READ! Read anything and everything, you'd be amazed what can give you
an idea for anything, poetry or otherwise.
Carry a notebook or a voice recorder around when you get an idea that
has to be set in writing.
Laura
Larissa, I'd love to hear the outline to this book you say you're
finishing with. I have so many!
One of them is titled Celina's Magic Jewell, it's at a publisher right
now - or the extended synopsis is at least. It's at Ellora's Cave
Publishing. I've had friends of mine go "Are you kidding?" Nope,
honest, they took all of three days to ask after the query letter, for
the extended synopsis. According to their guidelines, if it's a go from
there, they'll ask for the first five chapters, and then the whole
manuscript. Keep your fingers crossed. It took me a year to write that
manuscript to where it was even halfway decent, and I've done two
serious edits since then.
I also have e-books of poetry, two so far, and want to add more to that
number, but haven't had the chance. I've written poetry since I was a
little girl. I was all grown up when I started writing manuscripts,
LOL, 27 when I wrote my first one.
Laura
I gave you basics yesterday.
I'm not as bad as some could be, in regard to physical chaos that is.
I can still walk, though only at half the pace I used to manage. I
can still type, but there are days when even that is one tough
exercise. I read - a lot. I write about as much as I read, LOL.
I've had to learn how to pace myself because I can no longer go at
breakneck speed with everything. It's just not possible.
The site you sent me to is quite informative Larissa, thank you for
that.
A while ago, I started a Symptom Survey in another group I was once
part of. This Symptom Survey now has over 100 questions and some very
prestigious groups - (including the CDC) - are interested in seeing
our results when we have enough surveys filled out. We hope to gain a
lot of understanding into progression of the various diseases
connected to Fibromyalgia.
Now, no, I have never been diagnosed further than what I've told you.
Will they find more? Yeah, I imagine they'll find more when I
convince them to get some more complex screening done. I am getting
my eyes checked to figure out if there's a serious problem there -
it's getting very near frightening just to stand up and walk these
days, not just because of the rice crispy feeling I get, but because
half the time I feel like the floor's gonna smack me right in the
nose with me standing up. Definitely an eye thing, and definitely one
that happens regardless of speed at getting off my posterior.
I sincerely doubt this is in any way due to my medication, even the
one I no longer take. So many of my fellow sufferers have said
they're sissy drugs. Well, I'm not remotely large, perhaps sissy
drugs will work for a bit on me, LOL.
Laura
I do understand, I know several who have a terrible time just getting
to the keyboard because of their chaos - that's what I call it,
chaos - it's not just one thing that is affected by CFS, or Fibro, or
Poly or any of the rest, it's EVERYTHING. I've been part of other
fibro groups, but the creative half of me needs a place where I can
share what I can do and who I am in a more welcoming place, as this
would be.
Now, one of the groups I do recommend, if you have the energy, is a
new group that I helped create, but realized I couldn't be part of
because I don't have fibromyalgia, and don't want to just talk about
the illness, that group is named FibroHurts_SupportGroup. And they
are a wonderful bunch of people, including several from different
foundations and such that sponsor research in the dreaded diseases.
It is a Yahoo group, so shouldn't be hard to find.
I have learned to make it a point to stay away from my computer for
at least one full day. This is tough, and I mean tough, because on
average I get over a thousand email messages every day. But if I
don't "rest" I can't straighten everything in my brain in time
to "work". I work as a minister, online, and only online. I have
audio sermons through BlogTalkRadio twice a week and Bible lessons
the rest of the days written in blog format. It is awesome.
I also work as a writer/poet with a personalized poetry business.
That is fun, because I can help all kinds of people share good
things, remember their loved ones and all the rest. I, for one, am
glad to be here, and will definitely help keep the conversation going
if it ever gets to be a lull.
Laura A. Neff
A rainbow can be a simple view, one of eternity in every hue.
Hopefully a couple of the other members will chime in, but just to let you know a little bit about us... we are a fairly quiet group. For myself, I'm unable to type and therefore use dictation software. Part of my ongoing health issues that I continue to work through is difficulty speaking. It is often painful for me, therefore I'm not able to dictate nearly as much as I would like to.
I've been coming off the roughest six months of this problem (which I've had since the mid-90s) and am currently working on a couple of writing projects where I need to devote all of my writing/dictation time.
In a few weeks, hopefully I'll get these current project finished and can touch base with you again, but I don't ever do IM because my speech is too limited. Hope you understand and that you can get some other good feedback and
support here. Take the time to read the old messages. Several of us have posted some suggestions. I've also dealt with costochondritis and would like to wholeheartedly recommend the information you can find at the website: http://www.askwaltstollmd.com/ (I promise, there's enough to keep you busy here for weeks and weeks! especially if you check out the bulletin board & archives. I've learned a tremendous amount from him over the past few years.)
This is considered a significant amount of talking for me, so if you don't hear from me again for a while, please know I'm not ignoring you, simply applying myself to get this current writing project finished. Thanks! Larissa
--- On Thu, 2/5/09, Laura <poeticart169@...> wrote:
From: Laura <poeticart169@...> Subject:
[writing_beyond_fibromyalgia] I just found this group To: writing_beyond_fibromyalgia@yahoogroups.com Date: Thursday, February 5, 2009, 8:11 PM
I have Chronic Fatigue Syndrome and the way I deal with it has kept
me from remaining in several other groups. I write - a lot. I write
poetry, and so much more.
I am an ordained minister, and my CFS has, on many occasions, made it
hard to expand my ministry.
I have kept my ministry in an online forum - because I was told I
could not do much more than that as it were. I have been preaching
since 2007 when I was ordained.
I obviously write spiritual stuff as a result of my vocation. I am a
poet. I have had well over fifty poems published. A friend suggested
I consider a line of greeting cards, which I may do, because I do
have all-occasion poetry. I have already managed personalized poetry
and such.
I also have written a novel, though it would be for late teens early
adults, it's not as grown up as the one that may be in the works
soon.
Both of my grandmothers suffered CFS, but theirs wasn't diagnosed
until after they were diagnosed with more serious conditions,
including Polymialgia.
I was diagnosed with CFS 8 years after I was diagnosed with
Osteoarthritis and calcification of the bone structures in my body. I
have since been diagnosed with TMJ and Costochondritis.
I would love to share if any are willing to share as well. It is my
goal to have not only a line of all occasion cards, but a series of
cards and gifts specifically for the chronically ill to bring
awareness to this enormous population of human beings with
debilitating chronic illness.
And also what everyone has been doing with their writing. We may be a
small group, but I'd love to learn from each of you.
I was born in Texas, raised in the suburbs of St. Louis, and have lived
in Oklahoma, Illinois, Alabama and Georgia as well.
Now I am living in Georgia, with my husband, my four children and so
much more.
Laura A. Neff
I don't know if anyone else here would consider regular posting, but I
will try to keep the list active myself. I love to write, and I love to
interact with other writers. My doctor told me I couldn't lift, so that
pretty much cuts out any and all work of most genres. Good thing she
didn't say I couldn't type, I'd really go nuts.
Laura
PS. I read about hand/wrist braces worn at night. Is that for Carpal
Tunnel or Tendonitis? What kind of braces are they? I haven't been
tested but with my osteoarthritis it might be useful.
Larissa, I'd love to compare notes on writing. Find me anytime during
daylight hours 7AM to 6PM on Yahoo IM poeticart169 is my handle.
Would love to compare notes on writing techniques and even share
chapters of unpublished works if you like.
Laura A. Neff
--- In writing_beyond_fibromyalgia@yahoogroups.com, Larissa Lyons
<larissa_lyons@...> wrote:
>
> Hi all. I know the loop's been quiet, but I'm very happy to report
the recent release of my first novel-length book! :) Even though my
writing has slowed considerably the last six months, it's nice to see
such a tangible accomplishment, and to remind myself that I
*can*really do it. :-)
>
> An author on one of my writing groups just sent out the post below
(I'll paste it in its entirety) soliciting other authors and writers
who may have fibromyalgia and/or migraine headaches to participate in
a survey for an article she's writing. I wanted to pass on the
information in case anyone else was interested.
>
> Take care! Larissa
>
> Posted by: Charlotte Boyett-Compo
> I am writing an article on the proclivity of some writers to suffer
>
> from migraine headaches and fibromyalgia. If you are plagued by
either
>
> or both, would you have time to answer a few questions for me?
Please
>
> share this with your other writer acquaintances. I'd like to get as
>
> many responses as possible.
>
>
>
> If you would like to participate, please drop me a line offlist at
<<
>
> wndkepr @ iowatelecom. net >> without the spaces and put M.F.
Survey in
>
> the subject line.
>
>
>
> Charlee
>
I have Chronic Fatigue Syndrome and the way I deal with it has kept
me from remaining in several other groups. I write - a lot. I write
poetry, and so much more.
I am an ordained minister, and my CFS has, on many occasions, made it
hard to expand my ministry.
I have kept my ministry in an online forum - because I was told I
could not do much more than that as it were. I have been preaching
since 2007 when I was ordained.
I obviously write spiritual stuff as a result of my vocation. I am a
poet. I have had well over fifty poems published. A friend suggested
I consider a line of greeting cards, which I may do, because I do
have all-occasion poetry. I have already managed personalized poetry
and such.
I also have written a novel, though it would be for late teens early
adults, it's not as grown up as the one that may be in the works
soon.
Both of my grandmothers suffered CFS, but theirs wasn't diagnosed
until after they were diagnosed with more serious conditions,
including Polymialgia.
I was diagnosed with CFS 8 years after I was diagnosed with
Osteoarthritis and calcification of the bone structures in my body. I
have since been diagnosed with TMJ and Costochondritis.
I would love to share if any are willing to share as well. It is my
goal to have not only a line of all occasion cards, but a series of
cards and gifts specifically for the chronically ill to bring
awareness to this enormous population of human beings with
debilitating chronic illness.
Rev. Laura A. Neff
Co-Owner Poetic Expressions
http://www.poetic-expressions.net
Minister Covenant of Hope Ministries
http://www.mychurch.org/covenantofhopeministrieshttp://www.freewebs.com/covenantofhopeministries/index.htm
God puts rainbows in the clouds so that each of us-- in the dreariest
& most dreaded moments can see a possiblity of hope. Maya Angelou
Hi all. I know the loop's been quiet, but I'm very happy to report the recent release of my first novel-length book! :) Even though my writing has slowed considerably the last six months, it's nice to see such a tangible accomplishment, and to remind myself that I *can*really do it. :-)
An author on one of my writing groups just sent out the post below (I'll paste it in its entirety) soliciting other authors and writers who may have fibromyalgia and/or migraine headaches to participate in a survey for an article she's writing. I wanted to pass on the information in case anyone else was interested.
Take care! Larissa
Posted by: Charlotte Boyett-Compo I am writing an article on the proclivity of some writers to suffer
from migraine headaches and fibromyalgia. If you are plagued by either
or both, would you have time to answer a few questions for me? Please
share this with your other writer acquaintances. I'd like to get as
many responses as possible.
If you would like to participate, please drop me a line offlist at <<
wndkepr @ iowatelecom. net >> without the spaces and put M.F. Survey in
the subject line.
Hi Vick and Larissai: Sorry to hear you both are having a flare-up. I just got back from the doctor and it looks like I may have to have another operation on my left shoulder, but that is a bit down the road as I need more tests. Still, I'm blugging along. I hope both of you are feeling better really soon.
In our group we have two members, one blind and the other with severe cerebal palsy. Both us Dragon and love it. So it is something we should probably consider for the future, maybe even the shorter future.
Take care of yourselves. I'll be sending good vibes your way.
Carol Jo Kachmar
--- On Tue, 10/7/08, Vicki Lockwood <vickilockwood@...> wrote:
From: Vicki Lockwood <vickilockwood@...> Subject: Re: [writing_beyond_fibromyalgia] Larissa checking in and saying hi To: writing_beyond_fibromyalgia@yahoogroups.com Date: Tuesday, October 7, 2008, 9:54 PM
Hi, Larissa:
Yes, I've had some bad months, with no real writing. This week I received a message from an epublisher, that if I made some changes in my manuscript, they would be interested in a re-submission, so I guess I will try to do that. I've decided I can't do NaNo this year, so maybe I'll use November to do a revision.
I balanced the checkbooks today, which ended in pain. Ice paks, heat pads, pain pills. I'm trying everything. But even in pain, I'm keeping a close eye on the emails because I still have some queries out.
One day I may try the Dragon software.
You should be proud of yourself for those daily words. Every word counts!
Subject: [writing_beyond_ fibromyalgia] Larissa checking in and saying hi
Hi everybody. I know it's been a long time since anyone posted and I just wanted to check in and say howdy.
Vicki, I saw on the Roses Loop a few weeks back that you're having a rough time of it... I can really empathize. This summer has been the worst ever for me when it comes to talking and since I dictate my typing, I really felt silenced. Fortunately, I was able to get in a lot of handwriting and ended up with two spirals' worth of a story that I'm still working to get dictated. Even when it was only 100 words in a day, I felt really great just getting something out.
Dragon NaturallySpeaking just released version 10 and it's supposed to have much greater accuracy. When my voice is stronger, I'm hoping to give that a try!
Anyway, I have been thinking of everyone and hope that y'all are doing well. Larissa
Yes, I've had some bad months, with no real writing. This week I received a message from an epublisher, that if I made some changes in my manuscript, they would be interested in a re-submission, so I guess I will try to do that. I've decided I can't do NaNo this year, so maybe I'll use November to do a revision.
I balanced the checkbooks today, which ended in pain. Ice paks, heat pads, pain pills. I'm trying everything. But even in pain, I'm keeping a close eye on the emails because I still have some queries out.
One day I may try the Dragon software.
You should be proud of yourself for those daily words. Every word counts!
Subject: [writing_beyond_fibromyalgia] Larissa checking in and saying hi
Hi everybody. I know it's been a long time since anyone posted and I just wanted to check in and say howdy.
Vicki, I saw on the Roses Loop a few weeks back that you're having a rough time of it... I can really empathize. This summer has been the worst ever for me when it comes to talking and since I dictate my typing, I really felt silenced. Fortunately, I was able to get in a lot of handwriting and ended up with two spirals' worth of a story that I'm still working to get dictated. Even when it was only 100 words in a day, I felt really great just getting something out.
Dragon NaturallySpeaking just released version 10 and it's supposed to have much greater accuracy. When my voice is stronger, I'm hoping to give that a try!
Anyway, I have been thinking of everyone and hope that y'all are doing well. Larissa
Hi everybody. I know it's been a long time since anyone posted and I just wanted to check in and say howdy.
Vicki, I saw on the Roses Loop a few weeks back that you're having a rough time of it... I can really empathize. This summer has been the worst ever for me when it comes to talking and since I dictate my typing, I really felt silenced. Fortunately, I was able to get in a lot of handwriting and ended up with two spirals' worth of a story that I'm still working to get dictated. Even when it was only 100 words in a day, I felt really great just getting something out.
Dragon NaturallySpeaking just released version 10 and it's supposed to have much greater accuracy. When my voice is stronger, I'm hoping to give that a try!
Anyway, I have been thinking of everyone and hope that y'all are doing well. Larissa
Hi Bernice: I've been out of the country and so missed your message until now. I have a lesser case of fibro than Vicki or Larissa, but I do have a few suggestions to add to their excellent ones.
Be sure to check how your computer keyboard is set so the strain on your arms and wrists is not aggravated. Also, it's a good idea to type for short periods of time, say no more than 20 minutes, and then take a break and rest before typing again. It also helps to rest your eyes which can be strained by the computer screen
I would also agree with Vicki that the braces at night would be a great help. Larissa's idea of checking out physical therapy exercises for your hands and arms would be a great help though I found out you must keep them up to reap the benefit. Don't get discouraged if they don't help right away; they will if you keep at them.
You
also might get some relief from having a doctor prescribe Flexeril. It's a muscle relaxer which sometimes helps, but don't use it and then try to drive your body too hard or too long. If you do, the times without the drug will be a misery. Remember, the inflammation must heal before you can really put in time on the keyboard which is why the use of Dragonspeak and recorders to get down your ideas are such good ones.
Good luck and let us know how you do with these suggestions.
Carol Jo Kachmar
bwakefied <bwakefied@...> wrote:
Hello everyone, I am 18 and i love to write I have had a couple of stories published (only short ones, nothing major) but I found out today that i have carpal tunnel syndrome I found this group because I thought it would be helpful for me, I've been told by the doctor to cut back n my writing and ay advice or anyhing would be very much appreciated thankyou Bernice
Thankyou very much for the advice =)
--- In writing_beyond_fibromyalgia@yahoogroups.com, "Vicki Lockwood"
<vickilockwood@...> wrote:
>
> Hi Bernice:
> My doctor told me that wearing the stiff wrist braces during the night was the
best thing
I could do unless I wanted surgery. So I wear them and I do okay. I can't
write for hours
on end without pain. But I can dictate into a small recorder, get my thoughts in
order,
then type for a while. Then rest. It's working for me, so far.
> Vicki
> ----- Original Message -----
> From: bwakefied
> To: writing_beyond_fibromyalgia@yahoogroups.com
> Sent: Monday, June 30, 2008 1:19 PM
> Subject: [writing_beyond_fibromyalgia] Hello
>
>
> Hello everyone,
> I am 18 and i love to write I have had a couple of stories published (only
short ones,
nothing
> major) but I found out today that i have carpal tunnel syndrome
> I found this group because I thought it would be helpful for me, I've been
told by the
doctor
> to cut back n my writing and ay advice or anyhing would be very much
appreciated
> thankyou
> Bernice
>
My doctor told me that wearing the stiff wrist braces during the night was the best thing I could do unless I wanted surgery. So I wear them and I do okay. I can't write for hours on end without pain. But I can dictate into a small recorder, get my thoughts in order, then type for a while. Then rest. It's working for me, so far.
Hello everyone, I am 18 and i love to write I have had a couple of stories published (only short ones, nothing major) but I found out today that i have carpal tunnel syndrome I found this group because I thought it would be helpful for me, I've been told by the doctor to cut back n my writing and ay advice or anyhing would be very much appreciated thankyou Bernice
Hi Bernice! Overall, we're a fairly quiet group, but I do know if you check the old messages, there's been a lot of great suggestions shared. I also posted a couple of tips that really help me on my website a couple of months ago. I'll copy them below. I had the surgery for CTS Release and it didn't help a lick, so I strongly recommend checking out physical therapy or any other exercises you can do that will strengthen your hands and arms in general, and agree with your doctor about cutting back. Every individual has their own "tolerance" level that they can write to without pain, or at least with manageable pain. The trick is finding yours so you can keep writing without harming your body!
I wish you the best of luck. :-) Larissa
NEW WRITING TIPS
Actually, these are the first writing tips ever, but I guess they still qualify as being new. :-)
As an author dealing with a disability, I thought I'd share a couple of my best writing tips—tricks of the trade, that allow me to write and keep the voices in my head from bubbling over!
Dragon NaturallySpeaking—dictation software. If it weren't for this, I wouldn't be able to write my stories at all. Typing is out of the question due to pain and swelling, but when everything is working as it should (thanks to Mr. Lyons!...yes, my dear spouse is used to responding to the occasional "Help! It's not recognizing my words" pleas for assistance and fortunately, he's very good at keeping everything operating in top shape) I "talk" my story and characters into the computer. This software has made significant strides over the years. I've been using it since 1996 and the recent versions have come along tremendously, only I still have to teach it all of the "naughty" words!
R.S.V.P. fine point pens by Pentel—the best pen I've ever used, bar none. Granted, I've never tried truly expensive pens, but I wasn't able to write more than a sentence or so with Bic and the like, and for several years I despaired of ever being able to write letters, much less chapters, again. Then I discovered this wonderful writing instrument. It fairly glides over the pages. I write almost every bit of my stories longhand and then dictate from spiral-bound pages.
--- On Mon, 6/30/08, bwakefied <bwakefied@...> wrote:
From: bwakefied <bwakefied@...> Subject: [writing_beyond_fibromyalgia] Hello To: writing_beyond_fibromyalgia@yahoogroups.com Date: Monday, June 30, 2008, 1:19 PM
Hello everyone,
I am 18 and i love to write I have had a couple of stories published (only short ones, nothing
major) but I found out today that i have carpal tunnel syndrome
I found this group because I thought it would be helpful for me, I've been told by the doctor
to cut back n my writing and ay advice or anyhing would be very much appreciated
thankyou
Bernice
Hello everyone,
I am 18 and i love to write I have had a couple of stories published (only short
ones, nothing
major) but I found out today that i have carpal tunnel syndrome
I found this group because I thought it would be helpful for me, I've been told
by the doctor
to cut back n my writing and ay advice or anyhing would be very much appreciated
thankyou
Bernice
Hi everyone. I was so happy to read Vicki's post and suggestion about staying in touch (and the e-mails that spawned!).
I apologize for being MIA both recently and last fall. Right after we all agreed to start this group, I had the biggest "fibro-flare" I've had in a couple of years and just had to get off the computer for a while. It seemed as soon as that cleared, we had some work done on our floors and the chemicals knocked me out again. I've been doing significantly better this year, other than a week-long bout with the flu I'm just now getting over. It's ironic, but it seems that since being diagnosed (mid 90s) and cleaning up my diet and environment, I hardly ever get "sick" with colds and stuff. Yeah, the day to day existence is often very painful, but it's amazing how catching a cold/virus can really slow you down.
Okay, for the good stuff -- What helps me with overall feeling better -- eating plain, simple foods without chemicals or extensive preparation; I keep proteins and starches separate and that has helped my digestion/IBS symptoms all but disappear. with WRITING -- I use a touchpad by Cirque and highly recommend it (regular-style mouses [mice?] are murder on my wrist and hands after just 3-5 clicks) . Secondly, I don't type as even a single sentence can be enough to spark significant arm and wrist pain...I use dictation software. The price is low enough I think anyone can give it a shot and thank goodness it has improved like it has the last few years. This is the only thing that truly enables me to write on a professional level at all.
I also hand write all of my stories in a notebook. That way, I can dictate the story when I'm feeling up to it and as my throat allows.
Now I'll throw out what I have the most trouble with and see if anyone has any suggestions...
Honestly, it's e-mails. I made a commitment last fall to always write first, and surf the Internet/check e-mail second, which means I often don't get past my writing goal for the day.
I've been thinking of dedicating one day a week to e-mails, but I try not to be on the computer every day, and just haven't been sure how to balance writing and storytelling with promotion and business-keeping. Any suggestions there?
Reading over Diana's e-mail and remembering how I felt the first few years after being diagnosed (often very hopeless and depressed), I also realized I found a nontraditional chiropractor (ironically, another doctor altogether recommended him...after reading my 3 page typed list of symptoms and diagnoses) anyway, he was able to identify that a lot of my fibromyalgia-attributed pain was caused by lingering viruses and bacteria. Once we cleared that together, a good percentage of my symptoms lessened significantly. I tried a number of medications the first 5+ years, and after taking them and having a lot of side effects, I've chosen to go the natural route as much as possible. When I hurt, I do my best to stop (don't always succeed...) because I feel like our hurting isn't normal, which means my body isn't reacting normally, and I have to keep reminding myself that it's OK not to push trying to do a "normal" output.
And now I've gone hoarse :) so it's time to stop. Larissa
Well, I'm glad that there are at least three of us who might be able to stay in touch. I don't know Larissa, so I can't contact her. I'm glad the timer and the notebook idea helped you two. Here's another idea for you. I wrote an article on using two Energy Bank Accounts--one like a checking account and one like a savings account. It takes a littel work in the beginning, but it works really well. Just give everything you do a number, positive if it makes you feel better and negative if it makes you feel worse. Start the checking account in the morning by giving your sleep a positive number, then start subtracting as you work and adding as you rest. This is a project that will take you at least a week to get the numbers right. The Savings account is for when you end up with a good positive number at night, you have excess energy. Transfer the number to the savings account. When your savings account hits a really high number, you can use it to do things like take a vacation, or do something that takes a lot of energy.
I give myself 10 energy points for every hour that I sleep, then subtract two points for each of those hours that something woke me, even if only for a couple minutes. And if I have above sixty points at bedtime, the number higher than sixty gets transferred to the savings. This is a way to track your pace and keep you from overdoing it.
Think it over, and if you want to try it, start on a day that is normally an easy one, because this will take its own energy.
Okay, it's back to bed for me. This is my easy day.
Sorry I couldn't answer right away. I got myself in a real bind of too many online classes in one month. Ridiculous, I know, so I go swamped. I still have one class to finish, but finally have a bit of breathing room.
I would hope we could keep the group going though I don't think, with all the writing I have to do in March that I could write each week unless it was just a note to say I'm still here and kicking.
Vicki, I wanted to thank you for the timer idea. It really does help as I sometimes get so into my writing that I lose track of time and find I've written for hours only to pay dearly for it later especially when the pain keeps me from sleeping.
Has anyone heard from Larissa? She is in my contacts list as being one of us also, but I haven't seen an answer from her. I think I have her regular e-mail in my contacts and could send it along if you wish.
I wish you all a great March and hope to hear from you all again.
Carol Jo Kachmar
--- In writing_beyond_fibromyalgia@yahoogroups.com, "Vicki Lockwood" <vickilockwood@...> wrote: > > Hi, Diana: > I think we all feel that way. Rather than fill a message with 'woe is me', we choose to not send a message. Maybe we could share what works for us sometimes, or what we tried that didn't work. I'll go first. > The timer works great, if I make myself us it. Tramadol helps sometimes, if the pain isn't horrible. If the pain is horrible, I use ice on the burning pain, and heat on the shooting pain. Also, I can't afford Lyrica, but my doctor got me a seven day trial pak and it seemed to help with both the pain and the fog, so I contacted Pfizer and submitted an application for a free Rx. > And for the writing? I take a 70 page spiral notebook to bed with me. I make notes. I plot, I plan, I do character sketches, even though I'm not a plotter or a planner. > Okay, your turn. > Vicki > ----- Original Message ----- > From: Diana Bolling > To: writing_beyond_fibromyalgia@yahoogroups.com > Sent: Thursday, February 21, 2008 11:51 AM > Subject: Re: [writing_beyond_fibromyalgia] Hi All > > > > I never really know what to say. Yes I hurt and my head is foggy more times than not. During my few brief minutes of clarity I do get a great idea...it is the following up on it that causes me to fall flat. > > I dont want to appear as a whiney person so I dont let on about my pain most days. I wish that there were a cure for this. It is really a hellish existance at times. > > Diana > > twelvestoneslady <vickilockwood@...> wrote: > I'm just wondering if this group is dead. I love the idea of staying in > touch with others who understand how hard it is to write and deal with > pain at the same time. But I checked my Yahoo groups today and had 56. > So, are we going to use this space? I've eliminated six groups that are > just sitting there, doing nothing. I'm a member of several groups on > health and several on writing, and I think this one could really help > all of us. Except, we're all ignoring it. > I'm willing to put one day a week on my calendar to post a message, if > everyone else will do the same. Whadayasay? > Vicki >
Hi Again:
Found Larissa's e-mail. Its larissa_lyons@...
Vicki, forgot to say that I hope you get the free Lyrica but be careful
with it as it has some whopper side effects as it was designed to help
epileptics orginally.
I really like your idea of a notebook by the bed. I often get an idea
just as I'm going to sleep, but sometimes lose it when I wake up. That
is such a simple idea to stop the frustration that I wonder I didn't
think of it before. Thanks!
Carol Jo
Hi Vicki and Diana:
Sorry I couldn't answer right away. I got myself in a real bind of
too many online classes in one month. Ridiculous, I know, so I go
swamped. I still have one class to finish, but finally have a bit of
breathing room.
I would hope we could keep the group going though I don't think, with
all the writing I have to do in March that I could write each week
unless it was just a note to say I'm still here and kicking.
Vicki, I wanted to thank you for the timer idea. It really does help
as I sometimes get so into my writing that I lose track of time and
find I've written for hours only to pay dearly for it later
especially when the pain keeps me from sleeping.
Has anyone heard from Larissa? She is in my contacts list as being
one of us also, but I haven't seen an answer from her. I think I
have her regular e-mail in my contacts and could send it along if you
wish.
I wish you all a great March and hope to hear from you all again.
Carol Jo Kachmar
--- In writing_beyond_fibromyalgia@yahoogroups.com, "Vicki Lockwood"
<vickilockwood@...> wrote:
>
> Hi, Diana:
> I think we all feel that way. Rather than fill a message with 'woe
is me', we choose to not send a message. Maybe we could share what
works for us sometimes, or what we tried that didn't work. I'll go
first.
> The timer works great, if I make myself us it. Tramadol helps
sometimes, if the pain isn't horrible. If the pain is horrible, I use
ice on the burning pain, and heat on the shooting pain. Also, I can't
afford Lyrica, but my doctor got me a seven day trial pak and it
seemed to help with both the pain and the fog, so I contacted Pfizer
and submitted an application for a free Rx.
> And for the writing? I take a 70 page spiral notebook to bed with
me. I make notes. I plot, I plan, I do character sketches, even
though I'm not a plotter or a planner.
> Okay, your turn.
> Vicki
> ----- Original Message -----
> From: Diana Bolling
> To: writing_beyond_fibromyalgia@yahoogroups.com
> Sent: Thursday, February 21, 2008 11:51 AM
> Subject: Re: [writing_beyond_fibromyalgia] Hi All
>
>
>
> I never really know what to say. Yes I hurt and my head is foggy
more times than not. During my few brief minutes of clarity I do get
a great idea...it is the following up on it that causes me to fall
flat.
>
> I dont want to appear as a whiney person so I dont let on about
my pain most days. I wish that there were a cure for this. It is
really a hellish existance at times.
>
> Diana
>
> twelvestoneslady <vickilockwood@...> wrote:
> I'm just wondering if this group is dead. I love the idea of
staying in
> touch with others who understand how hard it is to write and
deal with
> pain at the same time. But I checked my Yahoo groups today and
had 56.
> So, are we going to use this space? I've eliminated six groups
that are
> just sitting there, doing nothing. I'm a member of several
groups on
> health and several on writing, and I think this one could
really help
> all of us. Except, we're all ignoring it.
> I'm willing to put one day a week on my calendar to post a
message, if
> everyone else will do the same. Whadayasay?
> Vicki
>
I think we all feel that way. Rather than fill a message with 'woe is me', we choose to not send a message. Maybe we could share what works for us sometimes, or what we tried that didn't work. I'll go first.
The timer works great, if I make myself us it. Tramadol helps sometimes, if the pain isn't horrible. If the pain is horrible, I use ice on the burning pain, and heat on the shooting pain. Also, I can't afford Lyrica, but my doctor got me a seven day trial pak and it seemed to help with both the pain and the fog, so I contacted Pfizer and submitted an application for a free Rx.
And for the writing? I take a 70 page spiral notebook to bed with me. I make notes. I plot, I plan, I do character sketches, even though I'm not a plotter or a planner.
I never really know what to say. Yes I hurt and my head is foggy more times than not. During my few brief minutes of clarity I do get a great idea...it is the following up on it that causes me to fall flat.
I dont want to appear as a whiney person so I dont let on about my pain most days. I wish that there were a cure for this. It is really a hellish existance at times.
I'm just wondering if this group is dead. I love the idea of staying in touch with others who understand how hard it is to write and deal with pain at the same time. But I checked my Yahoo groups today and had 56. So, are we going to use this space? I've eliminated six groups that are just sitting there, doing nothing. I'm a member of several groups on health and several on writing, and I think this one could really help all of us. Except, we're all ignoring it. I'm willing to put one day a week on my calendar to post a message, if everyone else will do the same. Whadayasay? Vicki
I never really know what to say. Yes I hurt and my head is foggy more times than not. During my few brief minutes of clarity I do get a great idea...it is the following up on it that causes me to fall flat.
I dont want to appear as a whiney person so I dont let on about my pain most days. I wish that there were a cure for this. It is really a hellish existance at times.
Diana
twelvestoneslady <vickilockwood@...> wrote:
I'm just wondering if
this group is dead. I love the idea of staying in touch with others who understand how hard it is to write and deal with pain at the same time. But I checked my Yahoo groups today and had 56. So, are we going to use this space? I've eliminated six groups that are just sitting there, doing nothing. I'm a member of several groups on health and several on writing, and I think this one could really help all of us. Except, we're all ignoring it. I'm willing to put one day a week on my calendar to post a message, if everyone else will do the same. Whadayasay? Vicki
I'm just wondering if this group is dead. I love the idea of staying in
touch with others who understand how hard it is to write and deal with
pain at the same time. But I checked my Yahoo groups today and had 56.
So, are we going to use this space? I've eliminated six groups that are
just sitting there, doing nothing. I'm a member of several groups on
health and several on writing, and I think this one could really help
all of us. Except, we're all ignoring it.
I'm willing to put one day a week on my calendar to post a message, if
everyone else will do the same. Whadayasay?
Vicki
Hi Vicki:
Great to hear from you. I wondered if the group was still in
business. Also, that is a great idea about the timer. I will be sure
to use it.
Hope all is going well with everyone in the group. I, unfortunately,
have a flareup of my fibro and a terrible cold at the same time but am
recovering.
Take care of yourselves, all of you.
Carol Jo Kachmar
Hi All:
Just wanted to share one thing that I do to help me pace myself. I
bought a kitchen timer to set by my screen and when I sit down to work
on a long project, I set it for thirty minutes and when that time is
up, I stop for a moment and go do something else--anything that makes
me move around some.
I hope this helps someone else as much as it does me. Your brain
doesn't have to stop just because your fingers do. Stand up. Do a yoga
pose. Fill the sink with hot water and put the dishes in. walk on the
treadmill for five minutes, or sit down and just take a break.
Can't wait for this group to take off. I think it's really going to
help members who struggle with chronic pain and fatigue.
Have a great weekend.
Vicki Lockwood
Hi Larissa: Well, your plans sound fine to this computer neophyte. I love that you have started the group, but also like you, I cannot be inundated with tons of email as it interfere's with my writing. The files on topics sounds great.
Thanks for all your work on this.
Carol Jo Kachmar
Larissa Lyons <larissa_lyons@...> wrote:
A quick hello to everyone that signed up -- and thanks!
Over the next few days, I'm going to review
the posts from the 50 Books group and send invitations to join us to those folks that posted on any of the health-related threads. If you know of anyone else that might appreciate or be able to contribute to this group, please tell them about it or e-mail and let me know so I can invite them too.
I've been thinking of a few ways to make this a productive, beneficial group without anyone feeling inundated by e-mails (raising hand :) -- one idea I've had is to utilize the Files section for different topics such as "bodywork", "Critique or Writing Tips", "introductions", etc. While the group is small, it will be easy to get to know one another and hopefully exchange positive ideas, but as we grow, I thought it might be easier for new members to reference information if we're able to organize it by topic using Word documents that are updated regularly (maybe monthly), with primarily questions posted on the group. I'm
all ears if anyone has comments or other suggestions. Please let me know what you think of this idea and anything else you'd like to share.
I'm really excited about networking with other authors dealing with similar health issues. I don't live near any RWA chapters and my primary writing buddy is 1700 miles away :-) so I'm looking forward to getting to know the folks on this loop.
A quick hello to everyone that signed up -- and thanks!
Over the next few days, I'm going to review the posts from the 50 Books group and send invitations to join us to those folks that posted on any of the health-related threads. If you know of anyone else that might appreciate or be able to contribute to this group, please tell them about it or e-mail and let me know so I can invite them too.
I've been thinking of a few ways to make this a productive, beneficial group without anyone feeling inundated by e-mails (raising hand :) -- one idea I've had is to utilize the Files section for different topics such as "bodywork", "Critique or Writing Tips", "introductions", etc. While the group is small, it will be easy to get to know one another and hopefully exchange positive ideas, but as we grow, I thought it might be easier for new members to reference information if we're able to organize it by topic using Word documents that are updated regularly (maybe monthly), with primarily questions posted on the group. I'm all ears if anyone has comments or other suggestions. Please let me know what you think of this idea and anything else you'd like to share.
I'm really excited about networking with other authors dealing with similar health issues. I don't live near any RWA chapters and my primary writing buddy is 1700 miles away :-) so I'm looking forward to getting to know the folks on this loop.