- Messages
- 33
- Location
- United States
Hello Possums!
I have not posted for several years - life got in the way....which actually sounds like a good thing when dealing with CFS/ME/Fibro.....right?
I have been on Cymbalta for 7 years. It has vastly improved my life. It gave me to strength to re-enter the world of other human beings, and the ability to love them again. I was so isolated before Cymbalta and truly felt like another species of person living among aliens. It relieved so much physical and emotional pain. I was even able to create a nice little business in that time, that allows me to work from home and choose my hours.
But after having gained about 50lbs (approx 22 kilos) from the side effect of extreme carb craving AND after going through the torturous symptoms of withdrawal after missing just one pill, I've decided that I am done with this drug. The extra weight cannot be helping my ME/Fibro pain issues! It certainly doesn't help my self-esteem and depression.
I have successfully ramped down from 190mg to 30mg over the last 4 months. On 30mg the withdrawals have started and it's not pretty: flu-like fatigue, all over body pain, major brain fog, head and neck pain, sore throat, fever flashes, muscle weakness, sudden weepiness, and a very tender stomach. I have spent two full days in bed during the past week on 30mg. Some of this I realize, must be my "base-line"....but the rest is pretty intense.
One thing that is helps is that I started taking 2.5 mg of a cannabis edible every 3 to 4 hours during the day (normally I only use it for sleep). Luckily, I live in a pot-friendly state and I can purchase 10mg recreational edibles and break them down into small bits. This helps "round the edges" especially regarding the loss of energy and depression.
I have read several other posts about Cymbalta here on Phoenix Rising, and it seems to affect everyone differently - but the common complaint overall, are the withdrawal symptoms.
Any other tips? I welcome all suggestions...and thank you in advance
P-Kat
I have not posted for several years - life got in the way....which actually sounds like a good thing when dealing with CFS/ME/Fibro.....right?
I have been on Cymbalta for 7 years. It has vastly improved my life. It gave me to strength to re-enter the world of other human beings, and the ability to love them again. I was so isolated before Cymbalta and truly felt like another species of person living among aliens. It relieved so much physical and emotional pain. I was even able to create a nice little business in that time, that allows me to work from home and choose my hours.
But after having gained about 50lbs (approx 22 kilos) from the side effect of extreme carb craving AND after going through the torturous symptoms of withdrawal after missing just one pill, I've decided that I am done with this drug. The extra weight cannot be helping my ME/Fibro pain issues! It certainly doesn't help my self-esteem and depression.
I have successfully ramped down from 190mg to 30mg over the last 4 months. On 30mg the withdrawals have started and it's not pretty: flu-like fatigue, all over body pain, major brain fog, head and neck pain, sore throat, fever flashes, muscle weakness, sudden weepiness, and a very tender stomach. I have spent two full days in bed during the past week on 30mg. Some of this I realize, must be my "base-line"....but the rest is pretty intense.
One thing that is helps is that I started taking 2.5 mg of a cannabis edible every 3 to 4 hours during the day (normally I only use it for sleep). Luckily, I live in a pot-friendly state and I can purchase 10mg recreational edibles and break them down into small bits. This helps "round the edges" especially regarding the loss of energy and depression.
I have read several other posts about Cymbalta here on Phoenix Rising, and it seems to affect everyone differently - but the common complaint overall, are the withdrawal symptoms.
Any other tips? I welcome all suggestions...and thank you in advance
P-Kat