Posts Tagged ‘alternative cancer clinics’

Well I was going to post about my first chemo week last week or over the weekend. But it got a little wacko last week, so I just didn’t get to it. So I began my IPT last Monday and had twice, on both Monday and Wednesday. Here, I am getting a nasty four-drug cocktail of 5FU, epirubicin, cytoxan, and gemzar. The first day was a little rugged while I was in the hole. I went a little too low. My heart was thumping against my chest and I was sweating up a storm. The real downside was that, when I was doing this before, when I was given the green light to eat, I could solid chow down. The only time I was really able to chow down. But not this time around. That was a definite disappointment but oh well .. maybe Wednesday would be better.

Or not. Tuesday I had received a bag of amino acids, then went back for chemo on Wednesday. I was already just feeling a little down physically. I was given my insulin and settled in for the ride. About 20 in, the nurse asked how I felt and I said I was probably 5-10 out and she said I was getting that look. So they checked my sugar and it was in the 60s with one glucometer but they didn’t believe it, so they used a different one and sure enough, my sugar was in the 40s. Needless to say, the other glucometer went in the garbage that day. So they administered my chemo drugs but that push takes quite some time. So down I went … like a rock! Damn but I was panting, sweating and my heart was ready to come out of my chest. All I could do was just sit there with my eyes closed and try to just breathe through it. The nurse kept asking if I was OK and I just nodded. When it was time to eat, I drank juice, ate some fruit, and thought I could eat some deviled eggs. Nope, too dry. So I proceeded to drink an Orgain and that felt like a fist in my stomach. That was it.

That day, I didn’t get my insulin until around noon and I was fasting. I also declined my dexamethasone because it messes with my vision. This was something I may never do again … refusing dex. I was done eating by around 1:30 but I never felt right the rest of the day. There were two things I did, that day, that I don’t usually do. There was this energy guy there who can actually create magnetic fields with his brain. He is from the N Georgia mountains (re: Deliverance … honestly … claimed to have gone to high school with one of the Dueling Banjos boys .. yikes!) and he is actually measurable. He has been heavily studied and he goes up to Duke once every other month to knock Lyme disease out of folks. Anyway, he put the palms of his hands about an inch away from the bottoms of my feet, with my shoes on, and the soles of those feet heated up immediately. He jolted me a few times and then there was a guy selling these machines called Theragem and he put that over my brain and my spleen for a bit.

Later, at home, boy did I get hit! I was freeeeezing and sweating, dry heaving, nauseous, feverish, YUCK! It dissipated during the night and when I woke up, I only had a headache right between my eyes … but the next day, it was time for my liver biopsy which was anything but smooth.

My showtime was 10am and it was, of course, fasting. What I didn’t realize is that my biopsy wasn’t supposed to occur until 1pm. And what actually transpired was it didn’t happen until 3pm. Fasting. And, true to form, my blood pressure was low … very low. I was dehydrated and have been for weeks, so they would not sedate me fully due to the blood pressure. This wouldn’t have been so bad if they only needed one sample. But they needed six.. OMG, I was raising hell and whining like a little girl! Finally it was over, but with so many sticks, they then had to observe me for four hours for possible bleeding. Didn’t get home till 8 or so.

So now those samples go to pathology to determine estrogen and progesterone receptor status as well as Her2neu. They also go to a lab called Caris for some genetic determinations of which chemo drugs will, or will not, work for me. Let’s hope the drugs I am on will match the ones I need to be on. Along with all this, I started getting my cold again.

Today, I got my bag of Vit C after deciding not to do chemo today because I just didn’t feel well all weekend. I got labs drawn today, so without knowing if my body was able to handle it, I just didn’t feel comfortable. Now I am back at the room and lying in the bed, exhausted. I am still getting weaker because I am still getting skinnier … losing more muscle. So now I am on the hunt to resume TPN because, without the fluid I am carrying, I am betting I am about 110, which is way too thin seeing I am not looking for a new career as an old, wrinkled supermodel.

So we will get lab results in a couple of days and hopefully all this discomfort is about cancer dying; not cancer winning. Boy, has this every been a ride y’all! And obviously, it is not over yet.

On a better note, this weekend I got to meet with yet another Southern cousin … this time from my mother’s side. I have only met him once before as a teenager. It was wonderful spending time with him and his wife. Here we are at the condo.

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My first day at Progressive. Got off to a little bit of a slow start because I was an unexpected add-on to their schedule this week. But the vibe here is so wonderful that I couldn’t have cared less! Before long, I was escorted back to my first Hyperbaric Oxygen Therapy (HBOT) session. I spent an hour in the chamber. I guess claustrophobic folks might have trouble with it, but it was much more spacious than, say, an MRI or CT scanner, but it is totally enclosed. There was enough room to where I could almost sit up, so it didn’t feel too enclosed. It was much like being in an airplane in that my ears popped while we were starting up, much like an airplane taking off. Same thing when we were done. Quite nice, really. I just plugged my earbuds into my iPad and listened to Darlene Zschech and had a wonderful time.

When that was over, we were served lunch. The organic chef was wonderful. She had a chicken-based veggie soup on tap and since I have such a hard time with food repulsing me when it’s in my mouth, she pureed it for me and it was so good. I was so happy that, though I couldn’t eat much of it, it wasn’t stressful for me!

Then I went back for my first IVC with them. It was just a small bag, but we will up that probably tomorrow. They had planned for me to have an ozone sauna but then we realized that since my port is going to stay accessed for the week, I couldn’t get in a sauna at all due to the sweat. Can’t get moisture behind that tape. So we figured we could sauna me first thing on Mondays and last thing on Fridays, before the access me and after they de-access me. They wanted three times a week, but two will have to do. Those port needle sticks hurt. And though we could spray some stuff on it to numb it, not real sure how well my skin would hold up, in that one small spot, being accessed all week and stuck 3 times each week. So no, we won’t be going that route. Not as big a wussy as I am!

One of the times I was taken to a different area, the gal was helping me get settled in. I was getting ready to hang my IV bag on the hook and she stopped me. She said I need to slow myself down and let her do it. I started laughing and told her, shoot, I had been traumatized for the past seven weeks where I had to fight for every little thing and hope to God they had it right because I saw them making mistakes all around me all the time. And lest you mistake, that wasn’t because the nurses didn’t know their stuff. It was just that the word had not been passed from on high in time for the nurses to get it done. This place? Oh no. They’re all about keeping you comfortable and keeping your stress levels down. Everyone there just goes out of their way for the patient.

I think it’s so cool that this miracle came through for me and my friend on the week before Jesus took that beating and those nails in His hands for my healing, as well as everything else. How perfectly timed is that? Might not be for everyone, but I love the fact that there is worship music in the infusion room … works for me!

I didn’t really get to look at my protocol today, but I’m supposed to tomorrow, so will have more of a feel what my weeks will look like. So tomorrow I get an IV first thing and we go from there. One of that gals I met at that other place was having just as much trouble there as I was and they weren’t even cutting her a good deal, so I encouraged her to at least have a look at the place. She did last Friday. She was there for treatment today! I had told her it was night and day different … she disagreed. She thought that was an understatement! So here is me in the HBOT chamber this morning. Not a great shot … was a bit dark in there … but hopefully you can see my happy smile!

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