Monday, February 9

Shout-out to all who are loved

It occurs to me that the ones we love never get to hear it enough, so for all those of you that check this blog regularly, I LOVE YOU! I TRUST YOU! I MEAN IT!

I have had a chance to relax this morning and appreciate stuff. I got to talk with Laura Siegrist, a collegiate friend who recently moved to frozen Indiana. I ate dessert for breakfast (yummy apple squares, mmmm), and looked around to see that the laundry was done and the house was pretty clean. I think I heard angelic voices just now.

Thank you Jesus for opening my eyes to see so many folks within whom you are at work. Thank you Jesus for giving me your love through them. Thank you Jesus for showing us your grace when we don't trust you. Thanks for taking away my job, because I have been so blessed by new lessons and new friends.

Thank YOU for thinking of us, we are doing well and setting our minds on things that are good, pure, noble and worthy of our time. The office is clean-- thanks Matt! The garden is full of potential, and we are really enjoying all the warm weather recently.

I cannot believe that this Saturday marks our FIVE YEAR ANNIVERSARY. We actually call it our "Valentersary." Am I getting old? Am I really 5 years older? I've stopped waiting for an epiphany-- life moves too fast to process them anyway.

Watching John's Memorial service DVD has really solidified the gigantic ripple effect of one person's life. He was treasured. We have been burning copies all week and it has been emotional, special and hard. You can watch it by clicking on the link below:

http://www.facebook.com/video/video.php?v=1108032059856

Sunday, January 25

A New Year, lots to share

It's been a long time since I sat down to write. I just haven't been ready, like I was scared to think about everything and force myself to put it into words.

Matt's dad left his body behind on the way to Heaven almost three weeks ago. He died on my father's birthyday: January 6. We had just returned to Virginia from our Christmas visit to New England. There was a wedding in DC that stalled our return by a few days, and it gave our hearts & minds a reprieve from those nagging, forboding thoughts of loss. So we drove back to Rumney and stayed a week. We were gone about 3 weeks. I got laid off just before we left, so things have been helter-skelter. Loss of job, loss of parent, loss of structure and lots of change.

Time with the Horkeys was short, but fun. Christmas seems to always a time of abundance and near-glutony, but this time seemed modest, balanced and easy. Hoo-rah! My brother and his family were there, so it was awesome to spend time with them. Michelle is a saint and their son is just so precious. So good-natured and sweet for a two year old. We all went to a butterfly conservatory in Massachusetts which will stay in memory forever. Here's a little piece of it.



Then we traveled on to visit Matt's family. John was spending more time sleeping each day, so we spent a lot of time hanging around the house with nights out to enjoy the snow and local friends. I spent a day sick with some nasty kind of puke-inducing virus. We visited with lots of family and had a great visit from John's doctor. Leaving was very hard; we knew that these had been our last days with earthly John. But the doctor encouraged us to go to the wedding, trying to guess which day John would pass was like shooting at the stars.

The wedding in DC was wonderful. We were surrounded by 'ole collegiate friends. The support, love and merriment was fresh air to us. Matt's best friend was the groom, and Matt was in the groomsmen lineup. Here he is with the rest of the guys. Such a loving, crazy bunch. And of course, DC is a great city.

The wedding was great, and we headed home with minds full of memories and tummies full of good food! Unfortunately, Matt soon cam edown with the vomit-inducing virus and spent the drive back home experiencing the symptoms of said virus. It took him two days to get back on his feet. The morning he was ready to go back to work was January 6th. We got the call at 1:30 am and were on the road back to Rumney by 8am.

Saturday, December 13

Merry Christmas


I want to say thank you to the economy, for giving this gift! The trip to New England has never been so cheap! $1.47 -- Holy Canolli! I can fill my tank for $20, like when I was in college!!

Saturday, November 29

From pen to pan



We had a great Thanksgiving. Of course, we were up late the night before in food preparations. The DeWevers brought buttermilk biscuits, cranberry jello salad, chocolate torte (from scratch!!) and a few games to the celebration.

Next day was the main event: the Turkey Slaughter. Both of us had taken chickens through this process, but a turkey seemed slightly more complicated. So we consulted with the experts and had set the strategy with the guidance of fathers, neighbors, friends and cousins.

This turkey was not phased by much. We let him fall asleep upside down before pulling the plug. It took about an hour from start to finish and another hour for him to be fried for dinner. While not a big fan of meat nor of butchering, it sure is nice to know where the food came from. When all was said and done, however, I probably ate one mouthful of turkey... but I've never eaten much of that on Thanksgiving anyway.

Saturday, November 1

God is Sufficient

Can I just give a shout out: God is doing AMAZING things!

Details aren't important, but have ever seen God "show up" all over your life... like in your best friend, cool giving opportunities, financial blessing, and good worship? Well, that's what is surrounding us right now. Such amazing grace.

Matt leaves on Monday for about 10 days in NH. It's going to be a great opportunity for him. I'll be following next Friday and we return home on November 16th. I'll get to hang out with my mom for a few days, which will be very nice as well.

Everything seems to be falling into place for us. I'm looking at an in-home business opportunity which is very exciting too. Bottom line: I sense the presence of the LORD all around our family.

Saturday, October 25

A Weekend with Family

The second weekend in October was a great opportunity to visit NH again. We traveled with our favorite companions: Bernie & Martha and the van. Saturday was a barn raising, another step in Isaac's summer-long project in central VT. It was a beautiful time of year and an good time with John & Priscilla. We also got to spend a lot of time with Nate, Veronica & the boys. Here's some pics for your enjoyment. For those curious, I've included a video at the very bottom: intense! :D



Sunday, October 5

It's Been a While...

Well, as I imagined would be the case, we haven't had much time off since the last post. From May-October we keep quite busy with our jobs; not enough time for decent blogging.

This weekend is a casual one for the DeWevers and as the work week begins to slow, we've begun to take back some of hobbies. Today was a nice time to mosey around the house and work on previously-ignored projects. We finally moved the office downstairs, installed light switches in the basement, and Matt tackled the apple pie featured in last month's edition of Southern Style magazine. This is his Paula Dean picture. He also made a coffee cake and served me breakfast in bed: faboulous! I found a use for all the donated brie I still have in the fridge... yummy savory tarts. We are hosting cell group tonight.


On Wednesday we'll drive to New Hampshire for Isaac's birthday, a barn raising & some time with John & Priscilla. The months have been pretty status quo, but John is eating less these days and we wanted to grab a quick visit before the Christmas pilgrimage.

What have we done this Summer?
  • Random house projects: drip hoses galore, gutter caps, bits of landscaping...
  • Visited Jason in DC, meeting his fiance. The wedding is sometime in January.
  • Hosted my mom for 10 days. Also visited Colonial Williamsburg for the 1st time.
  • Installed HVAC!! Yes, friends, we'll have heat this winter!
  • Matt is taking a community college class for business management.
  • Fianlly bought a lawn mower & a ladder.
  • Recently did a liver cleanse.
  • I baptized the cordless phone in the washing machine... so we bought a new one.
Here are some photos:

Wednesday, May 14

A weekend planned by God


We left Virginia this past Friday after work and split the 12 hour drive into 2 parts, staying overnight at Montage Mountain, PA. It was a nice opportunity to drive with Bernie & Martha, and their van was also a nice change; more leg room is good!

We pulled into John & Priscilla's driveway at 3pm to see that Mark (John's younger brother) and Becky were already there, with Italian sandwiches from Maine. But Priscilla was crying and John was on the phone with his doctor. His other leg has slowly become swollen throughout the day and by 3pm it was showing discoloration in the foot. John's doctor was very persistent in having John taken to Dartmouth Medical Center's ER, as they had a 24/7 ultrasound dept. We tried to enjoy the sandwiches, but it was obviously a tense situation; John was angry & Priscilla was worried. Not too long after, we had commandeered Bernie & Martha's van to transport John to Hanover, NH and Dartmouth Medical Center.

After quite a while, John was diagnosed with another series of blood clots and admitted to the hospital's oncology ward for the night. The next morning we learned that his blood pressure had dropped to 60/40 and that he was dehydrated to the point of near hypothermia. After a series of blood tests, transfusions, several bags of liquids, etc... he had regained color and was feeling almost normal. Then we had consultations with the doctors.

It's tricky to explain, so I'll give you a nut shell version about John's situation. Due to the polycystic kidneys, John can't have tests normally used to diagnose the progression of his cancer or the location from where his kidneys are bleeding. Blood thinners have been useful and are now necessary for maintaining a fine line between keeping blood clots from forming and must be controlled so that the kidneys will not bleed uncontrollably. The doctors wanted to take John off the blood thinners before starting his chemo pills, as a side effect is internal bleeding (not good when that's already an issue).

After talking with several doctors and specialists, John has decided to maintain the blood thinners and hope for the best. It was also decided that since John is still in the hospital, he should begin his chemo pills (Sutent), so they can monitor and catch any issues that may pop up. This is a great thing: even though he'd rather not be in the hospital, he is getting excellent care & Priscilla is glad to have all the resources available to them there.

John has been getting a suspended dose of pain medication which also helps to control his coughing. A massage therapist will spend about 45 minutes with him 3x this week and that's really helped relax him. The nausea is staying at bay most days due to medication, so he is eating at regular intervals and enjoying it for the most part. We all met with the Palliative Care team which is helping with paperwork for dissability, advance directives, etc. They are great people!!

We praise God for this weekend! Although there are hospitals closer to Rumney, Dartmouth Medical Center is very therapeutic for patients and their guests. Extensive grounds are available for picnic lunches, casual walks, and there's even a trail system for when you just need to step away from it all. John's room is on ground level and has a huge picture window that looks out into a small garden. Down the hall is a waiting area with a patio and picnic table, and the food options are extremely diverse.

John has his own room. We (Priscilla, Mathew, Isaac, me, Bernie & Martha) were able to visit from 9am -3pm almost every day without discomfort or feeling crowded, and would switch out for lunch and to let him sleep. We went to Subway for Mother's Day, at 'Cilla's request, & my parents came for a short stay while we were in the area. The drive home was nice and the work week is already 1/2 over!! That's nice.

Leaving New Hampshire was difficult, but everything in life is uncertain... we have no guarantee that our loved ones will be with us forever. Each day with John was a gift to see God's hand of peace in his heart. It's so much easier for us because John is not trying to evade this part of the journey. And Matt even said that he would not be as much at peace if we hadn't moved here and been growing as God has directed. It's amazing. Nobody wants to loose John, but it's not a good-bye-- only a "see you later."

Saturday, May 3

A much-anticipated update

  • John, Priscilla & Isaac met with a kidney cancer specialist at Dartmouth-Hitchcock (university med school) this past Wednesday to see about different treatment options. Because John is so weak, and because both his kidneys are not functioning well, he has no good options for strong and/or invasive treatment. This rules out high-doseages of chemo and any sort of operation or transplant.

  • He is a great candidate for at-home chemo, which is a prescribed pill that you take on a set schedule. Sort of like an "on again/off again" doseage. Side effects include nasea/ vomitting, diarhea, etc... and hair loss. So big changes for John there!! The pill has been ordered from their local pharmacy and should arrive within 10 days or so (I think). When they delivered the script from the doctor, they learned that the co-pay would be about $25/month. Without insurance, this Rx can be as much as $7,500/month!! Can you only imagine...
  • John continues this up-hill battle with all the grace & humor for which he is known, but his body is not regenerating itself at all. He continues to be on standby at the local hospital if his levels indicate a need for new, fresh blood. He is weak, fragile-looking, and battles coughing if he engages in conversation. This is most likely due to fluid build-up around the heart, a common problem with cancer.
  • Priscilla is holding up well, taking time in the morning to get out of the house & put in a few hours at the boys' home accross the street. Most of the boys and staff know John & Priscilla very well and it is a great relationship that Priscilla can maintain, combatting the feelings of helplessness. Her mantra remains the same, "God is in control." At this point, it is the only thing that keeps her going.
  • Isaac is back from Alaska, returning to main land culture, and keeping busy in the afternoons when Priscilla returns home from the Beckett House. We haven't spoken too much, but he remains hopeful, knowing that God has it all under control.
  • Matt & I are planning another trip for an extended Mother's Day weekend. Bernie & Martha (Priscilla's sister & brother-in-law) have made plans to visit, so we will carpool and help out with the driving. Matt has had to work through some low emotions recently, so this will be incredibly good for him. It's a rare opportunity for me, because I won't be able to break away from work all summer with any ease.
There is a website I found helpful:

Tuesday, April 22

Renal Cell Carcinoma

I spoke with Mom and Dad today and found that the meeting in Laconia was a little long... (the last two weeks have been very long, so that's no surprise.)

At 8 o'clock AM, Dad and Mom arrived at Lakes Region General Hospital to meet with Dr. Friedlander, an oncologist on staff there. Approximately 4 hours later they left the appointment knowing two things;

  • One - Dad has been diagnosed with Renal Cell Carcinoma (Kidney Cancer).
  • Two - Dad has an appointment on the 30th of April with an oncologist at Dartmouth Hitchcock Medical Center who specializes in RCC. After the meeting next week at DHMC, the oncologists from both Laconia and Dartmouth are going to meet and determine the road for treatment.

I asked Mom how she was feeling after the long day. I think she is relieved to finally have a diagnosis.

Dad sounded much better tonight; he was prescribed a very good medicine to relieve the persistent cough he has. Talking to him today was much easier and he stayed on the phone quite a while.

I want to thank everyone, friends and family alike, who has supported my family in the last two weeks and who is continuing to support my Dad and Mom both present with them and in prayer and phone calls, etc.

This has been quite a trying time for me, though God has never been closer and Christ never so fair as in these last two weeks. Seeing my father physically stretched and thinned, yet so spiritually vibrant, is fantastic. (We truly are weak earthen vessels through which Christ wants to shine to the world.)

Thank you all again.

MATTHEW


Sunday, April 20

Still no results


Well, we're back in Virginia. Although the trip was absolutely worth it, we are glad to be back home to routine and familiarity. I thought those of you who hadn't seen John recently should be prepared for when you see him next. The timing of this photo was when John was experiencing some chest pain, so he's not smiling like he normally would. In fact, he smiles less often now, but his witt and grace are the same as ever.

The time spent with Priscilla & John was really good. Because the weather was so nice, we were able to return some curb appeal needed for today's real estate market (raking, mulching, etc). The next 2 months will probably be the "hot" time for their area, so we wanted the yard to be ready. It was also warm enough to enjoy some sunshine and warm breezes on the porch and in the yard with John. That day he was experiencing significant chest pain, so we returned to the local hospital ER in case the blood clot had moved itself into his lung.

The team of doctors & nurses determined that he was not having a heart attack, but could not perform a CAT Scan, because of the sensitivity of his kidneys to the contrast/dye. The ER team called in his primary doctor and we all had a good chat. Basically, John has cancer, but the type is still undetermined. Hopefully this will be resolved by Tuesday morning's meeting. He has fluid around his heart (most likely due to the cancer) and low blood pressure. His blood is thinned perfectly, so the likelihood of a clot at all is extremely low. His primary doctor couldn't perform any tests because it was Friday night/Saturday morning and the only hospitals that could were in Boston. The bigger hospitals would put him through every test he's already had again, trying to figure out where the cancer was stemming from and what to do next about chest pain and/or low blood pressure. So, the primary doctor gave some helpful advice and allowed John to return home until Tuesday's meeting with the oncologist. He did mention that he'd call the lab & pester them to be sure that John's case was prioritized. He's a great doctor and was very candid that because John was so young, any treatment would be worth a try.

The doctor also told us that the probability of John having Histiocytosis X was a likely misdiagnoses, because statistics show that the majority of complex diagnosis with strange names (ie: Histo X) are extremely rare and often a case of common oversight of a more "normal" problem. It is very likely that John has kidney (Renal) cancer. Renal cancer doesn't take normal chemo treatment and an operation wouldn't work, but chemicals similar to chemo are often used with varied results. Because his kidneys are already compromised with tumors, we do not know what can be done... we look forward to knowing some answers Tuesday.

Isaac returns home from Alaska this week, which will be a great comfort to us all. While Matt was there, the lawyer was contacted and trusts, POA, etc was settled and done. The taxes were also filed. Matt found an error in John's calculations, resulting in $1,000 less they owed Uncle Sam. Dinners have begun arriving daily and Priscilla is holding up pretty well. John is most often tired by 2 pm and dozes off throughout the day. He coughs regularly, a chest cough that starts like a tickle and takes the energy right out of him. But he still chuckles at my jokes!

Priscilla's parent hope to visit this week which should be a comfort to her. They recently retuned from their winter home in Virginia and are getting their lake house up to snuff after a long Adirondack winter. All prayer are going right to the source, thank you all for your cards and gifts of love and care. Matt & I are planning to return for a long weekend for Mother's Day, but are "on call" in the meantime. Wisdom will be needed as the time passes.

Thursday, April 17

Still Waiting

Alicia (that's me) left Virginia on Wednesday morning with the Nate Myles family, who were en route to their home in New Hampshire. The 13 hour trip was uneventful, made enjoyable with good company and fast food. We were also pleased to learn that John was "released" from captivity at Lakes Region General Hospital with instructions to get blood work done the following day to determine appropriate medication doseage. Once back at home on Depot St, Matt stopped in to see some old friends & work colleagues at Harris Family Furniture. They knew about John's condition and asked if he would appreciate an ajustable bed (which they had in stock and could easily donate to the family). What a blessing!!! Halelujah, the LORD knows what we need before we even ask. John can sit up, raise his legs, lie flat, or whatever... because the bed was delievered & set up in the same day! John is currently lounging on a queen-sized bed downstairs in the TV room. He has a good view of the kitchen too.

We anticipated a prognosis & diagnosis meeting today (Thurdsay) at 2pm with the doctors, but received word that the tests were still being done on his tissue samples taken earlier in the week on Tuesday. This was frustrating, but we are thankful he is able to really rest at home and comfortable; it's so nice to be together as a family! I must confess that seeing John in this state was a shock-- in the 4 months since Christmas, he has become very frail looking & boney. His eyes have a very dark pool look to them, but he's the same old John... always making us chuckle.

The meeting has been reschuled for Tuesday, but Matt & I will be back in Virginia by then. We plan to head out early on Saturday & enjoy breakfast with my parents on our trip back to Virginia.
Tomorrow we will be taking care of loose ends around the house... such as mulching the flower beds and replacing screen on a few windows and the porch doors. The weather should cooperate though, there's almost no snow left on the ground! Eveyone here is looking forward to consistantly warmer days.

Monday, April 14

Firstly, let me (again) thank everyone who has made intercession for John & his loved ones. It is obvious that this is God's show... and he's got everything under control. We watch him orchestrate such marvelous wonders daily.

Here's a quick update; I just spoke with Matt...
The tissues taken from his biopsy are insufficient to determine the cells growing in his lungs, theefore a second biopsy is scheduled for tomorrow. Luckily, there is a lymphnode in his neck which will make this procedure less invasive. That's good. The meeting scheduled for Tuesday (a full scale report & diagnosis) has been pushed to Thursday. I will be able to get a ride to NH and be with the family either Thursday or Friday. Matt & I plan to travel back to Virginia over the weekend and be back to work Monday.Matt & Priscilla generally leave to go to the hospital (Lakes Region General Hospital: Laconia, NH) by 8am and are home by 8pm. If you want to call and speak with any of them, please do... they will be happy to get your call!
The ph# for John's room is: (603) 524-3211, ext. 2402

Sunday, April 13

Recent Meditation

Praise to the Lord,
The Almighty, the King of creation!
O my soul, praise Him,
For He is thy health and salvation!
All ye who hear,
Now to His temple draw near;
Praise Him in glad adoration.

Praise to the Lord,
Who over all things so wondrously reigneth,
Shelters thee under His wings,
Yea, so gently sustaineth!
Hast thou not seen
How all your longings have been
Granted in what He ordaineth?

Praise to the Lord,
Who doth prosper thy work and defend thee;
Surely His goodness
And mercy here daily attend thee.
Ponder anew
What the Almighty can do,
If with His love He befriend thee.

Praise to the Lord,
O let all that is in me adore Him!
All that hath life and breath,
Come now with praises before Him.
Let the Amen
Sound from His people again,
Gladly for aye we adore Him.

A Few Thank yous

To everyone in the family, fellowship, or proximity of John, Matt, Priscilla (and me) I want to say thanks. I really should have written about 1500 thank you notes thus far... you'll have to settle for a public session of me getting all the appreciation off my chest:

Thank you for:
  1. Offering your thoughts of health and prayers for the same.
  2. Giving small gifts of cookies, juice, coffee, dinner, etc...
  3. Looking up fares for flights, just in case (Sarah)
  4. Asking if there's anything we need (Mom & Dad Horkey)
  5. Being sensitive about offering space or providing extra companionship
  6. Paying for my lunch (thanks Bernie & Nate)
  7. Building up good energy through laughter
  8. Letting us cry (Ashley)
  9. Letting us talk (Elisabeth)
  10. Helping out with transportation (Eleanor)
  11. Providing helpful information when we need wisdom
  12. Taking us out on walks (Linda)
  13. Inviting me to your sleepover (Abby)
  14. Expressing your own thoughts & feelings (Martha)
  15. Asking if we need any cash
  16. Impromptu acts of kindness
  17. Calling to check in
  18. Helpful reminders
  19. E-mails
  20. Understanding
“Praise Him for His acts of power; praise Him for His surpassing greatness.” Psalm 150:1-2

Saturday, April 12

What I recently learned about cancer

Cancer Update from Johns Hopkins

1. Every person has cancer cells in the body. These cancer cells do not show up in the standard tests until they have multiplied to a few billion.When doctors tell cancer patients that there are no more cancer cells in their bodies after treatment, it just means the tests are unable to detect the cancer cells because they have not reached the detectable size.

2. Cancer cells occur between 6 to more than 10 times in a person's lifetime.

3. When the person's immune system is strong the cancer cells will be destroyed and prevented from multiplying and forming tumors.

4. When a person has cancer it indicates the person has multiple nutritional deficiencies. These could be due to genetic, environmental, food and lifestyle factors.

5. To overcome the multiple nutritional deficiencies, changing diet and including supplements will strengthen the immune system.

6. Chemotherapy involves poisoning the rapidly-growing cancer cells and also destroys rapidly-growing healthy cells in the bone marrow, gastro-intestinal tract etc, and can cause organ damage, like liver, kidneys, heart, lungs etc.

7. Radiation while destroying cancer cells also burns, scars and damages healthy cells, tissues and organs.

8. Initial treatment with chemotherapy and radiation will often reduce tumor size, however prolonged use of chemotherapy and radiation do not result in more tumor destruction.

9. When the body has too much toxic burden from chemotherapy and radiation, the immune system is either compromised or destroyed, hence the person can succumb to various kinds of infections and complications.

10. Chemotherapy and radiation can cause cancer cells to mutate and become resistant and difficult to destroy. Surgery can also cause cancer cells to spread to other sites.

11. An effective way to battle cancer is to starve the cancer cells by not feeding it with the foods it needs to multiply.
  • Sugar is a cancer-feeder By cutting off sugar it cuts off one important food supply to the cancer cells. Sugar substitutes like NutraSweet, Equal,Spoonful, etc are made with Aspartame and it is harmful. A better natural substitute would be Manuka honey or molasses but only in very small amounts. Table salt has a chemical added to make it white in colour . A better alternative is Bragg's amino or sea salt.
  • Milk causes the body to produce mucus, especially in the gastro-intestinal tract. Cancer feeds on mucus. By cutting off milk and substituting with unsweetened soy milk cancer cells are being starved.
  • Cancer cells thrive in an acid environment. A meat-based diet is acidic and it is best to eat fish, and a little chicken rather than beef or pork. Meat also contains livestock antibiotics, growth hormones and parasites, which are all harmful, especially to people with cancer.
  • A diet made of 80% fresh vegetables and juice, whole grains,seeds, nuts and a little fruits help put the body into an alkaline environment. About 20% can be from cooked food including beans. Fresh vegetable juices provide live enzymes that are easily absorbed and reach down to cellular levels within 15 minutes to nourish and enhance growth of healthy cells. To obtain live enzymes for building healthy cells try and drink fresh vegetable juice (most vegetables including bean sprouts) and eat some raw vegetables 2 or 3 times a day. Enzymes are destroyed at temperatures of 104 degrees F.
  • Avoid coffee, tea, and chocolate, which have high caffeine. Green tea is a better alternative and has cancer-fighting properties. Water-best to drink purified water, or filtered, to avoid known toxins and heavy metals in tap water. Distilled water is acidic, avoid it.
  • Meat protein is difficult to digest and requires a lot of digestive enzymes. Undigested meat remaining in the intestines become putrified and leads to more toxic buildup.
  • Cancer cell walls have a tough protein covering. By refraining from or eating less meat it frees more enzymes to attack the protein walls of cancer cells and allows the body's killer cells to destroy the cancer cells.
  • Some supplements build up the immune system (IP6, Flor-ssence, Essiac, anti-oxidants, vitamins, minerals, EFAs etc.) to enable the body's own killer cells to destroy cancer cells. Other supplements like vitamin E are known to cause apoptosis, or programmed cell death, the body's normal method of disposing of damaged, unwanted, or unneeded cells.
  • Cancer is a disease of the mind, body, and spirit. A proactive and positive spirit will help the cancer warrior be a survivor. Anger, unforgiveness and bitterness put the body into a stressful and acidic environment. Learn to have a loving and forgiving spirit. Learn to relax and enjoy life.
  • Cancer cells cannot thrive in an oxygenated environment. Exercising daily, and deep breathing help to get more oxygen down to the cellular level. Oxygen therapy is another means employed to destroy cancer cells.
And while you're thinking about it...
1. No plastic containers in micro.
2. No water bottles in freezer.
3. No plastic wrap in microwave.

Johns Hopkins has recently sent this out in its newsletters. This information is being circulated at Walter Reed Army Medical Center as well. Dioxin chemicals causes cancer, especially breast cancer. Dioxins are highly poisonous to the cells of our bodies. Don't freeze your plastic bottles with water in them as this releases dioxins from the plastic. Recently, Dr. Edward Fujimoto, Wellness Program Manager at Castle Hospital , was on a TV program to explain this health hazard. He talked about dioxins and how bad they are for us. He said that we should not be heating our food in the microwave using plastic containers. This especially applies to foods that contain fat. He said that the combination of fat, high heat, and plastics releases dioxin into the food and ultimately into the cells of the body. Instead, he recommends using glass, such as Corning Ware, Pyrex or ceramic containers for heating food. You get the same results, only without the dioxin. So such things as TV dinners, instant ramen and soups, etc., should be removed from the container and heated in something else. Paper isn't bad but you don't know what is in the paper. It's just safer to use tempered glass, Corning Ware, etc.

He reminded us that a while ago some of the fast food restaurants moved away from the foam containers to paper. The dioxin problem is one of the reasons. Also, he pointed out that plastic wrap, such as Saran, is just as dangerous when placed over foods to be cooked in the microwave. As the food is nuked, the high heat causes poisonous toxins to actually melt out of the plastic wrap and drip into the food Cover food with a paper towel instead.

What the doctors are thinking

It is believed that John has Histiocytosis X as well as cancer. This progressive diagnosis is still inconclusive, so nothing you read until Tuesday is confirmed fact. I will explain Histiocitosis X below, let me clarify the cancer issue first, just because it's easier! The doctors are trying to determine between three different forms of cancer. They have concluded that lymphoma is NOT a factor any more. We do not know what other cancers they suspect.

Histio-what?!
Histiocytosis X, (Hsto X) is a condition of the immune system. It is characterized by an abnormal increase in the number of certain immune cells, called histiocyte cells. Histiocyte cells include monocytes, macrophages, and dendritic cells. (T-cell lymphoma is a related condition... so the doctors were definitely on the right track)

Hsto X has typically been thought of as a cancer-like condition, but more recently researchers have begun to suspect that it is actually an autoimmune phenomenon, in which rogue immune cells attack the body, rather than fight infections. Some forms of the disorder are genetic. Hsto X occurs in 1/200,000 per year.

Another type/name of this disorder, pulmonary histiocytosis X, is characterized by inflammation of the small airways (bronchioles) and the small blood vessels in the lungs. It is most common in adults. The inflammation leads to stiffening and destruction of the walls of the alveoli (parts of the lung). The cause is unknown. People 30 - 40 years old are affected most often. Cigarette smokers make up 90% of patients. Yes, John did smoke for some years. 50% with pulmonary Hsto X improve, while the other 50% loose lung function.

Symptoms:
  • Cough
  • Shortness of breath
  • Chest pain
  • Fever
  • Weight Loss
  • General discomfort, uneasiness, or ill feeling (malaise)
  • Increased amount of urine output
  • Thirst and increased drinking of fluids
  • Bone pain
  • Rash
The tumors produce a punched-out appearance on bone x-ray. Tumors in weight-bearing bones, such as the legs or spine, may fracture spontaneously. There is often systemic (whole body) involvement as well, causing rashes, lung problems, gum infiltration, lymph gland swelling, hormonal problems, enlargement of the spleen and liver, and anemia. Not surprisingly, with a disease that affects so many systems and organs, Hsto X may be deadly.
This disorder is treated with corticosteroids, which suppress immune function (including the dangerous cells). Radiation therapy
or limited surgery may also be used to treat bone lesions. Patients are also treated with supportive care to reduce symptoms and treat infections that may occur when the immune system is compromised. Treatment may include antibiotics, breathing assistance with a respirator, physical therapy, selenium-based shampoo for scalp problems, and hormone replacement to deal with hormonal dysfunction.

So, how is the family?
It's a balancing act. How to temper emotions against new medical conclusions every day is a struggle, obviously. The regular routine can be a wonderful thing. Tonight the decision was made to enjoy a stir-fry dinner with basmatti rice (a new found favorite for Matt & me) . After Matt & Priscilla bought the rice, veggies & bottle of sauce, Matt called me on my cell phone in VA. They had bought the rice from a bulk container... no cooking directions! So we all laughed as I tried to recall the ratio. I'm sure it was good.



Friday, April 11

I am Rosie... right?!


So we have a lawnmower now, which is great. Ever since my days on the Horkey farm, I was a little petified of having my own house and needing to take care of the grass. Lawnmowers don't like me, they always break, and it's a task like washing the dishes... people inspect your job and the spots you missed stand out real bad.

Last summer there was no rain, so mowing wasn't such a huge deal-- we had benevolent neighbors (crackheads who needed some cash) and we got by just fine.

Since Matt's been gone, the time to mow has arrived. And who doesn't love that smell of fresh-cut grass? So I did a fair amount of it earlier this week and planned to finish last night. Well...

The blasted machine wouldn't start!! I kept pulling the start chord (a whole lot) and checking t o see if I was doing everything right. I called Chris & Bernie (Matt's cousin & uncle); they said that I was doing it right, like the throttle, priming it, safety mechanism engaged. They recommended I "kick it a few times, throw it in the ditch, cuss, then walk away to enjoy a beer. 15 Minutes later, she'll start right up." And wouldn't you know it? I must've put the fear of GOD into our Toro!! HA HA HA Take THAT!

However, my tricep and upper lat are sooo sore from pulling that stupid start chord. What an imbalanced work out. I should have kicked it more.

The funny thing is that I've also gotten a flat tire this week. And Matt took the patch kit with him to NH. So I called Chris that time too. He came right over. I can only imagine if I tried to take on the Explorer!

Thursday, April 10

There's no place like home


John now weighs about 170 lbs, which means he's probably lost over 50 lbs. I think John stands 6' 2'' or so. Even so, the doctor says it's very likely he will be able to return home to Depot Street by Saturday. The blood clot must be almost completely dissolved. He was on 2 different medications for blood thinning. Coumadin was given as a tablet and Heparin through an IV. Matt & Priscilla have set up a mini bedroom downstairs for John and I'm sure he's looking forward to the peace and quiet.

They had some good laughs as Matt & Priscilla tried to persuade John that he had been inappropriately candid after coming out of surgery yesterday. Of course, neither Matt or Priscilla have a good poker face, so John knew they were lying almost immediately. Towards the second part of the day John went through some rough spells of nausea and needed some oxygen, but maintained a positive attitude through it all!

Wednesday, April 9

The "Bobopsy"

General News
Matt reports that when John is fully awake and rested, he is his normal self... jolly, but weak. They've placed an iPOD in his room with all kinds of his favorite music. Both Matt & Priscilla spent most of the day with him and the energy was good overall, though it seems to be an emotional roller coaster. When new friends come to see the family, many get emotional and the tears begin to flow all over again. It is obvious that John & Priscilla have touched many lives while living in New Hampshire, because once everyone has collected himself/herself -- a new well-wisher arrives!

At this point it seems that Isaac will continue at his job in Alaska as planned. He should be back home by the 25th unless he changes his mind, but the money he's making is very, very good. I spoke with him just a few minutes ago & he's thinking that the extra funds will be helpful in these next few months. It is obvious that this was a difficult decision, but he calls in regularly and talks to John throughout the day.

The System Sucks
Matt spent a lot of time today making inquiries into Medicare/Medicaid, insurance, disability, and so on... it was very frustrating. We now understand why so many people desire a national health care system, because the one we've got is "really messed up. I needn't go into details... let's just say that most people are high and dry for 6 months unless they suddenly find themselves in renal failure or a similar fatal condition.

The Biopsy
The oncologist (cancer doctor) says that John's cancer might actually be lymphoma, a much easier form of cancer to treat. This being said, when they operated to get tissue samples for testing, the doctors saw some abnormal growth in one of his lungs. They won't have the results until next week and the appointment with the doctor is scheduled for Tuesday at 2pm. This is when plans will be made and steps will be taken.

Laughter does good like medicine... click on the above title of this post (or paste this link into your browser) for a favorite line from My Big Fat Greek Wedding.
http://www.youtube.com/watch?v=mWispEM3900