Mecfs and the golfswing model I developed

Published 2024-02-02
I had Mecfs for 24 years. Today people usually call it Long covid, different names same shit as its a energy deficiency illness.

I developed a swing model that is the only one that actually works.
You need and must shift to a new grip (Hans version) if you want to follow the instruction I laid out.
You can NOT use thumb on shaft modern grip in any form they teach you out there as it wont work. If you still do, go somewhere else as my golf instruction is built around the grip Hans use the guy you see swinging here.

Due to illness, I cant work, I cant go for a run, I cant read a book nowadays as it requires to much energy and focus.

So, Hans grip version, thicker grips and more layers ( 5-7) of griptape on your clubs are needed and a must.
Then, tilt and lift and a wide open stance.
This is done first without a club, then with a club.
You need to relax and pay attention to club turning after impact.

If you use a ball, it wont work.
Your brain will then acess old bad habit the ones your learn from various golf gurus.
So, no club then a club and NO ball.
You go back and forward with that until proficiency is reached (6 months give or take) then a ball can be introduced if old habits kick in (video is needed to check) then one go back to club and no ball a few times and then try again with a ball.

You can plan for 6 months of work give or take for benefits to happen.

I wont respond much if any due to the framework here works and I wont go into details here as it would require to much work I dont want to do.

You can either follow and find out here and do this or go elsewhere.
but if you do that then you will keep struggling with your golfswing forever.

Physicsgirl mecfs/longcovid 24/7 bedbound. This illness is not fun and the prospect of surviving when its this severe is not good.

   • An Update On Dianna's Health  

The amateur kid that has tour level accuracy as he never been able to do that previously so, my stuff works.

   • My instruction works  

All Comments (5)
  • Robert I would like to work with your drill and use your approach.i understand that you cannot work with with me personnalti will d what you say. Can we make a deal? Dennis Guffey
  • @adamlofving2071
    Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (CFS), while often grouped together under the ICD code I93.3, are distinct conditions with overlapping features, not to be confused with post-COVID syndrome. It's important to note that ME/CFS is a rare disorder, with evidence suggesting a significant portion of diagnosed cases—up to 84%, according to Norwegian studies—may actually be misdiagnoses of treatable conditions. Your description suggests a milder form of the condition, raising the possibility of a misdiagnosis. Typically, ME/CFS is thought to follow viral infections, not bacterial ones, with historical roots in what was once termed "Post-Polio syndrome." This highlights the century-old origins of its classification. Currently, there are promising treatments and therapies under investigation, but they are in the research phase and not widely available. Participation in clinical research may be necessary to access these experimental treatments. I encourage you to explore this avenue further, as it might offer some relief
  • @jaybee7890
    oh great another golf swing model and theory ROTFL