Monday, July 26, 2010

7-26-2010

Lord what a night, no sleep at all. Denise said it was the predisone, that I had took it too late. Saturday night I like to not have went to sleep, started in bed and woke up freezing but soaking wet on the couch about 7am. Personally I think small elves carried me in there and bathed me. Now here it is Monday and I wish they'd have knocked me out, lol. I believe that I sweated out a lot of the infection though, other than tired I feel pretty good.

I didn't go again to HBOT and I will not go until I know the infection is gone and I can clear my ears for the dive. I go to Dr Rathfoot tomorrow for a check up, man I hope my sinuses are clear, if not they will give you stuff that will. Stinks but not too bad. I got only two visits in last week. I am hoping that I am done with the treatment. It isn't bad but you never know what mood the doc will show up and that causes stress. I have a problem with people that start a sentence screams look you G.D. S.O.B., then it gets worse. Its like Dr Jekyll and Mr Hyde and the way I figured it so far is that he knows that the people there are at his mercy and I'm sure that God is keeping score, I know I am. That kind of stress placed can reverse or at least detract from the benefit. I should have been doing Vit C. I have read that your body uses more under stress. I guess the law of averages just caught up with me. Look at the excellent doctors I have had so far plus the ones that read this. The has to be a bad apple in the bunch somewhere, sometime. So I really can't complain, I have been blessed.


Its sad really that someone has to be that way. Like the ones before though, I have remained silent on here and at the hospital... but it is hard. It is a shame really, Hyperbaric Oxygen Therapy is such a great tool. One of the few "conventional medicines" I think shows greatness. I have faith in it. I have not only experienced what it can do but saw others benefit from it. Over the course I have remained silent on this about it, I had no other choice. Usually Chad or John dive and both are compassionate and caring. Credits to their profession. I actually don't see how caregivers keep a heart as much as they see, and some don't, but these do.

I am slowly starting back my herbs and vitamins now, being careful as I don't get choked on them. It is getting easier. I still plan if all goes well to restart all the herbs plus the one that I am sorta leary of, the B-17. A friend on CC turned me onto a website that is pretty good. There is a therapy there that bears looking into, I've read about it over the years on other sites. I plan to look it over. It is at http://doctoryourself.com. Not that I will not walk away from this care but add to it. I have had too many kin folk die of cancer after they thought it was gone, too many. If mine is gone, I will still go through for prevention.

Friday, July 23, 2010

7-23-2010

It has been a long day, a painful one. I did finally get the oil changed in the truck and the cucumbers and some tomatoes picked. Rather than taking them to everybody I had them come and get it. I did get the chance to browse the web and chat with my friends at ConCen.

I should be down to one of the last few patches and so I am taking the advice of my friend Kim. I will wear these last 2 patches an extended day each and follow-up with pills for a few days then my system should be weaned. There is a lot of pain that shows, more than I thought was there. Not that I'm into pain but before I ate and swallowed whatever and whenever with occasional break through pain, thing is, it masked far too much pain. That allowed me to eat and do whatever and that ain't a good thing. It isn't the mountains that wears one down, it is the hills. I knew when I done really bad but not when I done bad... I do now.

My neck is hurting on the outside more than the inside after a few minutes unprotected in the sun. The sun has become my enemy with this and yet is my friend with the Non Hodgkin's Lymphoma. Speaking of which, the ones that read this please remember my good friend Sally tonight who is hurting and say a prayer for her. She is one of the sweetest, smartest, strongest people I have had the honor of calling friend. If one reads on CTCL it looks like a walk in the park, but in reality it is far, far from that. I love on one board when someone says they are hurting and the doctors say they are not. It is by the Grace from God that the roles aren't changed.

I finally got some meds for my cold today that Dr Rathfoot called in. It has taken from last Friday til now, but at least I have them. I've suffered some with this cold but this is life, I've seen a whole lot worse times and I'm sure I will again. I have an appointment with him next week and I pray that he will say good job. I grow tired of this battle.

Thursday, July 22, 2010

07-22-2010

I still have some kind of bug I caught off mom so I haven't been to the HBOT treatments since Wed. I feel like crap, just drained on strength, head stopped up and ache all over. It reminds me a little of Chemo but not the bad days, the good ones, that depresses me a lot. So I have once again been inside the house doing nothing and sleeping on and off. Since last Friday we have tried to get a hold of Rathfoot but to no success. This is the first time he has dropped the ball. Tomorrow will be a week and still nothing as this stuff gets worse and trys to go on down in my respiratory track.

I am so over being helpless in so many areas, I would love my independence back. Next month will make a year for this to be going on. I have had enough already, enough for 2 lifetimes.

Wednesday, July 21, 2010

07-21-2010

I stayed home today due to an infection in my sinuses and ears, both were stopped up and I felt like crap. Tomorrow I will stay home again just to make sure this stuff leaves even though I feel a little better tonight.

My right shoulder is acting up, I think the tear I did 20 years ago has torn again, either that or I've injured it again. I will wait until all this calms down and then maybe go for a shot into the shoulder and see if that helps.

My neuropathy gave me a fit today even though I kept off my feet and kept them elevated... strange. My throat seemed a little less painful today after I woke up, but then again I didn't talk much today. It still isn't too bad. I think if the saliva glands would start to work and this sinus thing would quit, and the reflux stop I might have a chance to have a voice.

August 9 is still in the back of my mind though. I look forward to it yet at the same time I can wait. If they give me the all clear I'm buying a boat, a cheap fishing boat... and I mean cheap, lol.

Tuesday, July 20, 2010

For My Family and Friends



07-20-2010

   I awoke decent today but in a lot of pain. I think I may be getting mom's cold and just my luck, it is in the respiratory and sinus region. For the last few days I've felt rough. The hissing, like an airline is leaking, and it is loud has came back. HBOT was one of the hardest yet, I was already about to throw up before I got there and it got worse as we pressurized. Thank God it was a good movie, Cinderella Man. I would not have watched it on my own but it turned out to be an excellent movie, one of the best ones I have seen and it helped me to focus. I almost asked several times to come out.

  Me and Charlie ate and discussed his upcoming heart cath, I think I filled him in pretty well, had a bunch of those, lol. Nobody was happy that I drove myself down yesterday, but I made it. The Chemo has left me where I fall asleep, almost like pass out easily, but I know the warning signs. He will be absent when he has his heart cath and I plan to drive myself then. far to long have I been a burden.

  I slept today after I got home and tonight I will have no problem sleeping more. Again I meant to change the oil in the truck and again it didn't happen, lol. Maybe tomorrow. My throat is so tight inside tonight it is hard to breathe and enough break through pain I resorted to about 10mg of Morphine. My God that sounds like a lot yet it barely eases it off. I think I will be in for a Hell of a ride when the patches come off.

  I still get frustrated that I cannot do what I want and what I once did. How is all this junk suppose to get done? How did I do it all before? I failed at doing all the gardens, I was in hopes that I could do enough so that if this is my last season everybody would have plenty of food stored. One thing is for sure, they all have eaten Tomatoes and Cucumbers till they were full. At least they will have enough seed for net year and some to share if I am not here. We will find out August 12th if it is gone or not. I pray it is for I could not physically, mentally, or emotionally withstand any more. If it ain't, I pray I go fast.

Sunday, July 18, 2010

07-18-2010

  I woke up this morning about 10am, took the barrage of pills I have to take, then went right back to bed. I didn't get up again until 5pm. I had planned to pick the beans, tomatoes, then change the oil in my truck...didn't happen. Mom has a cold and I may be getting a touch of it. I ache all over.

  My right shoulder is going out. I tore it about 20 years ago and it healed, maybe I built up muscles to compensate for it like I did my left. When I woke up both times my mouth was covered over with something that felt like glue but tastes horrible. It takes forever to get that junk out and then getting it out of my throat is almost impossible and painful. Afterward though it feels better.