Hi Everyone, I am guest blogging on my Mom's site because I just got back from Tijuana where I got to spend a few days with her.
And you are in luck...I am quite detail oriented. I know you come here looking for details, so let me paint them for you. But first...a little 'snapple fact': Did you know that you could feed the fish on the right hand side of this blog? Just put your mouse over the fish tank and click to drop in some food. The fish will happily eat it up.
Ok, back to the big show. I arrived in Tijuana on Friday and walked across the border to THE WILLIAM HITT CENTER where my Mom is being treated. She was just finishing up her daily IV therapy and she was quite happy to see me. I was quite happy to see her and that beautiful smile of hers. She certainly seemed to have some energy and quickly ordered me back to the waiting area to introduce myself to Ruth, who is also staying at SADIES and being treated at the HITT CENTER.
Ruth is a fantastic person, and I am so glad that she and my Mom have connected and are sharing this experience. Ruth is in her 70s and is from Mendicino (where Mike and Tanya got married). This is her second time at the HITT CENTER. The first was for breast cancer (she has no cancer cells in her body any more and attributes it to her treatment at the HITT CENTER), and now she is back being treated for Lyme Disease.
Anyway, my Mom and I went in to see her Doctor, and check to see if she needed any changes to her medication. She did need some adjustments, and the Doctor looked at her slide (they swab inside her nose to look at a sampling of her cells) and seemed pleased that she was heading in the right direction. He remarked that she had inflammation. He felt that was a good thing, though I had always heard that was bad. He told us she came in here with no activity in those cells and they have been trying to get them to show some inflammation for the last week. I am positive the Doctor knows better than I do, so I did not question that part any further. We asked how long he felt she would be in treatment for. He started looking at his calander and doing math. I was quick to point out that we were asking for an approximate date considering that we are looking for a cure, and not a cancer management strategy. He let us know that there is indeed a difference, and told us she should be in treatment for at least 6 weeks. This places her at a return trip to Marin in Early March. Well beyond the time frame she desired, but well within a reasonable limit. We are curing cancer after all. I am sure they will continue to monitor her and send her home early or keep her a little longer if things look like they are changing from our scheduled healing.
After the meeting, we shuttled in their regular taxi (driven by a nice man named Hector who picks them up both ways each day) and got to SADIES BED AND BREAKFAST. The place is amazing. It's large, comfortable, elegant, and filled with warmth and love...two things the hotels can not offer. The proprieters of SADIES are really looking out for Carol, and make sure she is comfortable and well fed. They prepare meals that are not only delicious, but also fit in with the specialized diet she is on...though I did catch her cheating once, and as my 4th grade teacher, Mrs. Smolski would say: 'Shame Be On Thee'
I was delighted to see how much energy my Mom had gained. Surely she is not back to normal speed, but someone finally kicked the clutch in from these last few months. My sister in law, Tanya, had been staying with my Mom the better part of the week, and she had warned me that my Mom's energy was very low and that her body temperature was extremely high. Well, this day, we walked four flights of stairs and talked to everyone in the house without wearing down. The coughing was still there, but so many other things had improved.
Time for her to change her medication a bit, and by morning her body temperature had returned to normal. When Tanya was there, the house was freezing (there was a real winter storm). Everyone wore their jackets inside, except Carol who strolled downstairs in a short sleeve t-shirt. But not this morning. Breakfast was served while Mom wore her parka. More evidence that she is reacting to her perscribed medication, as this was an obvious reflection in the change she made the night before.
The thing about this treatment, is that each day builds upon the last. This is why I was not happy when she took a week off for a trip. But now, just a day after Tanya saw her with no energy, the time came for her body to start reponding, and it really did.
Napping is still an important part of the day, because her body is working so hard to heal that it is just exhausted. Forcing it to stay up when it really needs to refresh is not wise. So Carol is very diligent about making sure she gets the rest she needs.
On this second night of my visit (Saturday) something really cool happened. As I saw my Mom sleep during her nap, I noticed she was sleeping on her back. That may sound very small to you, but for the last 4 months she has only been able to sleep on her left hand side curled up in the fetal position. Anything else would have her coughing up a storm. This fetal position on the left was the only thing allowing her any peace. We talked about it briefly, and sure enough, this was the first time she had slept on her back. When I woke up in the morning...the sight was even better. Carol was laying on her RIGHT side! This was also a first, and another wonderful sign of changes happening in her body.
There are still some challanges, though. The Candida diet is strict. It is a hard diet to follow, though very important. My Mom has lost a whole lot of weight (and you know she did not have a lot to lose in the first place). It is critical that she puts some weight on...but this is not a diet that is accomodating to that. It is a very lean, very healthy diet. It also contributed to a heavy round of constipation for her. This would be very uncomfortable for anyone. For someone in my Moms condition who must conitinue to consume nutrients even though they have no room for it...it can be quite unbearable. But she is trooper and handling it better than I could.
Some of the meds can also cause Nausia. So each day is a balancing act. But thankfully, we know she is on the right track, healing with the right doctors, and relaxing at the right place.
Carol, as most of you know, is a care giver. She is always taking care of people, taking care of problems, and taking care of 'stuff'. If this cancer is a wake up call for anything...it's that she needs to take care of HERSELF first and foremost. That's the one positive about her treatment being far from home. She is not distracted by 'stuff' and she is finally allowing people to take care of HER. And that's awesome. The Doctors look after her medical regimen and the people at Sadies make sure she is relaxed. So there is no guessing at this game.
Once healed, she will continue to check in with the doctors every few months to evaluate her progress. So when she gets home, its even more important that she is eating right, having fun, and taking time for herself. Sounds like a perscription we should all follow.
Sunday, January 24, 2010
Tuesday, January 19, 2010
Day 2 - Tijuana
Tanya and I made it successfully down to San Diego in the wee hours Monday, January 18th. Sonia, the soul of Sadie's Bed and Breakfast, met us at the airport and took us to Tijuana, and then waited in the car for an hour so I wouldn't be stranded at Dr. Hitt's Center before it opened. Tanya continued on with Sonja to the B&B, and unpacked all my stuff for me.
So now I have completed my second day of treatment. Ozone and IV Vitamin C. Suddenly I have some color in my face and a bit of energy. Not much energy, but enough so that I don't immediately have to take a nap.
My supplements have changed. No more liquid zeolites, now I have liquid copper and liquid paladium. I'm up to the second phase of candida supplements.
And each day, my cough changes and my symptoms change. I'm still coughing, but today it is not hurting, and very little phlem is coming up. And thank goodness, my constipation seems to be over!!
Thank you all for the wonderful birthday greetings! Sonia made a desert and put a candle in it for me to blow out, and then I passed the desert to someone else at the dinner table.
Tanya is appreciating the B&B, and checked out the open air market with Sonia on Monday. And doing lot's of reading. She has signed us up for a massage on Wednesday afternoon. Sonia has a massage room and a facial room in the B&B, so now all she needs are more clients, and a bit more help around the B&B to keep up.
Tanya leaves on Friday, a direct flight on Volaris airline from Tijuana to Oakland. Seth comes on Friday and stays for the weekend, and then George will fly down on the following Monday.
Thank you for all your support! Love, Carol
Tuesday, January 12, 2010
Florida family reunion
Dear Family and Friends,
Florida is wonderful. Not warm, as it is experiencing this cold snap for the first few days we are here, but friendly.
My brother Norton, my cousin Barbara and husband Paul, and George and I are here visiting cousin Patty and her sweetheart Larry. We have seen Gert, my alternate mother, and Marcy and Jeff and the kidlets.
And Patty has turned somersaults to be sure that I had organic foods and bottled water and all the things I need for my new restrictive diet.
For those of you that I have been whining to about my constipation, I am still having some problems, but am no longer in pain. And I am sleeping well here.
Norton, Barbara and Paul all returned home on Sunday, so now this week it is Rest and Relaxation (and Eating). We played Yahtzee last night, and Patty won 2 out of 2 games, with a Yahtzee in each game. We went to a flea market (an annual treat for me),
We leave on Friday, and meet up with my sister-in-law Ellen, who is staying over in San Francisco just to see us. She and I will go to see Darcy and Terry and children, and then she leaves on Sunday to go back to Boston.
And I return to Mexico early Monday, with Tanya, so I can resume treatment.
Life is good! Thank you, Patty, for taking such good care of me!
Love, Carol
Tuesday, January 5, 2010
Coughing substantially diminished!
Yowsa, Yowsa!! After my first treatment on Saturday, I was doing some mighty fine coughing. And then on Sunday and Monday, the coughing was much less. Significantly less!
Yesterday, after my treatment, I came back to Sadie's B&B and climbed into bed and napped until dinner, ate, and then went back to bed. Today I came back and went up to the patio to eat my lunch, and here I am updating my blog. The bed is in front of me, but is not calling to me. Another Yowsa!!
So is it the candida diet? the supplements? the liquid zeolites? Sonia's cooking? the auto-immune vaccine I get shot in the butt with every morning? I don't kow the answer, but I do know that I am very happy - sure that I am at the right clinic and at the right place to be staying. I'm so pleased with the changes!
I have 8 supplements: a liquid, sublingual drops, drops to put in water, pills to take on an empty stomach, pills to take before meals, pills to take in the middle of meals. And more to come...
I'm not answering phone calls until after dinner these days, just out of priorities, and not responding to very many emails. I'm just in major gratitude. Thank you, G-d!
And thank you, Family and Friends, for being there and supporting me. I love you all very much!
Love,
Carol
Saturday, January 2, 2010
Happy New Year from Tijuana
Mike and I flew down to San Diego as planned, and just as planned met Seth, who had driven down from Los Angeles to spend New Year's Day with us. We arrived at noon, and went directly to our motel, so I could lie down for awhile. Then we went for a lunch foray to a good Thai restaurant, came back for more Carol's rest time, then went to dinner at Souplantation and had great make-your-own salads. Then back to the motel for more Carol's rest and to be lasered. Watched a movie. I had no energy.
Saturday morning we repacked our things and took the motel shuttle across the border to the William Hitt Center. They gave me an Ozone treatment (take 1/2 cup of my blood, add Ozone, then give it back to me), then 1/2 hour of waiting for the ozone to circulate, then an IV drip of vitamin C. We waited around to talk with Dr. Humiston, talked about their treatments, did a bit of muscle testing on supplements (I only need one of the many supplements that I brought with me), and left with 3 new supplements and a candida diet. Well, a modified candida diet that seems to allow pasta and flour tortillas. hmmmmm.
We had called for a shuttle, and Hector appeared with his taxi to ferry us around. First we stopped at the bank for some pesos, then to a taco stand for lunch (2:30 pm), then to Sadie's Bed and Breakfast.
Sadie's is beautiful. There is a fountain area outside behind the dining room. Our room has a jacuzzi bath tup and a nice shower head. We have wireless internet service.
For $15 more per night per person, they will serve dinner. We had an exquisite cream of vegetable soup, followed by a salad, and then a steak, brown rice, and asparagus with slivered almonds. Delicious!
Dear ones, I'll keep you informed. I don't know whether I am crashing out of energy or having a nice energy period. We'll see as it unfolds.
Mike leaves very early Monday morning, to go back to work. We have a free day tomorrow. Sadie's doesn't serve dinner on Sunday, but they said that there is a really good Japanese restaurant nearby. So we will plan to go there.
Happy New Year to you, and our wishes for a very healthy one as well!
Love,
Carol
Wednesday, December 23, 2009
Decision is made... Tijuana on Jan 1st
My last post was about the pressure - oh, the pressure.
A compromise has been reached. I will fly down to San Diego on New Years Day, meet Seth to celebrate the day, then start William Hitt's clinic in Tijuana on January 2nd. I will continue there through January 6th, and then head to a San Diego airport hotel for an early start on my planned trip to Florida to play with my cousins and brother and aunt. I return to California on Jan 15th for a fast 2 days, then fly back to San Diego to resume treatment on January 18th.
I'll be staying at Sadie's Bed and Breakfast in Tijuana, which looks like it is pretty and has a swimming pool. Seth will think about joining me for the first week if he can and if he needs the healing.
So the healing journey continues.
I felt really good today, so of course I wore myself out. And now at 7 pm I feel exhausted. Tomorrow is Christmas Eve at George's family, and then Friday the family will be at our house. My kitchen is looking great, and everything but the doors are in place. We're starting to drop things into drawers and get more organized, but we have so much Stuff! Wow! We are kitchen Stuff collectors!!
Have a wonderful Holiday, and a very healthy and happy New Year!
Love,
Carol
Tuesday, December 22, 2009
The pressure is on
Dear Friends and Family,
Had my very first ever transfusion on Monday, December 21st. I "pinked up" right away, and today I have much more stamina. I should have done this a week ago, when it was first offered!
As my strength has been improving, I'm being more attentive to the doing the things that support my healing. I am pretty faithful about the 1 hour in the morning and 1 hour in the evening on the Q1000 laser, and have not missed my Essiac tea. I'm up to 15 drops, 3 times a day of the liquid Zeolite, I'm taking amino acids and extra l'arginine, proteolytic enzymes, and all my vitamins. My green drink is including chlorophyll, colloidal minerals, and spirulina. We're juicing the carrots and having that regularly. Also young coconuts, which are so refreshing.
Although Bill Henderson's book "CancerFree" says that the CA125 marker will go up with cancer die-off, as well as with cancer increase, that does not seem to be good enough for my boys, Seth and Mike. I am getting a lot of pressure to take additional action, especially to go to the William Hitt center in Tijuana or the Burzynski clinic in Houston. I am not happy with the Burzynski clinic, so it is the William Hitt center for me. The question is timing.
My preference is to enjoy the holidays, go on our planned trip to Florida to see my cousins and brother and aunt, and then to return, and leave on the 18th or 19th of January to begin the William Hitt treatment.
Seth is pushing for immediate action. From looking at the calendar, this means flying down this Saturday or Sunday to San Diego, starting William Hitt on Monday, Dec. 28th, having 7 days of treatment before returning to Oakland on January 6th, so I can join George and fly to Florida as planned on January 7th.
I say that I am feeling good. Seth says that the blood tests and the CA125 marker are not good. Who knows - my next entry may be from Tijuana and I may miss the rest of the holidays...
Love to you all,
Carol
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