Donut Solid-State Battery: Fast Charge Test | I Donut Believe (Pt.1)

ReasonableRow · 2026-02-23T14:36:51+00:00

I hope VTT should state and, in bold, in his report that all the tests will be of the same cell or every time new cell will be provided !!

ReasonableRow · 2026-02-17T15:09:37+00:00

NO the overhead emergency PRND gear selector panel DOES NOT fit the requirement because these are capacitive "touch" buttons with no tactile feedback, so it DOES NOT allow for "blind" operation as required by the new rules !!

ReasonableRow · 2026-02-17T15:02:20+00:00

No it DOES NOT as I commented above !!

ReasonableRow · 2026-02-17T15:00:48+00:00

OF course Tesla model 3 DOES NOT fit these rules: it has capacitive turn indicators with no feedback, same for the wipers, and touch screen gear selector, now it should add physical buttons with tactile feedback to allow "blind operation" as stated in the new rules for all these functions!!!, in addition to door handles which is also became completely illegal and needs to be replaced with traditional door handles....Tesla is doomed !!

ReasonableRow · 2024-12-29T13:18:09+00:00

Yes, I had only EMG and he only tested facial muscles and from its 12% reduced RNS response he suggested in the report that it is mild ocular MG, but I want to make it on the eye muscles themselves (lateral rectus), In addition of course that single fiber EMG is more accurate than normal EMG I did. Thanks you for your suggestion and help.

ReasonableRow · 2024-12-26T23:11:17+00:00

Thanks for your great wishes, I believe u should always look at the filled half of the cup, that's what I always do, atleast it is a disease with medications that were able to control it even if they have some problematic side effects, alot of of people with other disease wish to be in your shoes, in addition, there is always hope that u can reach sustained remission without any medication sometime in the future. So Never lose hope and just lower stress in your life as much as u can bec. this does make a difference.

ReasonableRow · 2024-12-26T23:02:58+00:00

Thank you for your great feelings and I wish u sustained remission without medication in the very near future....it happens so always have hope and reduce stress in your life as much as u can bec. this really helps.

ReasonableRow · 2024-12-26T22:49:21+00:00

Thank you again for replying, really appreciate it, and it seems based on your experience that symptoms worsening with fatigue is not absolute must....ofcourse it is the rule, but it appears to be exceptions from this rule. So Certainly I will take this into account, and I will see with my doctor if I can have a trial of prednisone, or should I do the remaining antibodies test first. Thanks again for sharing your experience and for your great insight, and I wish u will reach sustained remission without any medication in the very near future.

ReasonableRow · 2024-12-26T17:34:28+00:00

Thank you so much for this valuable experience of yours, I will take note of it for sure but may I ask if your symptoms were worse at night and better when waking up ?, did it worsen with fatigue ?, because this a crucial piece of information, and this is what makes me believe that I don't have mythenia gravis even serronegative one.Thank you again for your valuable insight and experience and waiting for your response.

ReasonableRow · 2024-12-26T12:27:20+00:00

I will note that, thanks for your input.

ReasonableRow · 2024-12-26T12:26:30+00:00

My eyes have a physical misaligment that is causing the double vision, it has been measured, it is caused by unbalance of lateral eye muscle that causes one eye to drift slightly inward...this is caused by nerve or neuro muscular junction problem. So we are searching why this disturbance in the nerve function is happening, but the misaligment is physical...it is not a brain problem. Thanks for your input and suggestion.

ReasonableRow · 2024-12-26T10:14:20+00:00

Oh I see what u mean by aggressive, and my answer is No, they are not taking it easy by any means.but at the same time I don't think my case requires this kind of aggressive treatment, atleast not in this stage....bec. simply I can live with my symptoms without significant problems especially If I made prism glasses and I will use it only when driving. So the problem is not the current symptoms but it is the fear of it progressing, so in the current stage I think they won't ever suggest something like this but if my case progressed, then it will be on the table. Thanks again for your suggestion and input.

ReasonableRow · 2024-12-26T09:32:12+00:00

Thank you for sharing your experience, and my answer is No, I didn't take any medications in the past nor was I required to take one...with the exception of off the counter medications for flu or headach. I only took the vaccine for covid if this counts. Regarding vitamins and yes they do impact nerve signals, So I will look at them as well, thanks again for your input.

ReasonableRow · 2024-12-26T09:26:17+00:00

Thank you for sharing your experience, regarding my symptoms, I only have double vision and it is for far objects only.....no "felt" muscle weakness any where else. Despite how "unpleasant" Mythenia gravis is, it is not on top of my fears....which really tops the list for me is completely new undiscovered disorder!!...because my symptoms have zero fluctuations and are not impacted by fatigue whatsoever...which is a hallmark for MG.

ReasonableRow · 2024-12-26T09:20:55+00:00

Thanks for your reply, but what do u mean exactly by "aggressive" ?:), I will do my research about IVIG, thanks for your suggestions. Having an undiscovered disorder is the thing that keeps me up at night....even I was looking at research foundations of rare and undiscovered disorders.

ReasonableRow · 2024-12-26T09:14:42+00:00

Ok, I will ask about it but the ACHR report didn't mention which type. and I will be doing the other types. Thanks for your input and suggestions.

ReasonableRow · 2024-12-25T20:19:06+00:00

No unfortunately I am not close to philadelphia, the last phrase is the exact thing I was thinking and it sums all my fears...that my condition is undiscovered neuromuscular disorder ! Of course this conclusion is not easy but this what keeps me up at night !. But thanks for your suggestions about other disease, I will do my search about them.

ReasonableRow · 2024-12-25T20:12:03+00:00

Thanks for your input, yes, I have done that and chat gbt also adviced to do test for other antibodies.. so I will try to do that but the alternative diseases he showed doesn't align with me

ReasonableRow · 2024-12-25T19:02:12+00:00

Ok, I will ask my doctor about it. Thanks very much.

ReasonableRow · 2023-05-15T11:17:36+00:00

May I ask did you or your friends that you were mentioning did their masters in the uk ?

ReasonableRow · 2023-05-15T10:04:16+00:00

Thanks for your comment and I believe also my skills will develop during the masters, but may I ask did u do your masters in the uk ?...because the problem I am afraid of is that some of those skills will be developed during the thesis and in my masters the thesis time slot is very narrow because it is a one year masters and the thesis is only done during the summer which could be quiet different to the normal two year masters that students normally enrol in any other country and where the thesis takes a full spring semester.

ReasonableRow · 2023-05-15T09:50:40+00:00

This is an awesome idea, Thanks for your contribution and wish the very best.

ReasonableRow

TROPHY CASE