@clairesam Sorry for the delay, I didn’t see this question for some reason! Here my update for everyone:
It has been exactly one year and I’ve tried DNRS, ANS Rewire, the Curable app, and several other bits I’ve collected here and there from similar “neural retraining” sources. With DNRS, I immediately noticed (since using happy memories is a huge part of the program) that I could not find a memory to dwell on that only brought me happy feelings, because every memory and every person in my life was associated with stress. This was a huge revelation because it showed me that my brain was really stuck interpreting many things in my life traumatically (I'm defining trauma as any sort of stressful experience that keeps the nervous system in fight or flight). I did some research and decided EMDR could be useful in moving these memories out of the fight-or-flight parts of my brain. I am now seeing a therapist who I will start EMDR with very soon, but to my surprise, the "happiness" in my memories/associations has started to come back already, and I believe it's from doing work on self-compassion (Kristin Neff), forgiveness (Fred Luskin), mindfulness (I know you're sick of hearing that lol), and shame (Brene Brown).
@xebex I couldn't agree more that DNRS demands way too much of PwME. It was primarily designed for people with Multiple Chemical Sensitivities (as you know), who do not usually have the amount of fatigue we have. I believe MCS is similar to MECFS in that it involves post-traumatic dysautonomia, but MECFS is almost infinitely more complicated BECAUSE the initial trigger in MCS is simple: a chemical/organic toxin exposure set their bodies into dysfunction. For us, it could be so many different kinds of triggers: toxin, virus, bacteria, surgery, pregnancy/labor, accident, general mental stress, psychological trauma, structural issues, brain/spinal lesions, etc. Whatever the initial triggers were that made you sick will determine what you need to address to get better. For me it was: connective tissue disorder (hEDS) which led to Chiari malformation, scoliosis, SIBO, and other stressors on the nervous system (I don't think these are usually enough to cause issues on their own until additional stressors come along), long-term mold exposure, and longterm mental stress. I am now strongly of the opinion that using brain training alone is NOT a solution for 99% of PwME!! There are simply too many stressors on the body, and trying to "retrain your brain" while those stressors remain is like mopping the floor while the sink is still on. I agree the best way to go is to learn what you can from these brain retraining sources and use them in they way that's best for you WHILE you address each stressor.
So I saw little to no progress in my physical symptoms from taking a purely brain retraining approach this past year. The only thing I can say is my headaches seem to have gotten better and there may have been a tiny improvement in fatigue that didn't last. But like you,
@xebex, I believe the theory is valid! Not only valid, but I still believe this trauma/neuroplasticity model is THE explanation of MECFS. The question is: How do you use that to get better then? ANS Rewire takes a much more holistic approach than DNRS, and is specifically for MECFS and Fibromyalgia. However, it drove me INSANE that Dan promises such quick results (50% better in 6 months!) and although I think his program can be useful, if you have a good functional medicine doctor with a knowledge of ME, you're probably already doing most of the things he suggests (except the actual "rewiring," which he spends very little time on and is not that profound).
So here's what I'd say: Practicing these techniques for the last year has not improved my physical state much, BUT it has opened my eyes to so many INCREDIBLY important things that I think will be necessary to my recovery, including:
1. My brain truly is stuck in trauma (unable to think of 'happy' memories/loved ones without feeling my nervous system triggered)
2. I am incredibly out of touch with both physical sensations and my emotions
3. I have a host of coping habits that put an enormous amount of stress on my body including: lack of boundaries, perfectionism, anger, need for control, avoidance of pain, etc.
4. My entire illness can be categorized as dysautonomia, or an inability to regulate my autonomic nervous system. I even came up with my own name for MECFS since the current names suck: Post-traumatic, exertion-intolerant dysautonomia (PTEDS)
Just because I have these issues, does NOT mean you do! You have your own cocktail of stressors that neurplastically changed your NS, and the goal is to figure out what they are and address them, and I think including neural retraining techniques is hugely helpful in that process.
So my current game plan is this:
1. Continue mental/emotional work including self-compassion, forgiveness, mindfulness, etc. with therapist
2. Address SIBO with a nutritionist (dietary changes, antimicrobials, etc.)
3. Use EMDR with therapist to allow my brain to "unlock" the trauma (this is highly researched based btw)
4. Continue to use Curable, DNRS, and similar neural retraining modalities to change the way I process things
5. Continue medication and supplements that help me (progesterone, T3, T4, LDN, lexapro, propranolol, magnesium, B12, D, iron)
6. Keep my house clean of mold (discovered it in air vents over the summer and had them cleaned and got an air purifier) - did notice improvement in symptoms after this
@Abrin I agree, and it is infuriating. Once I start getting better, I plan to put all of this information on Youtube for free because it makes me livid that it's not available easily for free. I find that unacceptable. If you want me to make another post summarizing what each of these programs actually contains, I can.
@tttttttt I have the Spanish copy of Gupta, message me your email and I will send it to you!
PS - I'm sorry for anyone who tried these programs and it hurt their mental health. I understand that. If it is discouraging you more than encouraging you, don't do it. Wait until you find something that works better for you or until you feel like you can have a mindset that allows you to do neural retraining without getting discouraged (that's been work for me). Most importantly, DO NOT push yourself outside your window while doing it! And if anyone says that's how it should work, it shouldn't.
PSS - Even if you don't have pain, I highly encourage you to check out Lorimer Moseley's work:
This will show you the science behind how the brain gets stuck in chronic symptoms, even in the absence of actual "pathology" or danger
Sorry if I missed anything/anyone! Hopefully I'll stay up to speed better on here from now on.