Lynn shares her thoughts on how to recover from fibromyalgia based on her fibromyalgia recovery

Lynn shares how she lost an amazing amount of weight during her fibromyalgia recovery & the amazing turning point in her journey!

Lynn Lennon fibromyalgia weight loss & recovery

For Recovery Story Disclaimer, please see the main page!

Having recovered from CFS/ME & Fibromyalgia some years ago, it might sound strange to hear that I was inspired by this interview, but that is exactly what happened.

If you listen carefully, you will hear some critical distinctions in Lynn’s story of recovery that will be useful to anyone still afflicted with Fibromyalgia or Chronic Fatigue Syndrome.

In this interview Lynn openly shares her darkest moments and shares what she believes it takes to recover.

What makes this Fibromyalgia Recovery story even more exiting is that when Lynn started her journey, she had no concept of why she was ill or what she needed to do, but her instinct and determination allowed her to recover anyway.

Regarding Lynn’s thoughts on;

How to Recover from Fibromyalgia

Here are some interesting highlights to look out for:

  • How did Lynn turn around from hitting rock bottom?
  • What does she think is the key to recovery?
  • What is her Mantra that was powerful enough to give her the resources to dig her way out of Fibromyalgia?
  • What is the most amazing power that Lynn recommends everyone should tap into?
  • What did she do 3-5 hours a day to help her recover?
  • What did her doctor who prescribed morphine for 4 years to her say when she went to him fully recovered looking so fit and healthy she was barely recognisable?
  • How did Lynn come to turn around her ability to deal with pain?

NOTE:  Lynn’s thoughts on exercise obviously may not apply to you if fatigue is your predominant symptom as opposed to pain.

 

 

Lynn Lennon Interview April 2013 FACEBOOK

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May 25, 2013
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Alex Hall
Guest
I LOVED this interview, such an inspiration and such insight – really helpful. Again this repeats the idea of taking a multi-pronged approach to recovery. Mainly I found her shift in attitude seemed to be the most helpful for her – I believe that hitting rock bottom really can be a very helpful place for many of us. I loved her idea of making the right choices in every area of her life and every time – hugely helpful. I’m not sure the approach to exercise would be ideal for people with CFS which is different to Fibro, but so… Read more »
Dan
Guest
Hi Alex! Yes hitting rock bottom seems to be a common theme amongst those that recovered. Something changes from a want to a must which Lynn articulated so well. It was my experience also. I think before that, we only make haphazard attempts (hence the cupbouard full of half used supplements!) and without enough positive feedback, we simply don’t follo through on anything. Fibro and CFS (because of having the predominant symptom being different), work slightly different and hence Lynn’s approach with exercise is not a good idea for those with ME/CFS until they make a fuller recovery. I think… Read more »
Christine
Guest

Thank you Lynn for sharing your story. True inspiration and hope for others. Totally resonates and sounds almost identical to my jouney, both pre and post stories of it. Thank you xox
And Dan, thank you again for sharing the love!

Dan
Guest

You’re welcome Christine! Thanks for sharing it right back – 🙂

Kim
Guest
Part of what she said is really good – about making the best possible choice every time. However most of us don’t know what that is. For instance people believe that triathalons are a smart thing to do. They are not. The put undo stress on the body that is absolutely not needed for good health and fitness. A hour half walk each day outside is sufficient. If she keeps up with her admitted high stress lifestyle, her fibromyalgia will come back. She made a lot of good choices but is still making some bad ones without realizing it. When… Read more »
Dan
Guest
Hi Kim – glad you got something out of it. I hear what you are saying about Triathalons and I share your views about extreme endurance sports. However, the wonderful thing about the story is that it really demonstrates that Lynn has made a full recovery! It strikes me that she is fully on top of her health and given how she recovered, I would be extremely surprised if she ever suffered any significant relapse. Yes, GET is not a good idea for people with CFS, and I describe why in CFS Unravelled. However, where fatigue is not your dominant… Read more »
grace gilroy
Guest
This was so utterly inspiring & with much wisdom & a deep awareness coming from this lady. However I am a little puzzled by the fact that she suffered from Fibromyalgia & yet your interview with her assumed she had ME. From all I have read these are not the same thing. I have a friend diagnosed with Fibromyalgia. He suffers severe pain but does not have the multiple symptoms that I have ( diagnosed with ME). I actually have very little pain in that sense – extreme headache & severe flulike symptoms – I could go on.. Lynn seemed… Read more »
Dan
Guest
Thanks for your comment Grace – I am so glad you found it inspiring. Yes, her diagnosis is Fibromyalgia and Yes, the predominant symptom is different to ME. The reason for the comparing reference is that in my view ME, CFS, CFIDS, MCS and Fibromyalgia all have the same underlying dysfunction driving them, even though different symptoms or triggers are manifested in the person experiencing the illness. If you watch my video explanation, hopefully you will feel a little less confused. I go into more detail in the book. See my comments above about pushing physically – you are right… Read more »
Ruth
Guest

Great interview – it sounds so simple to make all good choices and something I will keep in the forefront of my mind from now on.

Dan
Guest

Thanks for the +ve feedback Ruth. Yes, the simplest things are often the best! 🙂

Julie Lee
Guest

Thank you so much Dan for creating this wonderful website and giving patients access to such inspiring stories of recovery! Your work has played an important part in my own recovery process,particularly in relation to the feeling of isolation which comes with this illness.I am definately not alone and even though I have a little way to go I know that I CAN recover and that in itself is the magic bullet for me! Thank God for people like yourself.Believe me you have a huge positive influence when it,s needed the most.With my absolute gratitude,Regards and God bless.

Dan
Guest
Thank you for your lovely comments and feedback. You know Julie, a few years ago I felt exactly like you in terms of the isolation. Nobody seemed to recover, it was all just negative out there. In fact, so many people on facebook and the web still say things like “if you recovered, then you never had it” – that’s how powerful the beliefs are. I hope to turn that around for as many people as possible, because what one can imagine, one can achieve, what one can’t imagine, one can’t achieve. I smiled a bit at your comment, because… Read more »
Juan
Guest
It is important to untdrseand that yoga is not a competitive practice. You need to tune into your own body and how it feels. There may be people in the class who are able to do certain poses that are difficult for you. Don’t try to do them if it hurts. Ask if there is a modification that you can do instead. You may also be able to use props such as blocks or straps to make it easier for you to get the correct alignment in the pose. It takes time for your body to open up in a… Read more »
Sharlene Mackie Ferizi
Guest
Sharlene Mackie Ferizi

I enjoyed the interview and I am hoping that I can do some of the things she did and what your book says. I like to start with what is the best choice I can make. I need to see some positive changes in my life and this is encouraging to me to hear and see that there is possible success, I need to try and see what I can do to kickstart this road of recovery and hopefully it will work for me too. Thank you

Dan
Guest

Glad you enjoyed it Sharlene!

If you ever read my book Discover Hope, you might have come across the poem ‘little steps’. That’s what it is all about, lots of little steps, consistently taken adding up to real results.

Dig deep and find your personal triggers and your personal roadmap to recover. Remember as I always say, treat the cause, not just the consequences.

Graham
Guest

Hey Dan. Thanks for taking the time to record this; I appreciate the encouragement today. Cheers, Graham

Dan
Guest
Hi Graham. Thanks for the appreciation, all this takes much more time than people realise – just the graphics and processing and uploading and so on – lots of work! So I am glad that it is making a difference and people are finding encouragement. When we are making progress, kicking goals, then our beliefs are strong and we feel confident. When things go wrong and we have setbacks, our confidence quickly falls apart. I think only someone who has tried for years to get over this horrid illness can truly appreciate how little it takes sometimes for us to… Read more »
Graham
Guest

Thanks again Dan; I realize how much work goes on behind the scenes to make this happen! 🙂

Dan
Guest

Thanks Graham – yes, nothing is quick or simple! You should see the challenge in trying to get the book to print format stage – it all takes a lot of time and money, but at least it’s appreciated out there on the most part – so that makes it worth it! 🙂

Teri Cutting
Guest
Very inspiring interview. After having CFS for so long, I was diagnosed in 1991, I am starting to believe that recovery is possible and that is key! Once again a multipronged approach seems best! I have been using your book Dan and gradually making changes. Thank you for the wonderful work you are doing! ‘m using your book and gradually making changes. It’s kind of funny though, I have never dreamed about participating in a triathalon, I’m trilled that I can walk 10 minutes each morning! Thank you Dan for the work you are doing. You are helping an “army”… Read more »
Dan
Guest

Wow Teri, that’s a long time – you are doing great to remain positive! The multi-pronged approach made sense to me which is why I used it and wrote about it in CFS Unravelled, but it is interesting to hear it over and over again when I speak to people that have recovered.

Thanks for your positive feedback – glad someone out there is listening – 🙂

grace gilroy
Guest
Thanks Dan for bothering to reply to an ‘annoyed woman’ I guess my irritation (dissolved thanks be to God & all the others…) is really if I look at it about all this confusion round names for this bewildering illness. This vagueness is not helpful when dealing with the medical profession. it simply encourages doubt to creep in.. anyway besides that I so appreciate all that you’re doing & having read your book I’m about to find myself a good naturopath & get well. You’re a total hero to have done all this research -I have great confidence in this… Read more »
Dan
Guest
Thanks for your positive comments. You know, it’s normal that you are an ‘annoyed woman’. I was an ‘annoyed man’ for a long long time. That’s why I get it when people say what they do, even the stuff I don’t like to hear. Truth is, it could have been me at one point! – 🙂 I hope you listen carefully to the interviews. Virtually EVERY recovery interview will talk about meditation and for good reason. It’s not about ‘chilling out’ or not ‘stressing out’, it’s about directly affecting the central nervous system, which of course is where the ANS… Read more »
Angela
Guest
I listened to the entire interview. While I am glad she has made a full recovery, I feel that she is blaming the patient a bit. Maybe she really had Depression or a Somatoform disorder and the increased endorphins due to exercise pulled her out of it. I was told for years that it was Depression and all in my head. I pushed myself trying to exercise, work and go beyond the envelope. This did major damage. I had sepsis due to a non-functional immune system due to ME/CFS. My NK cells function is a 3.I didn’t slowly decide my… Read more »
Dan
Guest
Hi Angela – I often get this blaming comment myself and never relate well to it because I never blamed myself for being ill, even though I realised my part in it when I reached a deeper understanding. Once those that recover realise how they got ill, they recognise how their behaviour has contributed to the problem. From this they usually take responsibility which is very empowering because it allows them to change towards improving their health. However, blame is not helpful. There are usually many external forces that occur to bring about the illness, which nobody can have any… Read more »
Angela
Guest
Hi Dan, I read your book and wholeheartedly agree with your ideas. I know that MASSIVE, unrelenting stress helped push my already vulnerable system over the abyss. Life happened: new baby, husband massively sick with a then unknown illness, surgery for me, then a virus…all came together in a perfect storm that could lead nowhere other than ME/CFS land. Thankfully, in your book you take the approach that, regardless of how you got sick, there are things that can be done to get better…VERY EMPOWERING. When I was listening to the recording, I was very inspired. However, today I was… Read more »
Dan
Guest
When you have Fibro or ME/CFS, tthose “positive choices” can seem like they are a mile away sometimes don’t they? I totally hear you! Thank you for your positive feedback Angela. You are right of course, you don’t choose your way into the illness, few people want to be sick! And it isn’t always bad choices that get us there, sometimes it’s just a bunch of stuff that happens. Well done for staying positive. I don’t think Lynn meant any offense. I think she just wants people to realise that often we don’t actually do the things we know we… Read more »
Angela
Guest

Just watch, I’ll have my own recovery story for you in the future The title will be “From Sepsis to Strength”. 🙂

Dan
Guest

Sounds fantastic! I really look forward to sharing recovery stories of people who were helped by CFS Unravelled – ultimately, that is what this is ALL about. 🙂

Susan
Guest
Dear Lynn and Dan, Thank you – thank you – thank you both for your commitment to sharing your details of recovery! Since being introduced to the concepts detailed in your book, Dan, I have started working with the Optimal Health Clinic via phone in London, England (I reside in California, USA) and have listened to MANY recovery stories posted on their website. Lynn’s recovery story, as well as your own, fall right in line with those. I think recovery stories are a vital part of the recovery process; I feel deeply grateful to both of you for bringing this… Read more »
Dan
Guest

Great to hear about your progress, I look forward to sharing your story when the time comes!

Several people have mentioned this clinic – I am still not fully sure what they do, but at first glance they certainly seem to be in line with what I am saying.

The more recovery stories we collect, the easier it is for people to have faith and then confidence in their own possible recovery!

Thanks for sharing – 🙂

Kim
Guest
As a result of using supplements I didn’t need as ‘prescribed by the book, Treating and Beating Fibromyalgia, my health deteriorated and led me down a path of destruction. I developed tinnitus that caused severe anxiety from taking supplements so I was prescribed a tranquilizer. I was never informed as to how addictive they are. I kept taking them for years for anxiety, Restless Leg Syndrome, and insomnia. I took them on an ‘as needed’ basis and in a child-size dose. This year I realized that I was having new symptoms that were caused by the clonazepam. I have been… Read more »
Dan
Guest
Dear Kim Thank you for sharing your experience, I share many of your concerns about treatments, which is why it is important to always get a qualified second opinion from a doctor if you take any drugs. Realise that no matter how bad things may seem, the can turn around. Please seek help from a friend or family member as well as a professional counsellor! People have a variety of symptoms, but most people I have interviewed tell me afterwards about other symptoms which they forgot to mention, so we don’t always get the full story. Regarding a difference in… Read more »
Kelly
Guest
Sorry Dan, but I feel compelled to add my voice to the chorus of folks who aren’t too impressed with Lynn’s story. Of course it was ‘easy’ for her to make choices if she was actually eating several donuts a day and/or drinking beverages loaded with high-fructose corn syrup. She was clearly poisoning herself…and I think most people with half a brain could figure that out. I truly don’t mean to be rude, but the choice she made was choosing to not be so incredibly ignorant IHMO. What about the folks who eat healthier diets, yet may have been exposed… Read more »
Dan
Guest
Thank you very much for speaking up, I really appreciate you making a comment Kelly! By chorus of folks, are you referring to the people on this page or who are they? If only recovery from Fibromyalgia was as simple as positive affirmations! I suspect you haven’t read my book and perhaps not even seen my video explanation – the recovery process is clearly more complicated than just positive thinking. In my book CFS Unravelled, I advocate focussing on treating what I describe as the cause of the illness, whilst creating a healing environment. Let me be clear here –… Read more »
Kelly
Guest
I appreciate your reply Dan. Sorry for my late one. Also sorry if I came off a bit snippy or judgmental. It just seemed to me that her case wasn’t too complicated since she was eating such an obviously terrible diet, but when I think about it, there are people who eat the same way and don’t become chronically ill. I do in fact believe that attitude, and forgiveness, and releasing anger towards others does play a role in healing. Your kind and thoughtful reply helps reinforce my need to continue working in that area. Having said that, I do… Read more »
Kim
Guest
I appreciate your response, Dan but I tried what you suggested long ago without success. Four doctors prescribed clonazepam for me so getting a second opinion didn’t help. They are in denial as to how addictive and dangerous they are and hand them out like candy. They should only be used for a couple of weeks but the standard is to prescribe them for many months or years. This has been going on for decades despite public outcry and class action law suits. I suggest you educate yourself on this matter by going to utube and watching videos by people… Read more »
Dan
Guest
Hi Kim I hear what you are saying. Like I said, for M.E., pushing into exercise is clearly not the idea, but the RIGHT exercise can actually be VERY helpful. Also, I am not quite sure what you think I am suggesting, but simply eating the right diet alone is rarely going to lead anyone to recovery, it wasn’t the case with me, I haven’t seen others succeed that way. I fully appreciate the challenge in recovering from ME/CFS or Fibromyalgia. However, I believe that the odds depend a lot on what we do and how we do it. I,… Read more »
Kim
Guest
To be clear I know you are not suggesting that diet alone cures M,E., I was just making a point that diet is a complex thing and it seems to have been one of Lynn’s primary strategies. For instance, many people around the world live on only two or three foods and still have the energy to work hard every day. Nomadic Mongolians eat only meat and milk, they have no fruits, veg, or grains. Ethnicity plays a role in what is good for a person. First Nations do well on a high fat, high protein diet. There was a… Read more »
Dan
Guest

My view is that there are many ways towards recovery, but the key thing to focus on is treating the cause, not just the consequences.

I understand how you feel – sorry my views didn’t resonate with you.

Hope you find something that does resonate with you and that you keep working towards recovery.

I wish you all the best with your health.

🙂

Selma
Guest
I was diagnosed with fibro 15 years ago-managed it by keeping stress low, diet, exercise and supplements then things turned scary neurological 7 years ago with on set of optic neuritis. You name it I have done if for treatments- herbal protocols, homeopathy, every form of bodywork, acupuncture, healing prayer, meditation/mindfulness, yoga and walking-only to get sicker with each attack some of which were caused by the treatment. Is it lyme? I don’t know or some autoimmune variant. But I have read that some FMS patients have numbness ,muscle weakness and neuropathy as do some CFS patients I believe. I… Read more »
Dan
Guest

It is my view that endometriosis is often a result of having CFS/FMS due to the problems with hormone levels.

Selma, the key is working out your personal trigger and doing any program with full 100% committment. I hope you get some help to dig deep, consider keeping a diary to find out how you are triggered in your flares. I would also urge you to restart your meditation!

Note that Lynn is fully recovered. The neurofeedback from memory wasn’t for herself!

🙂

Selma
Guest
Thank you! Yes, I do it all-diet, exercise, juicing,meditation and now mindfulness. and other therapies…. Lynn did not say she used neurofeedback, but she mentioned using it for her clients to reset the flight/fight response-so I was curious on what she is finding in regard to how effective that is. It is also supposed to help with sleep and chronic pain–so I thought maybe that is something worth looking into to help retrain the brain, assuming the brain is the source of the problems. As far as my triggers they do seem to be chemical and stress induced (like fear… Read more »
vicky
Guest
I found this interview really inspiring and it gave me a lot of hope, I would like to thank Lynn for taking the time to share her story in such detail. I found that many of the changes Lynn shares here reinforce, to me, the wisdom of changes I have made in my own life. I am starting to feel like I am recovering, but I am at the stage of having a day or two where I almost feel like myself, but then I am not so well again for a while or even crash quite badly for no… Read more »
Dan
Guest
Hi Vicky Thank you for your positive feedback, I am so glad that you found this interview helpful. You sound like you are doing well. I encourage you to dig deeper however. As you can see with Lynn and most recovery stories, it is usually a multi-lateral approach tailored to the individual. So other triggers need to be considered also. You might like to keep a diary to try to identify if anything else triggers your symptoms. A common one for people who have been ill a long time is their concern about the illness (need to direct the mind… Read more »
vicky
Guest

Hi Dan,

I guess my reply didn’t make it clear that diet is only one of a number of things I am working on, it’s just that I have found a simpler diet to help me in improving my sleep patterns, practicing mindfulness and meditation, and it even makes yoga and walking more comfortable as I have less aches and pains, presumably due to ingesting less toxins and less foods that cause digestive difficulties.
I find funding for practitioners very problematic, but I see them when I can, and I have been sharing the links 🙂

Dan
Guest
Hi Vicky You are clearly making great efforts, so it’s nice to see you gain ground! I understand about the funding challenges. It’s really both about the effectiveness as well as the cost of assistance. I wonder if a one-off payment (even though higher) that then gives you a package of support is the way to go? (like $1,500 for a 3 day seminar with 6 months worth of fortnightly support) I focus on this because I think this has a much higher chance of actually creating breakthroughs. The problem with a pay as you go approach is that you… Read more »
vicky
Guest
Hi Dan, I have been thinking about what you have said and I feel that a 3 day seminar would be too intense, and that maybe one day per month for 3 months (or even half day x 6) with weekly support between and after might be more useful? My reasons for this are a) the exhaustion issue and the attendant difficulty concentrating and b) the feeling of pressure to conquer everything at once. Its like reading a book about how to meditate and reading ahead eagerly without taking the time to do the practice. If people are travelling for… Read more »
Dan
Guest
Thanks Vicky, I don’t know what other people think, but certainly share many of your feelings. Unfortunately spreading the course into more smaller sessions is not commensurate with reducing the cost from my point of view. Another issue is the possiblity of people not fully committing to the program – so upfront payment is important also, but that is not easily afforded. This is why originally I thought about delivering an internet course, however that has high upfront costs and lacks personal intervention which I feel is very important. Whilst it might work for some, many will just cruise along… Read more »
Christina
Guest
This interview was so long and drawn out forever. very odd there are studies showing FM patients have a decrease in symptoms during pregnancy then the pain all floods back within a week or two of giving birth. I had this experience personally as well. Also there are other strange parts of her symptoms that don’t sound like fibromyalgia, sounds more like chronic major depression. who knows. This obviously does not happen to the majority of patients. I really question this whole thing, especially when someone is selling something. I will say I have had great success eliminating gluten, dairy,… Read more »
Dan
Guest
The reason why the interviews are longer, is because I try to ensure that I establish the person experience so that people don’t think they didn’t have it, because people often want to say that when someone has recovered, but I agree, I need to try and make these interviews a little shorter! It is surprising to me that you would label her experience as depression, whcih is what many doctors used to do before they learned about fibromyalgia. Depression doesn’t cause severe fibromyalgia pain. I understand what you mean about exercise, hence my comments as many people especially with… Read more »
Rachel
Guest
Thank you Dan for posting recovery stories and responding to everyone’s comments. I am half way through CFS unravelled and feel like I have learned so much about CFS, which no one has been able to tell me since I’ve had it. (I have had CFS one year, the main symptom is fatigue..) I have been doing a graded exercise program for the year with an exercise physiologist who has also had CFS. I have improved to a point but lately I have come to a stop of no improvement. Very frustrating… However since starting your book I’ve looked into… Read more »
Dan
Guest
Hi Rachel – thanks for your positivity! The issues you find are some of many that people with ME/CFS have. And treating such and other imbalances will certainly help you move forward. So yes, this is by no means a surprise at all. You can even improve your gut function through a variety of treatments with your doctor/naturopath which all help. However, my main message of the book which is sometimes missed is TREAT THE CAUSE, not just the consequences. I cannot emphasise this enough and hope you see this as you finish CFS Unravelled. Best of luck with it,… Read more »
Rachel
Guest

Thanks for your quick response! I really hope that this is my ’cause’ because I don’t know what else could be making me feel so fatigued everyday.. Fingers are crossed. Thank you for your inspiration, research and motivation. Would love to share my recovery story when it comes!

Patricia Simon
Guest
I don’t know if anyone will understand this, but I feel like life broke my heart snd st 60 years old it is very hard to come back from that. Lynn’s story is great, thanks for sharing with us Lynn. It was inspirational and I did get something out of it, it prompted my own thought processes and for me to digest my own experiences with doctors. When I was first diagnose the specialist literally said to me ” what do you want me to do sbout it there is no treatment” he didn’t even seem to understand that getting… Read more »
Dan
Guest
Thanks for the comment Patricia. I think you will find that the people that have recovered have found it far from ‘easy’. If access to particular treatments is unavailable, don’t despair. There is no reason to think that these are compulsory as you will find people have recovered without these (I nver used sauna or massage for example). But yes, other factors not known to you are likely involved and exploring these are critical. In CFS Unravelled I speak about the various triggers and that ALL of our triggers must be addressed. Some of the key ones to consider are… Read more »
Phoebe Thomasson
Guest
Hi Dan Many thanks to Lynne and yourself for bringing us this article. Much inspiration to be gained. One note to your other contributors, especially the ‘annoyed’ types; I myself used to be annoyed at everything! This is definitely part of the expression of the illness itself, and isn’t a true reflection of the person, so don’t beat yourselves up, though it can feel unpleasant to say the least. I had pretty serious mental problems myself so believe me I know what I’m talking about. I was diagnosed with Schizophrenia at the age of 26 and my high stress levels… Read more »
June Doogan
Guest
Thankyou to Dan and Lynn for sharing this story. It has just been what I needed to hear at the time I needed to hear it. Everyone has a different situation and this was so right for me at this time. It wouldn’t have been a couple of years ago but for now its inspirational and hope-filled. Dan I especially want to say thankyou to you for all the time and effort you are making to help others understand the possible health issues related to these conditions and to find a path through the mist and fog. The amount of… Read more »
Dan
Guest
Thanks for the positive feedback June. Yes, timing is everything isn’t it. Living with ME/CFS/FMS goes on the premise that things don’t get worse. Interestingly I have seen the pattern regularly where things get drastically worse and people can no longer ‘live with’ ME/CFS or Fibromyalgia. Usually at that stage, I see lots of action! You will probably recognise this pattern in the recovery interviews. It seems it’s human nature that we only get motivated to take things to the next level when we can no longer tolerate the status quo! Stay connected – I hope to have some exciting… Read more »
Maria
Guest
My comments got deleted after I wrote a long letter so here is a short one instead. For Angela, the note I saw about nk cells. You should take a western blot or better test for lyme just to rule that out. Lyme is often much worse than viral or fungal reasons for cfs for example. It gets worse with emf all around us, and also Children can get autistick in the womb already from all the emf penetrating into the womb. Then it only gets worse with vaccines. There are so many man made viruses today and environmental causes… Read more »
Elaine
Guest

I have a firm diagnosis of Fibromyalgia, but fatigue is a huge problem for me. I have heard from other Fibromyalgia sufferers that, as well as pain, fatigue is another disabling issue.

Dan
Guest

The fatigue is part of the SYNDROME. The key to recovery is to treat the syndrome rather than the symptoms. I suggest you watch the explanation on how recovery happens: http://cfsunravelled.com/how%20recovery%20happens/

Tina
Guest

She says exactly the same things that I would say 🙂
I hope to one day be able to say like her that I fully recovered, more than half of the way right now

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