Peripheral neuropathy????

Had it since I was 35 years old and tried everything, including surgery to get rid of it, by mistake quite often. It can stop the heart, been there as well.
 

yes the very outer dried peel usually - just any suitable amount? - I tried it for a while but being an impatient fella sometimes didn't give it much of a chance. The guy that put me onto it was adamant it made a collosal difference to him - and he is someone I would trust on the matter
 

Well here's one recipe I found. It icludes more than just onion peel, but addresses much of our concerns. Note; it states that red onion & peels are best.


Dominican Té de Cebolla​


Rated 4.4 stars by 5 users

Category​

Traditional Medicinal Tea


Ingredients​

Directions​

  1. Fill a large pot with 9-10 cups of water
  2. Add all the fruits, herbs, and spices and boil at high heat until the onions and apples are fully cooked.
  3. Strain the tea before storing in a large glass jar in the refrigerator. Heat up over the stove when ready to enjoy.
  4. Squeeze fresh lemon juice before drinking.

Recipe Note​


We recommend having at least a glass a day!
 
wow that sounds like it will pack a punch - just wondering if the boiling will kill any chemicals?? - but certainly worth trying for fun - problem is taking it alongside normal medication like lyrica ??? full glass a day sounds good - who's goin first??
 
davey said:
wow that sounds like it will pack a punch - just wondering if the boiling will kill any chemicals?? - but certainly worth trying for fun - problem is taking it alongside normal medication like lyrica ??? full glass a day sounds good - who's goin first??
Click to expand...

I need to place a grocery order soon ... think I'll get a couple of onions & some apples, I have cinnamon sticks.

Just boil up a small batch ... it might taste horrible ?
 
I have pain, tingling, burning, cold sensation in feet, legs, arms and hands as a result of an autoimmune disease called Transverse Myelitis. It can be caused by several things including a bad flu or yes, A flu shot or vaccination. Mine was caused by vaccines I took in the late 80s to travel to Asia. It was made worse by flu shots and yes, the Covid vaccines. Mild cases of TM are more common than the literature says. True diagnosis requires full MRI of the spinal cord including gadolinium dye. Costs would start at $20,000 and go up from there. So you can see why chasing a diagnosis for neuropathy is not always done. Especially when the treatment options are basically nonexistent.
 
rgp said:
I won't waste your time reading all that i have tried for it. Allot of it very aggravating / expensive . None of it helped.

I was @ one time even told that ... if I could loose just ten pounds [which would change my A1c] the change would be felt almost immediately . Well I lost 60 pounds , my last A1c reading was 6.5 ....... Not one damn bit of change in my neuropathy.

Not trying to be discourging ... Just being truthful.
Click to expand...
Thank you for your truthfulness. I was diagnosed with PN 3 years ago. And there is NO CURE for this cruel disease. I'm looking for a truthful support group in and around the Mansfield, Ohio area.
We, with this disease, do need to talk with someone that is going through the very same thing that we all are experiencing....as it helps to talk to or with someone.
And, as you know, that pain never, never goes away. Is there anyone in the area that has PN that would like to start a support group for this disease? We just need to connect and talk to someone and get their feelings about this disease as I sincerely believe that talking about this helps me and others. Many thanks for reading this.
 
I probably have a mild case, so I don't know if this is helpful. My first symptoms began several years ago with pain mainly between the knee and ankle when walking. I could only go so far before needing to sit down, or at least stand still awhile. I couldn't make it from one end to the other of a shopping mall without breaks. I didn't know it was PN until my doctor explained it. I make sure to walk 1-2 miles a day, and it's made a big difference toward less leg pain. Last year, I was sick in bed about a week, couldn't walk, and the old pain returned as before, until I got back into my routine.
 
Biscuit said:
Thank you for your truthfulness. I was diagnosed with PN 3 years ago. And there is NO CURE for this cruel disease. I'm looking for a truthful support group in and around the Mansfield, Ohio area.
We, with this disease, do need to talk with someone that is going through the very same thing that we all are experiencing....as it helps to talk to or with someone.
And, as you know, that pain never, never goes away. Is there anyone in the area that has PN that would like to start a support group for this disease? We just need to connect and talk to someone and get their feelings about this disease as I sincerely believe that talking about this helps me and others. Many thanks for reading this.
Click to expand...
Your so right on about seeing and talking with others who have PN. I am a member of a support group hosted by the Western Neuropathy Association. It meets through ZOOM meetings 3 times a month. For more info go to pnhelp.org, and click support. The mayo clinic, and several other sites have support groups...with a little searching you might find one that suits your needs. Good luck! ( there were over 50 people in this last Saturdays meeting. ) a couple years ago there were about 10. PN seems to be a growing problem in our society. I have no idea how to cure it, or slow it down. I hope they figure it out soon.
 

You must log in or register to reply here.

Back
Top