Showing posts with label bipap. Show all posts
Showing posts with label bipap. Show all posts

Sunday, March 6, 2011

Re: Bipap- READER QUESTION

I get lots of questions in my email, and I am going to start being better about posting them as an FYI...
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On Sat, Mar 5, 2011 at 11:59 PM, Tess wrote:

Hi i was wondering if you had any advice on choosing a bipap mqchine.  Or living with ot!! Im going to jave to go on one soon andbrememered that.you had used one

Tess


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Yes, I used a bipap for about a year prior to my transplant, and though it was hard to get used to, once I got used to it, I loved it!!! I don't really have knowledge of a lot of different machines, they are all pretty much the same, I think. I used a huge one at the hospital and a tiny one at home, and really the only thing that matters is the mask, that you get a size that fits well and that you adjust it til it is tight enough to make a seal but comfortable and not pulling at your neck.  If you doctor recommends one, I would go ahead and do it right away. You will sleep much better and the rest will be good for your body!!!
--
~Beth

Friday, July 2, 2010

40,000 UNIQUE VISITORS!!!!!!!!

40,000 unique computers
and probably human beings
have viewed Cystic Gal!

I am so very grateful!!


Statcounter tells me that the 40,000th UNIQUE READER was from

Newnan, Georgia, United States

CONGRATULATIONS, NEWNAN!

I feel compelled to, Seinfeld-style, also say, Hellooooo, Newnan!

Please also enjoy my new fave-o banner image from my first dry run. Now that's one casual sexy foot that's ready to give it a-go again!

xxoo, cg

Monday, May 31, 2010

Rock Star Lifestyle ... or Outfit

One of the only perks about being out of work right now (other than that I keep getting better and preparing for my transplant, ahem . . . ) is that I can feel the little voice in my/your/one's mind that says, "Am I dressed conservatively enough for work?" "Does this outfit look professional?" or "Do I need to add a sweater to this?" slowly dying away. I am using this time of my life to embrace the rock and roll fashions that I have always admired.

(But, you know, don't have crazy expectations)

Thursday, November 26, 2009

Cluck Cluck Says the TBird


Ho Ho Ho! Merry . . . Thanksgiving!

2 lists: My personal Top Ten List of Things to be Thankful For, and
My CF List of Things to be Thankful For

Ten Things I'm Thankful for This Thanksgiving:

1. My family! They are truly always there for me. When I need them, they literally come running, flying, driving to get to me. My Dad would move a mountain to help me and my mom would beat up a WWF wrestler with her bare hands if she thought is was necessary for my health. My brother and sister are the best humans on the planet and accept me in all my different ways of being.

2. My friends! I am blessed to have a lot of friends. I am even further blessed to have a handful of friends that I feel so close to, I feel that they are family. I have been directed toward people who fit with me, and I seem to fit with them, from the moment I meet them.

3. My cats! I don't care who thinks it's silly, my cat Beckett has been by my side for 10 years. She has often been the only one with me in some very dark times, and she has also been with me during times of great joy. She literally helps me get out of bed every day and is a big inspiration for me to get my transplant, get well, and come home. My 2nd cat, Samuel, is also a love bug and reminds me to live more cautiously (as he is afraid of most... everything.)

4. My career as a drama teacher. When I was a kid growing up, because I had read Alex: The Life of Child, and then because I lost a godbrother when he was in college, and then because it became easier to read medical studies online - I, like most CFers, often thought, "maybe I'll live 'til I'm ____." There are many days when I'm driving home from rehearsal in my car, to my home that I rent with my very own money, to cook dinner and watch a show and etc. - that I am amazed that I have made it so far in my career and with my life and that I'm like, "Hey wow, look at my life. I live here. I'm doing this! Cool." I am thankful that all the things happened that brought me here.

5. My writing. I am grateful that writing is an outlet for me, for the better or the worse and that all of you people are willing to read it whether its funny or not, complaining or not, swear words or not, poems or not. Yesterday I found my blog mentioned on a site listing inspiring blogs for Chronic Illness and for a moment I thought, "Really?! All I do is bitch and moan on my blog!" -so I'm grateful that all my bitchin' and moaning and some jokin' is inspiring :)

(Ok, the next 5 will be more practical thanks...)

6. I am actually ironically grateful for my BiPap machine that boosts my energy and is allowing me to be at home and not in the hospital.

7. I am grateful for the Jelly Belly Jelly Beans that my friend E-Teach brought me.

8. I am grateful for Pudding Packs that I consume daily.

9. I am grateful for text messages as they are my fave mode of communication during this pre tx time. No talking!

10. I am grateful for my penguin flannel pajamas that CysticMommy bought me.

My CF List of Things to be Thankful For
(some overlap)

1. My BiPap Machine
2. Prilosec
3. TOBI
4. Pulmozyme
5. My great doctor, Dr. U-Bird and nurse N-Pregg
6. My great social worker, S-Happy.
7. The treadmill I saved to buy that allows me to exercise every day.
8. Prunes.
9. Gatorade
10. NAPS!!

What are you grateful for? Happy Thanksgiving! Have a great day!!

Love, CG

Saturday, November 21, 2009

Health Update and Fun for BiPap Use


So things were sorta complicated this week, as I had two good sessions at Physical Therapy and was doing a good job of home exercise and meds and all that, as well.

Now, remember that when I was in the hospital in October, I ended up in the hospital because of hypercapnia, or high carbon dioxide levels, that were causing me to have severe headaches, delusional and illogical thinking, and a desire to sleep all the time (which compounded the problem). Eventually, this caused acute respiratory failure and I had to spend 5 days in the ICU reducing my CO2 levels using a BiPap machine, or assisted ventilation, to help me breathe more deeply and also clear my "used" air completely so that my CO2 levels would lower. I have continued to use the BiPap machine at home.

Okay- so then this Thursday, at Physical Therapy, I started to get the CO2 headache during exercise. The headache is a very specific, sudden, painful kind of headache that usually wakes patients up from sleep (like it did with me). It was striking me during exercise, which is odd. I went to the doctor that day, and my CO2 level had raised in one week from 63 to 86- not good, and most likely responsible for my headache. So oh no!

To see if this was a fluke, Dr U-Bird let me go home for a night and come back on Friday to see if my CO2 level went up or down overnight. Thankfully, it had gone down a bit to 75- good because the BiPap helped it go down, but bad because it showed that overall, my CO2 was increased from the week prior.

So there was a big debate and I was allowed to go home for the weekend with a change to my BiPap settings, to make them stronger, and with my CysticMommy to pay diligent attention to me. I will repeat the test of my CO2 level next week.


In the meantime, my oldest friend, S-Artee, is here visiting! I am supposed to stay on BiPap "as much as I can." Oh no! S-Artee is my very best friend for 29 long years, and I haven't seen her in at least 5 years. She is here to spend wonderful time with me!! We were, you know, planning to TALK during her trip. One problem when you're on the bipap, is that it is hard to talk through the mask. It is possible, but you have to talk really loud inside the mask, to be heard at all outside the mask. This is one reason that I burnt my voice out so badly in the ICU. I did not realize that I was yelling inside of the mask every time I tried to talk to someone, to project my voice through the airtight plastic.

This brings us to the weekend's theme: Fun on the BiPap. One fun thing you can do on the BiPap that involves little talking, is joke-telling.

Exhibit A: WARNING: This video contains cackling.



Exhibit B: WARNING: This video contains me wearing the BiPap which increases the pudginess of my face:) I am not this pudgy-faced in real life. :)



YAY!! Tell a lame joke with your best friend today!!

Love, Cystic Gal!

PS. I also have uploaded another video to count for yesterday's post. See below!

Monday, November 2, 2009

Thoughts I Wanna Get Down Before I Forget Em:

Being in this stage of illness is so strange. There are a lot of adjectives that go along with it. This stage of illness is sad, and maddening, and overwhelming- but most of the time for me, it is just slow, and strange. I know that I have moved very quickly from "severe lung disease" to "end-stage lung disease."Every article I read about my symptoms is about "end-stage" lung diseases. I wait for a transplant because without one I will not live. On the one hand, I logically understand that. But it wasn't until this month in the hospital that I got any experience with this word, "dieing" as it pertained to me and the body I live in now.

What I know now about my point of view the weekend prior to going into the hospital is that I was already extremely hypoxic. So in addition to the lapses of logic that come along with feeling extremely ill, and not being able to breathe, my thoughts were actually altered. I remember sitting around my house in my pajams the entire time, and sleeping a lot, which must have worsened my hypoxia. Looking back, my mother says that I was already being sort of out of character over the phone. By Sunday, I was practicing active cycle breathing to keep my oxygen saturation around 92 on 5L of oxygen, and I knew Dr. U-bird was going to put me in the hospital.

This is where my memories start to get all messed up. Much of the rest of the week doesn't matter in relation to the point I want to make tonight - but I will say this -a lot of bad things happened that first week in the hospital and mostly because I was not my usual diligent self, overlooking my own care because I was all crazy hypoxic. Also, my own doctor was out of town, which bred a series of medical personnel self-righteous indulgences that I will write about at greater length some future day. So, yadda yadda yadda, a bunch of shit went down and I was just getting sicker.

[Sidenote to CFer readers: only on CF blog can you "yadda yadda yadda some scary medical stuff went down" in order to get to your point. I am reminded of that episode of Seinfeld, "You yadda yadda'd the sex?" "I yadda yadda'd the sex." I have, above, yadda yadda'd what is usually the most interesting part of the typical hospital story.]

A lot of bad things happened and by the end of the week, I was laying fetal in my hospital bed, which was propped up almost to sitting, and trying desperately to breathe: in . . . 1 . . . out . . . 1 . . . in . . . 2 . . . out . . . 2, until I reached 100. Then I would start again. I stayed up all night this way, counting my breath and occasionally stopping to see if my oxygen would stay stable. It didn't. I don't know, with the chain of events, if I had already seen a doctor, or I was afraid to call for the doctor, if I had tried the BiPap, or not. I only remember laying in the bed, counting my breaths, forcing them in and out.

This was when I realized, this is part of dieing. This is what it feels like. Before, I was ill. And now, I am dieing.

Around four in the morning, I started sending texts that said, "I really need someone here now. Someone should come here now," and some others that I don't really remember. I texted them to my parents who were planning to arrive only 4 days later as it was. I didn't want to be alone for four more days. All of a sudden.

At some point in the night, I was laying, counting my breaths on my fingers and trying to read with the book laying next to me. I was re-reading a book I have referenced here before called, "Sick Girl Speaks!" by Tiffany Christensen. On her list, "Top Ten Opportunities of Illness," she writes, "9. Going to an internal place that is so deep pain cannot find you there." In my state, I found this phrase very meaningful, and I decided to meditate on it instead of counting my breaths. I started to breathe to, "(Inhale) Take me to a place inside (Exhale) Where pain can never find me."

I wanted to find a place so deep and quiet inside myself that my tired lungs and breathing muscles could continue to do my breathing, while my mind and the rest of my exhausted body could get some rest. I started to also think about everything that lies ahead of me, not even knowing of the immediate threat of respiratory failure.

I wanted to find a place inside where pain would never find me. By the morning, I found it.

CG

Sunday, October 25, 2009

I Did Not Notice the Passers-by, And They Did Not Notice Me.

Dear CG Readers,

I was having such difficulty deciding how to communicate with you again as everything unfolded over the past week and a half. I decided to make my Newsflash! to get the word out there, and then did not know what to say. (Not something I usually experience;)

All I can say, so far, is this: When I got so sick two weeks ago, I spent some time mentally preparing. I thought I was prepared to come into the hospital, and to get better so that I could continue my journey to transplant. my transplant if I had to, to stay well. I never thought that things would get so much worse before my transplant. I thought my health would get a little better before the transplant.

Now, my biggest hope is that my health stays just the same. I will look at every day of slight improvement or plateau as a victory. I am no longer demanding leaps and bounds, they could lead to setback. I am demanding one day at a time of same or a little bit more manageable.

(More to come in later posts...)

There is a long story to tell and many lessons learned and many doorways opened . . . opening still.

Tonight, in the middle of the night, settling into wear my BiPap over night, and feeling unsettled, confused, enlightened and downtrodden about how far down the rabbit hole I went, and how hard it was to come out. Scared that I could not do it again . . .

I had the pleasure of hearing this song and was suddenly clapping and swaying on my bed, enjoying the rhythm and lyrics of the song and how closely the words echoed with my journey last week. Perhaps these words will help explain while I am too tired to write all the other ones. I invite T-Money, CysticDad, CysticMom, or even J-Proffie to offer submission. CysticLady is charged with filling in the gaps.

I don't want to be dramatic, but I believe that this past week had the potential to be the 5 days that would save my life, or take it. That does sound dramatic, but I believe it to be true right now. I want to remember the skills I used so that I can use them again and waste less time finding them.

ANYHOW! The song:

Moment Of Surrender
U2

At the moment of surrender

I folded to my knees
I did not notice the passers-by
And they did not notice me

I’ve been in every black hole
At the altar of the dark star
My body’s now a begging bowl
That’s begging to get back, begging to get back
To my heart
To the rhythm of my soul
To the rhythm of my unconsciousness
To the rhythm that yearns
To be released from control

I was punching in the numbers at the ATM machine
I could see in the reflection
A face staring back at me
At the moment of surrender
Of vision over visibility
I did not notice the passers-by
And they did not notice me

I was speeding on the subway
Through the stations of the cross
Every eye looking every other way
Counting down ’til the pain would stop

At the moment of surrender
Of vision over visibility
I did not notice the passers-by
And they did not notice me
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sorry to borrow some song lyrics, but there they are!

Goodnight, I have to dance and cradle myself to sleep, I wish the same to you.
CG

New Blog and Site

Yo Old Friends!  It's me, Beth Peters / CysticGal  / the artist actually known as Mary ElizaBeth Peters . I am moving on from this bl...