NeuroTalk Support Groups

NeuroTalk Support Groups (https://www.neurotalk.org/)
-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Morton salt gel? (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/190220-morton-salt-gel.html)

debbiehub 06-18-2013 06:20 PM

Morton salt gel?
 
What was that moton salt gel ish stuff? Looked on amazon ,,nothing came up

Ty
Deb

Kitty 06-18-2013 07:36 PM

Deb, I think you might be thinking of the Epsom Salt lotion. mrsD is very familiar with it and I'm sure she'll post here soon.

Is this the product? http://www.amazon.com/Morton-Epsom-L.../dp/B008X365AU

painman2009 06-18-2013 08:19 PM

Quote:

Originally Posted by Kitty (Post 993300)
Deb, I think you might be thinking of the Epsom Salt lotion. mrsD is very familiar with it and I'm sure she'll post here soon.

Is this the product? http://www.amazon.com/Morton-Epsom-L.../dp/B008X365AU

hey Deb. I dont have a bath tub but I use the epsom salt in luke warm water . and a wash cloth to apply. it has been helping a little. granted I just started but.

Brambledog 06-19-2013 04:00 AM

Didn't know there was a cream!

I put a couple of tablespoons of epsoms in a bowl of lukewarm water and soak my feet when they're really bad, and it does give me some relief, although it hurts initially to feel the water... For my knee, I wrap the epsoms in a damp cloth and lay it on the skin. I don't do it all the time, only when things are bad - anyone know if there is a cumulative effect with them? Is it worth doing every day?

Bram.

mrsD 06-19-2013 06:14 AM

Yes, you can do it every day. It is a lotion in an 8oz bottle.

No fragrance and it rubs in quickly to the applied site.
If applied over veins (like in the foot and hand) more will get into the blood stream to work systemically.

You don't slather it on, but use about a quarter's diameter on the site needed. A little goes a long way.

Magnesium is an NMDA antagonist, reducing pain. Also it dilates
blood vessels improving circulation to the site. Studies have shown that up to 70% of US residents do not get the RDA of magnesium in their diets. Magnesium is an essential mineral in about 100 biochemical reactions in the body.

mrsD 06-19-2013 06:31 AM

Magnesium also relaxes muscles and helps with cramping problems. ;)

Brambledog 06-19-2013 07:51 AM

Thanks for this. After much searching, I've ordered a tub of Magnesium Sulphate Cream (Epsom Salt preparation) made by Kirkman. 4oz tub (113g) for £20. It seemed to be the best value, and when it comes I think I'll put some into a smaller tube for carrying around.

Yay!!! Hope it's as good as I want it to be :winky:

Bram.

mrsD 06-19-2013 08:32 AM

The Kirkman product comes with a measuring spoon... 100mg of magnesium/ gram measure.

This is handy, because adults should aim for 200mg a day to start.
Adults need about 400mg of mag a day, and if you eat some mag rich foods, you don't need the full RDA from the cream. Those who avoid nuts, beans, leafy greens, should use more of the cream/lotion.

I found that this lotion lowered my high blood pressure to more normal levels. So if you take blood pressure drugs, you should test yourself often to see if your medication becomes too strong for you.

Discuss any changes with your doctor. If you skip or stop using the magnesium topical your blood pressure will go back up if you have hypertension.

debbiehub 06-19-2013 09:12 AM

Ty
 
[QUOTE=mrsD;993441]Magnesium also relaxes muscles and helps with cramping problems. ;)[/QUOTEi just ordered it from amazon...Ty!

mrsD 06-19-2013 09:15 AM

The muscles that run your fingers are in the forearm... that is where you want to rub in the lotion...not on the fingers per se.

I usually rub the last bit of lotion left on my hands, into my fingers at the end. But the majority of the lotion should go on your arms. I also like putting it on my inner wrists and under the forearms...as that helps it get into the blood stream faster for other benefits, like lowering blood pressure.

Brambledog 06-19-2013 09:21 AM

So who will get theirs first?! :winky:

I saw the little spoon, looked like a good plan to know how much I would be using. I didn't order the one in the link near the top of this thread because I'm in the UK, and that's from the US. Couldn't find the same product over here.

Bram.

mrsD 06-19-2013 09:28 AM

Kirkman was one of the first to make magnesium into an OTC cream. It is a reputable company.

The Morton's is really new...just hit the US shelves just over a month ago.

KathyUK 06-20-2013 01:06 AM

After my weird and painful reaction to the epsom salt bath, I daren't try again with the magnesium sulphate. Does anyone know if there is a difference in efficacy between the sulphate and other types, eg. citrate? Also do different mediums make a difference as there are a lot of magnesium citrate "oil that isn't oil" sprays on eBay. Thanks!

mrsD 06-20-2013 03:48 AM

Perhaps you put too much in the bath or made the water too hot?

This is a salt after all..and too much will sting like salt water can.

Magnesium sulfate is not typically used orally...it is a laxative.
To get oral absorption you need magnesium glycinate or citrate (in small doses because citrate is also laxative.)

Because most magnesium can have a laxative action orally, people vary in response to it. The topical forms in cream and lotion I believe are better absorbed as the base carries the mag thru the skin. I am leary of the spray oils (which are not oils at all), because plain water solutions are more limited in absorption.

Here in US we have SlowMag which is a delayed release oral form that works well too.
http://www.slowmag.com/

There are good food sources if you want to do it that way.
Suggestions are on the SlowMag website.

KathyUK 06-20-2013 07:46 AM

Hiya - I followed the instructions from one of the threads on here, and didn't have quite enough to do it as strong as many do on here. It did say to have the water as hot as you can stand, which isn't very hot for me, so it was my usual bath temperature. My feet swelled and turned purplish red. I was ready for the stinging as I'd read a fair bit on here, but I wasn't ready for my feet turning to balloons and changing colour like that, and wow the pain was bad. My feet aren't my main area of CRPS, although I was starting with mild symptoms in them. Since that bath they have been much worse. I can't remember if it was Bram who suggested it might be down to the sulphur or someone on another board (my head is really bad today, sorry for my terrible memory). It makes sense as since this happened I've looked into the foods that set off my IBS and they are sulphur rich too (onions being the worst culprit lol).

I've found "magnesium oil" on eBay and they sell it in Holland and Barrett, so I'm going to try that. It's magnesium chloride in water. If I have the same reaction to that then it blows my theory out of the water lol. Definitely won't touch epsom salts again. It's funny as I haven't had that reaction to the generic aromatherapy bath salts, are they generally based on something else? :)

mrsD 06-20-2013 08:07 AM

We don't use hot water on the Peripheral Neuropathy forum here.

Lukewarm only. Heat can flare us with PN.... we avoid that.

I've been doing epsom salts for many years, never had a reaction to lukewarm water.

There is also a limit to how much can be absorbed from water...
here is a link:

http://www.epsomsaltcouncil.org/arti...um_sulfate.pdf

I know that topical absorption does change with the product used.... The old CVS lotion did work for me a bit...but the new Morton Epsom Lotion is really good. I've been able to come off 3 blood pressure pills and now only take a small dose of beta blocker as a result. It also takes down my swelling left foot within hours! Something in this lotion base is improving absorption. It is creamier than the old CVS (which was discontinued).

Brambledog 06-20-2013 09:41 AM

Mine came today!! Brilliant service. I haven't used it yet aside been out, but will try it this evening...

KathyUK 06-20-2013 12:17 PM

Quote:

Originally Posted by mrsD (Post 993765)
We don't use hot water on the Peripheral Neuropathy forum here.

Lukewarm only. Heat can flare us with PN.... we avoid that.

I've been doing epsom salts for many years, never had a reaction to lukewarm water.

There is also a limit to how much can be absorbed from water...
here is a link:

http://www.epsomsaltcouncil.org/arti...um_sulfate.pdf

I know that topical absorption does change with the product used.... The old CVS lotion did work for me a bit...but the new Morton Epsom Lotion is really good. I've been able to come off 3 blood pressure pills and now only take a small dose of beta blocker as a result. It also takes down my swelling left foot within hours! Something in this lotion base is improving absorption. It is creamier than the old CVS (which was discontinued).

Yep, I can't tolerate hot water so the bath was luke warm, I was worried that I wouldn't get a good effect but wasn't expecting a really bad one like that, it was scary to be honest. I suppose it was just some sort of allergic reaction and given my IBS the sulphur theory rings true, but we'll see. I wouldn't risk trying it again to test my theory, it caused so much pain and swelling and I'm in a long flare at the moment now as it is without adding to it. I'm going to try the magnesium chloride sprays/flakes as I'd really like to be able to give the magnesium a proper shot. If I react badly to that too, I'll have to rethink. I'm not convinced the dietary supplement route is for me given how much less you get through to your system, how much longer it takes to build up levels and how it effects the stomach. Just going to play it safe for now. Thanks for all the info! I wonder if the chloride or other forms are available in creams? I will have a google.....

pyro 07-26-2013 10:36 PM

Quote:

Originally Posted by mrsD (Post 993765)
We don't use hot water on the Peripheral Neuropathy forum here.

Lukewarm only. Heat can flare us with PN.... we avoid that.

I've been doing epsom salts for many years, never had a reaction to lukewarm water.

There is also a limit to how much can be absorbed from water...
here is a link:

Lukewarm baths also applies to neuralgia symptoms? I though it was okay.. Please can you point me to the water temp discussions..


All times are GMT -5. The time now is 01:43 PM.

Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.