Chronic Pain & Fibromyalgia

The last part of January and the first week of February have been a bit rough. I was diagnosed years ago with Fibromyalgia and for almost 10 years I spent a good majority of every day trying to just cope with the chronic and incessant pain. For the better part of the last 3 years though I have had a huge decrease in pain to the point it was not top priority anymore. However, the last 2-3 weeks has been a bit rough. I am sore all over, my muscles and joints throughout my body hurt. I think maybe the pain in my hip and leg and the falls are what brought it on/brought it back.  That and sitting 10 hours a day or more typing doesn’t help. I tried Lyrica again but at the same time my doctor also put me back on metformin to see if we could get better control over my blood sugar and the side effects of the two made me miserable. Lyrica causes me severe vertigo. To the point, I won’t drive, and I need to drive so I am not going to take it.  My doctor wasn’t thrilled that I refused to take any medication for the pain so instead, he suggested I look into CBD oil, which I am not thrilled about so after researching it a bit I decided that was a no-go as well. Too expensive, not covered by insurance (obviously), etc. Just not an option.

On the plus side, we were able to afford insurance, only for me though and not Eddie which I am also not thrilled about. He will have insurance in another 9 months through work anyways I think, so we were more concerned about me at the moment and making sure I can still afford insulin, my Libre, metformin, etc. The insurance is only going to cover 80% to a maximum of $1000 a year towards medications and for the medical equipment such as my Freestyle Libre sensors it will only cover 80% to a maximum of $1000 in the first year, $1500 in the second and then $3000 in the third year onwards per year which means the first year it will only cover about half of the year for my sensors, but hopefully at that point I will have secondary insurance through Eddie’s work which will cover 50% but again it’s better than nothing at all.

Since I am not taking anything at the moment for the pain which is pretty bad, like 8 out of 10 pretty much continuously all over, almost every muscle and joint, I have been searching for other alternatives and I think the only thing that seems to help relieve and make me comfier, or in other words 4 out of 10, effectively halving it, is heat. I had Eddie buy me a heating pad the other day and it seems to help. So does having the wood fire going, I think it’s maybe the dry heat. I want to get a heated throw blanket. I think I am going to get one next time I have a little extra if I can find one for a decent price. Tea seems to help too. I think it’s the cold. This cottage is so bitterly cold sometimes, it isn’t insulated very well and it’s damp. The weather has either been quite cold, like -20 with snow or it’s been around 3 and raining out. It seems to go back and forth between the two, which isn’t helping at all.