Newsletter Archive

Sophie Newsletter July 1998-Tummy Troubles

Sophie Prunty Newsletter

July 1998 (Sophie is 4 ½!)IMG_3400

Howdy Everyone!!

What a Spring!! As most of you know, Sophie has faced a very challenging 1998 thus far. She spent all of February and most of March and April in the hospital. Just last week she spend another four days at the hospital. She has had two surgeries and three ambulance rides. In all, Sophie has been admitted and released from the hospital six times this year. She is on monster IV antibiotics and is happily rocking and rolling at home now. Sophie is currently getting most of her nutrition from a permanent IV line called a “central line”. This is an intravenous tube that goes directly to a large vein that feeds into her heart. Through her central line “food” (dextrose, proteins, lipids, etc.) and medicine are pumped directly into her circulatory system.

What Happened?

What started as the flu ended up being what the docs call “pseudo-bowel obstruction.” Although there was no evidence of a physical blockage, her gastro-intestinal system began to spasm and her GI tract shut down. Our “gal with a lot of gas” had a belly as big as a soccer ball, and emergency surgery saved her life. She spent the month of February in the hospital and was given a cecostomy (this is a hole in her ascending colon) for drainage.


From this visit Soph experienced numerous complications. She had a second surgery. In this surgery she received a G-tube that goes into her stomach. This tube is there to relieve pressure (gas) and for supplemental feedings. At this second surgery, her central line was put in. She is doing great with her new apparatus. We thought she was high-maintenance before!!


Just when you think it is safe to go back in the water…

This past Saturday (July 18), Sophie had a seizure and her second and third ambulance rides. She was back home Tuesday night. The diagnosis was an infection in her “central line”. An infection in the area around the heart is just plain terrifying. The seizure is believed to have been caused by a fever spike that accompanied the infection. Once again the people in Rush Presbyterian St. Luke’s pediatric intensive care unit(PICU) were fantastic! If you have to be really sick, disguise yourself as a little kid and go there. We just can’t say enough, especially about those nurses!IMG_3397


Speaking of Nursing

Jody has now added the title of full-time nurse to her career, as good ole’ insurance doesn’t cover home nursing care. With all of the health care issues being examined by the government these days, Rick is threatening to become a Democrat since they seem to be looking at our needs more closely. Hopefully these issues will be worked out to our advantage before Sophie is in college or Jody needs to be committed.

And the beat goes on…

We’re still learning to live with a kid with serious medical issues. Without her central line Sophie wouldn’t have made it. She has gained over 15 pounds and grown 5 inches! In spite of our recent return trip to the hospital, we are slowly tapering her off the central line and increasing her feedings as her system tolerates it. So far she’s doing well, although progress is slower than her docs would like it.

Now that some of the “crisis-management” has tapered off a bit we can finally spend a little time together as a family and continue to strengthen Sophie’s program. She is currently getting home-therapy (less germs to throw her system wacky.) The volunteers are also back on their schedules. We as a team continue to challenge her in the playroom and she’s doing well!IMG_3403

All of the time Sophie spent lying in bed fostered the concern that she would loose some of the physical progress she had made prior to Hospital-Mania. Fortunately, she has gained muscle mass with the weight. The only glitch has been her back is more rounded from all of the lying around. Where she used to be more floppy, she is now tighter, and this has created a little more of a challenge for her therapists as she’s a big, strong girl now.
Thank You! Thank You! Thank You!

As usual, all of you angels out there have been so supportive. We don’t know how we would make it without all of your thoughts, prayers, time, and gifts. You really are making a difference in a little girl’s life! Our volunteers have been so incredible – they helped out at home and at the hospital with time and support, and kept us thinking positive thoughts. They have bravely met and conquered their discomfort with Sophie’s new apparatus.

Special thanks go out to Annette, Jill, Jan, Denise, Deborah, Holly and Lori for giving us a few hours of relief at the hospital.(We apologize if we have forgotten anyone!) Our neighbors, the Lemanski’s once again have helped us each time with watching the house and caring for our dog and cat.

Rick’s parents came up from Arkansas for two weeks to help us. Rick and Jody alternated nights at the hospital, so we really had no time together for most of the Spring. Jody’s parents helped in numerous ways that allowed us to get away one night and just be a couple. Everyone in the family was blood-typed or donated, and friends in Oak Park kept us supplied with food. Rick’s brothers and Jody’s sisters and their families have been forever helpful and special—thanks, guys.

Finally, a special thanks goes out to Allan  for helping Rick while Sophie was at the hospital. His help enabled Jody to go to the Option Institute for additional training. Rick had to push Jody out of the hospital room to go to the training (it is only held one time a year.)

Sophie was selected to be a beneficiary of the Mulliganeers fund raiser this Spring. What a fantastic group of individuals! Those Mulliganeers are really making the difference in some children’s lives. We were one of 5 families selected to benefit from their St. Pat’s dinner/fund raiser. Sophie was still in the hospital at that time and Jody was at the Option Institute. However, thanks to some special volunteer help from Annette, Rick was able to attend. These people really know how to throw a party!

As Jody’s Mom said, “it is so nice to know and have faith that the money you send to a group actually gets to the intended recipient.” Our portion has enabled us to pay off some very overdue therapy bills. In addition, some accessibility improvements around our house are now closer to a reality. Thank you for your generosity.

Sophie’s most recent fund raiser involved Teresa, and old roommate of Jody’s and Susan, a new friend. The Partylite/Pampered Chef event was beautifully done. Sophie and Jody were able to attend, and as a bonus Jody’s sister, Jan,  was there with her outstanding porcelain ornaments. It was a beautiful day and Jan, Teresa, and Susan had some wonderful things to sell.

And speaking of generosity…PLEASE know that we include you in all our mailings so that you are aware of all that we are doing. Please DO NOT feel that you need to contribute to each event!

And on that note…

Susan, who is a new crusader for Sophie’s cause (Susan had a similar disorder that was cured and experienced life with a central line for a short period of time,) and who is the Pampered Chef rep, has just let us know that she is doing another fund raiser for Sophie. During her selling months of September to December 1998, she will donate $1.50 for every “Welcome Home Heart” Mold. This is an exclusive stoneware mold that can be used for cookies, chocolates, crafts, or displaying. It is a great gift or keepsake. By purchasing through Susan, $1.00 goes to your county’s Second Harvest National Food Bank, and $1.50 goes to Sophie’s Fund. This special gift can be purchased for $8.00 plus shipping and taxes. What a unique way of remembering YOUR special little friend. Thank you!!

But wait… There’s more:
The Sophie PruntyIMG_3402
“One In A Million” Charity Golf Outing
Friday, September 4, 1998
Indian Lakes Resort, Bloomingdale, IL

12pm registration
1pm shot-gun start
7pm banquet

golf tournament and dinner: $125 per person
dinner only: $35 per person

Limited number of players, so call now!

Please call Bill Prunty for details!


Thank you everyone, once again, for everything. Your concerns and support are so very, very helpful to us. We hope that this letter finds you happy and healthy. Please hug your kids (no matter how old!,) kiss your significant other, call a friend you haven’t spoken to in ages. Just remember—life is so very precious, enjoy it to the fullest!!!

We love you,

Rick, Jody and Sophie

Sophie playing with volunteer and friend, Terri.

Sophie playing with volunteer and friend, Terri.


One thought on “Sophie Newsletter July 1998-Tummy Troubles

  1. Jody,
    We met you and Sophie at Bob and Eleanor’s 60th. We grew up in Charles City with the Prunty’s. I’ve had an assortment of medical problems through the years including sleep disorders. I was recently diagnosed with peripheral sensory neuropathy. Im awaiting further testing at Baylor Houston. Can you call me?
    Mary McDonald Hanel

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