Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

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Old 09-10-2009, 08:07 AM #1
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Default Are those with hot RSD still experiencing vascoconstriction?

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Originally Posted by GalenaFaolan View Post
SB, that is why I typically will mention "hot" and "cold" rsd when it comes to people talking about ice or how to make something feel better. Us "cold" people are some hurtin' puppies with cold, but of course "hot" isn't bothered by ice or cold and is perfectly fine for you because you're not restricting already constricted blood vessels like mine are being a "cold" rsd. :-)

This is very true because even everyone with cold or hot rsd have different experiences somewhat because we are all individuals. So it will remain.

Hugs,

Karen
Hi Karen, since I have cold rsd, and the vascoconstrition is very obvious my question is If you ahve hot RSD isnt the same thing happening to you, vascoconstriction, as it is with me? your body is just reacting differently? In the begining my legs were red hot, as the stages advanced they went cold, but the underlying problem was always vascocontrition. So is it the same. sorry for my awful spelling. cz
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Old 09-10-2009, 10:13 AM #2
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cold RSD: vasoconstriction
hot RSD: vasodilation
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Work related (car) accident September 21, 1995, consequences:
- chondromalacia patellae both knees
- RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008
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Old 09-11-2009, 09:12 AM #3
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Quote:
Originally Posted by CRPSbe View Post
cold RSD: vasoconstriction
hot RSD: vasodilation
Marleen,

Thank you, that is very succinct. From here, we can picture:

vasoconstriction (constrict - Verb: to draw or press in; cause to contract or shrink; compress) -- smaller blood vessels, less flow

vasodilation (dilate - Verb: to make wider or larger; cause to expand) -- large, open vessels, more flow

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Old 09-12-2009, 09:40 AM #4
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I was told at one time that the vasodilation/vasoconstriction that occurs in RSD has to do with the tiny nerves on blood vessels. The nerves make it possible for a blood vessel to react, to either constrict or to open up automatically under cold or warmer circumstances - it's a very finetuned system that can instantaneously react. The RSD makes these nerves act totally out of control. That's why you get constantly opened up blood vessels in first stage RSD, then the nerves sort of don't know what to do anymore in stage 2 and they start to vary between constriction and dilation, then in stage 3 it goes the other way and they cannot keep the blood vessels open enough anymore. That's why in late stage RSD often vasodilators are given as meds, to make the blood vessels open up more, to allow for more blood flow and to warm up the limb from the inside out.
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Work related (car) accident September 21, 1995, consequences:
- chondromalacia patellae both knees
- RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008
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Old 09-11-2009, 02:12 AM #5
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I have cold rsd too. Here's an explanation between the hot and cold. They aren't the same thing at all. One, cold, is vasoconstriction. Hot is vasodilation because there's too much blood flowing through the blood vessels, versus cold where there is a lack of blood flow.

Quote:
Vasoconstriction reduces blood flow (area is usually cold, white or dusky in color), vasodilation iincreases blood flow (area is hot, red or excessively pink).
Here's a link that explains it as well, Heat/Cold Adaptation. It says what the quote above says. "Red skin indicates vasodilation and the pooling of blood near the surface for release of heat."

Hope this helps clear it up. :-) Some people start off with hot rsd and it gradually changes to cold, but cold usually stays cold and sometimes people can have both at the same time.

Hugs,

Karen

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Originally Posted by CZZ74 View Post
Hi Karen, since I have cold rsd, and the vascoconstrition is very obvious my question is If you ahve hot RSD isnt the same thing happening to you, vascoconstriction, as it is with me? your body is just reacting differently? In the begining my legs were red hot, as the stages advanced they went cold, but the underlying problem was always vascocontrition. So is it the same. sorry for my awful spelling. cz
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Old 09-11-2009, 05:14 AM #6
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Default thank you for the correction.

Quote:
Originally Posted by GalenaFaolan View Post
I have cold rsd too. Here's an explanation between the hot and cold. They aren't the same thing at all. One, cold, is vasoconstriction. Hot is vasodilation because there's too much blood flowing through the blood vessels, versus cold where there is a lack of blood flow.



Here's a link that explains it as well, Heat/Cold Adaptation. It says what the quote above says. "Red skin indicates vasodilation and the pooling of blood near the surface for release of heat."

Hope this helps clear it up. :-) Some people start off with hot rsd and it gradually changes to cold, but cold usually stays cold and sometimes people can have both at the same time.

Hugs,

Karen
Karen, hi, im so surprized that we would have both components through the duration of rsd- that it can be so extreme in the spectrums. I was incorrect, I thought that whether hot or cold, we both suffered from vacoconstrition. I thought it just changed with the life cycle of rsd. I went through the heat in the early stages. Now with the cold, I still have excessive sweating its a huge problem requiring potassium replacment reguarly, I really try to watch it as nothing burns more than an IV of potassium. do we both have the blood pooling, I understand that our nerve cells literally leek blood. I have had lesions that look like blood blisters, so so painful. If i knew how to post pictures i would show you. Dr. S has told me that our edema is different, its in the nerve cells or rather its the nerve cells holding the fluid and leaking the fluid. the blood goes down to my extremeties but does not return,as my body considers them as lost cause. it still seems so odd to me that the disorder is on both ends of the spectrum vasoconstriction and vasodilation..and I agree we may have them both at the same time in different parts of our body. thank you for you post, hoping you have a good day, cz
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Old 09-12-2009, 04:13 PM #7
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Glad to help you with understanding the difference. I hadn't seen Marleen's post or Sherri's before I post it. lol Those who start cold stay cold, those who start hot may, like you did, turn cold eventually. That "used to be" the criteria for rsd. Skin was hot first and cold later, which isn't true for everyone and I found most people have cold rsd and hot rsd is a minority. I'd have to dig up the stats on my survey again for the %'s.

Sweating, blood pressure problems and such are all due to the rsd wreaking havoc with both voluntary and involuntary systems. We can't regulate our body temperature anymore and get cold or hot when we shouldn't be. I only deal with some sweating at night that is mild but get worse at "that" time of the month. lol I think part of the reason for my lack of sweating as some do is because I'm very underweight now. I know it's hormones making the sweating worse at night near my period. Potassium burns you, seriously? Wow, I've never heard anyone who experienced that...interesting.

Maybe not so much blood pooling...it's the lack of blood flow that causes skin color change for me, but I think it's the excess blood flow, blood pooling in hot rsd though. I have blood blisters, known as petechial hemorrhages, all over my body, have since the beginning that turn into lesions. Even tiny ones take forever to heal. I thought I read somewhere what causes it but can't remember where or when! LOL

Hugs,

Karen

Quote:
Originally Posted by CZZ74 View Post
Karen, hi, im so surprized that we would have both components through the duration of rsd- that it can be so extreme in the spectrums. I was incorrect, I thought that whether hot or cold, we both suffered from vacoconstrition. I thought it just changed with the life cycle of rsd. I went through the heat in the early stages. Now with the cold, I still have excessive sweating its a huge problem requiring potassium replacment reguarly, I really try to watch it as nothing burns more than an IV of potassium. do we both have the blood pooling, I understand that our nerve cells literally leek blood. I have had lesions that look like blood blisters, so so painful. If i knew how to post pictures i would show you. Dr. S has told me that our edema is different, its in the nerve cells or rather its the nerve cells holding the fluid and leaking the fluid. the blood goes down to my extremeties but does not return,as my body considers them as lost cause. it still seems so odd to me that the disorder is on both ends of the spectrum vasoconstriction and vasodilation..and I agree we may have them both at the same time in different parts of our body. thank you for you post, hoping you have a good day, cz
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Old 09-13-2009, 06:22 AM #8
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Quote:
Originally Posted by GalenaFaolan View Post
Glad to help you with understanding the difference. I hadn't seen Marleen's post or Sherri's before I post it. lol Those who start cold stay cold, those who start hot may, like you did, turn cold eventually. That "used to be" the criteria for rsd. Skin was hot first and cold later, which isn't true for everyone and I found most people have cold rsd and hot rsd is a minority. I'd have to dig up the stats on my survey again for the %'s.
Some people actually move more slowly or even faster through the stages but it's also possible to skip a stage. It also largely depends on treatments given and how you react to them. That's why RSD is so different for everyone.
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=====================
Work related (car) accident September 21, 1995, consequences:
- chondromalacia patellae both knees
- RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008
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Old 09-13-2009, 09:09 AM #9
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Lightbulb

We are just discussing this on the PN forum.

I am going to try it too, since winter is almost here.

http://healthifeet.com/

This might help those who struggle with "cold" and poor circulation.

The l-arginine and magnesium in it are known vasodilators. But I cannot endorse it yet. I just thought I'd put it up here for those wanting a non-invasive thing to help with comfort.

Here is an edit... I am finding different ingredients listed on various websites today for this product... but it appears that capsaicin is in it.
For those who cannot tolerate pepper extract...which may cause burning, then this is not for those patients.
Here is our thread:
http://neurotalk.psychcentral.com/thread102849.html

This one has arginine with NO capsicum (pepper).
http://www.butaicosmetics.com/en/foot_cream.aspx
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Last edited by mrsD; 09-13-2009 at 10:01 AM.
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Old 09-13-2009, 10:06 AM #10
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Default No Biofreeze for cold rsd

Quote:
Originally Posted by mrsD View Post
We are just discussing this on the PN forum.

I am going to try it too, since winter is almost here.

http://healthifeet.com/

This might help those who struggle with "cold" and poor circulation.

The l-arginine and magnesium in it are known vasodilators. But I cannot endorse it yet. I just thought I'd put it up here for those wanting a non-invasive thing to help with comfort.

Here is an edit... I am finding different ingredients listed on various websites today for this product... but it appears that capsaicin is in it.
For those who cannot tolerate pepper extract...which may cause burning, then this is not for those patients.
Here is our thread:
http://neurotalk.psychcentral.com/thread102849.html

This one has arginine with NO capsicum (pepper).
http://www.butaicosmetics.com/en/foot_cream.aspx
Hi thanks for this, I went to PN and read the thread, I did want to mention that biofreeze is a big NO for my cold rsd, the initial "cold" feeling it creates is unbearable for me. It really increases my pain.the capsaican may be different?
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