CPPS is Actually TMS (Mind Body Syndrome)

If you’ve done the tests, the scans, etc. and still haven’t found answers for your CPPS, it’s time to look elsewhere 🧠

Research shows that CPPS is often rooted in a complex interplay between the mind and body-- known as mind-body syndrome (TMS). Understanding this mind-body syndrome offers new insights into holistic approaches for diagnosis, treatment, and long-term healing ❤️‍🩹

#menspelvichealth #tms #mindbodysyndrome #CPPS #pelvicpainrelief
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Transform You, and Your Pelvic Floor Transforms.

[albertoperez]

100 percent true! That’s the only way I was able to get rid of CPPS symptoms I had for 4yrs

[PhillipMadden-ukfy]

I'm a disabled vet with ptsd and it took me over a decade after I got out to figure out that the worse I thought an episode was gonna be the worse it was. Eventually I trained myself to believe that it's not going to be a bad one and it works! Also my symptoms were very physical like loss of limb movement erratic heartbeat and vomiting so yep mind and body are very connected.

[camlendrim]

Avoiding prolonged sitting, controlling stress and anxiety, consistent pelvic floor stretches, aloe supplements to prevent constipation

[andrefilismissingtooth]

What are methods to put this into practice?

[Moonless]

My question is still trying to come to grips with if I should be doing body movements like PT/yoga or not to untrain the brain that something is wrong

[anthonyguiot]

Hey Michael, in the video you mention that cpps is due to mind body syndrom, which was discovered by Sarno. But is the process from your program about rewiring the brain properly? I see lots of exercises related to relaxing positioning, fascia release, ... Can you give more insights please? Have a nice day!

[Jay-fze]

Could this be the same with dyssynergic defecation/ pfd

[d.aardent]

I've found through looking up research studies that they are finding covid, and in my case long covid syndrome keeps affecting the neurological system as it can keep affecting and interfering with immune system causing inflammation and keeps causing brain fog and memory issues and exacerbates depression and such.
I just started finding out about this TMS thing and wondering if long covid is a big factor of that also. I know i used to be able to heal myself up from most things, but after i got the first covid in early 2020, it was rough and i never had a flu like that ever and the subsequent variants i had some version of every year since and just all kinds of continuous messed up systems in my body. Ive never been right since.
It was a complicated set of circumstances back then also where i was having a nervous breakdown from exhaustion taking care of my dad and mom 24-7 and i wasnt hardly sleeping for like couple years and i was so burned out and dead brained, i wasnt taking care of myself, then i got sick after i hadnt been sick for a few years as i always took all kinds of supplements for immunity, but i just got lax as i didnt have time to deal with it when i was doing so much for them everyday and running them to med appointments almost daily.
But ive finally built up resistance to covid variants i think as i got semi sick last fall but my reaction was fairly mild, i still went to bed and slept a lot but im always infinitely fatigued anyway.
But i wasnt ill for very long it seemed, not at all like what ive had in the past years.
But i still have a lot of brain and nerve issues, muscle weakness, boggy slow thinking, like it feels physically taxing and tiring to think about and worry about too much at one time.
I never got time to really mentally heal from the stress and anxiety of my business and trying to be caregiver to parents, i never was able to take time off and just rest my mind. But i feel like im still always on the edge of brain crisis and overwhelmed and just so tired i can never sleep enough. I just want to cease to exist these days as i have so many problems and weird pelvic pain issues that didnt really exist until i got covid.

[shahjadsiam]

Hey Michael/Shanon, I have been with you guys for a while but I am commenting first time today…I have been suffering from UTI/CPPS/PFD/SD i don’t know which one for almost 2 years….My life has become doctor to doctor and honestly speaking I even don’t think I will be alright someday…Even if doctor prescribe something I will say what to do if this doesn’t work….or changing doctors every week….I have lost everything my career my life…..I wake up in the morning with severe depression and all day searching online what could it be what is the solution…..nothing seems to work….my urine c/s prostate smear c/s all negative and finally one doctor said I have CPPS…..I have forgotten how normal urination feels like I have severe painful urination feeling of tightness in the urethra hesitancy urgency frequent urination and symptoms worsen whenever nightfall or ejaculation occurs…..I am devastated and lost myself to this pain emotionally mentally physically everywhere….help me

[AG-nnlp]

What about numbness in the saddle area and horrible sciatica type symptoms 😢

[anthonyguiot]

Hi Shannon, how can I work with you? Let me know!

[ChristianAddeo]

my PT said there was lots of tightness in my pelvic area, do u think its the mind causing this?

[indigosky]

I understand the tms concept and i have tension in my pelvic floor which is triggering my bladder. With pt i had gotten my pelvic floor to finally stay pretty relaxed but I've developed new tension spots and back to having bladder problems again.(she gave me kegel exercises that i guess my body wasn't ready for.) I know you include stretches etc on your channel to address the physical aspect as well as the mental stuff (most tms channels say to stop all pt which doesn't make sense to me.) But I'm confused how to heal this. I do my pt exercises and massage as well as meditation and breathing. Any suggestions or insight would be appreciated. I want relief. 😢 i hadn't gotten 100% better but was at least having several good days in a row. Now I'm struggling again and some days it affects my quality of life. I would love advice. Thank you.

Edit to add: i am female if that makes a difference.

[sk]

But how can the brain tighten the pelvis so extreme? I feel like I have pudendal nerve entrapment because it’s so tight down there and it feels that something in my pelvis is indeed entrapped

[Vxnxio]

Have you heard about Wise Anderson protocol? They did lot of experiment and found out that this CPPS is caused by Pelvic floor dysfunction and psychological issues. But there is a new theory suggesting that this is purely psychological. My Urologist said that my prostate is inflamed by touching it. I don't know what to believe anymore. I'm so lost.

[nitinmajoka]

I had swelling in the left testicle 8 years ago that went away by medicines but the pain never gone....all reports are normal always...now pain in the left testicle...pelvic area ...flares ..groin..thighs...it is really cpps ..already 2 urologist said its cpps...not able to live normal life😢

Please help

[HR-ljcy]

Dear micheal, I had this and you saved me. Since 1 month i have costochondritis, should i threat this the same way. I think its similar.. keep up the good work.

[MBison-octc]

okay. so this is your new perspective? because in the past you said, its a muscle problem (stretching as solution...)

[mudwiser]

Why is it TMS if it's Mind Body Syndrome... Shouldn't it be MBS?
What am I missing ?

[Mraymankarate]

My cpps developed after an injury from excessive masturbation.
I did MRI for pelvic, penis and lower back....all came normal.
I did prostatitis culture and no bacteria.
I also been give Cipro antibiotics for one month and no benefits.
I took pregababentin.
Nothing really helped.
My symptoms now is nerve pain in pelvic area.
Muscular tension in anal
dicomfort in testicle and penis .
back pain
hip pain.
sexual issue
anxiety
aching
I also did physical therapy many times .
I am confused