Saturday, May 15, 2010

This Grandma is Exhausted

Enjoy the cake - love Suzi

Good news!

Yesterday, we experienced an awesome answer to prayer - Emma had her cast taken off and didn't need another ! She has the cutest little shoes to wear.

Today, at Emma's debut we raised nearly $500 to cover medical bills currently at $5,000. Thank you for helping with your financial gifts!

Please continue to stand with us in prayer. I'm asking for normal spine and brain functioning, the ability to hear her sing praises to God, and see her children!

Sunday, May 9, 2010

God is AND Emma is My Gift of Faith

A while back, I left Amber's home rather exhausted. It was a warm day and I felt the spasticity in my neck, throat, and shoulders. I spent some time caring for Emma and Payton while Nick and Lexi worked in their back yard.

As I watched little Emma, I noticed that she was having difficulty sleeping for more than a few minutes at a time. It was as if she was jolted out of her sleep - startled. I'm pretty sure we have all had this experience at one time or another. You know the kind - when falling asleep and your entire body jumps and wakes you up. But usually this only happens once or twice - right? Well poor Emma - every time she fell asleep - about 4 or 5 minutes - she would startle and then start crying. I held her and prayed. I placed her in the stroller and prayed. I researched Chiari, hydrocephalus and sleep apnea on line. I discovered that the combination is common among most babies with Chiari II.

I went home rather exhausted. Most of you know I can sleep a lot - 12 to 14 hours a day - but for some reason I was not able to fall asleep. As I laid in bed I began to pray for baby Emma. I prayed for her healing. I prayed for her left leg that was in a full leg cast. I prayed for the formation and function of her brain to be as perfect as His original design. My prayers seemed to be words and thoughts without effectiveness.

THEN the most amazing thing happened. In my discomfort and limitations, I prayed for healing of my brain, neck, and spine. As I prayed for myself, I felt relief from my symptoms. This caused me to think that there must be a spiritual connection among all we experience and with those we live among.

I do not understand but can tell you that God is and hears our prayers. PLEASE continue to pray with me for healing and personal growth to become everything God designed us to be during our life.

Sunday, April 18, 2010

On the way to visit Cassie


Friday evening I was on a flight to Charlotte, NC when I passed out. The combination of warm temperatures along with a few hot-flashes were more than I could handle.

I had dressed warm with layers of clothing. I did not take the ice vest. Never, ever did it occur to me that the temperature in the cabin of the plane might be a problem for me.

About an hour into the flight, I started feeling uncomfortably warm. Then I had a couple of hot flashes and started sweating. I turned the cabin air on full blast BUT it was warm air. I started to feel awful so I got up and asked to use the restroom in the front of the plane...

NO WAY - the front of the plane is for 1st class!

The walk to the back of the plane seemed impossible BUT I did not feel well so I turned to walk to the back of the plane. Moments later things became a blur - I could not understand what a man was saying and I could not coordinate or focus my eyes. I was down for the count!


YUP - right there on the plane, I collapsed. Finally, I could stretch out and be comfortable in the over-crowded plane. The next thing I hear :


"Is there a medic on board?"

"Maam, are you traveling with someone?"

"Do you have chest pain?"


"Nooo - I'm too hot" was my reply.

I was thinking - I want to stay on the floor - it's much more comfortable than my seat. And I'm glad my kids aren't with me - how embarrassing.

With a moist cool towel, a bag of ice water on my neck, and some orange juice - I began to feel better. Darn if they didn't make me return to my seat.

Then about a half hour later, I remembered I was wearing my glasses. I called the stewardess, she looked and found them under a seat. They looked as though they had been walked on and will need a major adjustment before they fit on my face correctly - I didn't get to the restroom until I was off the plane in Charlotte.

DO YOU THINK THE FLIGHT ATTENDANTS WOULD HAVE FOLLOWED UP and possibly had an someone go with me as I changed flights in Charlotte? THEY didn't and IT DID NOT OCCUR TO ME TO ASK... Fortunately, I made it to my next flight, which was much more comfortable (less crowded and cooler temps).

Tomorrow, I have to fly USAir to get home. I hope and pray that my flight will be more comfortable. At the very least, I promise you that I will speak up when I don't feel well - and I WILL ask for assistance!

Wednesday, April 7, 2010

Remember - nothing ever stays the same


I remained strong, adjusted to the changes in my health and was able to support my daughter with the birth of Emma. Developing pneumonia, which exacerbated the Multiple Sclerosis the month prior to going to San Francisco was not good. My daughter remained positive and was glad to have my company even though I slept a lot and we had some problems with my scooter - for mobility - while in SF. God blessed us in so many ways and answered so many prayers.

Through this experience I have learned how truly amazing my friends and family are. Thank you for your kind words, encouragement, and support. Emma's life and health is an answer to many of your prayers. I am so blessed to have these experiences. I feel that she belongs to all of us. Thank you again for your prayers and support.

I am doing better too - walking more and sleeping less. Today, I met with Shari and Karen at Kyrene District Office to discuss work. I am hoping to pick up a couple of evaluations prior to the end of the school year - about 8 hours each week. I feel better just thinking about the possibilities. Also, today I met with a mortgage officer about obtaining a loan for a condo in Scottsdale. With the additional hours - I should qualify.

Things are looking up!

Thursday, February 25, 2010

We are home!

Finally, after 34 days in San Franscico we are back in Phoenix. We will let you know when you can see Emma. Her appointment with her pediatrician is this Monday.

I have my follow-up appointment with my neurologist on the 8th. I continue to have significant problems with fatigue, sleeping 10 to 12 hours every day and on ocassion I have slept 16 hours.

Sunday, February 21, 2010

About Emma's Shunt

This is part of the shunt that controls the flow of CSF from the
ventricles into her abdominal area. This is placed under her scalp on the right side of her head.