RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (Full Version)

All Forums >> [Community Discussions] >> Gorean Lifestyles



Message


slavejale -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/10/2008 9:46:27 PM)

Greetings to the Free
greetings to the properties

well i have scoliosis, which thankfully has not put me in a wheelchair, but i have to work hard not to gain alot of work because (1)most of the family on my father's side has this slow metabolism thing and (2)if i were to gain about 20more pounds, i might actually be in a wheelchair. 

other than that, sometimes i have anxiety issues, especially if i am in a place where i do not know, but i dont like freak out totally or anything. i just start talking really fast and rambling alot.

when i was born i was legally blind, and legally deaf but after about 20 surgeries on my eyes, i can see with glasses and i can hear.

yea, i think that is about it.

well wishes to All and all.




Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/10/2008 10:25:09 PM)

Greetings jale

I can understand the weight gain becoming detrimental to you in regards to weight bearing, I think you've done good to maintain a weight that keeps you out of the "wheels". Since December of 2006 I've gained alot of weight from a medication called Lyrica (nearly 30 pounds in 4 months,) and it's only made it worse for me. Have only lost 10 recently and it was very hard. I've been off the med for nearly 8 months now.

You said "when i was born i was legally blind, and legally deaf but after about 20 surgeries on my eyes, i can see with glasses and i can hear."

My heart goes out to you for all the surgeries you had to endure, but if you believe in God as I do, the good Lord has blessed you in giving you your sight and hearing back. (I'm sorry for bringing up religion, if you do not believe, I do not mean to offend)

Sincerely,
~twinkle








Malkinius -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 1:56:48 AM)

greetings twinkle.....

quote:

ORIGINAL: Hiskajirah

<snip>

Master Malkinius said "Perhaps online chat venues are largely responsible for that? You can be anything and do anything online even when you can not hope to do it offline."  -  You are right Master. Infact I have been invited to online chatrooms to dance and while the man who invited me meant well............       I can't bring myself to do it.

<snip>

Thank you all for listening to me

Respectfully,
~twinkle


I am going to do something I don't often do. This is a case where I will make an exception. Go online and dance, serve and if your Master allows, even cyber a little bit. <grins> Go play and have fun. Treat it as play and mental therapy.

Sometimes being able to do, even if only virtually, can be very therapeutic. Just don't lose sight of reality. Take it easy and just play a bit at a time. Sometimes it is good to play. <smiles>

be well.....

Malkinius





Karynn -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 3:31:01 AM)

Tal again ya'll,

I thought it might be fun to recollect the positive moments before the pain, if you can recall one. I have a series of CDs my father found for me that are suggestive therapy, where the people talk in calm and very pleasant voice tones, and lead my brain on journies away from the pain. In the midst of one of them, the two voices say, "Remember a time when you were not in pain." then a voice echoes, "Or remember a time when you were in less pain than you feel you are now."

I was struck by several of you recounting your activity level at some time in the past, and the difficulty that we face trying to find ways to cope with that severely hindered freedom now. My case is not so different. Though some of my illness resulted from birth defects and kidney disease from the very beginning, there were many very well managed years of life that I was more in control than out of control. Those are the years that my brain returns to when I'm in that hypnotic therapy.

In 1996, I had my 11th surgery as an adult. I had spent the better part of my children's youth healing from various surgical procedures. Slowly but surely, after all the reconstruction and wiggling things around inside of me or just cutting them out, they left my body alone long enough to give it time to begin healing, and I was in my 20s, still full of youthful energy myself, and ready and chomping at the bit to join life again. I did so. It was my very best year of adult life, my favorite reflective year, the year we have the most photographs of me taken, and a year all of us look fondly back to with full memories. Even my younger son though only 4-5 at the time can remember that year because of all the significant things we did together as a family.

1996 was the year I was a soccer coach 3 nights a week and 1 game a weekend, then ref'd at least 1 other game, then sat through 1 more game that my sons played in on Saturdays. It was the year we were Pre-school coordinators for a very large church program, and hosted the 11 o'clock hour with 75 3 and 4 year olds every Sunday. It was the year I had a membership to a really nice Y-type gym and was in shape, the healthiest weight of my entire life, and fit. It was the year things just seemed to flow smoothly. We had such a great time with our boys, with our peers, active in private M/s lifestyle group, and the list seems endless. It was a very good year.

When I need one of those nudges, a pick-me-up to help cheer me up, I pull out the photo albums from that year. I flip through the pictures, and remember the events, the holiday at the beach, the soccer teams in spring and fall, and all the people who's lives touched ours. And when I lay in the quiet of the night, working hard to get comfortable enough to relax, even if I can't sleep officially, and I've got one of those CD's playing in my ears to encourage calmness, somewhere in that year is my favorite place to visit mentally.

I don't know if any of you have coping programs that work consistently for you. We're at a place in life where I've been willing to try various things. I tried herbs as you may remember, and they had way too much ick for way too little comfort. I've tried CDs with hypnotic therapy. I've tried sleeping on the floor and upright in a la-z-boy recliner, and found neither improved sleep. So when I do find something that helps, I use it often. And I focus on the good times. They always bring a smile.

What moments are your favorite, the ones that remind you of a time when you did smile more often, or could cope better, or had life by the tail?

K




MontrealPhoenix -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 3:49:19 AM)

Greetings twinkle
 
I cannot thank you enough for starting this thread. While those in our lives without disabilities like ours try to understand, and i'm grateful for those in mine, i don't think they do as well as we do. I think having people who understand will be a great help to all of us no matter what our disabilities are.
 
Right now, my hip is my greatest problem and luckily it appears to be temporary. My doctor has told me that after physio (that whole nuther kind of torture) i should be back to 100%. So at least there is hope.
 
Thank you once again and please don't hesitate to contact me on the other side if you ever want to talk.
 
live well,
 
Phoenix




MontrealPhoenix -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 3:57:34 AM)

Greetings Karynn
 
For me, the happy years were those when i took dance classes. Most of the time i studied ballet jazz but the last few years i studied with a teacher who combined ballet jazz with aerobics. She used to "test" the new moves on her boyfriend first so we knew we were in for a hard time if he was in pain when he came to pick her up, lol.  I felt so free when i danced, as if i could just take off and fly if i so wished. It makes me smile just writing about it now.
 
Even now, i sometimes try to dance a bit here in my apartment but i pay dearly for it. Still, it's worth it for that short time of freedom.
 
Phoenix




Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 5:00:48 AM)

quote:

ORIGINAL: Malkinius

greetings twinkle.....

quote:

ORIGINAL: Hiskajirah

<snip>

Master Malkinius said "Perhaps online chat venues are largely responsible for that? You can be anything and do anything online even when you can not hope to do it offline."  -  You are right Master. Infact I have been invited to online chatrooms to dance and while the man who invited me meant well............       I can't bring myself to do it.

<snip>

Thank you all for listening to me

Respectfully,
~twinkle


I am going to do something I don't often do. This is a case where I will make an exception. Go online and dance, serve and if your Master allows, even cyber a little bit. <grins> Go play and have fun. Treat it as play and mental therapy.

Sometimes being able to do, even if only virtually, can be very therapeutic. Just don't lose sight of reality. Take it easy and just play a bit at a time. Sometimes it is good to play. <smiles>

be well.....

Malkinius




Greetings Master

I want so badly to do as you suggested, I want to have fun and play, and laugh, tease, flirt, dance, express my passion and sensuality and once upon a time I was able to pleasingly serve. Sure there were many better than me, but I was just me, I always used descriptions that really would be me offline. The true color of my eyes, the true shape of my body, the true several bracelets that adorn my wrists, the locked Turian style collar around my neck, the bina's or hemp strings around my ankles, my slave bells jingling on my left ankle, a belly chain laying low on my hips (the belly chain became an exception when I gained weight, so I did not describe it anymore)

I miss those days, and I left chat and forums for a year, last year or about as I returned just a couple of months ago. I was still online in messenger and turned all the energy I could raise up into research for chronic pain studies.Even when I did serve, I was always so very nervous, I would sit on my side of the computer belly flip flopping just typing because there is a sense of reality to virtual reality. For me there is, atleast. But now I am so scared to serve, my anxiety goes through the roof, I fear failing, and faltering, I fear erroring, even in a discussion room only those who know me would understand my sentences at times. I mix words up, sentences become misunderstood and then I immediately rephrase it by saying "she means......" And I repeat myself for clarification. I can be told something now and forget in the split of a second, so I'll re-read posts and try to understand. I use to be very good at writing and communicating and I've lost much of it. I believe you are right in that serving and dancing and even cybering (am a lil chicken and shy with that, see--->bawk bawk) is therapeutic, it's a diversion, it changes the mindset and when the mind can find peace often times the body will follow suit. Mental therapy can become physical therapy. I was able to handle most all of my hm.. disabilities. (am still not comfortable with that word, but I'm trying to accept it) until about 2 years ago when I reached a breaking point because there was no longer any stability. Nothing consistant, no order, denials and delays, medically speaking. I've done some bad things to divert pain. Things I'm not proud of. Things my Master had to restrain me and embrace me simultaneously.

I don't know anywhere to go online anymore to even try to re learn Master. I was a GCI first girl for over 2 years and my memory to all I knew is gone. I recall pieces and portions. If I'm not around someone enough for them to make it to my long term memory, chances are I will never remember them. I use to cam alot simply for the more real interaction. (I liked to flash too, grins) . The only room I've been in at all since leaving the GCI is the Thassa Light House and the Black Tarn and it was only for maybe a half hour of time. And I had to beg leave because I was scared and worried. It sounds crazy, I'm sure.

Thank you Master for thinking of me and making an exception, I will try to get up the courage to do so.

Respectfully,
~twinkle





Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 5:12:50 AM)

quote:

ORIGINAL: MontrealPhoenix

Greetings twinkle
 
I cannot thank you enough for starting this thread. While those in our lives without disabilities like ours try to understand, and i'm grateful for those in mine, i don't think they do as well as we do. I think having people who understand will be a great help to all of us no matter what our disabilities are.
 
Right now, my hip is my greatest problem and luckily it appears to be temporary. My doctor has told me that after physio (that whole nuther kind of torture) i should be back to 100%. So at least there is hope.
 
Thank you once again and please don't hesitate to contact me on the other side if you ever want to talk.
 
live well,
 
Phoenix


Greetings Phoenix

You make me smile. And you are so welcome. This thread belongs to all of you. I'll pray that your hip remains a temporary problem and that you return to 100% fixed up. There really are so many of us with a disability, ailment, illness of some kind and usually we don't bring it into the open.

I was thinking earlier after I posted my own illnesses and problems openly that maybe I should not have told so much and then I thought.... you know what twinkle? It doesn't matter, it's you and it's real. Who could be scolded for that. And if by chance I were? I'd take it. We're learning so much about eachother, all of us all ready. The most important thing that came to my mind after posting was........ I'll never be seen the same again.
Because online we create an image in our minds about someone. We do it by their words, actions, character, personality, etc.

I am glad that there are a few people still around online that knew me before I became so......&%$#****!!!.
They were able to know who I was back then and who I've become since. It's hard merging two lives.

Thank you for the offer to talk on the flip side the same offer applies to you as well. smiles warmly

Sending a pain free hug your way
~twinkle




Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 5:29:53 AM)

quote:

ORIGINAL: Karynn

Tal again ya'll,

I thought it might be fun to recollect the positive moments before the pain, if you can recall one. I have a series of CDs my father found for me that are suggestive therapy, where the people talk in calm and very pleasant voice tones, and lead my brain on journies away from the pain. In the midst of one of them, the two voices say, "Remember a time when you were not in pain." then a voice echoes, "Or remember a time when you were in less pain than you feel you are now."

I was struck by several of you recounting your activity level at some time in the past, and the difficulty that we face trying to find ways to cope with that severely hindered freedom now. My case is not so different. Though some of my illness resulted from birth defects and kidney disease from the very beginning, there were many very well managed years of life that I was more in control than out of control. Those are the years that my brain returns to when I'm in that hypnotic therapy.

In 1996, I had my 11th surgery as an adult. I had spent the better part of my children's youth healing from various surgical procedures. Slowly but surely, after all the reconstruction and wiggling things around inside of me or just cutting them out, they left my body alone long enough to give it time to begin healing, and I was in my 20s, still full of youthful energy myself, and ready and chomping at the bit to join life again. I did so. It was my very best year of adult life, my favorite reflective year, the year we have the most photographs of me taken, and a year all of us look fondly back to with full memories. Even my younger son though only 4-5 at the time can remember that year because of all the significant things we did together as a family.

1996 was the year I was a soccer coach 3 nights a week and 1 game a weekend, then ref'd at least 1 other game, then sat through 1 more game that my sons played in on Saturdays. It was the year we were Pre-school coordinators for a very large church program, and hosted the 11 o'clock hour with 75 3 and 4 year olds every Sunday. It was the year I had a membership to a really nice Y-type gym and was in shape, the healthiest weight of my entire life, and fit. It was the year things just seemed to flow smoothly. We had such a great time with our boys, with our peers, active in private M/s lifestyle group, and the list seems endless. It was a very good year.

When I need one of those nudges, a pick-me-up to help cheer me up, I pull out the photo albums from that year. I flip through the pictures, and remember the events, the holiday at the beach, the soccer teams in spring and fall, and all the people who's lives touched ours. And when I lay in the quiet of the night, working hard to get comfortable enough to relax, even if I can't sleep officially, and I've got one of those CD's playing in my ears to encourage calmness, somewhere in that year is my favorite place to visit mentally.

I don't know if any of you have coping programs that work consistently for you. We're at a place in life where I've been willing to try various things. I tried herbs as you may remember, and they had way too much ick for way too little comfort. I've tried CDs with hypnotic therapy. I've tried sleeping on the floor and upright in a la-z-boy recliner, and found neither improved sleep. So when I do find something that helps, I use it often. And I focus on the good times. They always bring a smile.

What moments are your favorite, the ones that remind you of a time when you did smile more often, or could cope better, or had life by the tail?

K


Greetings Mistress

Recollecting positive moments before the pain-- is an excellent idea and wonderful advice. You said "What moments are your favorite, the ones that remind you of a time when you did smile more often, or could cope better, or had life by the tail?" -- My answer would have to be all 3 at the same time.

I have some coping stratagies, I've been in Pain Management for 4 years. But for me because I live with a PL8 and a 7 is a good day even though it's still very tough. My next question to the board is going to be just that...Coping stratagies so that everyone will have the opportunity to learn from one another by the stratagies others use. I really just try to laugh as much as I can and most of all laugh it all off. Make jokes about box in my right butt cheek, try to lighten the reality. And it's okay when others make fun back. It doesn't offend me. I recall when we went to the bank one day and my young son tells the teller almost loudly, " my mommy has a box in her butt". I almost died in laughter, I had to hold it back and the teller (and then the others that heard) were like, huh? My Master shushed his son immediately after, but it had already been said. I blushed and moved on.

My best thoughts and I recall them often is driving the kids everywhere, with the radio loud, all of us singing. Karaoke on a foot stool at home, the year I was in a walking boot, when I was first allowed to start trying to weight bear, my little son only 4 at the time pushed me outside in the wheelchair, handed me my crutches and said dominantly, commanding, "momma stand, now!" and I did and it hurt and he was my inspiration, "momma just one more step, just one more step. And he did this with me everyday until I was off the crutches and walking in that walking boot on my own even though it was only a few steps at a time. About 3 months later, I was walking again. I think back on that often and even today he pushes my limits, or tries to. He just turned 11.

Thank you for the inspirational reply Mistress

Sincerely,
~twinkle




amphoraHMTC -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 6:33:39 PM)

















ìQuote from a CM post <http://www.collarme.com/Hiskajirah>Hiskajirah

I fear erroring, even in a discussion room only
those who know me would understand my sentences
at times. I mix words up, sentences become
misunderstood and then I immediately rephrase it
by saying "she means......" And I repeat myself
for clarification. I can be told something now
and forget in the split of a second, so I'll
re-read posts and try to understand. I use to be
very good at writing and communicating and I've
lost much of it.

end quote"

..................................................................................................................................................................................................................

That is a lot of what this one feels too. Not
that she wishes her problems on anyone else but
is helped by knowing someone else has the same
problems. As in her mind is not working right to
her but others see her as fine. hiskajirah,
amphora has always thought your writings were
very good. My family and close friends say they
can tell a difference as to how she was before
the stroke, to now. But others who do not know
her think she is just whining. It is more fear
than whine. To not be able to control your own
thoughts at times is terrible. She feels this
post may be full of goofs as she is writing this
with a lot of passion, which tends to not let
her cognitive process work right. She refuses to
do a lot of chat rooms, as they move too fast
for her and role-playing No way! not that brave.

She works hard and long on her post to try to
get them as clear as possible. And of course
Master Malkinius has to approve so he catches
any errors she has. She rereads and proof reads
then rereads 4-6 times before she sends them to
him, Does them on MS word first, uses grammar
check, then uses the spell check on her mail
server, then Master Malkinius does another check
so you get a very critiqued result. Her first
one is just terrible. Maybe one time for giggles
she will beg to post without any corrections. LOL

Maybe we should have a thread of post without
any corrections and see how they look. We might
be surprised at ourselves. We each would at
least get to laugh at our own silly mistakes and
maybe lose some of our fear.

................................................................................................................................................................................................................

Mistress Karynn to save Master another post she
is adding it here, to get her mind at peace she
listens to Celtic singing in the Welsh language,
or to Native American songs. Her happy memories
are the times her 2 sons were in a Campfire
group, it was when they had just allowed boys to
join, she was the leader of the group had 24
2nd-3rd graders 3 preschoolers to keep under
control, Her oldest was in karate, youngest was
in gymnastics at the same time, 2 different
places one was for competitions, was president
of the PTA, she worked a 40 hour job on top of
that. She loved her life it was full, and had
purpose. Now she can't even keep track of her
day-to-day life.

................................................................................................................................................................................................................

hiskajirah, you asked about being Gorean helping
to cut back on the meds. She thinks it has, as
she just quit about 9 months ago taking all the
Bi Polar meds, Lithium, Topomax, Zoloft, since
finding her place in this lifestyle has changed
from the 13 meds to just 4, she actually started
cutting back 2 yrs ago when she realized she was
not fitting in the vanilla world anymore. But
finding the Gorean side has really helped.

................................................................................................................................................................................................................

She wants to thank all for their support. We
need to not hide our selves and help each other
more, she thinks as females we need to nurture
each other better. No disrespect meant for
anyone.

Posted with Master approval

amphora {HMTC}




welshvixen -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/11/2008 7:48:01 PM)

Greetings A/all,
 
Reading through this thread makes a girl realise just how lucky she is.
 
i would hope if i had to face half of what some of you have, i would do it with the same bravery and dignity that you all show.  Y/you all have my utmost respect.
 
well wishes,
 
vixen 




MontrealPhoenix -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 5:45:12 AM)

Greetings All and all,
 
I must confess to feeling a little frustrated. I went back to work this week, much sooner than i should have but i feel i had no choice. You see i work in a hospital processing and typing chart notes for the Oncology and Hematology departments. Despite warning the powers that be 3 months in advance of my surgery, noone was sent to be trained to replace me. Since the notes/letters i produce are used to plan treatments for very sick patients, i felt i had no choice but to go back to work this past Monday, although i do admit that not getting paid was an influence, albeit a small one.
 
Thursday and Friday, i would have liked to call in sick because i was in a world of pain, especially Friday when i felt so drugged up from having taken a full dose of Dilaudid. Yet i thought about all the work to be done and in i went. Frankly, i resent having to go in on days when the pain is so bad that not even Dilaudid was working. Yet that's how it is working in Healthcare, concern for employees takes a back seat to saving money every time.
 
As a result of having gone in, i will no doubt spend most of my weekend drugged out on Dilaudid as i'm beyond the point where Tylenol or even Advil will work. Besides there is only so much of that i can take before my reflux disease is awakened and i have to stop taking it.
 
Anyway, thank God for having this place to vent my frustration, otherwise i might have said things i shouldn't to my manager or someone who doesn't deserve to be dumped on.
 
well wishes,
 
Phoenix




slavejale -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 7:25:53 AM)

Greetings to the Free
greetings to the properties
greetings hiskajira

first i would like to say, i do believe in a higher power because there must be SOMETHING up there watching over me. Believe me. lol.

Second, like you i had a hard time though, i did  survive, describing myself in the chatroom for the same reason as you. i used my real, skin color, eye color, emotions, and everything.  one day one of the girls made reference in the chatroom to having a nose ring i sent her  message like...wow how does it feel to have a nose ring. (i think it was a nose ring not sure). she told me the that she really didnt have one i kind of like "oh" *chuckles*.  anyways, yes that was kind of hard for me as well, basically because i want people to know who i really am be it online/offline etc. etc. The first day i went into a Gor chatroom and said that i had caramel skin, i was asked was i really African American or was i just playing. i didnt take offense to it at all but it kind of suprised me.

well wishes to All and all




jesszabelle -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 8:04:50 AM)

Greetings, Mistress Karynn,

thank You so much for Your thoughtful post describing why it is that You hide Your pain. i smiled and shed a tear to see what i experience so well explained. my son often decries this habit of mine, as i don't seek help until my problems are well progressed. i've gotten better about that and about speaking of my issues with good friends. i still go out of my way to minimise the issues. we don't speak of such things. "it's not the done thing," you see.

i confess that i occasionally must use a cane. i abhor it. it screams, "look at me, i have a disability!" how improper that is! i use it far less that i probably ought. a good friend recently sent me to a site where they sell all manner of canes, though. i found a funky leopard print one. perhaps i can wrap my brain around seeing it as a great accessory instead of an advertisement  for my limitations.

i've had my issues since childhood, so i can't honestly remember living without them very clearly. as a child i studied classical piano, though. it was my haven and my heaven. nothing bad could touch me when i was in the living room playing my piano. even my siblings were forbidden to enter! in high school that ended when my problems progessed to the point where i could no longer play to my satisfaction. i gave it up in frustration.

having given this thread some thought, i've made a resolution: it's my goal to have a piano in my home again within a year's time. i'll never be able to play like a virtuoso, but i will be able to play like a jesszabelle. that's good enough.

i wish everyone well,
jesszabelle




sweetnessPP -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 9:35:19 AM)

Greetings to the Free,
Greetings to the slaves,
Greetings to guest of the board,

Thank you for starting this thread twinkle and thank you to all who have posted.  It is a help just knowing i am not alone in my feelings of frustration over not being able to do everything i want to/should do.  In addition to high blood pressure, i have arthritus in both knees and my back.  Both cause pain daily which at times is close to unbearable.  Also have severe lymphedema in both lower legs which causes pain and difficulty walking.  Raynaud's Phenomenon makes fingers ice cold, black, painful and close to useless at times.  i was diagnosed with young on-set Parkinson's disease 7 years ago and that is my biggest issue now.  It has progressed rapidly to where i have trouble walking, shake almost non-stop and lack of balance has caused several falls.  There aren't many options as i am almost peeked out on the drug dose.  There are other drugs but earlier on i tryed one and had hallucinations.  One of the medications i take is availble in patch form and we will probably try it to see if a steady release helps.  Other then that theres brain surgery which scares the bee-gee-be's outta me!!  Your awake during the operation!!!  Ekkkkk!!!!  Lately depression is setting in.   It takes me much longer to get things done around the house and i have had to admit that i just can not do some things anymore which hurts.  i remember days of running around finishing a chore list, running errands, volunteering at the childrens school and still having enough engery left to be pleasing to Sir after he returned home in the evening.  (In order to be awake in the evening now i need an afternoon rest, which feels like such a waste of time.)  Oh how i miss the old days!  

Thank you to those who shared their pain with us.  And a huge thank you to those of you who support us on a daily basis, letting us know we are still wanted/needed even if we aren't what we once were!

i wish you all well,
may you have more good days then bad,
and keep on smiling!
~sweetness~  :-)




Maahsatti -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 9:52:38 AM)

well twinkle,

I knew you back then and I know you now.
The only differance is that you have become more beautiful and pleasing in the eyes of this free.

serve and be well,
Mistress Maah




Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 3:31:07 PM)

quote:

ORIGINAL: amphoraHMTC

















ìQuote from a CM post <http://www.collarme.com/Hiskajirah>Hiskajirah

I fear erroring, even in a discussion room only
those who know me would understand my sentences
at times. I mix words up, sentences become
misunderstood and then I immediately rephrase it
by saying "she means......" And I repeat myself
for clarification. I can be told something now
and forget in the split of a second, so I'll
re-read posts and try to understand. I use to be
very good at writing and communicating and I've
lost much of it.

end quote"

..................................................................................................................................................................................................................

That is a lot of what this one feels too. Not
that she wishes her problems on anyone else but
is helped by knowing someone else has the same
problems. As in her mind is not working right to
her but others see her as fine. hiskajirah,
amphora has always thought your writings were
very good. My family and close friends say they
can tell a difference as to how she was before
the stroke, to now. But others who do not know
her think she is just whining. It is more fear
than whine. To not be able to control your own
thoughts at times is terrible. She feels this
post may be full of goofs as she is writing this
with a lot of passion, which tends to not let
her cognitive process work right. She refuses to
do a lot of chat rooms, as they move too fast
for her and role-playing No way! not that brave.

She works hard and long on her post to try to
get them as clear as possible. And of course
Master Malkinius has to approve so he catches
any errors she has. She rereads and proof reads
then rereads 4-6 times before she sends them to
him, Does them on MS word first, uses grammar
check, then uses the spell check on her mail
server, then Master Malkinius does another check
so you get a very critiqued result. Her first
one is just terrible. Maybe one time for giggles
she will beg to post without any corrections. LOL

Maybe we should have a thread of post without
any corrections and see how they look. We might
be surprised at ourselves. We each would at
least get to laugh at our own silly mistakes and
maybe lose some of our fear.

................................................................................................................................................................................................................

Mistress Karynn to save Master another post she
is adding it here, to get her mind at peace she
listens to Celtic singing in the Welsh language,
or to Native American songs. Her happy memories
are the times her 2 sons were in a Campfire
group, it was when they had just allowed boys to
join, she was the leader of the group had 24
2nd-3rd graders 3 preschoolers to keep under
control, Her oldest was in karate, youngest was
in gymnastics at the same time, 2 different
places one was for competitions, was president
of the PTA, she worked a 40 hour job on top of
that. She loved her life it was full, and had
purpose. Now she can't even keep track of her
day-to-day life.

................................................................................................................................................................................................................

hiskajirah, you asked about being Gorean helping
to cut back on the meds. She thinks it has, as
she just quit about 9 months ago taking all the
Bi Polar meds, Lithium, Topomax, Zoloft, since
finding her place in this lifestyle has changed
from the 13 meds to just 4, she actually started
cutting back 2 yrs ago when she realized she was
not fitting in the vanilla world anymore. But
finding the Gorean side has really helped.

................................................................................................................................................................................................................

She wants to thank all for their support. We
need to not hide our selves and help each other
more, she thinks as females we need to nurture
each other better. No disrespect meant for
anyone.

Posted with Master approval

amphora {HMTC}

 
Greetings amphora
 
I think sometmes we see ourselves as being worse or doing worse than we really are. In this, while I wish that you didn't experience the memory loss, the worry, the fear, the writing changes, I'm helped to that "someone else understands".

I fell asleep yesterday morning about 6:30 a.m after watching movies to fall asleep to. I just woke up about 2 hours ago. I've been wanting to make replies since I logged in and my mind is in scrabbled egg mode.

Mostly I make all my own replies, but from time to time when my Master isn't working, I'll read him my replies to others and that might be when he will say leave it out or give something else for her to add in it's place.

Online Gorean chatrooms had always made my nerves ramble because I knew I was being analized, watched etc. I could be over here having a real panic attack. lol

But also the best people I've ever come to know was through the internet and I'm happy to have met you now also.

Sincerely,
~twinkle




Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 3:45:59 PM)

quote:

ORIGINAL: MontrealPhoenix

Greetings All and all,
 
I must confess to feeling a little frustrated. I went back to work this week, much sooner than i should have but i feel i had no choice. You see i work in a hospital processing and typing chart notes for the Oncology and Hematology departments. Despite warning the powers that be 3 months in advance of my surgery, noone was sent to be trained to replace me. Since the notes/letters i produce are used to plan treatments for very sick patients, i felt i had no choice but to go back to work this past Monday, although i do admit that not getting paid was an influence, albeit a small one.
 
Thursday and Friday, i would have liked to call in sick because i was in a world of pain, especially Friday when i felt so drugged up from having taken a full dose of Dilaudid. Yet i thought about all the work to be done and in i went. Frankly, i resent having to go in on days when the pain is so bad that not even Dilaudid was working. Yet that's how it is working in Healthcare, concern for employees takes a back seat to saving money every time.
 
As a result of having gone in, i will no doubt spend most of my weekend drugged out on Dilaudid as i'm beyond the point where Tylenol or even Advil will work. Besides there is only so much of that i can take before my reflux disease is awakened and i have to stop taking it.
 
Anyway, thank God for having this place to vent my frustration, otherwise i might have said things i shouldn't to my manager or someone who doesn't deserve to be dumped on.
 
well wishes,
 
Phoenix


Greetings Phoenix

I hope that your frustration has eased and I hope that your pain is minimal. It was my intention when asking for this thread that we have a place to vent, babble, talk, discuss, all those things that may not be appropriate for other threads.

I'm happy people are using it as such. ~smiles

Sincerely,
~twinkle




Hiskajirah -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 3:54:48 PM)

quote:

ORIGINAL: slavejale

Greetings to the Free
greetings to the properties
greetings hiskajira

first i would like to say, i do believe in a higher power because there must be SOMETHING up there watching over me. Believe me. lol.

Second, like you i had a hard time though, i did  survive, describing myself in the chatroom for the same reason as you. i used my real, skin color, eye color, emotions, and everything.  one day one of the girls made reference in the chatroom to having a nose ring i sent her  message like...wow how does it feel to have a nose ring. (i think it was a nose ring not sure). she told me the that she really didnt have one i kind of like "oh" *chuckles*.  anyways, yes that was kind of hard for me as well, basically because i want people to know who i really am be it online/offline etc. etc. The first day i went into a Gor chatroom and said that i had caramel skin, i was asked was i really African American or was i just playing. i didnt take offense to it at all but it kind of suprised me.

well wishes to All and all


I have to giggle with you jale as my online chatroom experience was opposite, but just as funny. I do have several piercings, including a nose ring, now I understand that there were no um coochie rings in the books there were piered ear girls and those with nose rings, If I recall right, even some free women had the nose ring. So I described it as part of me (the nose ring) and was told not to use it in my descriptions. That tossed me back some as I just wanted to be me. The other part is that I'll describe my skin as either light caramel or lightly bronzed as I have a pigmentation of a darker color than caucasions. So I too have been asked about the heritage that comes with descriptions, but gosh, I've never (in reverse to the question you were asked) never been ask If I was white. Just starts laughing. wow at the things some people will say or ask.

Hoping you are having a good day.

Sincerely,
~twinkle




slavejale -> RE: Goreans with Disabilities- Support, Advice, Info, Venting & More! (4/12/2008 4:11:29 PM)

Greetings to the Free
greetings to the properties
greetings to hiskajira

A coochie ring? How's THAT for a true description *chuckles*. though i must admit that i while online i did receive an anklet with the three moons of Gor on it and i did "wear" it alot. but im not going to tell you that i was so bent on being true to what i typed, i actually went out to find a similar anklet. however, even that gift over the internent meant alot and it came from a special person whether She knows that i think She is special or not. 

call me crazy but i wanted to be so real, in the era of "fakes". i was actually appalled that one of the Masters in the room was strictly vanilla, but r/p His fantasies in the room. just be honest.

Anyways to keep this thread on track (cause i do have the tendency to go off on a tagent and derail things lol)...does having low self esteem a disability? Maybe not as severe as others, but still a disability all in the same?


well wishes All and all  (edited to add that)




Page: <<   < prev  1 [2] 3 4 5   next >   >>

Valid CSS!




Collarchat.com © 2012
Collarchat.com is a member of the Free Speech Coalition
Terms of Service Privacy Policy Spam Policy
0.3300781