Archive for the ‘ Personal Stories ’ Category

Yes, Chemotherapy is Evil ;)

Every three weeks I hope my chemotherapy session does not land me in bed. Every three weeks it does. I call it my “Crash” time. I don’t feel so bad that I can’t have my laptop and type, though. I still ran some ads for my business, still got my granddaughter out of bed and spent an hour with her. I forced myself to get up and drink my coffee on the back porch amidst the flowers until it got too hot. I had to take a nap afterward.

I may look like hell, but I’m still smiling. It’s not that I think I am exceptional, it’s just that I refuse to let it win. Besides, one can only watch so many Lifetime movies, or do so much to keep up with the Kardashians ;) I don’t even like television, really – there are too many other things to do in life.

It’s funny too, I go read all the Facebook updates from my friends since I have been away. The whiners are still whining. “It’s so hot out”, “I don’t feel good” they say. Are you kidding me? I’m not being mean, just real. I wish I could spread a little zest around, help them see how fortunate they are to have the (“crappy”) health they have. Come lie with me for three days honey, I’ll make you laugh :) The thing that bothers me most is these comments are usually from my daughter’s friends – my “adoptive kids”. They’re 20-something and feel bad. One in particular is pregnant. STOP THE PRESSES! She and a million other 20-somethings! Suck it up, baby. Wait til that child gets here! LOL

I think most folks just don’t understand chemo – I mean, it is pretty frightening! They think you get these intravenous drugs for a while, your hair falls out then grows back, then you either go into remission or die. Welcome to Limbo! Sometimes you are lucky and just have chemo for years, like me.

But alas, tomorrow is always another day! I sure wouldn’t want the alternative…… So I’ll continue to lie here every three weeks, reading how crappy others feel, smiling and hoping. Hoping the next time is only as bad as this time.

Stephanie :)

Day 8 on Immunocal

The pain in my back and legs is definitely subsiding after eight days of taking Immunocal. Whew! Hopefully I was right and the product just takes time. I felt fine all day, with plenty of energy and mental clarity. I was taking about 800 mg a day of Ibuprofen to supplement the prescribed pain medication I am on (Percocet 10/325), but yesterday I only took 400 mg at bedtime. I have not taken any so far today :)

Thursday June 10 is Chemo day. I may or may not feel like being online in the day that follow, but will continue to drink my Apple juice Immunocal cocktails. I will keep you posted on my progress.

Steph

Day 5 On Immunocal

After five days of taking Immunocal, I have to say it tastes great! I mix it with apple juice and drink it every morning. So far the only effects I am experiencing are some increased pain in my back and legs, my problem areas. I am hoping this is the product at work, attacking the spots on my bones. I will continue to take the product and make regular updates regarding its effects and my progress.

So this is what all the hubub is about….!

Howdy and welcome to my blog. If someone had
told me someday I would have a “blog” when I
first got online in 1998, I would have told them
they were crazy. Heck, if you told me last year
I would be blogging in a year I would have told you
the same thing. But alas, here I am. Writing a sort of
personal journal for anyone who wants to read it.

Actually, I am now a “Blogger” for purely selfish
reasons. I am blatently promoting myself,
Stephanie Remers. I want to be rich and famous, so
this is the first rung on a very high ladder I intend
to climb.

In the process, I hope those who read my blog may
find a bit of information, a bit of humor, and
a whole lot of hope.

So why not start things off with a bang? This is a video
of me in Las Vegas at a Marshall Sylver
Turning Point Seminar EATING FIRE! Enjoy!