Long-term Fibromyalgia Recovery Success Story (+ ME/CFS & IBS): Ela shares ANS REWIRE experience

Long-term fibromyalgia, long-term Chronic Fatigue Syndrome (ME/CFS) and long-term Irritable Bowel Syndrome (IBS) are often thought of as being impossible to recover from.
It's shocking to hear how long it took Ela to get diagnosed and the decades of frustration with long-term fibromyalgia, ME/CFS and IBS that she experienced.
As she puts it, the scientist in her made her skeptical and so she didn't want some online program offering some magic cure - hence the ANS REWIRE program strongly resonated with her.
She summarises ANS REWIRE as follows "this program and Dan has this focus on knowledge and doesn't claim to have THE solution, instead, there is a holistic view...it(ANS REWIRE) can help you find YOUR way to recovery"
It took her nearly 18 years to get diagnosed and she had tried many treatments for IBS, treatments for chronic fatigue and treatments for chronic pain, but these only helped slightly.
To learn more about the program, request the 4 free intro lessons here: ansrewire.com/... request/
The book she mentions is CFS Unravelled, you can learn more about it here: cfsunravelled....
Her full recovery interview will be published soon.
#ANSREWIRE #GetYourHealthBack #MECFSRecovery #FibromyalgiaRecovery #IBSRecovery #MECFS #IrritableBoweldSyndrome #IBS #Fibromyalgia #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
**MEDICAL DISCLAIMER**: Dan Neuffer, CFS Unravelled or ANS REWIRE do not provide medical advice, and the information available in this video does not offer a diagnosis or medical advice of any kind. The content is opinions and information presented for EDUCATIONAL PURPOSES ONLY, and MUST NOT be used as an alternative to a healthcare professional's diagnosis and treatment. Only a physician or other licensed health-care professional are able to determine the requirement for medical assistance. Please seek the advice of your physician or other licensed healthcare providers if you have any questions regarding a medical condition.

[@trishcovich1923]

Needed to hear that again, that it is possible to recover. Eight years in now.

[@kathystoner5239]

Great recovery video! Thanks, this does give me hope! I love the ANS Rewire program! I do love the holistic approach. This gives me hope as I can relate a little to her story..I was doing fantastic with the program for a while and then we moved into a new house and i had quite a setback. I took a break from the ANS Rewire and am now back to doing it again and am loving it.

[@kimwarburton8490]

:)

[@marcelguldemond2523]

Thanks for your story Ela, it really resonates with me. Especially the disappointment at yet another negative test result and not knowing why this was happening.

[@CFSUnravelled1]

So frustrating right!? How can she be ill for 20 years without a diagnosis and then only after reading the book and prompting the doctor it happens. That's not how healthcare is supposed to work!

[@ratfacekick]

"I didnt like her anymore, she wasnt positive, and certainly not strong." Completely relatable, but also completely untrue. We are the toughest sons of bitches on the planet.

[@CFSUnravelled1]

Totally right Timmy - it always makes me laugh when anyone suggest people with FMS/CFS are weak - the total opposite is true! It's a resource, but also a problem in many cases.

[@hollywebster6844]

If we weren't strong we would be dead. I think it's much more difficult for us to let go. Perhaps she was speaking of muscle strength. After 25 years of CFS I have much less muscle strength.

[@christiandeluxer2926]

@@hollywebster6844 You have 25 years CFS? How do you live,work, exersice etc

[@geethanair5803]

Every human is different , she had her own ways. Despite after a long time sickness. Some ppl are not in a position to present. We shd acept every person as how they are. I too like to hear abt recovery.as i am suffering since so many years...how can i get ANS rewire program??

[@marcelguldemond2523]

I dunno, I always feel weak when I consider my inability to cope with stress, and how I’ve disengaged with so much of public life because of that.

[@CocolimeFitness]

This sounds so familiar…wow

[@catherinecoppin6174]

Hi have me/cfs fibomalyagia. Went from always having energy high energy. Now just going to shop over road can make me poorly pain brain fog.

[@harrieta6961]

Ela talks about yoga. Is there any particular yoga that you can recommend? And when best to do it x

[@hollywebster6844]

Harriet, I have found restorative yoga helpful, especially during bad days. I try to do some kind of yoga every day. There is a KZbinr, Yoga With Bird, who posts gentle 5-10 minute yoga practices that are helpful to gently, slowly introduce yoga to our beleaguered bodies.

[@dommccaffry3802]

Why do you think you relapsed first time ? And do you worry about it happening again ? What was the most beneficial part of the programme for you ?

[@kirstensuhr7094]

I am bedridden cause of Lyme and coinfektions and coinfektions since over 4 years now. My Body does Not tolerate antibiotics or other treatments. I am desperate and hopeless. Can the Programm Help me?

[@CFSUnravelled1]

Hi Kirsten - I am sorry to hear that. The program is designed to help people diagnosed with ME/CFS, Fibromyalgia, POTS and related syndromes. See if you can connect with an integrative/functional medicine doctor that specialises in Lyme. I have seen others recover using a multi-lateral strategy as well as herbal protocols where antibiotics are not tolerated, but it's rarely from a single magic treatment.

[@kimwarburton8490]

i think you'll find info on sarah myhill's website. Lots of people with myriad extra complications, incl Lyme's on the Me/CFS fb group they run