Why wear a ribbon?

"Because I wish to make others aware that although I look ok on the outside, insi..." (oroman)

MDJunction to me

"MDJunction to me has been the helping friends of understanding that I have needed. I feel now as if someone else it the world understands the things that I am going through. I feel less alone and happier. Here I can let out all my emotions and get support from many people who have been in similar situations. It really has been a life saver for me!" (Amanda78)
We comply with the HONcode standard for trustworthy health information:
verify here.
Fibromyalgia Online Support Group
A community of patients, family members and friends dedicated to dealing with Fibromyalgia, together.
Join This Group
Group Home   Forums   Articles   Members (1756)   Diaries   Leaders   Guidelines
FMS Community FMS Support Forums General & Support How Fibro Affects Work...Besides the Obvious
Related discussions:
02/20/2008 05:31
rockmygypsysoul
Purple Ribbon
Posts: 26
New Member

Send a PM
Give a Hug
Hi all~ I'm new here, so be patient and forgiving if this has been talked about before (at least recently), but Im wondering how others who are able to work feel that their job or career has been affected by FMS.

More accurately, Im wondering if there are particualr things people have done that have helped them get through the day, especially related to certain symptoms. I'm also curious as to what non-narcotic drugs have worked for people who can't take them for their job...

Basically, my memory and focus is absolutely imperative for my job, so Im struggling a little with fibrofog - doing okay at work, but not great. I've been doing daily logic puzzles at night to try to encourage my mind to work, but Im wondering if there are any little tips or tricks anyone has.

Also, in my job I am periodically "on" but then can have some downtime between those times. When I have to be on, I absolutely have to be. And so far, Im pulling it off pretty well. What Im struggling with is what I can do in my downtime - while still being somewhat productive (so no sleeping!) to help refresh myself...?

Lastly (this has gotten lengthy!) I absolutely cannot take narcotics while I'm at work. Although Vicodin, etc. at this point really doesnt make me tired or dizzy, the mere fact that I was on a narcotic while at work, if it was found out, could destroy a case (I interview kids about sexual abuse). Does anyone have ANY ideas about ways to help take the edge off the pain while I'm at work so I can function but can't impair me?

Reply  


02/20/2008 06:49
truckin_angel
Purple Ribbon
Posts: 170
Member

Send a PM
Give a Hug
Hi, first welcome to the group.

I dont know if i can help at all because i quit my job when i was diagnosed with fibro but now i go to school full time although its alot different than work. I only take my muscle relaxors at bedtime and i also take Tramadol 4 times a day for pain. The Tramadol works good i think, i still have pain but i am able to get up and move around most of the time.

As far as the fibro fog, i have that really bad and i havent found anything that helps. There are times i just stare off in space, forget to write things down, forget about meetings, classes, etc...but thank the Lord i have friends who help me and covers my butt when they need to.

Sorry i couldnt be more help, hope things get better for u.

Hugs, Alicia

Reply  


02/20/2008 07:17
skynate
Purple Ribbon
Posts: 28
New Member

Send a PM
Give a Hug
my dumb doctor told me to take tylenol only, so i cant work right now,,, my job is a on your feet 8to 9 hour job which my body cant handle, hopefully that i will find someone to get me back to work, that is all i want to do , but have stupid rheumy that wont let me do anything, wanted me in his stupid date rape drug trial and wouldnt give me anything, i am praying for insurance and getting to dr in louisville, i want to work i want to get better to work but cant get no help from doc to get back to work and he is gonna get me fired because he wont fill my papers out for a leave of absence so i will have to find new job when and if i can work.
Teresa
Reply  


02/26/2008 07:55
angelcath6567
Purple Ribbon
Posts: 95
Member

Send a PM
Give a Hug
I am not sure I can help much either. However, I am a Customer Service Rep and am on the phones all day. Since I was just getting back to work after spinal fusion when this fibro started (or got bad) I only work part time right now, but I am trying hard to get back to full time and having a real hard time getting there! As a customer service rep, I have to be alert. I have a real hard time with the fibro-fog. I will forget, in seconds, what I was talking about or what the customer is asking. Its real tough. I am on Lyrica 3 times a day and take Lortab for breakthrough pain. Tramadol might be an idea since that is not a narcotic.

Your job must be so rewarding!! But I can imagine it must be quite stressful which can't help! Good luck to you! I know I am not much help, but this thread hits hard as I can't decide if I should continue working or apply for disability, so I had to respond.

Fibro hugs

Cath

Reply  


02/26/2008 09:43
mamanordy
Pink Ribbon
Posts: 2218
Senior Member

Send a PM
Give a Hug
I cant be much help here either, I had to quit my job because of the pain, memory loss, and depression/anxiety, plus heart problems. I had to be 100 at my job, I was a practice manager at a doctors office and if i wasnt a lot of important things didnt get done. So I gave it up and filed for SSD.

I hope you find something to help you.

Debbi

Reply  


02/26/2008 10:32
psk
Purple Ribbon
Posts: 272
Member

Send a PM
Give a Hug
Ive worked for myself for years and I can't qualify for disability even though I also have Lupus. I do a very physically demanding job and would'nt be able to work for anyone else because I need the $$$ and the flexibility to set my own hours. I'm afraid I can't do it anymore. I barely made it through last season. My husband and I are having financial problems now and said I should be delivering pizzas if I cant find anything else. I'm not ready to give up on myself yet. Sometimes I just need someone to cry to.

psk


Popular posts by psk
    Scared & Mad
    IBS
    Losing My Insurance
Reply  


02/26/2008 15:42
angelcath6567
Purple Ribbon
Posts: 95
Member

Send a PM
Give a Hug
Awww psk, so sorry to hear that! You can ALWAYS cry here!!
Reply  


02/26/2008 16:14
prince
Gold Ribbon
Posts: 176
Member

Send a PM
Give a Hug
Hello everyone! I have heard that for brain fog that natural therapies can offer help. These include herbs, vitamins, and detoxification methods such as sauna therapy, colonic irrigation and coffee enemas. Coffee enemas are particularly helpful and better than drinking coffee. Don't drink or eat foods that have sugar alternatives (equal, aspartame, etc...) Rest more,cut out junk food, wheat, dairy and excessive sugar. Hope this is of some help.
prince
Reply  


02/26/2008 18:15
Mydragonfly
Purple Ribbon
Posts: 1087
Member

Send a PM
Give a Hug
what is there left to eat?

Dragonfly

The Dragonfly brings the light and color of transformation into your life.
To learn more about Fibromyalgia
www.fmaware.org ***
www.webmd.com/fibromyalgia *** www.niams.nih.gov/hi/topics/fibromyalgia/fffibro.htm ***
www.painfoundation.org *** www.rheumatology.org/public/factsheets/fibromya_new.asp ***
Reply  


02/27/2008 08:37
sweetheartsuzee
Purple Ribbon
Posts: 1078
Senior Member

Send a PM
Give a Hug
LOL...Dragonfly!
~Suzee~
Only YOU can control your thoughts...
SO...
Change your thoughts and CHANGE YOUR LIFE!!!
Reply  



Start a New Discussion

Disclaimer: The information provided in MDJunction is not a replacement for medical diagnosis, treatment, or professional medical advice. Read more.
Contact Us | Bookmark Us | Add a Doctor | For Doctors | FAQ | Awareness Ribbons
About Us | Terms & Conditions | Privacy | Spread the Word | Advertise
Copyright (c) 2008 MDJunction.com All Rights Reserved