



I have tried few brands so far
All brands have different dosage
Tata1 mg - magnesium glycinate buffered with oxide - 440mg
Carbamide forte - 440 mg as well most likely buffered as it claims 22% elemental magnesium
Currently trying gnc - 440 g elemental magnesium from 3666mg glycinate
This is pure one .
Other pure glycinate brands dosage range from 82g to 350g.
I found gnc to be the highest when it comes to pure glycinate unbuffered. Just wondering do I need so much?
Should two capsule which roughly translate to 300g elemental magnesium?
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Everything cost so much nowadays.
A movie and cafe can easily cost 2k
Also feels like there isn't much do to that doesn't involve spending atleast 1 k per person for dates?
By no restriction I mean
- can eat and cook non veg
- can bring woman over for the night with no neighbours throwing tantrums
- the woman won't be his wife or only person . Most likely multiple woman
- can have friends over and have alcohol at home
- .play loud music
1-2 bhk is fine
Or any other options are also fine
Title
How do you know for sure if it's from autoimmune? Or mechanical issue?
Like indirect injury due to broad based hernibations annular tear etc?
My only problem so far has been si joints inflammation
Along small broad based hernibations and annular tear
No stiffness/night/morning pain at all
Rhemu has put me in upadacitynib 15mg
He says since I have no symptoms it's only to slow progression
My pain only exist when I bend down
I have guarding In low back due small broad based hernibations and annular tear
31m got diagnosed with nraxsla this year purely on basis on bilateral sacrolitis with no erosions etc
I have no stiffness or morning /night my pain only exist in bending down or when I stand up after sitting and slouching
My rhemu says I have a mild one
But I wondering how long do I have before I start seeing symptoms ?
Also I suffer from zero fatigue
Also I have disc hernibations and annular tear in extreme lower back . So no idea if my pain comes from that or si joints
My si joints definetly hurt in the sides
I have been given upadacitynib 15mg
Is it possible to have si joint inflammation Bilaterally as a secondary injury due to other issue other than autoimmune?
In 2024 I already had discussed buldge arigtj sacro which has turned in bilaterally along with small broad based herninations and annular tear in low back?
Is it common?
This chat is within a few text on apps
My story
My si joints is inflamed
But I have no stiffness/morning pain etc
However I simply can't bend down cause it hurts ?
Due to that its very hard to pick up things from floor or near impossible
I also have herniations small broad based akong with annular tear etc not sure which is causing the pain in low back
I am looking for guys where we can go to pubs ,clubs, cafes events etc and approach woman and have experiences
Stats
6'1
31 m
Woman usually check me out in street pubs etc and have been approached many many times everywhere
Looking for :
Similar age group 25-40 plus is fine in mumbai
Have some sort of disposable income to go to cafe pubsevents etc
We can all be friends and hangout as well it's not just only woman focused
Preferably single guys
Personal experience
From what I have seen competition is extremely low in real life as opposed to apps
So should be fairly smooth sailing most of the time
We can make a whatsapp group and talk about our experience as well
Edit : message me on insta ( link in my profile) or reddit . We can make a tele /whatsapp group
I am talking specifically for mumbai folks
Edit : here is the link for whatsapp group if anybody interested - MUMBAI ONLY
https://chat.whatsapp.com/BDDM0K50rJeGP9NyaZByEq?s=cl&p=a&mlu=4
When did your symptoms started? What age? How has it evolved over time
There are so many profiles that says hardly anything
What do you talk about? How do you start off conversation?
As soon as I found out what am I being dignosed for my heart straight up sunk
The fact that the disease is unhealable and progressive are absolute two worst things
The fact that it will only get worse as time progresses is horrifying
I just turned 31. If the disease stays for 30 years that's still makes me just 61
Even though the disease in fatal doesn't kill you doesn't stop the fact it kills you in other ways indirectly from depression, isolation, work
The lack of awareness makes it even worse
All the nonsense advice " you re normal , be positive, "
I am not even bad case
I don't have morning pain/stiffness
I eat whatever I want everyday
I only have pain in movement like bending etc no pain lying on bed
Rhemutologist says I have a "mild" case and promised me that ankylosing will never happen with me if i keep taking upadacitnyb 15 mg(current meds) etc