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-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Herbs/ natural remedies for RSD/ CRPS? (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/9620-herbs-natural-remedies-rsd-crps.html)

HubbyWithRSD 01-07-2007 10:39 PM

I've also heard....
 
I've also heard that sunflower seeds are a pain reliever. Anyone tried it? I'm sure it's not very strong but being that it's natural it might be worth a try. When I say sunflower seeds I'm talking the home grown natural ones, not those processed jobbies from the store. Think we'll have some pretty sunflowers growing this next summer! :D

lisashea 01-09-2007 08:09 PM

Quote:

Originally Posted by Vanessa (Post 56877)
I sure would love any info you have... :)

For how long did the acupuncture work for you?

Which teas do you reccomend?

Did you do the massages yourself?


The more info the better. Knowledge is power! TIA.

My accupuncturist removed all of my pain, needle by needle to each body part - starting at my ankle and moving up to my face. It was absolutely amazing! The best pain relief I ever had. Way better than any narcotic I ever tried.

Studies have shown that accupuncture is equal to narcotics for pain relief.
The issue is that you need to find the "right" accupuncturist. The one I went to was at www.newlifehealthcenter.com. I don't know how you would find someone like him. He has been practicing for many yrs(he's got to be in his 70's) and people who have no hope go to him and some get better from cancer and other terminal diseases.

PM me if you want to know more about going to see him. You can actually live there and be treated with meditation, teas, accupuncture, yoga, fasting,...all sorts of alternative treatments to get your health back.

He made me a special tea specific to my symptoms. It wasn't really tea but chinese herbs made into a liquid that he called tea but it was really medicine and tasted like sh..t! But I could feel it working in my body. A very strange experience.

Massages I got from a massage therapist who I would let work on my foot for a whole hour. Then my physical therapist did alot of massage too to my foot and ankle. After learning how they did my foot, I could do it myself but not nearly as good as them. They got in really deep where I couldn't do cuz it hurt and I'd stop before getting there cuz I was afraid to hurt myself.


Peace and hope,
Lisa

InHisHands 01-10-2007 04:55 PM

Thanks a lot, Jo55!
 
Quote:

Originally Posted by jo55 (Post 57015)
I googled "aches and pains natural pain relief"
i used the images search option- but if you click on a pic it will take you to the site where you can read more about the product-
http://images.google.com/images?svnu...ef&btnG=Search

Thank you VERY much!! :) :Thanx: I appreciate that.

septmystic 01-12-2007 06:42 PM

Natural Cures for RSD
 
My husband did some research on medical research sites and they said to try NAC (N-Acetyl-Cysteine) which is an amino acid. I tried it for 2 months, I saw a slight decrease in stiffness of my joints but was slightly sick to my stomach after taking the dosage. Not sure if it works but some swear by it. There is also DMSO cream, rubbed on my hands but for me this made the sensitivity worse. But there is research and each person is different. :)

InHisHands 01-12-2007 07:35 PM

Quote:

Originally Posted by septmystic (Post 58775)
My husband did some research on medical research sites and they said to try NAC (N-Acetyl-Cysteine) which is an amino acid. I tried it for 2 months, I saw a slight decrease in stiffness of my joints but was slightly sick to my stomach after taking the dosage. Not sure if it works but some swear by it. There is also DMSO cream, rubbed on my hands but for me this made the sensitivity worse. But there is research and each person is different. :)


Can you please tell me more about the DMSO cream? TIA!

Welcome here!! :) :) I read your other post, and I wanted to say "hi". I also have RSD in both of my arms. I know how that feels... Mine started in my right side and then moved to my left.

septmystic 01-13-2007 12:48 PM

Dmso
 
Hi Vanessa:

DMSO is used as an anti-oxidant and supposedly helps block pain signals just under the skin. So sensivity is lessened. Some people do react to it and you should always ask your doctor. It also is used as a transfering agent, so you must apply to clean skin, it will take anything applied on top of it deep into tissue so you have to be careful not to touch medication or such with this stuff on you. There is a lot of controversy on this medication but it can be bought online. I bought Nature's Gift DMSO w/Aloe Vera at www.herbalremedies.com. I researched which brand for about a week. This seemed the most pure and best
to try. My doctor approved saying it wouldn't hurt me.

This is something I saved from my searches "When applied to the skin, DMSO penetrates rapidly and will pass into the tissue below. Scientists believe DMSO may produce a wide range of pharmacologic actions, including anti-inflammation (reduces swelling), local analgesia (relieves pain), bacteriostasis, diuresis, cholinesterase inhibition, potentiator of the action of concomitantly administered drugs, influence on collagen, nonspecific enhancement of immunity, vasodilation, and lessening of adhesiveness of blood platelets."

Some online sources of information about this:
http://www.arthritis.org/resources/a...plorations.asp
http://www.medicinehouse.com/guidepages/PRrsd.html

Yes, it also is a type of paint thinner, but so are bugs! ;)
I hope this helps! Please let me know if you have more questions. I must have about 25 links on RSD.
Smiles,
Septmystic

Condor 01-13-2007 05:38 PM

MSM works for me
 
Along with other natural herbs, I take MSM. I believe it is in the same family as DMSO. Because it is sulfur based, some people cannot tolorate it. It works very well for me. I read about a 20 year study at OHSU in Portland on MSM and I liked what I read.
Stephen

Kali 03-01-2007 04:09 PM

Quote:

Originally Posted by InHisHands (Post 54630)
Well, at this point I am not too sure if/ how they are helping. But, I have only been taking them for 2 weeks.

I am making a teeny bit of progress in the right direction, but I am not sure if it is from the vitamins, or if it is a combination of: physical therapy, medication (neurontin 300 mg. in the morning, 300 mg. in the afternoon and 600 mg. at night. My PM Dr. just upped the dose at night to see if it would help with sleeping/ pain.), vitamins (the aboved mentioned ones), and I am no longer using the ice at PT/ home.

Just wondering... how old is your daughter? I am 16 years of age. It has been hard for me to find younger people with RSD.

Constrast baths are HARD on me, too.:( For me, though hot water bothers.

I'll have to look up those rubs. Maybe they would be of help to me. Might as well try. :)



Hi,

I'm new to this website. I am 15 yrs. old with RSD in the ankle, foot, and leg. I would love to connect with someone who may be going through similar physical and emotional experiences as me. Take care, I hope you feel better.

Kali

Annick03 03-01-2007 11:18 PM

Hi Vanessa,
I have used Skullcap tintcure for when the nerve pain does get to much. I take 10 to 30 drops, 3 times day. St. John's Wort in Virgin Olive Oil works, numbs the skin. I Have tried this too. But I don't use it much. Hope this helps.

Annick

artist 03-02-2007 10:43 AM

Hi Kali,

Just wanted say hi and welcome, we have a few people around your age here... just ask anything you want, make yourself at home :)
all the best!


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