, an uncle, three college students and 2 junior high girls bringing with them a giant turkey and lots of fun for our 2009 Thanksgiving gathering. 

The giant turkey was quickly set up in our front yard and my kids loved him.  Here’s a pic of the cousins:   

 

It was good to see everyone and a joy to be able to celebrate with Glenn’s side of the family.  The last time most of them had seen him was when he was first diagnosed with myeloma.  He’s looking great now and feeling so much more like himself. 

Laura, Lynne and I prepared the turkey early Thanksgiving morning and then I stepped back and let Lynne, Jaca & Laura take over in the kitchen.  Cooking is not my thing, as I made sure to remind them in an email before they came.  I love to set the table and plan the gathering but the actual cooking is not my favorite activity.  I learned from these gals and we had a good time in the kitchen.  Our meal turned out great and everyone was full and ready for their afternoon nap.  

Turkey Dinner!

They were not able to nap long.  Laser and Bookworm had been planning the first annual Backyard Bowl for weeks and put the ball in motion.  

The Prize

They had teams picked and plays ready to execute.  Everyone joined in, even Grandmother Jaca as a running back and wide receiver and Popeye as referee.  No one can say the McLaren clan doesn’t know how to go along with the fun and … 

 

make it a little competitive at the same time.  The 2009 Backyard Bowl was a blast! 

CHAMPS: Glenn, Irene, Katelyn, Princess, Laser, Taylor, Lynne & Temple

Friday morning the guys went to play golf and the girls headed to Gruene, TX for a little shopping.  We met up with the fellows at Adobe Verde for some good ole’ Tex-Mex and strolled around Gruene.

Alexis, Katelyn, and Lauren at Adobe Verde
Princess and cousin Taylor
Uncle Temple, Bookworm & Popeye wait on the ladies.

And of course, if you are in Gruene, you just have to go see Gruene Hall, the oldest dance hall in Texas.

Time for some great family pics down by the Guadalupe river …

The girls.

Saturday morning we were off to downtown San Antonio to see the Alamo. 

Never a dull moment when the McLaren clan is around.  Lots to do and memories to make.  It was a wonderful Thanksgiving holiday and I am so thankful they made the trip to be with us!

Moving Forward

Although Glenn is cancer free he will continue with chemotherapy for the next 9 months.  This will consist of a 2 week cycles involving dexamethadone, (oral meds) velcade (an injection chemo drug) and the daily thalidomide oral pill he takes.  He still takes a shot to the stomach daily for blood clotting and about 10 other pills a day.  So even though he is cancer free they want to ensure that the cancer does not have an opportunity to reappear.

My sister asked me why I didn’t sound more excited about his remission.  I am excited and happy and thankful, but for us there is the reality that Glenn has been given numbers.  Five to Ten.  That will be with us.  It won’t be how we live, but it will be in the back of our minds.  Most of us don’t know how long we have.  We take each day for granted.  For us it will be constantly searching the recent data hoping they are still progressing towards a cure. 

I am planning on Glenn and I living life with joy and happiness making memories with our children as if each day is our last.  Children help make life normal.  They share each new experience with you and give light when things seem to fade.  Maybe given “numbers” is a gift.  Hopefully, we will treasure life more and not forget that each day is a gift. 

I know that I am so thankful Glenn is here with me.  I never dreamed that when we made our vows 14 years ago that “in sickness and in health” would be a reality for us.  He has been my life and a part of me for so long.  It is hard to imagine a life without him and so, I won’t.  I will laugh with him and listen to him and argue with him and love him. Each day is a blessing and I am thankful.

Good News!

Glenn approached our appointment with a great deal of apprehension and concern.   While we were in SLC for testing he carried  the fear of the unknown with him.  I was not so worried just more concerned that Glenn would be disappointed he had not made progress or things had stayed the same. 

Without a great to-do, Dr. Tricot, dictated into his recorder what we had been waiting to hear.  “Glenn McLaren, diagnosed in October 2008, has achieved ’complete remission’ after two stem cell transplants.  That’s big news!  His tests revealed no signs of cancerous cells in his body.  His white blood cells are polyclonal, meaning they are making the different kinds of cells a normal healthy person makes.  With myeloma, the white blood cells become monoclonal and begin to overproduce to many of the bad cells leading to cancerous tumors (collection of cancer cells in one place) and destroying the body. 

Now with that, we asked what that means for his life expectancy.  Dr. Tricot told us that Glenn’s chromosomal make up of the Translocation 414 which makes his myeloma worse than others does not help him.  Individuals with this 414 translocation have a more likely occurence of the cancer to return sooner than others.  But, and this is a big but, because his body responded so well to the stem cell transplants and he was able to tolerate an additional round of 4 days/24 hours a day chemo after the transplants his 414 translocation is not as big a factor.  The fact that his body has fought the myeloma and achieved remission is a very positive sign for his life expectancy.  When Glenn makes it three more years without incidence his life expectancy will be expanded even more than the 5-10 years Dr. Tricot has indicated will be lived out. 

Glenn has had cancer, a rare bone cancer that will come back some day.  It is our hope that withing the next 5 years a cure will be found.  In the meantime, we are so thankful that he is officially a Cancer Survivor and no longer a guy with cancer.  All by the grace of God.

Testing in Salt Lake City

Glenn and I arrived in SLC late Saturday night to begin his 3 month testing.  We’ll be here until Wednesday.  They will be assessing his “myeloma markers” and see how his 2 stem cell transplants and chemotherapy have helped him. 

We are hopeful but for Glenn this is a reminder of the fact that he has cancer and will always be a cancer patient.  There is no cure for multiple myeloma at this time.  They are only hopeful of extending his life for 5 to 10 more years.  We forget that when we are toting kids to Scouts or planning camping trips or just working with the kids.  Our lives have changed and although being at home together all day is often challenging we are just living life and enjoying the little things. 

Glenn’s eyebrows have grown back and his hair is coming in and he looks great.  He has more energy but still lacks the strength he use to enjoy.  He gets bummed about his physical condition and limitations but is improving.  I have to remind him how blessed we are that he is recovering and enjoying time with us.  It is easy to forget  he was in ICU with acute kidney failure a little over a year ago.  His improvements are miraculous to me and truly a blessing. 

The kids are back home in Cibolo with Grandma and Grandpa.  They are enjoying spending time with their grandparents and even still plugging away at school this week with Grandma substitute teaching for me this week.  I’m not sure what our homeschooling future will be but I know that it has made life alot easier with all the transitions we have made in travel and treatment schedules. 

I sure miss my kids when I’m away and I wish they were here with us.  They are so fun to adventure with and Salt Lake City has so much to offer in hikes and sight-seeing.  The weather is gorgeous, cold and crisp.  I just love the mountains and the view that just never stops.  Bookworm and Princess tried hard to fit themselves into our suitcases.  I hope we can bring them with us again soon.

We’ll have test results and a conference with Dr. Tricot on Wednesday before we leave to find out Glenn’s status.  In the meantime, blessings to you all!

Catching Up Again

It feels like I am always catching up.  Most of you may think, “How can she be busy with both Glenn and her at home?”  Well, I wonder the same thing all the time.  It seems like there is never enough time and at the end of the day I wish I had done more or spent more quality time with the kids or accomplished something great.  I have been doing life.  Kids, husband, homeschooling, home, job hunting, community and church.  It doesn’t seem like much but it definitely fills my every moment.  What a gift I have been given. :)

CUB SCOUT CAMP OUT

Laser and Lego camped out at Lost Pines Camp Tom Wooton near Bastrop with their dad in mid-September.  It was packed full of activities and Lego earned his Archery and BB-Gun beltloops.  It still amazes me that Glenn is with us and able to do these things with his boys.  He did purchase an air bed that he thinks everyone who camps should have one.  It self inflates and then you roll it up to release the air for storage.  With his back problems from the cancer it was a relief for him to find a way to sleep comfortably on a camp out.


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FALL SOCIAL

For the past four years I have been in charge of our homeowner events.  I seem to be the only person willing to commit each year.  We had a few new volunteers this year but lost the ones from last year.  I do it for my kids.  The HOA pays for the moon bounce, popcorn and cotton candy and no matter who shows up, my kids always have a great time.

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Costume Parade

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Great weather, a good turn out and private bounce time before and after when your mom is the lady organizing!

HALLOWEEN

 

So, this is the first year that I did not sew a single costume.  I told the kids that this year we were going to dig into our dress up box and come up with our costumes this year.  My kids were completely fine with it and enjoyed dressing up in costumes they had not worn before.  Bookworm was the only one we had to create a new costume for because he literally had outgrown all our dress up things.  After brainstorming several low cost ideas we finally came up with Waldo.  All I had to do was get a white long sleeve shirt and paint red stripes all over it.  I sewed a felt hat(not a whole costume) and painted a yard art candy cane brown for his cane.  The result was great.  Laser dressed up as an astronaut which he really liked because it had a NASA baseball hat and he practically lives in baseball hats.  Lego was a Jedi and Princess was Belle, from Beauty and the Beast.  They all looked great and the trick-or-treating was plentiful. 

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Trick or Treat!

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Where's Waldo?

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Blast Off!

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To the bridge men!

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She's a beauty!

 

 

 

 

 

 

 

 

 

 

 

 

 

JOB HUNTING

 

Well, I had gone for almost 3 months without one single call regarding a job interview.  I have sent out resume after resume and nothing.  I was beginning to wonder if I would ever get a call but was secretly thankful I had not had to venture into the work world. 

Last week, I received an email from Trinity University for a position as an Administrative Assistant to the Associate Vice President of Academic Affairs-Budget & Research.  She asked me to come in for an interview.  I was horrified.  I had not been on an interview in 7 years.  I had been waiting and sending resumes but when it was really going to happen I was terrified.  It’s funny how I do alot of things in leadership positions in my community but not being in the work world day in and day out you lose your confidence when it comes to actually putting on the pantyhose and getting out there.  I felt completely unprepared and unqualified after being home for so long. 

As I got ready in my gray slacks, white shirt and black jacket Princess asked me if I was going to wear a tie.  And Laser looked at me dressed for my interview and said he had never seen me that way.  Lego was fascinated by my pantyhose.  I arrived on early and I managed to calm my nerves and appear cool and collect.  

A day later a second interview was scheduled and things were going extremely smoothly.  The AVP I would work for was really great.  She and I clicked and the other Admin. Asst. were very helpful and seem to be ladies I would be happy to work with.  I was offered the position.  I was crushed and excited at the same time.  Trinity was what I was hoping for, a new start in a new direction.  I discussed my start date and my upcoming trip to SLC with Glenn for his cancer trip and she said no problem, but she wanted me to be aware that health insurance at Trinity was high.  And high turned out to be right.  After looking at the insurance cost and out-of-pocket expenses for Glenn’s out-of-network doctors in SLC we decided that it could possibly cost me more to work then to stay home.  I declined the job offer and finally began to breathe again. 

The miracle in this whole situation is that Glenn’s unemployment was ending at the end of this month.  On the day she offered me the job, his unemployment was extended for another 20 weeks.   And to top it all off, the COBRA subsidy extension was introduced into the Senate for discussion and a vote.  They should be making a decision before Dec 1, 2009.  If all goes well, Glenn’s unemployment, disability and COBRA insurance should keep us afloat until May which is when he can go back to work.  I’m planning on finding part-time work but benefits should not be part of the plan. 

It is hard to express how difficult it was for me to consider going back to work.  I realized that I had to and that it was necessary, but leaving my children and not being with them was painful.  Yes, I know, millions of mothers send their children off to school each day and work outside the home, but for me, my heart is with them for as long as I can.  I’ll send them off into the big wide world someday, but while I can, I want to be with them, teach them and enjoy them for as long as I can.  A day will come that all this shall pass.

My sister told me that my experience of interviewing and being offered the job was like Abraham being told to go and sacrifice his son, but then once Abraham had prepared his altar and was ready to sacrifice his son, God told him to stop.  I felt like I was making a sacrifice that was great and then God said stop you don’t have to go to work.  I am so thankful that God has continued to guide me.  I may not always make the right decisions but I know God is there to help me make the best of what ever comes my way.

Status Quo

Glenn’s battle with cancer has gone as smooth as possible.  He will be continuing with his chemo treatments over the next year and returning to SLC for testing and evaluation every 3 month.  His strength has been improving but he seems to have periods of fatigue which is normal.  He takes chemo pills every night and other chemo drugs on a 2 week cycle.  Chemo is never easy on the body, but it is tolerable and he seems to be doing well according to his blood counts.

I am still unemployed although I am actively looking for a job.  Glenn’s unemployment was extended so that was a blessing.  We are doing well, keeping busy and enjoying the kids. 

I really do miss living in Utah.  We’ve been home for almost 2 months and for some reason I felt more comfortable there, at ease.   Maybe it was because the focus was Glenn and the kids and here at home it seems I’m scattered.  Homeschooling, looking for a job, our homeschool group, scouts, HOA and keeping up the house & yard seem to be consuming all my time.  I guess I miss the hikes and the walks to the library and the parks and spending time with the children without all the schedules.  It was simpler somehow.  I always feel cluttered here. 

Anyway, like my kids always tell me, “Our friends are in Texas!” and that is a huge plus for our home here in the great state of Texas.  Friends, please keep us in your prayers.  Pray that God’s plan for us will be revealed. :)

A girl and her dog.

Paisley is our family dog.  She is now almost 3 years old and has been a great dog.  We are not dog people, but she is loved in our own way.  My boys wanted a dog.  Read about dogs.  Learned about dogs.  Convinced me we needed a dog.  And so I thought, a boy and his dog.  Well, after almost 3 years, the boys rarely play with her and she mostly gets in their way as they play football, kickball or hit golf balls in the backyard.  It turns out that Princess is the one who really loves our dog.  It isn’t what I pictured.  Dogs being stinky and dirty and slobbery and well, dogs.  But Princess loves her and I find her often laying around talking with her galpal, Paisley. 

Paisly our Goldendoodle and Princess our Sweet Girl.

Paisly our Goldendoodle and Princess our Sweet Girl.

Princess loves her Paisley.

Princess loves her Paisley.

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