SSRIs as treatment for CFS?! Also Acupuncture question
Posted , 9 users are following.
Hi all, I'm a 52 year old man in the UK and my symptoms are exhaustion - heavy legs, generally tired out, brain fog. My GP after running lots of blood tests thinks its CFS and has referred me to a rheumatologist at the hospital to confirm the diagnosis (I don't get to see him for another 2 weeks). On the UK scale, its probably "mild" with the odd day of "moderate".
When my GP first suggested it was probably CFS the first thing she wanted to do was put me on SSRIs! I am naturally resistant to the idea of anti depressants to be honest - especially when I'm not depressed. I've been told boosting serotonin levels can help with CFS and its not JUST for depression - but I can't actually find much online to support that. I went back to a different GP partner the other day as I'm still not well enough to work after 7 weeks and the first thing HE said was for me to think again about SSRIs... So does anyone have any experience of that and it helping? I really am not in any way depressed - I've done a bit of meditation and hypnotherapy over the last few weeks and generally I am feeling quite laid back and stress/anxiety free (my employer is currently very supportive) - although the brain fog making writing and concentration more difficult is a nuisance, I am adapting to the lack of any energy thing and coping ok.
Conversely, a friend suggested acupuncture - and I can find a few articles suggesting it has helped with CFS. I am actually going for my first session with an experience and well qualified acupuncturist tonight. Has anyone any experience of that? And has it helped? I do have a friend in Switzerland who says its helped her a lot.
Thanks in advance for anyone's shared experiences.
1 like, 43 replies
GeorgiaS phil50852
Posted
When I first got ME a doctor tried to put me on SSRIs even though I kept telling him that I wasn't depressed. I didn't take them. I use 5-HTP for serotonin. I find it's very calming and I sleep well at night. I wake up feeling much better than when I don't take it.
I've never tried accupuncture but my friend, who has Fibromalgia, says it's helping her immensely! She keeps trying to get me to try it and I might.
phil50852 GeorgiaS
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Thanks Georgia, that's really helpful. I remember taking 5-HTP once before some years back and hadn't made the connection. I'll give that a try again.
GeorgiaS phil50852
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Excellent Phil! I came across it by chance when my friend visited me and he accidently left a bottle of it here. Fortunate accident.
I've been taking it for several years and although I've tried many, many different supplements it's one of the very few that I stick with.
Jk1952 GeorgiaS
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Hi Georgia, nice to see a post from you. Thanks for reminding me about the 5-Htp. I must try some. My sleep pattern is a mess at the moment.
I'm struggling to find an article about the diagnostic break through, I don't do face book. It sounds exciting for us all!
jackie00198 Jk1952
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Excuse me for jumping in on your conversation here. JK--I believe the article you're looking for was published by the University of California San Diego School of Medicine. Google "University of California Chronic Fatigue Syndrome," and click on "Researchers Identify Characteristic Chemical Structure..." At least, I think that's the article being referred to. If I'm wrong, someone please correct me.
phil50852 GeorgiaS
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Hi Georgia - I got a same day delivery from Amazon yesterday and took it last night - will give it a go for a month and see how it goes, ta
phil50852 jackie00198
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Thanks for that Jackie, I'll take a look at that too
Patrickgeoffrey jackie00198
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Patrickgeoffrey
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GeorgiaS Jk1952
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Hiya Jk! Yes it's always great to hear about when they learn something about ME.
I hope 5-HTP works for you; I find it excellent and I always try never to run out of it. I'll message you the brand I use seeing as we can't post brand names here.
GeorgiaS phil50852
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Patrickgeoffrey phil50852
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GeorgiaS Patrickgeoffrey
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Thanks very much for that info Patrick! Fascinating about cells going into hibernation, makes sense.
I get the ME research magazine Breakthrough from ME Research UK sent to me and there's an interesting article on a study in my latest one. It's about oxidative stress and the role of Nrf2.
'Low Nrf2 levels are found to play a central role in the increased oxidative stress found in ME/CFS patients, stimulation of Nrf2 could become the target of further research'.
Another,linked, article in the magazine found 'Abnormal connections among brain regions and reductions in white matter (in the brain) that continue as the illness progresses...white matter is thought to be highly susceptible to inflammation and its loss could well be the result of chronic oxidative stress or an ongoing infectious process'
There are certain foods and herbs that promote Nrf2 (the Master regulator) so help with oxidative stress, such as brocolli, Ginkgo biloba, blueberries, cabbage, sprouts, onions, milk thistle, green tea, turmeric, black pepper.
jackie00198 Patrickgeoffrey
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Thank you so much for posting information about that study. I've just read it. From everything I'm reading, we're finally entering into a time where ME/CFS is being considered as a serious illness, and good research is also finally happening. It's about time.
phil50852 Patrickgeoffrey
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GeorgiaS jackie00198
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Would it be possible for you to summarise what you read Jackie? Such as is there anything we can do about their claims, such as foods, supplements, herbs etc, and what exactly are they saying?
My brain hurts and I'm not up to reading it at the moment. Don't worry if you don't feel up to explaining.
cherie8218 Patrickgeoffrey
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