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Tonmya is a game changer for me!

Fibromyalgia | Last Active: 4 hours ago | Replies (24)

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@daisy17 been on 8 mg of LDN for a year. Never noticed much effect.

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Replies to "@daisy17 been on 8 mg of LDN for a year. Never noticed much effect."

@beejenigma I am taking 4.5mg of LDN a day. Being I'm not sure if I'm in fibro remission or not, I will keep taking it. I've cut back on my cyclobenzaprine and now only take it every few days.

My fibro was triggered by my first bout of Covid in 2021. But looking back, I think I've had short bouts of it for years, usually when the weather changed. When I got it in 2021, it hit me with a vengeance and my flares lasted months. I thank God every day that I feel good as the pain and lack of sleep from fibromyalgia was a nightmare.

Can you tell me what your out-of-pocket cost is for the Tonmya? If it's not covered by insurance, I don't think I could afford it even if I wanted to try it.