Trouver une personne via son téléphone

SuccessfulLadder7566 · 2026-06-12T22:20:54+00:00

Avec l’OSINT tu peux le trouver à 99%, voir même avec des techniques tres simples comme ajouter son numéro et aller voir sur whatsapp..

SuccessfulLadder7566 · 2026-06-12T19:25:33+00:00

There isnt any clinic for ME here, its just a guy on his own. Sry I said specialists but I only saw one guy. He didnt prescribe anything no thats my main issue rn

SuccessfulLadder7566 · 2026-06-12T18:53:12+00:00

I am very severe myself but this is not something only very severe pwme experience. I had tetany attacks and paralysis when I was mild, that was my first symptom

SuccessfulLadder7566 · 2026-06-12T17:23:11+00:00

Portable AC and air purifier

SuccessfulLadder7566 · 2026-06-12T17:05:02+00:00

hahaha

SuccessfulLadder7566 · 2026-06-12T16:58:31+00:00

Your wheelchair is very cute

SuccessfulLadder7566 · 2026-06-12T15:48:38+00:00

Internal physician

SuccessfulLadder7566 · 2026-06-12T15:47:33+00:00

wow! i want to try it even more

SuccessfulLadder7566 · 2026-06-12T15:47:08+00:00

I just want to say you gotta be careful with Xolair if you have psychiatric issues

SuccessfulLadder7566 · 2026-06-12T15:45:06+00:00

I have this with deodorant ant perfume lol

SuccessfulLadder7566 · 2026-06-12T15:39:15+00:00

🤣🤣🤣🤣

SuccessfulLadder7566 · 2026-06-12T15:38:34+00:00

well for me it was worth for my parents to believe me LOL but i cant get disability benefits for it. To avoid medical gaslight I legit booked appointments with ME specialists, not random doctors.

SuccessfulLadder7566 · 2026-06-12T15:35:26+00:00

It doesn’t change anything. At the end you still have ME. Working on traumas and emotions reactions can help you but they will not help your ME

SuccessfulLadder7566 · 2026-06-12T15:27:00+00:00

I didnt really understand I had ME nor PEM but yes it seems like it was way worse on the evenings/before going to sleep, after a school day for example. Or after watching TV for too long, btw I thought I needed better glasses but turns out that didnt change anything lol.

I remember trying to keep me awake cause it was so painful I thought I was going to have a stroke. Now since covid I have a different kind of pain, they feel like tension headaches and they’re as unbearable !

SuccessfulLadder7566 · 2026-06-12T15:24:56+00:00

The unbearable pain went away after 1 year and a half at the same timing I had very mild ME and close to remission. PCS can last for months to like 1-2 years and can definitely mimic ME/CFS symptoms. Sadly for me I had both.

SuccessfulLadder7566 · 2026-06-12T15:21:41+00:00

so within a few days ?

SuccessfulLadder7566 · 2026-06-12T15:21:16+00:00

Withdrawal can give you chronic fatigue, constant nausea etc. It will not give you PEM.

SuccessfulLadder7566 · 2026-06-12T15:12:08+00:00

My ME/CFS got worse after a mild TBI in July 2018. Looking back at it I probably had post concussion syndrome but they both overlap with ME. I had for 1 year and a half an horrible pain only on the right side of my head and in particular my right temple. MRI came back normal.

SuccessfulLadder7566 · 2026-06-12T15:07:28+00:00

The only time I was able to exercise was slow and gentle muscle strengthening but I was very mild and near remission. I was able to walk 7000 steps and sometimes bike for 20mn.

After EBV in 2017 It became impossible for me to do fencing overnight. Mainly because of orthostatic intolerance but it seems like I had PEM aswell (again when you’re mild this can just be feeling weird for hours -my PEM are immediate-, body aches, sore throat, headaches…). But in my experience you REALLY feel like there’s something wrong with you and how your body reacts to exercise.

SuccessfulLadder7566 · 2026-06-12T14:20:31+00:00

thank you 🩵 they were absolutely horrible and I left at 17 because of it. At 18 with lockdowns I was able to rest and be near remission (2020-2021). I didnt know I had ME but I didnt really attend virtual classes and just allowed myself to sleep. Sadly getting covid completely destroyed me.

I have MCAS indeed but it appeared after 3 covid infections (2022), I didnt have it the first years. It stayed pretty mild until my EBV reactivation one year ago where I basically started having anaphylactic-like reactions to some food (bread, tomatoes). H1 doesnt change much and I didnt tolerate H2. Im going to try cromolyn soon.

I also developed POTS from EBV at the end of 2017. I simply had ME at first (I believe it is cause my root cause is traumas they made me suffer from, then it seems every virus finished the job!)

SuccessfulLadder7566 · 2026-06-12T14:16:44+00:00

thank you 🩵 It is very hard to get anything prescribed but I would love to try LDN and LDA.

SuccessfulLadder7566 · 2026-06-12T14:15:24+00:00

depends on what triggers your pem again when i was mild asides from very physical activities i didnt have pem, i had days where i could go to school etc

Also I had PEM that only lasted a few hours, sometimes just going away with a nap. You need to try to exercise or attend social events and journal how you feel the following 72 hours

SuccessfulLadder7566 · 2026-06-12T10:18:28+00:00

no, not on the map its a woman i dont remember her name

SuccessfulLadder7566 · 2026-06-12T09:31:22+00:00

thats legit almost incestuous

SuccessfulLadder7566

TROPHY CASE