Fibromyalgia pain: Let's connect
Is there anyone here that suffers from fibro? I had the 'tender spot test' several years ago and I had 17 out of the 18. I try my hardest to get through the pain with my 4 hydrocodone/acetaminaphine pills a day, Tiger Balm rubbed into areas that are the worst, light exercises, and distracting myself with hobbies or chores, etc; but there are many occasions where none of that helps and I spend most of the day holding down the couch, getting up about 30-45 minutes after that, walking/standing around the house for 15-20 minutes, or sitting for about 15-30 min. I do not drive and my husband works 6 days a week, overtime almost every day, so I'm alone a lot. my wonderful husband is very supportive and I am very grateful for that, but my only other friends are online, out of state, and I will probably never even get to meet them. when extreme pain takes over, my depression takes over and it is so difficult to find hope. does anyone have tips for fibro, whether diet or over-the-counter meds (I've tried them all, I think), or anything, besides hobbies and such? I've tried every over-the-counter med, and the Tiger Balm does cover some of what the pain pill doesn't help, but I'm hoping one of our members might have some knowledge that could help. I'd really appreciate it.
hugz,
Clownscrytoo
Interested in more discussions like this? Go to the Fibromyalgia Support Group.
I already prayed for you. I was very specific for you. I understand the house cleaning. I moved from my huge home in Oregon to my son Guest House. I feel like I try the best I can to keep it in order
Love it. They are on every corner in Oregon. It is NOT habit forming.
Here in NY you have to go to a state authorized medical marijuana pharmacy. They just sell marijuana, nothing else. But first you need to get a year of your medical records, then go to a state authorized doctor who is licensed to write the script for med. marijuana, and then hopefully get him or her to write u a script. You literally have to jump through hoops and the drs don't take my insurance so you need to lay out a fair amount of money with no guarantee that you will even get the script. They just added chronic pain to the limited list of conditions. Prior to that I wouldn't have a chance to get it. You are so lucky to live in a decent state. If I was younger and stronger I would try to move.
Thank you so much!
Don't worry about Dr. Someday that charge will be covered by health insurance drug program. Remember the state makes money off you and your license, renewal etc. Please use it and feel the difference. I am stuck in Texas where not legal. I am using drugs that could kill me. If you have MJ available you are very fortunate.
@lynneb2110 It sounds like you and I have many of the same symptoms. I cannot tolerate it too hot or cold. I also have the sweats, red face etc 5 years after menopause. I thought it was just hormone changes due to menopause. Oh and my hands and feet can be so cold I can't warm them.
Hi @doxyjune I have not gained any weight from Cymbalta or Lyrica. My thyroid is normal. More than 10 years ago I had gastric bypass because I was diagnosed with a metabolic disorder. Like you, I gained weight no matter what. I was diabetic too. I lost 135 pounds and have kept it off. I'm sorry to hear you have tremors too. Have you ever been to a neurologist about the tremors?
We do have a lot of the same stuff, @sandytoes14. It took me a long time to mentally sort through whether my heat issues were hormonal or not. It was about 4-5 after menopause when that all started. I was frustrated with no one having any answers or suggestions for my misery. Previously, I thought maybe I had gotten away scot-free without menopausal hot flashes, mood swings, etc. This was way worse. >:-( Almost like a chemical burning sensation under my skin. Then this year, I began to have an aversion to touching cold things, even a frozen juice can. This year my Reynaud’s came galloping back, after a hiatus of several years. Didn’t miss it. However, I perceive the two issues (cold hands/feet) as likely separate things from the Reynauds, but I dunno.
@oregongirl, I have never seen such amazing dispensaries as in OR and WA. They are indeed on every corner.
I’m in MA, and we’re not as advanced and free-wheeling with the Taj Mahal-like dispensaries. But I’m facing a possible move to Virginia, the DC area, and VA DOESnt even have medical.
Just imagine if we did not have to take the killer drugs. And, that the pain literally seems to go away. I know it doesn't but when you are relaxed it is a better feeling. You can deal with the pain as you are getting a good night sleep.