This disease it’s true colours around age 40 its an excruciating genetic 🧬degenerative inflammatory disease.The barer can no longer sit, drive lie down or sleep . In the end they stand nearly 24 hours for hours everyday they live in sustained, energy drinks because they cant eat and then their bones start to disintegrate.
RLS is related to ADHD ,Tourette’s ,TMG .
Is your child or grandchild restless sleeper.
A lot of Women who suffer RLS during pregnancy 20 years later often come out of remission and start a horrible journey. Of course then they start to worry about their children 👧 🧒
RLS is not in the teaching curriculum for doctors , neurologists 70 percent prescribe DA’s which make it worse ,takes years to wean off often leaving permanent damage to the pleasure centre in the brain.
First it's not a disease but as the name says is a syndrome (A collection os symptoms which may have different cuses), but your right that is's degenerative and inflammatory.
What baffles me is that people don't realise is that these energy drinks are packed with sugar which causes inflammation, so the very foods that they are reaching out for is causing insensifying or perpetuiating the problem. Another common cause of inflammation is refined seed (vegetables like corn soya and sunflower) oils.
Yes RLS is connected to ADHD ,Tourette’s ,TMG because they all share the same cause the only difference is the individual patient's own genetics and how their body responds to the inflammation.
You are helping so much Shumbah, you understand how bad this is.
I’m in hospital, 5th day, the medication syrups and foods must have sugar added. My RLS is above the roof, I’m desperate no sleep, food sugar laden with everything.
Methadone not helping even 10ml x daily.
All of us are so grateful to your help, understanding and knowledge about what all of us are going through.
I applaud your efforts to educate those who should know how desperate we all are.
I hear u, sadly am in a bad way , and I can’t take a break and to be honest scared . However I am grateful I do not have RLS. .
I’m going to try do a post that I think you should research and consider. I’ve been holding back because I don’t want to give false hope however I am astonished at my results and it’s natural. I commitment. Actual I will try to record at put on you tube for all the non socials
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My Doctor really doesn’t seem to understand
The answer I received from my concern about the treatments on the RLS Foundation website
My first night on mirapex
RLS AWARENESS DAY 23 SEPTEMBER
My Opinion: Collateral Damage due to Discontinuance of Pramipexole
