Melatonin and PMR
After taking 40 mg or Prednisone for 3 days the PMR symptoms were mostly gone. However, once back on 20 mg dosage the morning pain and stiffness has returned not too mention during the night also (this has happened three times). Most nights I take 10 mg of Melatonin, I'm not confident in what I read on effect of melatonin on prednisone - so any feedback will be appreciated.
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I will have to look for it. I don't disagree that you know what you are talking about. I am by no means a medical expert. But I do notice that my achiness and stiffness get worse as soon as night time falls so I think our bodies become aware and something happens with the inflammation. I read this is one reason it becomes so painful for us overnight into the morning besides the fact that we are not moving.
I’m not a medical expert either. I was just sharing an article from a reliable source that was from a different perspective. That’s why I was wanting to read the article you mentioned.
There is evidence that people with PMR should take their prescribed dose of prednisone later in the day, even just before bed. After my PMR Diagnosis I was taking 15MGM of prednisone in the morning as directed by my rheumatologist and it wasn’t working after three days. So I switched to taking it before bed and bingo the next morning I felt great relief. I now take it after dinner so I am taking it with food to reduce digestive problems and it works well for me. The study I said inflammation occurs at night and you need the prednisone most at 3AM so you quell the inflammation and wake up feeling less stiff and sore. Just food for thought. Best wishes to all for good results.
I have Giant Cell Arteritis and ordered melatonin to help me sleep as the high dosage of prednisone I was on made sleep difficult. All melatonin bottles have warnings not to take if you have an autoimmune disorder, which both PMR and GCA are. I'm glad I read that before taking the melatonin. If I recall correctly, melatonin stimulates the immune system, but as both PMR and GCA are autoimmune disorders - with genetic markers -we want to calm down ou immune systems (with Prednisone), not overstimulate them. I had success sleeping better with lemon balm tea, and now that I'm on a lower dose of prednisone, 4 mg, I sleep fine. All the best, Teri
Ah hah. Interesting. Thanks for sharing that info!
Interesting. What you say correlates with what I was reading before also about Melatonin. and that most inflammation happens in the middle of the night around 2am - 3am. This is for the same reason that I also take my prednisone at dinner to help the mornings be easier.
We’ll I’m glad you figured that out too. It makes a world of difference. At least it did for me. Good luck in your recovery from PMR, Abbey.
I am having good results with Nighty Night Super Valerian Tea about an hour and half before bedtime. Melatonin was recommended by some and poo poo'd by others. I also have Valerian Tincture which I take about 1/2 a dropper with a little water earlier in the evening. I had to start taking a little earlier because it was not metabolizing by bedtime. After it kicks in, night night. I'm always leary about trying herbal remedies, but Teri who is a Mentor on MCC has used and recommended.
Thank you Teri. Having great results with Valerian/Lemon Balm Tea (Nighty Night Super) and Valerian Tincture. Much welcomed sleep and very rested in the morning.
My melatonin bottle instructions warned not to use it if on prednisone so I stopped using it. Interested in comment on prednisone in evening as sometimes it is said to cause troubled dreaming according to my rheumatologist. Will have to see if it would help me not get awake at 3 a.m. Magnesium tabs seem to help me sleep and restlessness.