Showing posts with label romance. Show all posts
Showing posts with label romance. Show all posts

Thursday, November 5, 2009

I Bet You Think This [Blog] Is About You

*in the post below, the name Jerkface has been used to substitute the identities of four different individuals.

So I have this problem. Every time that I deal with romance on this blog, all of my exes think I'm writing about them. Which is weeeird because a) I have a very detailed disclaimer dealing with this issue and b) I have written very little about romance on this blog and even put CysticLady to the task of covering romance during her guest posts (also because she is a romance-maniac right now). I got this email the other day that accused me of being all angry at one of my exes, which is weird, because, you know, I've had bigger fish to fry these last six months, you know? Not once sitting down in the ICU trying to figure out how to get from one end of the bed to the other without my oxygen dropping to 70, did I think, "Oh I am so angry at that man!", nor when being checked for hypoxia and struggling to pick out the commonalities between an apple and an orange did I say, "Now wait, let me tell you about [Jerkface]." And yet, oy vay, I get accused of man-anger when all have is lung-anger since August 11th.

And I have this other problem. A lot of my exes who are not particularly in my life anymore are writing to me and saying they are praying for me. Fine, pray away. I like praying. I do it every day. But it makes me wonder, if we cannot be there to support people in the real world, is it appropriate to try to affect them in the spiritual world? Perhaps, but I'm not sure. I also think this conundrum speaks to a great problem I have always wondered about with CF, which is the pressure that I have always felt to stay in contact with people only because they are curious about whether or not I am still alive. I know that sounds crass, but it's true. Perhaps other people have experienced this passing thought. For me, this means that I invited [Jerkface] to make peace with me before my surgery and he basically said, "nah, but I'm prayin' for ya," which is, you know, juuuuuust like making peace. ?

And then the other problem, the ultimate ex-boyfriend problem - that exes never believe that their exes can possibly be happy without them. I don't think that [Jerkface] can possibly be happy without me, mostly because he used to tell me that all the time. [Jerkface], in turn, cannot possibly believe that I have been fabulously happy, besides this whole my-lungs-are-dieing thing, mostly because I used to tell him that all the time. What fools we both are, as I am most definitely happier now than when I was all involved with [Jerkface]. Still, it takes a godly concentration to hold my fingers back from the computer where he writes, "I hope you're happy," and I want to write, "I'm fucking happy, I hope you're fucking happy too, jerkface!" If anything, these last six months have shown me that romantic love is not the highest thing on my priority list at all.

Watching things fall out of my life as I got sicker, and hoping for them to drop back in once I get well, I realize that romance is lower on my priority list than I ever expected.

Tuesday, October 13, 2009

Guest Blog by CysticLady: CF and Relationships Part II



Let me thank you for the nice comments on my first guest blog on Cystic Gal.  I am also grateful to be able to have a forum to share these experiences.

As such, I thought I'd write a follow-up.  There is another side to this story.  I will attempt to tell my version of it without using too many cliche's, but it may be hard because love is the most written and talked about topic in the history of the world.

Love is a wonderful part of life.  I think I can go so far as to say, it is the reason for life.  It is indeed a real shame to go through such lengths as a lung transplant to continue living, to then deny yourself the chance for love.  The same way that I weighed the risks vs. rewards of a lung transplant, is the way that I have to weigh the risks vs. rewards of love.

I have said before that I'd do everything again, the whole year of dying, the surgery, the recovery, for just one of those days after transplant that I didn't have to think about breathing.  Not even a special day, just a day when I get up, go about the day, perhaps dart to my car in a rain storm.  Then to sit at the end of the day and realize that not once I was fearful of being out of breath, of having to stop and check my sats, or bend over in a coughing fit.  I chose to have a lung transplant with the full knowledge that it would not be a cure that lasts forever.  I chose it knowing that everyday would not be perfect, that in fact, some days would be awful.  I've had those awful days, months, even.  Still, I am happy.

What I didn't share in my post last night was that I have a new boyfriend, a brand new shiny one.  With a lot of apprehension, I forwarded last night's post to him.  He called in the early morning, and, he's in.  I was speechless.  I was scared.  A few minutes later, I was relieved.  I believe him.  He is wonderful.

It may not last forever, and everyday will not be perfect, but I'm going for it.

In other news, CysticGal is doing better today.  She is a bit stoned due to a huge increase in her Marinol.  She has her first ABG ever tomorrow morning, so wish her luck.

 Teeda (CysticLady)

Monday, October 12, 2009

Guest Blog by CysticLady: CF and Relationships

I knew this day would come where I would post here, and I've had this idea percolating; however, I don't think that now, or any time in the near future will I know how to handle relationships and CF.

A bit of history:

I was married once.  We dated four years prior to our marriage and were married for six.  Around year four of the marriage was my lung transplant.  Before we were married I felt I had properly vetted the husband for many types of health issues.  He'd seen the gross hemoptysis, spent lots of nights in the hospital, changed a port needle, put the nebbies together.  Still, things fell apart in a complete and unsalvageable way in the two year period consisting of the year before transplant where I was dying all year, and the year after transplant where I was recovering all year. 

I think all the time really, what was it all about?  It was no secret I was sick, it was no secret that I'd eventually need a lung transplant.  I know for sure that the transplant was not the only reason for the end of the relationship, and for all I know it would be over now if I didn't have CF, or I didn't need a transplant.  Still, I always felt the need to isolate the final straw.  What I think it was, six years after transplant, four years after divorce, is that although my husband could deal with the illness, the hospital, the doctors, the coughing, the hours of therapies... really like a pro; that when it came time for him to actually give something up, change military bases to one he didn't like, give up being deployed, slow his career down - that it made him so mad, and in turn it made ME so mad.

So, what do I do with this information?  Can I trust enough to ever have another relationship?  I built up these walls, stay out, you don't want to come 'round here. 

Disclaimer:  I have Cystic Fibrosis, I had a lung transplant almost six years ago.  In the next four years I will probably need another one, or I might die of something else.  If I need another one I might not want one, but I might and either way it is up to me and me alone.  I will probably also need a kidney transplant one day, if I live long enough.  If we happen to procure some babies using one of the various methods babies come around, i.e., stork, adoption, emergency, then you will probably raise said baby by yourself one day.  And oh yeah, the biggest one, I am a survivor, and as such, I will pick me over you every day of the week and twice on Sunday. 

So, do you still want to date me?  I'm so cute.

Question one:  When do you tell them, in a way that makes the future relationship understand, buddy, this is serious?

Question two:  Once you tell them, and they have the moment where they think and say, "what kind of asshole would break up with someone because of their health?"  And you look over at them and think, "you would, and so would he, and him, and that one, and her too."  What now?

Because let's face it, when we think, "in sickness and in health", we assume that means a lot of health and maybe a little sickness, not mostly sickness.  And when we say "until death do us part", we mean when we're both really old, not in the next decade.

Personally, I have this idea that if the potential relationship is given the disclosure early, then they can walk away, no harm no foul, mitigate the damages, lessen the hurt feelings.  But, it never works that way for me.  Instead, it is the acceptance of the disclosure, and me proceeding like a green light GO.  Until the day that we both realize, yeah, he's that asshole we both denied he is.

I think that I need a yellow light, proceed with caution.

Teeda (CysticLady)

Tuesday, September 29, 2009

Randomling (A Poetry Post)

Skinny Silver Time

[This poest has been deleted because it is included in my chapbook, "Into the East."]

Thursday, August 27, 2009

CG and the Terrible, Horrible, No Good, Very Bad TODAY

Okay I made it through one bad day. One bad bad bad bad day.

Today, it was the sort of day where CG feels hopeless about her health and her personal and professional life in one big ball of sad sad sad, bad bad bad day.

The good side of today: I made it through the day without sending angry sad sad bad bad emails to my ex boyfriend across town, or the two friends I have lost in the last six months. Similarly, I did not make any rash family phone calls. I managed to delete the few snide comments on made on Facebook. I DID manage to take all my meds and do that whole regime, complete with a PORT needle change, with only one small anxiety type of situation about the needle's length. Also, I talked to the three people that I can talk to when I am in this slightly incoherent state of hopelessness and nose-blowing. Three. That's a lot.

The bad side of today: I slept most of the day. When I wasn't awake and crying, I was asleep. That can't be good. And I accomplished nothing nothing nothing that wasn't on my "health" list of to-do's. Also, the bad side to today was that I had today at all.

Tomorrow will have to be better. Because it won't be today. So that's good.

Love, CG

Tuesday, August 11, 2009

My Birthday Totally Blows

It is my 29th birthday today.

Girgle Girgle.

Last night I had a fun dinner planned with an attractive male companion.

Which is, you know, the perfect time for hemoptysis.

Girgle Girgle.

My night was ruined.

Later, getting ready for bed (alone, duh).

Girgle Girgle.

Sleep, ruined!

Today, on my way to rehearsal for a perfect

Oh wonderful play with a wonderful team of wonderfuls

Girgle Girgle Flood Spit Flood Spit Flood Flood Spiiiiit.

(Flashforward 12 hours)

To bed, in the ER, still waiting for a bed.

More tomorrow.

My Birthday Totally Blows.

(So just in case that wasn't clear, I had a lot of hemoptysis two times this morning, after 2 lesser times last night, and with my history decided to come on in. Now, waiting for a bed, started some IVs, tomorrow starting some hormones and getting my PORT put in. So keep those "your boobs'll be fine" comments coming. And I'll miss the rest of the play I'm directing with at least 2 new fabulous colleagues which was a wonderful opportunity to me that is now ruined, and and and I have to cancel a party on Saturday. And, it's my birthday. Have I said that already? So yes, I'm a brat right now. I'm going to bed now. So there.)

Love, CG

Saturday, July 25, 2009

Boobs vs. Port: Smackdown. A Call for Info!


I need info from other Cystic gals! I am considering getting a port (or port-a-cath, which is an entry way for IV meds that stays in a person, long term), but love my chest the way it is. Meaning, I am a boob girl. I am fine to admit it, my chest is my best asset. I wear v-neck shirts and necklaces and love love love my body from waist to shoulders. I am not interested in fucking it up. I like it. Not because guys like it (I don't have big boobs even,), I just like it for me. Always have. It's a staple of my fashion sense and my sense of femininity.

Boobs and Port. Give me the info!

Does it feel weird if a man hugs you with a port? Can you feel it pressing? Does it hurt?

Can a man feel it with his hands? (When it's not being used for IV meds, I mean)

Does it heal closed between treatments? Like if you had 3 months with no IVs, would it heal up?

When you are doing IVs, how much "geography" of your chest does it take up? Is it like a PICC in your chest? Are you destined to sweatshirts and woolie sweaters while on IVs?

GIVE IT TO ME STRAIGHT, GALS!!

Love, CG

Wednesday, July 22, 2009

There Are Nights

Disclaimer: I haven't really written any sad posts. Which is ironic, because I'm usually a sad sort of writer. I like sad topics and write sad lines and my characters are sad and boohoo. But this is my only sad post here so far. So, well, here it is.

And I didn't write it today, so don't go tweeting or emailing all crazy. I decided to post it on a different day than I wrote it so that it wouldn't be an overdramatic cry for help. Just a thought for out there- the bloggy world.

With Love, CG


There Are Nights

[This poest has been deleted because it is included in my chapbook, "Into the East."]

Saturday, July 11, 2009

Blogvitation

For tonight's blog, I invite you to read this particular post from one of my favorite bloggers . . .

The famous CF Husband!
http://cfhusband.blogspot.com/2009/07/reality.html

This post tackles something that has been a big issue in my life recently: "the big talk." What is the fine line in discussion with my loved ones, family and friends, about my health, my future, my plans? This is also, actually, an issue that I seem to be tackling with my medical staff right now too. They are sensitive to my emotional nature and my anxiety. In their sensitivity, I think our conversations are moving more slowly than either of us would really like.

Isn't that odd?

It's like being on a date where neither person wants to be there. Both people want to get up and leave but CAN'T!

In this situation, both parties want to have a discussion, but don't.

Humans are weird this way.

Deep thoughts by CG.
Goodnight!

Saturday, July 4, 2009

Saturday, In the Park . . . I think it was the 4th of July-y.


Happy Independence Day, U.S. of A! I have never been more proud to be an American than this year. I have never been more politically invested than this year (barring, perhaps, a year in middle school where I was really into politics which faded when I met J-hottie^, my first love).

In the spirit of this 4th of July, Independence Day, and in the spirit of this blog, "Cystic Gal," I would like to reflect upon the ways that CF has made me a more independent person, both when I was growing up, and today.

As a first point, I know that I am empowered over my body, which contributes to my Independence as a person, a woman, an artist, even dare-I-say-it, lover. From a very young age, I have felt this empowerment over my body which paused only for about 6 months in middle school while my breasts grew. This great empowered feeling is mostly a blessing, but as I grow into later stages of my illness, it is also, I find, a curse. I believe that I am empowered over my body largely because of CF.

I have been thinking on this over the past two days, as I read my friend Kathy Rooney's book, _Live Nude Girl: My Life as an Object_, in which Kathy reflects, as you can imagine from reading the title, about her upbringing and her world's dealings with her body. Though the book is focused on Rooney's work as a nude artists' model, the book analyzes other nude and naked means of employment. (If you are wondering what the difference is between "nude" and "naked," you should certainly read her book.) Assuming you have not read her book, though certainly some of my readers have, Rooney writes of the many messages she received about her body, like we all do, from her parents, her siblings, the "so-called slutty neighborhood girl," her friends, and the opposite sex in general.

I was stuck stuck stuck on this quote, the one above, about the "so-called slutty neighborhood girl," in that I was recently caught in a conversation or five about a friend's abhorrence that her son was dating THAT VERY GIRL at [...] school [...]. THAT GIRL, you know, "the slutty one." Now, my friend never actually said the word "slut" when talking about this girl. But it was, I felt, implied by the other things said about the girl. Perhaps I was influenced to hear this by the fact that other friends went ahead and said it - "slutty" from the comfort of their distance from the relationship itself. Torn between my feelings of confusion that a friend would judge another woman, well . . . girl, so openly, and understanding her very visceral concern for her son's well-being, I was dumbfounded trying to think of things to say to my friend.

I find it funny that every neighborhood, every school, every office has a "so-called slutty girl" that we are meant to be afraid of, titilated by, ashamed of, and sorry for at once. By describing as "so-called," Rooney admits "slutty" is just a distasteful label put on young girls who show too much leg, have breasts that are "too big" or who make out with boys "too early" on a comparative basis with their communities. However, Rooney's description of this girl and my recent ponderings over my friend's parental conundrum had me thinking, "Why is there always only ONE 'slutty' girl?" As far as I know, she always has friends, this slut-girl, and they always dress like her, and make out with boys like she does. Some of them are even blessed with the same great rack. [...] Yet there is always one leader of the pack that is The Slutty Girl you know.

The thing that The One Slutty Girl has that members of her harem don't is empowerment over her body. Actually, the MOST empowerment over her body among the girls. This is why there is only one girl, she has these features most of all, though others possess them. She wears the shorter shorts, and the revealing tops and she makes out with the boys "further" than she "should" because she is trying to figure out something about her body, the body that empowers her to control the boy she's with, control even her friends, perhaps control herself. The Slutty Girl IS her body, or she would like you to think that.

Sure, The Slutty Girl might have secretly low self-esteem, she might write sad things in her journal at night or be a coke-head on the side for all we know - or she might watch the History Channel at night and be into existential poetry. We do not know. All we do know about The Slutty Girl is that she doesn't mind if we look at her, and she doesn't worry about hiding her boobs every time she bends over, and she probably won't grow up to have sex with the light off. Whatever's going on with The Slutty Girl's inner-workings, she owns that body of hers and she's using it for something, whether sexual in nature or not. She owns her body in a fierce, independent, arrogant, flaunty, go-ahead-and-look-at-me-and-screw-you-for-looking kind of way that the other girls around her, try as they may, do not have. This makes her The Slutty Girl while the others are just regular "sluts" in the eyes of those that behold them and the mouths of the neighbors gossiping.

What does this have to do with CF? Hard to tackle in my remaining 12 minutes of bloggy time tonight. (That's right, blog readers, I'm trying to limit myself to only 1 hour of bloggy time per day! And that includes stat updates and viewer questions!! YIKES!)

[...] I can say that I [...] became aware of my body as something that needed to be used for specific purposes at a much earlier age than other people - men or women. I think that most people don't think of the usefulness of their body until at least adolescence. By "usefulness" I mean the active posing of questions regarding the body's ability to complete a task for the mind, as in "Can my body do this? Can my body do that? What must I do to my body so that I can eventually do that thing-I-wanna-do? Can I run? Can I swim? Can I hold my breath as long as her?"

Non-CF children grow up and they do or they don't accomplish tasks with their little bodies. These accomplishments are inherent. They are learned through observation. They are mostly unconscious. CF children grow up and they learn to-do-to their little bodies. It is taught, it is rarely observed, it is not inherent, unconscious, or even natural: Put the big pills in your mouth and swallow: to-do-to-your-stomach what your stomach can't-do, digest; Inhale the mist into your lungs deeply: to-do-to-your-lungs something they can't-do alone, fight disease; Cough out the secretions: to-do-to-your-lungs/trachea/mouth/stomach what you'll rarely see another human do: force expectorate (to remove disease).

CF children learn very early something that others don't learn for many years, that their body is something that can be forced, coddled, calmed, assaulted, overwhelmed, and freed - and that sometimes the most painful acts against them are the best for their bodies, though sometimes, there are just painful acts. It's a very tangled message that forces a child, most hopefully in my opinion, to assert This Is My Body- a deep and powerful understanding that changes the way a child views her/himself and the other bodies s/he interacts with.

In closing as I see the clock . . .

CF children, The Slutty Girl and even, dare I say, Kathleen Rooney and the artists' models she writes of, have one shared understanding: As soon as they learned to empower themselves into their own bodies, to own their own bodies, to objectify their own bodies and to use them as freely as the world around them would - to feel better, to feel really good, to get reactions, to get sex, to be admired, to become art, to get money - whatever the use - as soon as they learned to use their own bodies in the way that the world used them, they learned that this self-empowerment was very, very bad.

More on this topic in future days. My bloggy time is up!

HAPPY 4TH!!

CG


Wednesday, July 1, 2009

Florence Nightingale Syndrome: What Can IT do for YOU?

I have a confession to make and I trust that it will stay within the confines of this blog posting and my blog's very exclusive, very private readership*:

I'm madly in love with my Valvoline service professional. He's so kind, so caring. He always calls me "sweetheart," he sends me correspondence if he hasn't heard from me in awhile, he is always honest with me - about the status of my air filter(1). He is honorable.

Also, I have this thing on the side with my laundry man. He does my laundry week in and week out. He is committed to me. He folds my clothes so nicely and he even lifts them into my trunk, he is unending in his laundry ways. He doesn't make eye contact with me because, well, he has a wonky eye (2), but still, I can tell he shares in my feelings. And for only a dollar a pound.

I have been considering a lifestyle change due to my lovely maid, Wanessa (3). She is adorable in her fitted sheet changing techniques. She bravely vacuums my curtains and behind my couch once a week. She shows her true strength of character in bathroom and litter box areas. She has changed all of my views - on cleaning.

And last night I had a short-lived thing with a waiter at Legal Sea Foods (4). It was a brief affair - over by the end of my surf and turf. I will always think back on him kindly.

Oh, and that guy from the Arby's who gave me the extra cheese sauce. He was so handsome. I wish it could have lasted - the cheese sauce that is (5).

And don't even get me started on Barack Obama.

I also have to confess, I do have this small thing for my CF doc, Dr. U-Bird^. He is always honest with me. He listens to me even when I'm a crazy coockie biotch. He always informs me if he talks behind my back - to the other CF Clinic staff - in creating my treatment plans. He also cares about how I feel. And he has earned my trust.

In all but one of these situations, I had a small, mostly fictitious crush on my caretaker, because you know what? It works for me. In the Legal Seafoods situation however, in full disclosure I must say, I had an actual crush on the guy.

I would like to encourage all of the CFers out there to ask,

"What can Florence Nightingale Syndrome do for YOU?"

a) It can make you more highly productive in getting things done like oil changes!

b) You'll never do laundry again!

c) You'll have less dust and pet hair in your house and not inahle fumes cleaning the bathroom. Bonus: less germs in the bathroom and kitchen!

d) Clearly, it can make you eat more by constantly seeking that Nightingale Waiter Love high.

e) You will become addicted to cheese sauce. This can only help your calorie intake because cheese sauce is only available in high calorie situations.

f) You will become more politically active and aware! YES WE CAN steal him from Michelle, you'll say.

More importantly . . .
g) It can make you more likely to attend clinic, and to do so with your healthiest, best self present.

Now, obviously I am not suggesting that I, or anyone, should develop actual romantic feelings for their doctors (or their Valvoline service professionals, for that matter). But you should develop a trust for them. If you find that your doctor is not honest, does not listen, does not properly inform you of your care, or doesn't care about how you feel, it is time to find a new doctor. The same is true for your Arby's cheese sauce administrator.

SEVEN Ways To Develop Florence Nightingale Syndrome
In Your Medical Environment:


1) Ask the doctor if you can call her/him by a former lover's name (one you still like).

2) Try to figure out if your doctor looks vaguely like any attractive famous actors. Then squint at clinic.

3) Get dressed up for clinic including perfume. Blatantly ask, "Don't I look great?"

4) Entertain yourself with inappropriate sexual jokes and/or advances during a bronch, PICC placement, or other procedure, then blame it on the "ah-ah-ah-ah-ah-Sedation Meds(6)."

5) At the beginning of your clinic appointment, boldly state, "Let's just keep this between us."

6) At the end of your clinic appointment, ask your doc, "Was it good for you?"

7m) Sneak out of clinic before it's over so you don't have to, you know, talk about it.

Okay that last one is just for the male CF patients out there. This alternative is offered for the girls.

7f) Stay at clinic 'til the next morning. Shower there and then make a breakfast even if your doc has left for "rounds."

Okay Okay Okay, so this might sound a little extreme. I guess what I'm trying to say here is, YOU need to find YOUR way to love CF Clinic. This is my subtextual way. It and Eminem. And the Valium. And it's working for me so far.

Goodnight, Y'All. Mystery Solved,
CG

Notes:
*Duh, everyone can read this blog in the whole world.
(1) Okay, so one time I think he was ripping me off.
(2) I think wonky eyes are adorable so this is not a put down.
(3) Her real name and I'm really straight.
(4) I would have actually done this guy if the topic came up. I waited, it didn't.
(5) My affair with the LS guy lasted longer than that damn cheese sauce.
^A pseudonym I made up according to the secret CG pseudonym creation equation. I sincerely hope Dr. U-Bird gets my tone here. And doesn't sue me for a little humor.
(6) This true CF clinic folklore submitted by Cystic Lady. Available via google chat: 12:01 a.m. 7/2/09


Note to all: I'm just kidding here. Go satire, get your groove on. Best of all, I think I'm the target of my own satire here. Ha!

Saturday, June 27, 2009

My Lungs Aren't On My Face

Newsflash!
Now you can REALLY get "CG" straight to your inbox!
Click to the left!
sorry for delay

This will be a very short post but I must certainly reserve my CG rights to use that title again when I develop this thought further. "My Lungs Aren't On My Face," has become one of my favorite things to say lately. I always get a laugh for it, and the reason I get a chance to say it so much is, in short, I have had a really really bad year. Almost every person I see says to me, "But you look great!" which is a great complement, and I'm happy to take it. And I DO, indeed, look really great! :)

Ironically, however, I'm having the hardest time with how this disease is now affecting my day-to-day doings and wondering if it wouldn't in some way be easier for me if I actually looked sicker right now? Maybe then I would have an easier time remembering to take better care of myself as the day goes on, and maybe the people in my life wouldn't be so confused about how I am making my decisions differently lately.

Ugh. A big topic to bring up before bed, but just like the writing above, I have to go to bed and try not to worry too much if you guys understand why or not- I'll have to explain it more tomorrow. Goodnight!

With love,
CG

Wednesday, June 24, 2009

Good Traveler (GT) versus Cystic Gal (CG): SMACKDOWN

Top Ten Differences In Traveling
as fictitious "normal" ideal world author lady (Good Traveler), and
as CG: who I really am.

1) Good Traveler packs light. CG needs lots and lots of stuff.

2) Good Traveler gets up early. CG sleeps in late.

3) Good Traveler leaves no later than an hour after waking. CG takes all the time she needs to clear the airways. (long time.)

4) Good Traveler says, "any hotel, fine by me." CG says, "Treadmill?"

5) Good Traveler says, "I got the bags." CG says, "Can you help me with my bags and o2-maker thingie?"

6) Good Traveler takes 1 or 2 days to go "17 hours" according to mapquest. CG takes three.

7) Good Traveler drives ALAP (as long as possible) before stopping. CG is hungry, say, every 2 hours :)

8) Good Traveler wants to stay out late with old friends. CG wants to go to bed early though she adores old friends.

9) Good Traveler walks through town romantically. CG says, "Is there parking? I'll meet you there," and wonders what could have been. Feels bad.

10) Good Traveler loses. CG wins.

WHY? CG writes this blog.

Goodnight from the road,
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...