A Health Setback

I recently met a Young Professional for a coaching appointment over dinner and to my surprise, I saw another Young Professional who had attended a home group we hosted during the time in our lives when Jen was really sick.

Baxter (left), was involved in a Home Group we led for Young Professionals several years ago. I happened to bump into her while meeting another Young Professional for a dinner appointment.

Baxter had moved out of the area a few years ago to take another job but recently moved back to Orange County. Though we had exchanged some texts and engaged on Facebook, we hadn’t actually had an opportunity to connect personally since she moved back to the area.

Having been around during the time Jen was struggling with her health, Baxter saw first-hand the effects of the disease and medications Jen was taking. Naturally Baxter was curious about how Jen was doing.

For the past few years, as I’ve been asked frequently about Jen’s health, I’ve been able to share about how well Jen is doing and how the condition that afflicts her (Vasculitis) is under control, thanks to the care she’s been receiving by her doctors at UCLA.

In fact, early last year, I wrote about how Jen’s condition was considered to be in remission and her doctors wanted to take her off her medication completely, which they did in May of last year (see April 26, 2019 post on Lowedown.com).

Unfortunately though, I was not able to give such a positive and glowing response to Baxter in that moment, as Jen has recently suffered a setback in her health.

Jen sports her Navy spirit on Christmas day!

Back in December, Jen received the results from some blood work which indicated elevated levels in her kidney. Jen has only one kidney so this was very concerning to her and her doctors. Shortly after Christmas, Jen experienced elevated potassium levels which forced her to spend the night in the hospital.

Last week, Jen made several trips to UCLA to meet with her nephrologist as they try to figure out what is happening with her kidney. The good news is that the ultrasound and CT scan that she had showed no abnormalities in her kidney. However, some of the most recent bloodwork came back indicating that the vasculitis that has been in remission for the last four years has returned.

We suspect that this is the reason for the elevated levels in her kidney, as these same symptoms were present back in 2014 when the vasculitis first presented itself.

To say there is discouragement with this development would be a huge understatement. Jen is not looking forward to going back on Prednisone as the reminder of the damaging effects it had on her body are pretty painful.

Enjoying a Philly Cheesesteak tradition while in Philadelphia visiting our boys over Thanksgiving!

We are hoping and praying that because we know what we’re dealing with and Jen’s doctors are extremely competent that the path to stabilizing this “flare” will be quicker and much less traumatic than before.

We don’t know why we continue to be faced with these health challenges, but we know God is good and He has blessed us in so many ways. We would greatly appreciate your prayers.

Specifically, we are praying for the following:

  • We are praying that this vasculitis flare would be quickly stabilized
  • We are praying that Jen would not have to be on Prednisone for very long.
  • Lastly, we are praying that Jen would not have to be admitted to the hospital for ongoing treatment but that whatever treatments are prescribed could be done on an outpatient basis.

We are grateful for you, our friends, whose prayers and encouragement have sustained us. Thank you for your ministry in our lives!

Casting Away 2019

A few nights ago, while channel surfing, I stumbled across the Golden Globes broadcast. Tom Hanks was being honored with the Cecil B. DeMille award for his lasting impact on the movie industry.

During the monologue outlining Mr. Hanks’ long and illustrious career, there were short clips of the many noteworthy films he has starred in, including Saving Private Ryan, Forrest Gump, Apollo 13 and Cast Away.

The short clip of Cast Away showed a scene where Hanks is talking to a face-painted Volleyball he has named Wilson.

Tom Hanks, paints “Wilson” the volleyball, in the movie Cast Away

If you’re not familiar with the movie, the following may be considered a spoiler alert. In the movie, Hanks is the lone survivor of a FedEx plane crash where he finds himself stranded on a deserted island with only a few salvageable packages, one of which is a volleyball.

Hanks paints a face on the volleyball and since it is a Wilson branded ball, he begins calling it Wilson. Throughout the movie, Hanks talks to the ball as if it’s a real person, even responding to the ball as if it has talked back to him.

Jen and Jacob share an embrace in August at the beginning of Plebe Parent Weekend at the U.S. Naval Academy.

This strange dialogue might lead the viewer to conclude that Hanks, being alone on a small deserted island with no human contact, is going mad. But as the movie progresses, it becomes clear that Hanks’ dialogue with Wilson doesn’t indicate a step into insanity, but instead it’s a step to prevent insanity.

Hanks becomes so connected to Wilson that the movie-viewer can feel the anguish as Wilson begins to drift away beyond reach during Hanks’ attempted island escape.

As weird as this may seem, I can relate a bit to that feeling of anguish as the ball floats away. Numerous times this past year, we’ve had to say goodbye to our boys, and they have had to say goodbye to each other. Each time, there is a profound sense of sadness as we go our separate ways.

Jacob (left) and Joshua are all smiles after seeing each other right before Thanksgiving for the first time in months.

Even with amazing technological advancements such as texting and video chat, there still exists a deep longing and profound desire to to be with the people you love.

It appears that as humans we’ve been created with a deep need for human connection; our souls long for the physical presence of others.

In our ministry to Young Professionals, we know that this need and longing for connection IS the biggest need and challenge that they face. All of the most recent research and our own experience affirms that this is the case. Young Adults are desperately seeking meaningful connections with people who are in their life-stage.

Pray for Jacob (left) and Joshua as they enter the 2nd semester of their frosh year apart from each other.

In the past few years, we’ve positioned ourselves well to minister to Young Professionals by providing Leadership Development, Vocational Discipleship and professional level coaching. Yet a primary need and problem is helping Young Professionals develop significant connections with others.

As we reflect back on the lessons of 2019 and look forward to 2020, we would appreciate your prayers in these areas:

  1. Pray for Jen and me to pursue and maintain significant relationships that would feed our souls and encourage us to press on as we face new challenges.
  2. Pray for our boys to develop deep relational connections with others at their respective academies. 
  3. Pray for us to help the Young Professionals we encounter forge solid friendships with others that will spur them to continue to walk with Jesus and serve Him wherever they are.

We are grateful for you and your ministry to us. May you be richly blessed in 2020!

A “Healthy” Look at Thanksgiving

Last Thursday, Jen battled the Southern California traffic to make the day-long trip to see her Rheumatologist at UCLA. In the nearly three years she’s been seeing specialists in Westwood, this was the first time that I didn’t make the trip with her.

My absence was primarily because of a volunteer commitment that could not be changed.

Jen poses with Jacob and Joshua after the OC Champs Cross Country Race in mid October

Earlier in the fall, Jen and I committed to be volunteer coaches for a group of high school students in Santa Ana. Our group meets every Thursday and it just so happened that Jen’s Rheumatology appointment was scheduled for the same day as our coaching group. Changing the appointment to a different day without delay would almost take an act of Congress so it seemed prudent for Jen to keep the appointment and make the trip without me.

To be honest, when we first started making the trips to West Los Angeles, there was a sense of urgency and unknown because of Jen’s health condition at the time. I went to be a moral support and to gather as much information as possible about the condition we were dealing with.

A side benefit of the trip was being able to use the carpool lane, which could cut our travel time down by as much as an hour each way!

So how is Jen’s health? I get this question frequently and I realized that it’s been a while since we’ve updated you through our newsletters. As we reflected on Thanksgiving this year, one of the things we are extremely grateful for is our health. The boys are both healthy and not in the midst of any runner’s injuries and my health has been pretty good for the most part.

Jen shares with a group of Cru Leaders during a Leadership Development Conference in October 2017

For Jen, the good news is that her health is stable. For about two and half years now, she’s been taking an immunosuppressant  that has kept her immune system at bay, eliminating the flares that put her in the hospital 5 times in a 9 month period. As a result, she was able to get off Prednisone along with all the nasty side effects that it brings.

Jen has returned to a somewhat normal routine, including being a mom to our twins and working full-time with me in reaching and ministering to Young Professionals in Orange County. In addition, Jen has been able to resume her part-time role with Cru in helping to develop and shape leaders through the Senior Leadership Initiative Program, which is influencing and preparing some of the best emerging leaders within our organization.

Life isn’t perfect, however, and though the health outlook for Jen is much better than 3 years ago, there are still challenges. For one, the medicine Jen takes has some undesirable side effects, including a continued loss of appetite and general upset stomach.

Jen (2nd from right) poses with her Process Group – a group of leaders who meet regularly to process and discuss the things they’re learning and implementing

Additionally, Jen has been dealing with an issue of Frozen shoulder that requires multiple visits to physical therapy a week at times. And of course there’s the ongoing diabetes management that requires constant attention.

Maintaining good health requires attention and discipline for anyone but for a diabetic with a long-term auto-immune disorder, it adds to the complexity of life. All things considered though, we are extremely grateful for the Lord’s goodness and provision. We have much for which to be grateful!

We’re especially thankful for you, our friends and partners who have encouraged us and shared with us in our burdens and struggles! Thank you for continuing to journey with us as we navigate the challenges of ministry, parenthood and life. We would greatly appreciate your continued prayers for us and our family!

Overcoming June Gloom

Jen shares about her year-long struggle with health issues at our church's Sunday service.
Jen shares about her year-long struggle with health issues at our church’s Sunday service.

The weather in Southern California is great almost year round. While much of the country was under several feet of snow this past winter, we had almost spring like weather conditions here. It’s one of the things that makes Southern California such an attractive vacation destination and it’s also why so many people want to live here, which in turn explains why it’s so expensive to live here.

In June, however, most of the the Los Angeles and Orange County basin experiences a phenomenon that has come to be known as June gloom. I’m not a meteorologist, so I can’t explain all of the meteorological conditions that contribute to June gloom. I just know that for much of June, for some reason, a thick marine layer often creeps in off the coast and envelopes the southland, creating overcast skies in the morning that often burn off by late morning or mid day.

Because our house is located up against the Saddleback mountain foothills at about 800 feet elevation, we often will walk out of our house in the morning to clear, sunny skies. But as I drive down the hill to take the boys to school, it’s not uncommon for us to drive right down into that marine layer where it’s overcast and the sun is not directly visible.

This last year for us has felt a lot like June gloom. It’s as if one day everything was going great and it was sunny outside, but then we experienced some health issues that felt a lot like driving down into that thick marine layer.

For the last year, life has not had the clear, sunny outlook that we would want. Instead, it’s been overcast and even foggy at times. Life has been challenging and at times we’ve wondered if we would ever see the sun through the dark clouds.

These last few months have given us hope that perhaps the June gloom clouds are beginning to burn off and dissipate. We are beginning to see signs of the sun peeking through.

Several months ago, when we started seeing experts at UCLA, Jen was put on a new immunosuppressant that seems to be working. As a result, she has been able to slowly taper down on the amount of Prednisone she’s taking and that alone has helped her to begin to feel more like herself each day.

A few weeks ago, Jen was able to be on a conference call with a work group with which she’s been involved. That was a big step forward since she’s had to disengage with much of her work load for many months now.

Jen-Crossline4
Jen is interviewed by JP Jones, Senior Pastor of Crossline Church.

Last Sunday, Jen was asked to share in front of our church congregation a bit of her journey this past year with her health and how God has met her in the midst of the challenges of life. It was another key moment in her recovery, not just physically, but emotionally and spiritually as well. (You can watch the video interview online at: vimeo.com/130399778)

Things aren’t back to normal by any stretch but there is more hope now than anytime in the last 8 months that perhaps this disease can be managed and we can fully resume the mission to which we’ve been called.

We’re so grateful for your prayers and the way you’ve cared for our family this past year. Would you please continue to pray for our family and for Jen’s continued recovery?

Pray specifically for Jen’s blurred vision to clear and for her lung capacity to increase. Pray too that the side effects of long-term Prednisone use would continue to dissipate.

We continue to trust the Lord for this road we’re on and we pray that the Lord might find us faithful and fruitful as we follow Him and serve Him.

Starstruck

Waiting at UCLA to meet with the Rheumatologist
Waiting at UCLA to meet with the Rheumatologist

This last week marked the one year anniversary of the current health journey that we have been on. I remember vividly being in Nashville when Jen began experiencing sharp pains in her chest that landed her in the ER. I remember my friend Mark Short, who was a student years ago during our University of Arizona days and who also happens to now live near Nashville, adjusting his schedule on a moment’s notice to come and visit us in the hospital. I also remember my fears and anxieties being relieved when the doctor told us that he believed that Jen was suffering from walking pneumonia.

Of course that was just the beginning of the journey. There have been 5 hospital stays, countless doctor visits, chemo-therapy infusions, biopsies, endless tests and procedures and enough blood drawn it seems to fill an empty blood bank.

After Jen’s last flare in January landed her back in the hospital for a week, we were advised by our Pulmonologist to seek more advanced medical care and treatment from experts at a teaching hospital. We ended up setting up some appointments at UCLA and that has been very helpful for Jen in the course of her treatment.

Last month, we had two appointments at UCLA that were helpful and encouraging. The first appointment was scheduled during the first day of spring break so it became an all day family event. We made the best of our time in L.A. by spending a day at Universal Studios, which the boys were pretty excited about.

Joshua (left) and Jacob in front of the Scooby Doo Mystery Machine at Universal Studios.
Joshua (left) and Jacob in front of the Scooby Doo Mystery Machine at Universal Studios.

The next week we were back at UCLA for a full day of tests followed by a consultation with the Pulmonologist. Jen got a CAT Scan of her lungs and also had a Pulmonary Function Test.

When we met with the doctor, he showed us the image of the CAT Scan and compared it side by side with the image of her lungs when she was in the hospital in January. The difference was noticeable. Her lungs now look more clear.

However, Jen’s Pulmonary Function Test results showed that there is still some kind of restriction. The doctor said that could be the result of some lingering inflammation or it could be the result of nearly a year of being pretty inactive and sedentary. We remain hopeful that Jen’s lung capacity will increase over time.

Near the end of our appointment, we met with the head of the Pulmonary group, a doctor named John Lynch. Apparently, Dr. Lynch is one of the leading experts on Vasculitis in the United States. He told us that Vasculitis is pretty rare, with only 3 to 7 cases per million each year. That means there are probably only about 1000-2000 cases of it each year in the U.S. Because of that, he said it’s good to get treatment from doctors who are very familiar with the disorder.

He also told us that based on his observations and Jen’s test results, he thought she might be in remission. That was certainly good news – probably the most positive news we’ve heard in the last year!

Later in the week, when Jen met with her local Pulmonologist, he seemed star struck when Jen told him that we had met with Dr. Lynch. His comment, in an excited tone was, “You met with John Lynch! Wow! I spoke with him at a conference once!”

After our appointment, Jen and I went to dinner at a local mall in hopes of avoiding the rush hour traffic on our way home.

Dave & Jen pause to take a picture with Millhouse from the Simpsons at Universal Studios.
Dave & Jen pause to take a picture with Millhouse from the Simpsons at Universal Studios.

As we were exiting the restaurant, I walked right by Bob Newhart, who was walking with his wife into a different restaurant. Jen had already walked past him without noticing. Starstruck, I caught up to her and in an excited voice exclaimed, “Jen, we just walked right past Bob Newhart!” I guess it’s just a fun footnote of our trips to L.A.

Jen is continuing with her current treatment and continues to lower her dosage of Prednisone, which is now being reduced at a slower rate. She is now taking 9 mg per day.

The main issues now are continuing to build lung capacity, while hoping and praying that the many side effects of Prednisone will begin to subside. Among the side effects we are hoping will dissipate are blurred vision, bursitis in the knees, water retention and weight gain, and loss of hair.

Please pray with us for Jen’s continued recovery. Pray both for increased lung capacity and also that her body will be healed of the many negative side effects of Prednisone. Pray especially for perseverance as the recovery process often feels like 2 steps forward and 1 step backward.

Please pray for healing from a minor surgery Jen had to remove a skin cancerous mole as well as a tooth extraction and permanent implant that will be coming up in the near future.

As always, we are grateful for your continued prayers, support and many notes of love and encouragement!

Click here to read the pdf version of The Lowedown.

A Setback for Jen’s Recovery

Jen-ReaganLibraryFriends,
Thank you so much for your continued prayers for Jen. Please, please, please continue to pray for healing.Today, Jen was readmitted to the hospital for more tests. Let me explain why.

After Jen’s last infusion 4 weeks ago, she had some blood work done that seemed to indicate that things were going well with her lungs and her kidney. We were encouraged.

However, 2 weeks ago, Jen unexpectedly started experiencing some low grade fevers off and on and also was dealing with some shortness of breath.

Last week we visited Jen’s rheumatologist who was concerned when Jen shared about the symptoms she was experiencing. The possible causes of her symptoms could be a return of the vasculitis or maybe an infection that she has developed in her lungs.

Today, Jen saw her pulmonologist who determined that her lung functioning is only at about 50%. Because of that, Jen has been readmitted to the hospital for further testing to try to determine the cause of her lung issues.

Would you take a moment and pray for Jen right now? Pray that the doctors would have wisdom to correctly diagnose what is happening. And pray that she would be able to get treatment to correct her condition. Please pray that the Lord would heal her and restore her health.

We serve a mighty God who is able to do exceedingly more than we ask or imagine. Pray that God would be glorified through Jen and that He would choose to bring healing to her body.

Because Jen’s health issues have been ongoing, we’ve decided to set up a Caring Bridge site where we can post regular updates about Jen and her health. Please check out her site and register to receive updates whenever a new journal entry is posted.

The site is: http://www.caringbridge.org/visit/jenlowe

Thank you so much and God Bless!
Dave & Jen

The Waiting Game

Dear Friends,
Jennifer and I are so encouraged and overwhelmed by the love and support that we have received during these last few months as Jen has been undergoing tests and treatment for her Vasculitis condition.

Many have asked how Jen is doing now and what lies ahead.

Jen-ReaganLibrary
After four infusions, we’re waiting to see if the medication has taken effect.

The short answers are that Jen is doing well and we’re not quite sure what is next. Please read on for the more full explanation of what is happening.

Jen continues to do well and feel well as a result of the Prednizone (steroid) that she has been taking for the last 9 weeks. The steroid has reduced the inflammation that was causing a lot of pneumonia-like symptoms. As a result, she has felt a lot more like herself.

But the goal now is to get off the steroid (because of some of its negative side effects) without seeing the symptoms return. To do that, she’s received 4 weekly infusions of Rituxan, which is designed to put the vasculitis into remission so that when she is tapered off the steroid, the symptoms do not return.

Last Wednesday Jen received her fourth and final infusion. Her doctor also has begun tapering her off the Prednizone.

Where are we now in the recovery process? We don’t really know. We really have to take a wait and see approach.

Jen had some blood work done this week which we hope will show positive signs with many of the markers that the doctors look for when analyzing her condition. Specifically, they’ll be looking at inflammation rate, kidney functioning and the presence of certain anti-bodies.

Over the next 6 months, Jen’s immune system will begin to break down as a result of her infusions. In about 3 months, she should reach the low point of her immune system being compromised and as it builds itself back up, the hope is that the vasculitis will not return.

Please continue to pray with us. Specifically, pray that the Rituxan medication would be effective and that her symptoms would not return as she is slowly tapered off of steroids.

Pray too that Jen would not get sick during the time that her immune system is compromised.

Lastly, please continue to pray that we would trust the Lord as we navigate the various issues associated with this disease.

Thanks again for your continued prayers and your notes of encouragement. We feel loved!

God Bless!
Dave & Jen

Nazi’s, Codes and our Ongoing Medical Journey

What does a Nazi and a code have to do with Jen’s medical condition? Read on to find out.

Frederich Wegener was a German pathologist who in 1936 and 1939 was the first person to give a full description of the disease that is now afflicting Jen. It came to be known as Wegener’s disease or Wegener’s granulomatosis. However, in 2006, two doctors investigating Wegener’s past, determined that at some point he was involved in the Nazi regime and was even wanted by Polish authorities for possible war crimes. Given his professional past, there has been a desire by the medical community to refer to this disease as P-Anca Vasculitis rather than attaching it to Wegener’s name. (Read more about Wegener in this 2008 New York Times article)

Jen and I take a day to celebrate her birthday by visiting the J. Paul Getty museum.
Jen and I take a day to celebrate her birthday by visiting the J. Paul Getty museum.

By faith, we have scheduled an infusion of Rituxan for Jennifer for this Thursday. I say “by faith” because we still have not been approved by our insurance to cover this treatment. This despite the fact that we have been waiting for 3 weeks for an approval that should probably take 3 days or even less.

So what is the holdup? A code. That’s right, a code. Not a Nazi code but a medical code. Somehow, the insurance company was given a code that represents Jen’s condition that is not accurate. The code is not correct for the diagnosis she has. So we’re scrambling this week to get the code corrected so that Jen can begin the infusions to treat her disease.

While it all seems like a simple thing to correct, somehow when dealing with insurance companies and approvals such as these, nothing is quite as simple as it would seem it should be.

So we ask for your prayers this week. Pray that we would get the approval for the infusion BEFORE Jen gets the infusion. Pray that we would be able to get our doctor and the insurance company to communicate the right information with one another in an expeditious fashion. And lastly, pray that these infusions (she’ll need one per week for four weeks) will put the vasculitis into remission and that Jen will be on the road to managing this disease.

Thanks so much for your continued prayers. We are grateful for your love and support.

Please let us know how you are doing and if there is any way we can pray for you as well.

God Bless!

Dave & Jen

The Ups and Downs of Dealing with Medical Issues

 

Dear friends,

HumeLake1
Jacob and Joshua prepare to head up to Hume Lake with their youth group!

Jacob and Joshua are at Hume Lake this week with their church youth group so Jen and I are spending the week alone! We are praying that they would have a great time in a great environment and that this week will be pivotal for them in their own spiritual growth and development!

It’s been two weeks since I sent out any significant update on Jen’s health status. We want you to know how grateful we are for you during this time in our family and we wanted to give you an update so you can continue praying for us.

The last two weeks have been filled with more doctors visits, more lab work and even a trek to UC San Diego for consultation with another rheumatologist.

What we know for sure is that Jen has a lung disease known as Non Specific Interstitial Pneumonia (NSIP). In layman’s terms, it means that her lungs are really inflamed. The doctors have been working for months to isolate the source of the inflammation. We know for certain that it’s not viral or bacterial. She doesn’t have an infection that can be treated with antibiotics.

ScrippsSign
The “new” Rheumatology offices at Scripps are located in the basement. Ugghhh!

Instead, it’s been determined that Jen has a vascular disease known as Vasculitis. This is a rheumatological condition, meaning that it is being caused by her own immune system, which is not functioning properly.

A few weeks ago, Jen’s rheumatologist prescribed a steroid for Jen to begin taking in order to deal with the inflammation in her lungs. Though it has really helped Jen to feel a bit more back to normal, there are side effects. For one, the steroid makes it more difficult to maintain your blood sugar level, which is very critical for a diabetic. Jen is working very hard to manage her diabetes. We are really thankful that she has an insulin pump, which has helped tremendously.

The other noticeable side effect is that the steroid has made it more difficult to go to sleep and to get good rest.

So one prayer request is that Jen would continue to maintain her blood sugars while on the Prednisone and also that her sleep would be minimally affected.

The goal is to treat the vasculitis and to get it into remission. To do that, Jen’s doctor wants to prescribe a chemo-therapy grade drug (Rituxan) that has proven to be very effective. We don’t know when Jen will begin treatment because the doctor needs to get approval from our insurance company before administering the drug since it’s quite expensive.

Scripps1
Jen checks in for her appointment with the Rheumatologist at Scripps. Her diagnosis and proposed treatment plan were confirmed.

The good news is that this drug has shown to have minimal side effects compared to other chemo-therapy drugs. We’re told that most people adjust rather well to the drug, allowing for a more normal lifestyle during treatments.

Please pray that we would get approval from our insurance to cover the drug and that by taking this drug, the vasculitis would be put into remission.

The drug is given intravenously at an infusion center, so no hospitalization will be required. That’s good news for us as we’ve encountered a number of problems with our insurance covering the two different hospital visits that Jen has had over the past few months.

Honestly, one of the biggest prayer requests right now for us is that we would be able to get some of the insurance stuff straightened out. I can honestly say that dealing with insurance and some of the medical bills that they don’t seem to want to cover has been far more stressful than the medical issues themselves.

Pray for us to continue to trust the Lord during this time. Pray for healing and please pray that our insurance would cover the hospital visits for which they are currently denying coverage. I probably don’t have to tell you that the amount for those two hospital bills is quite obscene.

We are so grateful for your prayers, cards and notes of encouragement. It has been so comforting to know that we are not walking through this alone.

God Bless!

Dave & Jen

For the PDF version of the newsletter, click here.

 

An Update on Jen’s Health

Thanks to all of our friends who have been praying for Jen and her health. If you are unfamiliar with what’s been happening with Jen, please check out our latest newsletter, which explains more of the history of her condition.

Last Thursday, Jen was admitted into the hospital for a lung biopsy. The doctors felt this was necessary to try to diagnose what is really happening with her lungs. The procedure was not long or incredibly complicated, but it did require a short stay in the hospital for recovery.

Jen spent two nights in the hospital and came home Saturday afternoon. She is home recovering and though she is very sore from the incision, she is showing improvement every day.

She has several follow-up doctor visits this week but we don’t expect results from the pathology report really until early next week.

hospital2
Saddleback Hospital has become very familiar to us in the last 2 months.

Please pray specifically for two things – first, that Jen would recover quickly from the procedure she had. The incision was near the rib cage and I guess there are a lot of nerve endings in that area so it can be quite sensitive to pain.

Secondly, pray that the biopsy would enable the doctors to make an accurate diagnosis and corresponding treatment. Up until now, the doctors have been eliminating things that they know are not part of the problem. Our hope is that the biopsy would show clearly what the issue is and that it can be treated simply and quickly. We hope that Jen’s body will return to normal as soon as possible.

Thanks again for your love and support during this time of uncertainty. Your notes of encouragement, your prayers and concern have meant a lot.