For People With Multiple Conditions

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For People With Multiple Conditions

This is a support group for people with multiple medical conditions.

Members: 75
Latest Activity: on Monday

Discussion Forum

Mistreatment Discussion

Started by pinkyspurse. Last reply by Eileen Apr 27. 1 Reply

This is for people who feel like they've been mistreated with their medical conditions and would like to talk about it.

Prurigo Nodularis (skin disease) and Diabetes

Started by Tinkersmom. Last reply by Mohanned Oct 29, 2012. 4 Replies

I'm searching for a connection between PN and Diabetes. The "experts" say the cause of PN is unknown. It presents as a "bite" that causes extreme itching. Next, lesions appear and the itching…Continue

Introduce Yourself!

Started by pinkyspurse. Last reply by Mohanned Oct 24, 2012. 36 Replies

This category is for introducing yourself and explaining what medical conditions you have and how they affect your life or whatever.

General & Misc. Discussion

Started by pinkyspurse. Last reply by Yvonne Aug 11, 2012. 15 Replies

If you feel like talking about something that won't fit into any of the broad categories I created, post it here!

Comment Wall

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Comment by PaulaO on January 11, 2012 at 7:29pm

Restless Leg Syndrome is often confused with Periodic Limb Movement Disorder. RLS happens primarily during the day and can happen as you are first laying down. PLMD happens at night and is the body twitching mostly in response to low oxygen although there can be other causes. It also mostly happens during the deep REM sleep and will wake you up, even though you may not remember it. Many people with untreated sleep apnea have PLMD. It is possible to have both RLS and PLMD. Yay.

I have kicked my 85lb Rottweiler over the foot high footboard of the bed during a kick caused by PLMD. She was not pleased. LOL

RLS is nerve wracking. I have been tempted to cut my legs off. Without anesthesia. The pain would be better than the sensations.

Comment by Robert Miles on January 11, 2012 at 6:05pm

I've heard of Restless Legs Syndrome. Is that it?

Comment by Natalie ._c- on January 11, 2012 at 6:05pm

Yvonne, it's Restless Legs Syndrome, soon to be known as Willis Ekbom Disease. It's a creepy-crawly, continuous electric shock, ants in your bones and muscles kind of feeling that starts when you are at rest and is agonizing, and the only relief for it is to move and keep moving the affected area. Obviously, THAT makes it impossible to sleep. At its worst, it affected the whole back side of my body, and lasted all night long, which is disastrous when you have to go to work in the morning. I'd spend all night jumping out of my skin, and then was a wreck at work!! After having it all my life, I have finally found a med regimen that works about 95% (and I'll forgive the last 5%) which consists of Xanax (actually an anti-anxiety drug, which has sleepiness as a side effect), melatonin, an iron supplement (because they have found that the brain is deficient in iron in RLS) and valerian root. As soon as I run out of the valerian root, I'm going to stop it because I tend to be suspicious of herbs, but my psychiatrist, who is the one treating me, recommended it. And if the RLS symptoms come back again after I've tried stopping it, I can always start it again. In my family, RLS is genetic, but it can also occur in conjunction with neuropathy and renal disease, so diabetics are at increased risk of it, too.

Comment by Yvonne on January 11, 2012 at 4:45am

Natalie, what is RLS?

Comment by muleman on January 10, 2012 at 4:58am

Hi Natalie and the Chaplain. I wrote to Chappie a while back. I wrote as a vet, Airborne! but didn't get a reply!
Sure sounds like the Chaplain has had a bad time. real sorry!
I have wild type 2! Had 2 miner heart attacks and have a stent in an artery to my heart. Hi BP, Eurhythmia, and sleep Apnia. I stop breathing over 1.000 times a night!
October 2008 I crashed my driving mule. Got an open fracture of my ankle. Dislocated it and broke my foot!
Got an infection in my ankle for 6 months and has Necrosis in it now. Both part of the Ankle bone are dead and decaying. They are talking about either pinning my ankle or taking my left foot off. I have the burning shines and heavy freckling of my legs. My foot has turned black once, but I worked on it hard with one of those small paint roller with the long handle and massaged what I could reach. It came right, kinda! I have a short deformed left arm after a parachute accident! So massaging a left foot aint easy. There is no support in the Free Health service here according to my Doc. I know my life is in God's hands, and the rest is up to me!

Comment by Liz on October 15, 2011 at 10:16pm
"Comment by PaulaO on Monday"
"We ought to make business cards with all our acronyms listed like degrees. Make people think we are edjamakatid when, in fact, we are just fubar."

& "Degenerative Disc Disease. A catch-all name for what they can't name yet. Like 'metabolic disease'."

You're so right, PaulaO! Lupus, DDD, fibromyalgia... It's all the same to me! I can't distinguish one from the other...
Comment by Natalie ._c- on October 14, 2011 at 6:35pm
I have a high pain threshold, too. I don't ever remember being in pain from my thyroidectomy enough to want meds; I just used them to get to sleep. And I've broken toes and received no treatment. I think Geo and I are related! :-)
Comment by justgeo1 on October 14, 2011 at 5:35pm
I have a very high pain threshold, so I don't need as much pain medication. When I had my neck dissection I only needed meds at night so I could sleep and that was only for less than a month. I've broken bones that never got set or had a cast because the pain never got me attention. Everyone is different.
Comment by PaulaO on October 13, 2011 at 10:51pm
LOL It's the face.

But seriously, don't stretch it. Take it on schedule to keep the pain away. By waiting until you HAVE to have it, you are causing yourself harm and making the pain harder to get rid of. By keeping it under control, you may find yourself actually using less than you think. Since pain medication is hard to get, I take my vicodins and snap them in half. I take a half when I can tell it will be one of those days and use the other half later if needed. I have found that on days when I do that, the pain is less than on days I wait until it is "bad enough". By keeping it under control, it is, well, easier to control! It is akin to taking diabetes medication on schedule vs waiting until your the glucose level is "dangerous enough".
Comment by Chaplain ET on October 13, 2011 at 9:07pm
I wonder at those individuals who say they don't "feel" pain, when I sure do! I started out with this thing called Chronic Veinous Stasis Leg Ulcers, down on my shins, where it ate the flesh almost down to the bone. I had to have these wet wraps placed on both legs, and when they came off, the pain was excrutiating! But having the leg open to the air, was also very painful. So, the doctors placed me on Vicodin, and although my legs have healed over, they are still red (like a burn), and painful, so my doctors still prescribe it, knowing that I won't abuse it. As a matter of fact, I try to stretch it out, time-wise, until I HAVE to take it. I don't know if this is because they know I'm a retired Chaplain, or if I have an honest face! Does my picture help?
 

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