Christmas Eve Update -- 97-12-24

Dear Friends,

It's Christmas Eve. Just moments until Christmas. Our anticipation is heightened..., and soon will be fulfilled. The big day is coming. Our prepartions are done.

It's Christmas Eve at the Fenters. In the last few hours it has become a day of anticipation unlike any other. It's the day before. Something is about to happen. With each uneven breath of Gail's dying body our hearts leap beyond the annual celebration of the Incarnation to the once and forever experience of Glorification. Christmas fulfilled. Jesus come to get us to take us home. And that's where Gail is headed. Home.

The last few days have been both agony and ecstasy. Agony at watching Gail suffer,  her cries of unrelieved pain rending the night, exploding the stillness into a cacophony of  distress and consuming hurt. Agony. Agony at my own bitter helplessness. And, yes, unbelievably, ecstasy. A grounded certainty that this woman, the finest person I've ever known, will soon enter a glorious life, never again to be touched by pain, helplessness, separation or grief. Ecstasy at watching the fruit of her life, Marta and Rachel, shine like the jewels of heaven's foundation. Ecstasy at watching her beautiful blue eyes glow with joy as her children slide into her bed, cradling her in their arms, and sweetly kissing her shaven head. Those eyes speak the words, paragraphs of words, cruelly stolen from her since July.

Friday through noon today were endless. We could not discover the source of Gail's pain. Often she would go for only moments before the pain contorted her. Other times she would smile that glorious smile for several minutes before her eyes hooded in retreat. Bill and Betty Tracy, dear friends from San Diego, saw both the agony and ecstasy and left in tears. Yet minutes later, when Max and Denalynn Lucado from San Antonio were here, Gail glowed with "Gailness," a remarkable sweetness indefinable by any other word. Shortly after their departure the agony began again. 

And then today, sometime around noon,  the pain stopped. She closed her eyes and drifted into sleep. Except for momentary eye flutters, and a rare lopsided grin, Gail has been unresponsive for about twelve hours. She lies beside me quietly. Sweetly. Peacefully. I do not believe that I will ever look into her eyes again. Death normally comes within twenty-four to forty-eight hours of this stage of the disease.

It's Christmas Eve. The anticipation of Incarnation. And for the Fenters, the anticipation of Glorification.  Gail going home. Gail glorified. Gail welcomed by the Father.

It's Christmas Eve. Though sleepless for days, I will not sleep tonight. I will hold her hand. I will catalog our memories. I will thank God for the gift of this incredible woman. I will honor him for the two astonishing young women molded by her goodness. And when the time comes I will let her go home where she belongs.

Randy Fenter

Pre-Christmas Update on Gail -- 97-12-22 

Randy and Gail returned from Dallas earlier this month with discouraging news. Gail's tumor has continued to grow and she had been removed from chemotheraphy. The tumor's growth has impacted further Gail's speech, mobility and eye sight. Please keep Randy, Gail, Marta and Rachel in your prayers over the holiday period that God will provide them with special blessings during this very difficult and challenging time. Thank you for your love and support to family.

Update on Gail. Update 8 -- 97-11-01 

We returned from Dallas this week with difficult news. Gail's tumor continues to grow unabated. While there may be some dead cells in the middle of the tumor, the tumor continues to expand putting pressure on multiple parts of the brain. 

Gail's movement of her right hand and leg have been due to the massive dosages of decadron (a steroid) which reduces the swelling around the tumor. The swelling (built up pressure) is as debilitating on brain function as the tumor itself. However, we can only reduce this swelling for a time. As the tumor grows, concomitant swelling also increases. 

We're glad to still be in the temozolomide study group. Though we have little to no hope of this chemo killing the tumor, we do believe that it has slowed its relentless growth. However, since Gail's tumor is already at the maximum size allowed in this group, this will probably be the last round of this particular chemo. 

Of course the problem with any chemotherapy is remarkable ineffectiveness on brain tumors. The brain-blood barrier, a natural defense mechanism, isolates the brain from such treatments. Too, the kind of tumor that Gail has (a glioblastoma multiforme, phase 4) cloaks itself with a outer sheath which hides it from any attack. 

Medically we are at the same place that we were the first week of December, 1996. Gail has the most aggressively malignant form of brain cancer (glioblastoma multiforme) at the highest phase of development (phase 4). There is no medical cure, nor does there appear to be any on the horizon.

Though Gail is unable to speak (our last true conversation was July 19, 1997), we've "discussed" where we are at length in past few days through "20 questions." We know what we're facing. We know there is no medical hope. And we both had suspected for some time that her improvement was due to the mega-steroids. Facing this is actually easier on us that riding the emotional yo-yo of hoping against hope. We cherish each day. With the grace of the Lord we purposefully make every day a good day. We review the good things the Lord has done for us...today. We thank God for you, for our girls, and for our time together. We entrust ourselves to the One who loves us more than life itself.

Gail has had a difficult week physically. It's difficult for her to sleep. We're often up multiple times for trips to the restroom or for additional medication. Her headaches have been severe and she wrestles with nausea and heartburn. It's hard to see her in pain.


In spite of all of this Gail is Gail. Sweet. Understanding. Patient. Smiling. Loving her family. She is an amazing person. I'm blessed to live with her.

We're taking chemo through this Tuesday. Keep us in strong prayer through the next few days.

Marta and Rachel are stunning. Their care for their mother is a beautiful thing to watch. They face each day with courage, confidence and a goodness maternally inherited. In the worst of times they bring smiles to our faces and pride to our hearts.

I return to the pulpit this week beginning a series, "The Heart's Hunger for Home: The Promise of Heaven." Although I have not yet been able to put the amount of time and effort into this series that I want, it has already blessed our family.

For each of you, we are grateful. Now, and forever.

Randy, Gail, Marta and Rachel



 

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