Showing posts with label crps. Show all posts
Showing posts with label crps. Show all posts

Tuesday, May 18, 2010

Air Force colonel claims lack of oversight in reserve health care

by David Ham

13NEWS / WVEC.com

Posted on May 13, 2010 at 11:41 AM
Updated Thursday, May 13 at 12:19 PM 




HAMPTON -- An Air Force reservist is pleading to Congress for help.
Col. Doug Strand injured his leg in a motorcycle accident two years ago while reporting for duty at Langley Air Force Base. Now he suffers from Reflex Sympathetic Dystrophy, a painful nerve disorder.

Saturday, February 27, 2010

Change the World

This is a very unique video, please watch it all the way through....
You will understand it better once it is completed!!




Sunday, December 20, 2009

Freedom From Pain

Freedom from pain

A 24-year-old Christiansburg woman is regaining mobility and making plans to attend graduate school after treatment put her in remission from years of pain.



CHRISTIANSBURG -- Brandy Sachs smiles more these days, even after gaining 30 pounds in one year.

For this 24-year-old, weight gain is a blessing and the least of her concerns.

In October 2008, Sachs weighed 76 pounds after she spent seven days in a ketamine-induced coma. She was the 55th patient to undergo the treatment in Germany. She emerged from the procedure with few memories and couldn't perform natural tasks, such as shivering. 

The coma was designed to reboot her nervous system, and, doctors hoped, rid her of the decade-long bouts of pain associated with reflex sympathetic dystrophy, known now as chronic regional pain syndrome. The little-known condition she was diagnosed with at age 13 caused her to cringe in pain with any touch even as slight as a flutter of her brown hair. Walking was difficult, and her right foot had turned inward and would often swell.

Today, after a year's worth of ketamine boosters, doctors say Sachs is in remission. She's been RSD-pain free for a year and won't have to return to Philadelphia for infusions of the drug for another year, unless any changes occur.

While she isn't entirely pain, or medicine, free (she is on strong painkillers as a result of a back surgery that touched nerves, but that pain is not related to the condition), Sachs said a little pain is better than her previous state.

Always cautious, she prefers to say the condition is dormant, but she's pleased with her progress.

"I have RSD, and I'm always going to have it," she said.

She walks on two crutches and has become more active. She started driving on her own, went rock-wall climbing and can make two full laps around Walmart.

Mentally, Sachs said she still feels stuck at 16. Many of her memories -- and skills -- are fuzzy. Doctors said some memories may never return.

The physical progression also has been slow, although Blacksburg therapist James O'Connell said Sachs has made great strides. She's now working on the stationary bike and the treadmill to gain strength and tone her unused legs. He's trying to get her to wear regular shoes, instead of the orthopedic shoe created for her in Germany.
Sachs goes to physical therapy twice weekly. Just last week, she took her first steps in years without bracing herself.

"I'm so proud of her," said her mother, Lisa Sachs. For years, the mother and daughter could barely hug. "It still makes you smile every time you see her stand up," she said.
Around the house, Brandy Sachs still often uses a wheelchair. That's mostly to navigate the crowds of cats, dogs and people who swarm her parents' small Christiansburg home.

"It's just easier," she said. If she bangs any part of her body too much, the RSD could flare, and the pain might return.

In August, Sachs hopes to enroll in graduate school at Virginia Tech to study sociology.
Her parents said that step will be good for their daughter, whose life was overtaken by the condition.

Sachs' story has inspired many. In July, People magazine featured part of her story.

The family said the breadth of knowledge about RSD and CRPS is growing.

"When we first started with it, they knew nothing," Lisa Sachs said.

Brandy Sachs spent seven days in a ketamine-induced coma and went through months of ketamine boosters to ease chronic pain. Her physical progression has been slow, but she is strengthening her legs by riding a stationary bike and walking on a treadmill.
Brandy Sachs spent seven days
in a ketamine-induced coma and
went through months of ketamine
boosters to ease chronic pain.
Her physical progression has been
slow, but she is strengthening her
legs by riding a stationary bike and
walking on a treadmill.
James O'Connell applies resistance to Brandy Sachs' foot during a physical therapy session as her mother, Lisa Sachs, looks on.
James O'Connell applies resistance
to Brandy Sachs' foot during a physical
therapy session as her mother,
Lisa Sachs, looks on.
Brandy Sachs, 24, takes unassisted steps Monday for the first time in years during a physical therapy session with James O'Connell in Blacksburg.
Brandy Sachs, 24, takes unassisted
steps Monday for the first time in years
during a physical therapy session with
James O'Connell in Blacksburg.

Photos by JUSTIN COOK The Roanoke Times Source 

Tuesday, December 8, 2009

Hotel Blamed for Complications of Apnea

 Hotel Blamed for Complications of Apnea 
By NICK DIVITO
December 8, 2009

LAS VEGAS (CN) - A man says he went to bed with sleep apnea and woke up with a wrist disorder, because the hotel where he was staying failed to tell him about a planned power cutoff. Andrew Gold uses a breathing machine that delivers oxygen while he sleeps.

     Gold sued the Palazzo Hotel in Clark County Court. He claims hotel officials failed to warn him when he checked in that they were planning a power outage in the early morning hours of Dec. 17, 2008.

     Gold says that when the power went off at 3 a.m., the machine stopped and he woke up. He says he stumbled through the dark room to find a light switch, but tripped and hit the palm of his right hand on a nightstand, causing him to develop Complex Regional Pain Syndrome, or Reflex Sympathetic Dystrophy.

     Gold says had he known about the planned power outage, he would not have stayed at the hotel.

     He demands at least $50,000, and says the hotel failed to warn him of the power cutoff, and failed to provide a flashlight in his room for such emergencies.

     He is represented by Ralph Rohay.

 View actual court papers HERE

Source

Tuesday, October 6, 2009

Couple ready to hit road in customized van

By Wayne Laepple
The Daily Item


Published October 05, 2009 11:19 pm 



Barbara Schaffer and her husband, Paul, arranged for Harvey, their customized van, to have enough room for trips to music festivals around the country.
Liz Rohde / The Daily Item








NORTHUMBERLAND — If you happen to see a large white van parked outside Paul and Barbara Schaffer’s King Street home, you’re looking at Harvey. Harvey is actually a Sprinter van that’s been customized to accommodate Barbara’s wheelchair.

“We named it Harvey after the big white rabbit in the movie,” Barbara said with a chuckle. “Maybe we’ll paint a pink nose and whiskers on it some day.”


Actor James Stewart starred in the 1950 movie, “Harvey,” about a man who befriends an invisible six-foot tall rabbit, or pooka.


The Schaffers never thought they’d ever be interested in a recreational vehicle or a second home, but after a visit to Arches National Park in Utah a couple of years ago, they changed their minds.


“We really wanted to sleep out under the stars,” said Barbara, “but we just couldn’t do that.”


Since 2001, the couple has enjoyed attending half a dozen music festivals every year, and they wanted to be able to join friends who camp at the events and take part in the after-hours jams they’ve only heard about.


“We started thinking about it, but no one builds any that are handicapped-accessible,” Paul said. “What we wanted just didn’t exist.”


Barbara, 60, who suffers from Reflex Sympathetic Dystrophy Syndrome, a debilitating nerve condition, has been using a battery-powered wheelchair for a number of years as her condition has changed. Paul, 63, took early retirement to care for her following her 1987 injury.


They did see a few motor homes that could have been adapted, he said, but they were all very large luxury units, so large that they would have had to tow their Dodge Caravan behind to transport Barbara from the campground to an event. Besides, those units were way outside their price range. Even an Internet search for a used vehicle came up dry, since their particular needs couldn’t be met in a used vehicle without extensive modifications.


“We decided we had to start fresh,” Barbara said.


She decided they should find the right lift unit to get her and her wheelchair into the vehicle. However, they didn’t want a unit that would occupy space inside the vehicle. She finally found a company, Creative Controls, in Madison Heights, Mich., that assured them they could mount their lift beneath whatever vehicle they chose for their motor home.


Next they found a custom builder of motor homes, Sportsmobile, in Huntingdon, Ind.


“They make custom vans, not RVs,” said Paul. “These are the people who, in 1961, modified the first Volkswagen vans into campers.”


The Schaffers found a perfect ally in Sportsmobile. The company provided an online floor plan that allowed the couple to develop a floor plan using the components the needed where they needed them. For example, instead of a right-hand front seat, a power-operated tie-down for Barbara’s wheelchair was specified.



Because Barbara cannot step over the entrance to the bathroom, they changed the layout so the commode is next to the doorway. She can sit on the commode, then lift her legs and pivot into the space. To make that change work, the hot water heater had to be downsized and relocated.


Working closely with the design team at Sportsmobile, it took nearly two months to get the interior layout completed.


“There was a lot of problem-solving by phone.” Barbara said.


They had already settled on the Sprinter, a vehicle designed by Mercedes and sold by Chrysler in this country, but it took some time to locate a 24-footer, the largest one made, and then have the necessary windows installed. The vans are shipped into the U.S. with only the windshield and door windows, so other doors and windows had to be installed after they purchased it.


The truck was purchased in Michigan and delivered to Creative Controls for installation of the wheelchair lift, then taken to Indiana for the rest of the work. The Schaffers went to the Sportsmobile plant to be present as workers installed the bathroom and kitchen modules to be certain the wheelchair would fit where it was supposed to.


“They were wonderful to work with,” Barbara said. “They wanted to be sure everything was right.”


At one point, the locking mechanism to hold her wheelchair would not work correctly, and a technician from Creative Controls came to Indiana to correct the problem. They wound up having to take the vehicle back to the plant to get it right, which held up work at Sportsmobile for a day or so.


The results, the couple agree, have exceeded their expectations.
They demonstrated the lift, which folds out from beneath the vehicle. Barbara backed her wheelchair onto it, and it hoisted her up to floor level. She backed in and turned around near the folding table where they can take meals. Then she moved forward and the electronic lock snapped into place. She pulled on her seat belt and was ready to go.


In the middle of the unit, the compact kitchen, complete with stove, refrigerator, microwave and sink, faces the lavatory, which features a sink, shower and commode. Behind them are two couches that quickly convert to beds.


“We’ve also got air-conditioning and a furnace,” Paul said, as he swung the rear doors wide to reveal a fabric screen across the doorway that will let them indeed sleep outdoors. There’s also a generator for lights, and they will be able to use it to charge the batteries on Barbara’s wheelchair.


“People told us we couldn’t do this,” she said. “We were persistent, and we found the right people to help.”


The couple drove the unit back from Indiana, and Paul said the 5-cylinder, three-liter diesel engine with a five-speed automatic transmission gave them better than 20 miles per gallon.


“A piece of you asks why you’re doing this,” he said, as he contemplated the cost of Harvey. He wouldn’t say exactly how much it cost them. “This cost more than either of the homes we’ve owned, but will let us do something together that we both enjoy.”



 Source 

Monday, June 29, 2009

Where have I been?? =)

I have received numerous emails from you, my readers and followers, asking where I am; what I'm up to; and if I am doing alright. I can't begin to tell you how very sweet that is of you, and you know who you are, and how blessed it makes me feel. I couldn't believe it once I got to each of those emails and read the words of encouragement, prayers of well being, and outreach of concern - support, and all around love that each one held. I was so moved, they brought tears of joy along with a few chuckles, and I loved them all!!

So I am going to update you all on what all I have been up to that has kept me out of pocket for so long....

As you know, at the first of the month I participated in a Sleep Study to try and get some solid answer as to why I keep uncontrollably falling. I did that on the 3rd through the 4th and on the 10th I went to hear the results, here's how that went;

I woke up at 6:30 am to start getting around and ready because my appointment was at 10:15 am and the drive over is about an hour. So I showered, fixed my hair, got dressed, and went into the kitchen with my make-up kit (it looks like a make-up artist should own this kit...hahahaa) and sat at the table with my mom, enjoyed the a/c & fan blowing in the room - but not on me, and put my make-up on. We talked, drank coffee, and ate some toast, and we both took our meds at the same time, of course her's are different than mine, but it was kind of funny that after we finished our toast we both reached for our medicines. Usually my mom goes with me to my doctor appointments, but this morning she wasn't feeling very well so she decided to stay home. So about 10 minutes to 9:00 am I left out starting my drive with all the other morning drivers, and man there was more than I thought there would have been.

I get to the doctor's office, check in and begin reading a couple of magazines. One of which was called "Fort Worth, Texas - The City's Magazine" and the cover had these huge words "Top Docs 2008". Well of course I had to check to see if any of my doctor's were listed and if this Sleep Medicine doctor was listed. Much to my delight, all of them were listed and this Sleep Medicine doctor was the number one in the area....I was feeling pretty confident about what this sleep study was going to provide. Good, bad or indifferent, the results would be pretty definite one way or the other....in my mind anyway.

Finally I was called back to speak with the doctor, yes....I took that magazine with me into his office!! I walk into his office, which is something new for me; usually it is into an exam room when you have a follow up. Anyway, I walk in his office and look around this really beautifully decorated office. There were two chairs in front of his desk so I sat in the one on the left, while I was waiting for him to come join me in his office, I continued to look through the magazine. Why is it that you always have to wait 10 minutes or more for the doctor to join you, either in the exam room or his office?? UGH!!

When he came in he sat in the chair next to me instead of behind his desk, which I thought was so odd..comforting, concerning, but still odd. hahahaha. He started by asking how I liked doing the sleep study and if I had any questions about it before we get started on the details of it all. Of course I had to tell him how much I loved the mattress..hahaha, and how nice everyone was to me and I appreciated that!! Then he asked me to go over to the computer so we could look at the graph reading from all the electrodes that were placed all over my body, and take a look at the actual video. Talk about interesting!! To see yourself sleep is really something everyone should experience!! I really don't move around much, just my head and one arm or the other is all that really moved....which I knew I didn't move very much because it hurts, but I had no idea just how still I could be. He began to tell me that during the night when I was sleeping that I did go into REM sleep multiple times, and during the day with the naps every 2 hours that I did go to sleep 3 of those times and very quickly and 2 of those times I did go into REM sleep.
Ok, so now I bet you are asking the same question that I had....What does that all mean?

Well, it means that I do have signs of Narcalepsy which goes along with the diagnosis my other doctor gave me of Cataplexy. He went on to say that the reason for my unexpected and uncontrollable falling is due to Cataplexy. I felt really good to finally have a definite answer for all that has been happening to me for the past several months. I asked if I could have a copy of the video, graphs, and his findings. Yes, I also asked if I could have the magazine of the Top Docs, to which he said yes to all. YAY!!

I walked out of there with my head in the clouds and my eyes set on DSW Shoes again....but I didn't stop this time...hahahaha. I drove back to my mother's, but first I stopped at Subway and got foot long subs for my mom, dad and myself. I was excited to let my parents know that we now have an answer for which could be controlled.
But once my Neurologist heard of his diagnosis, she totally disagreed....greattttt, just great!!!!
Which means I still have to keep my appointment with UT Southwestern Medical Center on July 31st. I sure do hope they can come up with either the same diagnosis or something that can be controlled as well!!

I stayed at my parents house through the weekend, because I had another doctor's appointment on the following Monday. I let him know of the results from the sleep study and he was pleased with himself because he was the one who had that thought in the first place. So he prescribed Imipramine and I went merrily on my way back to my parents house for the night. But I didn't leave until Wednesday because I was exhausted and didn't want to rush to make it home before doing my radio show or leave afterwards and be driving in the dark, so I hung out with my parents one more night. =)

Wednesday morning I loaded up my suitcases, yes that is plural....I had been there for a couple weeks ya know.....anyway, got all my things packed up, got the dogs things packed up and ready to be loaded up in the car. My dad and I toted everything outside and sat things beside my car, I went back in the house for the last little bit of things - my purse, cell phone, keys and to give out hugs. Only one problem....I couldn't find my keys!! We all searched everywhere for them, and I do mean everywhere, but couldn't find them. After an hour of searching and bringing everything back in the house because it was way too hot for them to be left outside for long, I searched through my purse one more time....which made it the 9th or 10th time.....and what do ya know....I found my keys in the outside pocket of my purse....someplace I never put them!!
So....my dad and I toted everything back out and in the car, I got the dogs in and straped in, gave out my hugs and kisses, and away we went, making our way back home.

Three hours later we arrived home to find all my plants in the house from the greenhouse because they weren't tended to the way they needed to be....go figure....They all looked half dead or at least headed in that direction. But I was way too tired to fuss with it right then!! So I unloaded everything out of the car and dropped it all off in the closet and quickly changed my clothes for comfort and made my way into my nice, comfy bed!! WOW did it ever feel nice to be back in my own bed again!! I raised the feet up and lowered the head, put the tv on relaxing music and closed my eyes.....I drifted off to sleep so quick!!

Ever since, I have been either sleeping.....babysitting my two grand-daughters, tending to my plants, or sitting out on the boat dock relaxing and watching the cows!!
Well, until this week that is!! This week has started off with me putting key notes and a speech (of sorts) together for my speaking engagement for the Abilene Holistic Association on Thursday evening. I am really looking forward to it and hope open the eyes of those who are blind to the effects Chronic pain, be from RSD or something else, causes on the mind, body and spirit. If any of you have something you would like for me to add to my speech, please email it to me and I will be sure to include it .... if I don't already have it!!

So, I guess that pretty much gets you up to speed with all that has been going on with me this past month....and for those of you who are on my mailing list for my Newsletter, sorry to have you read the same thing twice....that is if you read my blog also....hahahahaa.

Again, I appreciate all your emails of well wishes.....they truly made me feel so much better!! It is so nice to have you all as friends!!

~~God Bless You All~~



Monday, May 11, 2009

"If You Only Knew Syndrome" - Do You Have It Too?

If you are someone living with a chronic illness that nobody can see, you know what "If You Only Knew Syndrome" is!

When people say things like: "Wow, you are really looking good, things must be going well with you" or "So you must not be ill anymore because you are so active again, and you're looking better", that is when you just want to sarcastically say to those people: "If you only knew!" Right? Sometimes you just want to scream: "Buy a vowel already because you DON'T have a clue!"

But you hold that sort of response inside, biting your tongue so hard that you could draw blood, and smile and say something like: "Thank You! I'm doing pretty good 'today'!" or maybe: "Good thing I don't look like I am feeling inside!" and you just laugh it off. While in the back of your mind you are feeling frustrated, discouraged or you're fighting the urge to shake that person and explain how ignorant they are!!

You have felt those things, or worse, haven't you? Sure you have, all of us who are living with a chronic illness that doesn't show itself on the outside where everyone can see, goes through situations like that, it's inevitable! It's going to happen!

But....do they really mean it as a compliment with some understanding or knowledge of what you're going through?

How could you know this for sure?

You can't honestly think they are saying it to be mean or hurt your feelings can you? No, of course not!

So why is it that we take such offense to those comments?

I know, for myself - and many others, the answer to that question is because we are getting 'sick and tired' of being 'sick and tired' and we long to be "NORMAL" again.

We really don't want to park in those handicapped spaces. I mean, sure they are closer to the door and real convenient. But you feel a bit "guilty" when you get out of your car and people look at you like: "What the heck? That person can walk, there's no reason for them to be parking there" or they have an angry look on their faces as they watch you walk in the store. Ever experience one or both of those?

You also feel 'guilty' because of what you perceive to be your limitations. (e.g. cleaning, vacuuming, sweeping, mopping, making the bed, cooking, etc.) Right?

I remember life before chronic illnesses and pain, and how much I loved it. So when someone looks "down" on me because they 'assume' I don't do anything except sit around all day eating bon-bons and watching soap opera's, it would really upset me to the point of causing much undo stress and my slithering into depression over it. I use to think to myself, "Man, if this is how the rest of my life is going to be, then God....Take me now!!" And I know I'm not the only one who experiences those types of feelings, Am I?

With a chronic illness that is invisible to the eye, all you want is for people to understand how dramatically your live has been altered by what is causing your illness or pain.
You just want "Empathy" not "Sympathy"!!

How do you ever get that "empathy" that you want and need?

Unfortunately, to get the much needed support and sense of understanding from others, you first need to "accept" things as they are and begin your journey into wellness!

You are probably sitting there asking: "What does she mean by that?", aren't you?

Well, can you honestly say you have "accepted" the fact that you are in chronic pain, or you have a chronic illness that only you can see because you feeeel the affected area.
But to those who have never felt the type of pain you have, it is incredibly difficult to describe what or how you're feeling. Should you even try making them try to feel it? No, probably not. Why? Because unless they are diagnosed with the same illness, they will never come close to even imagine the things you go through on a daily basis!
So what then are you to do?

Share some of the things that have helped you "accept" things and move 'forward' in your journey and find that much needed sense of understanding and empathy!

Here are just a few of the things I have done when I sincerely didn't think there was anything that could get me to the next level of the relentless agony I was feeling each and every second of each and every minute of each and every hour of each and every day!!

1. Realized nobody could help me any better than I could, so it was completely up to me how my life would go, and I chose to Live!

2. Learned how to meditate and visualize my journey being in a much happier time and place.

3. Learned how to 'breathe' correctly so I could get the full benefit of all those deep breaths I had been taking.

4. Learned how to 'relax'! This one of the most important things you will ever do for yourself! I invite you to find a way to unwind and enjoy the beauty God provide for you each and every day!


Ok, your turn... =)


Looking forward to reading your tips that has gotten you to where you want to be....And if you aren't where you want to be, ask me, or someone, how you can!


~God Bless~
Coach Marla

Friday, March 13, 2009

Celebrating The "Women Of HOPE" - Journey # 4

~~Beckii's Journey~~


My name is Beckii and I am 15 and I live in central England and this is my story....


I have CRPS/RSD, Chronic Pain Syndrome and Irritable Bowel Syndrome (IBS).


I first fell ill in October 2006, at first we were sure that I had appendicitis, but when my temperature fell back to normal whilst in hospital and the lack of vomiting the doctors were completely confused about what it was. I was in hospital for two weeks, and it wasn't appendicitis.

One of the head consultants said it was a nasty muscle attacking virus that would last 6-8 weeks. We believed him and went away, in the follow up appointments I still wasn't any better, he then referred me to the pain management team at our local hospital (who are very good, the consultant and chronic pain nurse I'm under there are both Christians which is yay for me :D ) They diagnosed me with Chronic Pain Syndrome, (a rather nondescript title which just means that I'm in pain for a long time).

Then I plodded along for a while taking my meds and doing part time school, then Easter 2007 I got crushed in a door frame at school. This was when the CRPS occurred. It first appeared in my right arm, it was diagnosed within 2 weeks, which was amazing. ( It just so happened that the 5th time we went to accident and emergency the doctor decided to send me to the physical therapy department. The PT we saw took one look at my arm and diagnosed it. Looking at it really this was a minor miracle that everything got moving so quickly!)

Again I plodded along taking meds having physiotherapy (at this point my arm was purple nearly all the time, frozen across my body and my trigger finger twitched constantly)

Then in June 2007 I got a night cramp in my left leg. This also developed into CRPS. We took the same course of action only this time we went straight to the physiotherapist, we upped the therapy.

In august 2007 I went to my church's family camp, after much prayer I was completely healed and off of my meds within the week. But this is not where my story ends.

In September 2007 I scolded my hand whilst making a hot drink. I took Co-codamol for the pain, the A&E nurse said it was actually really bad (2nd degree covering about 1/4 of my left hand) and suggested the co-codamol.

By October this had sparked off pain and nausea in my stomach. The docs said this was the chronic pain syndrome back again (we later (august 2008) found out that it was also IBS) so we started back up on the meds, but not with opioid's as that's what caused it.

Again I plodded along until may 2008 when I got night cramp in both of my legs, the CRPS developed in my left leg again. To start with it was only my lower leg but now it's the whole thing. I use a stick to walk and I cannot walk very far most days, after about 50 yards I want to stop, after about 200 yards I need to stop and sit down to recover, if I don't it takes me hours to, after about 500 yards I'm on the verge of collapsing and it can take me days to recover.

I don't live as a normal teen girl would, I've been forced to grow up. But I've also been forced to fully rely on God - I mean even without pain walking on God's steam can't be a bad thing right?

Last weekend I went away with one of the local Christian youth groups, and I can say a good time was had by all. Though if I weren't actually counting on God to make my legs move properly and keep me smiling even through the agony I wouldn't have coped.

It sounds very odd to say this but If I could of course I would get rid of the pain, but If I were given the option of not having it at all, I would still take it. I've learn so many lessons through it the experience has been invaluable.


~~Beckii~~
Xx

Tuesday, March 10, 2009

Celebrating The "Women Of HOPE" - Journey # 3

~~Mar's Story~~

April 23, 2005

I was doing my job, my job that I loved so much. I was a nurse, and I worked on the med-surge floor at Medina Memorial Hospital. One of my CNAs asked me if I would please help her pull up a patient in bed. I said yes, that I would help her. When I did that, my left leg stayed attached to the floor. It did not move with me. As I did that, the top part of my leg (the thigh) went to the right. The bottom part of my leg (the calf) went to the left...instant pain, dropped to the floor. That night was so very busy. I got an icepack and used an ace bandage to keep it in one place. We had 30 patients and there were just two of us on the floor. No time for me to stop doing what I loved to do. When I got done with my 12 hours shift....... I thought my leg was going to fall off. I called my PCP when I got home that am, and went right over there to see him. He sent me for x-rays. Then he told me that I needed to go to an Orthopedic Surgeon.

May 9, 2005

I went to the surgeon and he said that I tore my Medial Meniscus and that I broke a huge piece of the end of my Patella.

June 22, 2005

I had Arthroscopic Surgery to fix what I had done to my knee....the recovery from this was pretty long, and a lot of physical therapy!!

December 26, 2006

The day after Christmas... .I went out to turn the outside lights on in the garage. On my way there....... .I fell on the patio. The cement patio. I tried really hard to guard my knee. That did not work out so well for me! My knee crashed on the patio. I was on the ground, in the snow...it was snowing. I had my cell phone with me THANK GOD! I called in the house, and Dylan was the only one that was here with me. He was playing with his new toys. I said to him, Dyl mommy fell and I am out on the patio and I cannot get up! He said mommy, I am playing with my new toys! hahahah I said Dyl I need you to call Gam and Pap (my parents). He called them and told them what had happened, but he forgot to tell them that I was still on the ground! My poor son, he was pacing waiting for my parents! They came and helped me in the house. I looked at my knee....it was an instant bruise a really bad one, the whole knee.

I immediately called my surgeon; He said to ice it, and that he would see me in the morning. I went, and he did an MRI...he said that it showed nothing. Well, months went by, and I kept having so many problems with walking, and the pain. I went back to him in July and said that something was really wrong in there. He then did another MRI and said that I needed to have another surgery that I had broke a HUGE piece of the Patella on the Medial side. He then said that he was going to do a surgery that was called Drilling and Coning....which meant that he was going to drill many tiny holes in my knee and hope that the cartilage would grow back.

August 1, 2006

The day that my WHOLE life changed....I woke from the surgery screaming, and crying. My knee was burning SO bad! He was the first face that I saw when I woke. He told the nurse to give me some more medication, and the nurse said that she just had given me some. He told her that he did not care, that she needed to give me some more....I was still screaming, that burning pain, that pins and needles pain....did not stop.......the recovery from this surgery was HORRIBLE! I had to do physical therapy, and I could not do it.....I could barley walk, and that burning pain...still there. After a while he said that he would do a cortisone shot. When he did that, it was soo bad, hurt so bad! The pain was intensified from that shot.

October 19, 2007

A year and two months later....... ..the surgeon finally said that he thought that there was something more going on in the knee...he sent me to about five other doctors to confirm what he was thinking that I had....they all agreed with what he was saying....He thought that I had CRPS.

He sent me to a Pain Management doctor....I was evaluated by him......at first he said that he did not think that I had it. I went back to him about two weeks later...he then told me that I had CRPS.....

After that we tried two Sympathetic nerve blocks. The first one lasted until I got out to the truck to go home. The second one lasted about one week. We have played around with my medication this whole time....nothing seems to be working out so well for me. He often talked about the SCS....I had a lot of thinking to do about that! I talked it over with my husband, and with my parents. My husband said that he thought anything at this point was worth a try. My parents said the same thing. I still was not convinced that I should do it....I did not know what to do. The flares for me were so bad, the discoloration, the burning, stabbing shooting pain, the hypersensitivity. I could not even wear pants, in the winter I was wearing shorts when I had to go out.

One night I had a horrible flare, it was the worst ever. I called my mom, and her and my dad came to my house. They were begging me to please try the SCS...there were a lot of emotions at that very minute. At that point, I decided that I had to try the SCS. I tried the trial surgery first. As soon as the SCS was turned on.....oh man, I felt relief!!! It was sooo nice! I had the trial in for four days....I did not want it to come out! I wanted to run away with it in!!

July 8, 2008

The date that my permanent SCS was put in....this surgery was different. I was awake for most of the surgery so that I could tell them when I felt it and things. Then I went to sleep while they put the battery in.
When I awoke, the pain was not so bad, but the battery site was BURNING!! They kept telling me that it would go away. Six months later they were still telling me that the burning pain would go away! I think that the SCS helped with my CRPS pain for about a month. Then things changed....and changed for the worse. I have had eight re-programming done....still with little to none difference.. ..

February 2009

At this point......the SCS is doing nothing for me. I tried to do what they call the "holiday". That is when you turn your SCS off for a week and see what happens and they say that it might reset the brain. Well, while it was off, the only things that I noticed about it not being on was that my legs and feet were very purple and red...also, I noticed that the spasms that I have in my calves were worse! The burning, stabbing shooting pain that I have always had......was no different with the SCS on or off.... The battery site......still BURNS
like crazy.

This last time that I saw
my PM he gave me some Lidoderm patches for that site. They seem to be helping some what...but the burning is still there... He also increased my Kadian (morphine) too. He said that maybe that would help through out the day. So far, I do not notice a difference at all.

Through this whole thing, I am trying to stay positive. My children.... .oh dear, I feel so bad for them. I was the active, sports mom. And now, I am not! It is hard for them to understand
why.......they ask, and I have to tell them that I cannot do something and it breaks my heart! Work........ oh, how much I miss working. I know that at this point, there is no way that I can go to work.

Depression.. .......sometimes , it is really bad. I feel sorry for myself, and I know that I can not do that. Everyone has bad days right? Well, my bad days seem to be more than that good days!

My marriage.... .I am not even sure that it can survive this. So many things have changed.... I will say, that I have met, and found some wonderful people that also have CRPS. They understand what I am going through every day!

I do have HOPE, and I will always have HOPE! It is a struggle everyday....
......but,
I will make it!!

~~Marlene~
~

Wednesday, January 28, 2009

Pain, Gates & Brain, Oh My!

As silly as this may sound, you have "Gates" in your brain. I know, I was just as surprised when I first learned about them. That's why I am so anxious to share this insightful information with you.

If you are anything like me in your suffering with Chronic Pain, you most likely 'feel' your pain more intensely during the night hours. When you are trying to go to sleep, you're trying to get completely relaxed, then all of a sudden, boom, you really start 'feeling' the pain stronger and in more areas, Yes?

The reason for that is because of the number of competing messages arriving at the "gate" is usually far less at night than it is during the day. Because of no competition many more of those pain messages get through. So what are we to do? Simple really, you have to do something that will excite the nerve center directly, something like acupressure! Acupressure is a lot like Acupuncture with the exception of the needles. Which works better for me, how about you?

The first and most difficult lesson to really grasp is that pain is natural! Don't raise your eyebrows at that statement, read on! It is the response of the body to both external (exogenous) and internal (endogenous) events, signaling us about danger or to take caution, and providing us with a survival mechanism that allows us to respond to an injury, be it a new injury or an old one.

One way to understand the mechanism of pain is to view pain as messages descending from the your brain or ascending to the extremities of your body through this massive highway of nerve fibers. Can you picture it? These nerves meet up at a "GATE" (actually a series of gates) where your spinal cord joins with your brain. Sort of like a 'bottleneck' in rush hour traffic, 'pain' messages crowd in with other messages it has gathered from your body along the journey down that massive highway. Then it sits and waits for a chance to get through, sort of like that person who sits through a green light but is more than willing to go right through the red lights. So what happens is some messages are received and others don't get through at all.

See, every experience you have in life is remembered by your brain. And that experience is attached to the emotion or feelings you had at the time of that experience. (e.g. fear, pleasure, pain, depression, loneliness, worthlessness, etc.).

So when you are confronted with a new situation, your mind attempts to make sense of it by scanning the deep recesses of every corner for similar experiences. Once it finds that experience, it also brings up the attached feelings that goes along with it.

If the attached feeling is uncomfortable or painful, your mind then looks for a way to get rid of the pain. It comes to a quick conclusion about what you should think or how you should act, then it does something really damaging for you, it 'justifies' that conclusion by pulling in evidence to support it.

Then you make a move that is based almost entirely on OLD experiences or things you had previously learned! What is so surprising is ALL of this happens in an instant, BEFORE the logical or rational part of your brain ever has a chance to "think it through".

So learning acupressure is something to be looked at as a NEW experience that can override everything, allowing you to control the opening and closing of your "gates". Wow, that possibility would allow you to be able to get into bed, lay back, get comfortable, and truly enjoy a good nights sleep. Is acupressure the answer for everybody? Probably not, but how do you know if it will work for you if you don't give it a try?

There are several options you have at your fingertips; acupressure, tapping, meditation, exercise, etc., but remember; if one doesn't work for you that doesn't mean another won't, so try and try again. I would also recommend you have someone who is familiar with your choice to help walk you through how it should be done to get the benefits to the fullest.

The secret of a better and more full-filled life is to cast out those old, dead, unhealthy thoughts. Opening those "gates" for the new, vital, nourishing, wholesome, faith based thoughts to come flying in. An intake of new thoughts will remake you and your life!



Monday, January 12, 2009

Local man dies after suffering 'devastating' disease

written by: Adam Chodak posted by: Jen Marnowski 1 day ago


THORNTON, CO. - In March of 2007, Nick Hoch broke his toe. The accident triggered a nightmare of a disease defined primarily by unrelenting pain.

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Hoch, 37, had been working for Budweiser, loading and unloading beer throughout the Denver area.

While on the job, he dropped a keg on his foot. Doctors removed two bones from one of his toes and replaced them with pins.

Hoch, a Thornton resident and father of three, should have bounced back quickly. He didn't.

"It got progressively worse," his father, Tom, said.

Tom watched as the pain not only intensified, but moved beyond his foot and into his legs.

"You touched him, he was in brutal agony," he remembered.

Hoch had what's called Complex Regional Pain Syndrome (CRPS). Doctors once referred to it as Reflex Sympathetic Dystrophy (RSD).

This is the same disease Leslie Fishbein - the Denver furniture magnate who died earlier this year - had.

"It's devastating and it can become all-consuming for patients," said pain specialist Dr. Mike McCeney. "It basically takes over their lives."

McCeney, who works in northern Colorado, said CRPS is usually the result of a relatively minor injury like a broken bone.

He said the nervous system, for some reason, goes haywire causing "pain that's actually way out of proportion to the actual injury that has occurred."

The pain can be managed, but there's no cure for CRPS.

McCeney said not many know about the disease, including those in the medical community.

"There's some doctors out there that don't know about the entity and unfortunately (some patients) don't get treatment going soon enough, which can be a problem," he said.

Hoch struggled with the pain for nearly two years. This week, Hoch went into the hospital to undergo a procedure that could have tempered the pain.

Early Wednesday morning, just hours before the scheduled surgery, Tom Hoch got a call.

"That was it," he said. "I mean 37 years old and he's gone."

Hoch still doesn't know what exactly killed his son, but he does know he'll continue to get the word out about this horrible disease.

"You wouldn't wish this on your worst enemy," he said.

(Copyright KUSA*TV, All Rights Reserved) Source

Please watch this video from the News:


Monday, January 5, 2009

Reflex Sympathetic Dystrophy Syndrome Association-RSD Coach™

I am raising funds for research and development of a possible cure to end the life shattering pain one goes through with this syndrome. If you were living with this extremely painful syndrome, wouldn't you want someone to raise funds to help you not hurt every second of every minute of every hour of every day?? Of course you would! So won't you please give to help someone else can feel better!

read more | digg story


See my FirstGiving Widget on SideBar for quick Donating or Click the Title of this Post!
Thank You & God Bless! We ALL appreciate your contribution in helping us FEEL better!!

Wednesday, December 31, 2008

Jacksonville Woman Develops RSD after Dog Bite

Posted On:
December 30, 2008 by Thomas & Lawrence




A Jacksonville woman developed reflex sympathetic dystrophy (RSD) after being attacked by a dog on her own property. The dog bit deeply in her arm, but the wound itself was not severe enough to require stitches. After being initially seen by doctors she was sent home.

Within days she developed a serious infection of the wound site. The infection was followed by the onset of severe burning pain, color changes, a cooler temperature in the arm, and abnormal hair growth on the arm. Unfortunately, all of these are classic symptoms of RSD.

RSD, previously known as Complex Regional Pain Syndrome, is a serious, usually permanent neurological condition that is usually caused by an injury to an extremity.

This situation highlights the very serious nature of dog attacks. Every year, we hear of people seriously injured or killed by pet dogs in Jacksonville. Children are the most frequent victims of dog attacks, accounting for 70% of dog attack injuries. In the United States, there are almost 600,000 dog bite wounds that require medical care each year.




Source

Friday, December 5, 2008

Are YOU Staying In Control??

Compared to most endeavors, controlling yourself is relatively simple and easy. And when you're able to control your own thoughts, words and actions, there is no limit to what you can accomplish.

To control yourself requires no other person's permission, cooperation or assistance.
To control yourself requires no special knowledge, skill or equipment.

What it does require is a compelling reason. When the reason why is meaningful enough, you will have no trouble finding the will and the means to control your own life.

That's why it is so important to have a clear sense of where you intend to go and why. Connecting with your purpose will keep you in control, and staying in control will carry you to achievement.

There is a purpose within you that is stronger than the temptations and distractions. There is a solid, meaningful reason that will compel you to carefully and effectively control all that you do.

The more fully you know and express that purpose, the more surely and reliably you'll be in control. And the more completely you exercise control over yourself, the higher your life will rise.

Wednesday, December 3, 2008

This Powerful Moment....

There is enormous power in this moment. The more fully you experience what is here right now, the more that power is available to you.

Are you angry or bitter, disappointed or resentful about what has happened in the past? Then much of the power of this moment will be out of your reach.

Are you anxious and worried about something that may or may not happen in the future? Then you will miss out on the opportunity to create real and lasting value from this powerful moment you are in.

Imagine that everything you are, everything you know, everything you care about, is focused into this very moment. And feel the enormous power of what you can, right here and now, do with it all.

Rise above the murky fog of what could have been and what someday might or might not come to pass. Focus the whole of your being on what is, and on the overflowing abundant opportunities this moment presents to you.

There is great and wonderful power in this very moment, in who you are, in where you are right now. See it, be it, and let yourself live it fully.

Saturday, November 8, 2008

Another RSD Tip of The Day!

If You Have Had, You Now Have!!

If you have the ability to complain about something, you also have the ability to take the positive action that will make it better. And taking the positive action is infinitely more effective than merely complaining!

If you have cause to get angry, you also can turn the energy of that anger in a positive direction. You can then resolve it better for all concerned.

If you have reason to be frustrated, you also have the motivation necessary to get beyond it. No frustration ever has to continue troubling you!!

If you have experienced disappointment, you also have learned valuable lessons. Look ahead, apply what you have learned, and transform your disappointment into a positive turning point.

If you have known loss and sadness, you also have gained a profound understanding of how very precious life is. Take the opportunity, for which you've paid so dearly, to raise yourself to a whole new level of meaning and fulfillment.

If you face a difficult challenge, you also have the opportunity to grow stronger, more capable, wiser, experienced, and resilient. Embrace those opportunities, for in them you will find the sweet substance of life!!

Courage is not limited to the battlefield or the Indianapolis 500 or bravely catching a thief in your house. The real tests of courage are much quieter. They are the inner tests, like remaining faithful when nobody's looking, like enduring pain when the room is empty, like standing alone when you're misunderstood.

~Charles Swindoll

Friday, November 7, 2008

RSD Tip Of The Day!

Help 'YOU' Feel Better!

When you are feeling down, focus your thoughts on this question:

"What can I do that would help me feel better?"

Instead of filling your mind with doubt, self-pity, resentment, regret, and despair, fill it with thoughts and plans for moving positively forward. There is something that will take your focus off of whatever has already happened and direct your thoughts firmly towards the best of what can be.

Pay no attention to how you are suppose to feel or how you expected to feel. Decide for yourself how good you would like to feel, and then take the steps that will get you there.

It will likely be much easier than you think. Then once you choose to feel better, it quickly begins to happen. It sounds too simple to be true, I know, but it works with surprising and delightful effectiveness. When you decide to help yourself feel better....you will!!

So, What can you do that will help you feel better? You are just moments away from making it happen!

"The very least you can do in your life is to figure out what you hope for. And the most you can do is live inside that hope. Not admire it from a distance but live right in it, under it's roof!"
~Barbara Kingsolver

Wednesday, November 5, 2008

When your pain has no name

Origins of chronic and debilitating pain remain unclear for many sufferers
ABCNews in Chicago By DAN CHILDS

-- Cynthia Toussaint was a ballerina. She was no stranger to the aches, pains and occasional injuries that came with the trade.

So when the pain from an injury to a right hamstring wouldn't subside, Toussaint, then 21, did what she could to endure it. After all, she had auditions to attend -- in particular, a promising role in the musical Fame.

When the burning, unrelenting pain was too much to bear, however, she sought a doctor's opinion.

"I was told that I wouldn't dance for eight weeks and I thought, 'No, they're wrong,'" she recalls.

But the pain would last for much longer than eight weeks. For months it persisted. A year and a half after the pain in her right leg started, she began to experience a similar pain in her left leg. Six and a half years after that, the pain had spread to both arms.

The spread of her condition was not always so gradual. One morning, she woke up to find that her left arm had bent itself into a state of permanent contracture.

"It was so shocking to wake up to find that one of my arms would not unfold anymore," she says.

Today the pain is everywhere. Toussaint describes it as a feeling as if she has "been doused with gasoline and lit on fire... burning from the inside out... It's pain like I never imagined."

The condition which ushered Toussaint into a life of chronic agony also gradually robbed her of her ability to dance, her ability to walk -- and, as it spread to her vocal cords, her ability to talk.

"Here I am 26 years later in a wheelchair," she says. "I had everything; my life was just starting. Suddenly I had this injury that never goes away."

Her voice would eventually return. But for years, Toussaint's battle with chronic pain and loss of function came spiked with the bitter reality that no matter how many doctors she saw, none could give her an accurate diagnosis of her condition.

Worse, without a solid diagnosis, she says many physicians refused to take her case seriously.

"I was told that I was crazy for 13 and a half years," Toussaint says. Once, one of her doctors told her to take a truth serum so she would admit that she was not truly in pain. Another suggested that she was fabricating her pain condition due to stage fright.

And a visit to yet another doctor was met with even greater insensitivity, she recalls.

"I said, 'What should I do?' and he said, 'Shoot yourself in the head.' He thought it was funny."

It was not until a year and a half ago that Toussaint found that she suffered from a mysterious condition known as complex regional pain syndrome (CRPS), alternatively known as reflex sympathetic dystrophy syndrome (RSD). The nature of the condition continues to baffle doctors, as does its exact cause.

But finally, her pain had a name.

"When I got my diagnosis, it couldn't have been worse," Toussaint says. "But it was the happiest day of my life. They could never say I was crazy again."

Patients Battle Pain, Stigma


Toussaint's struggle with her condition turned her into an activist against pain. She launched the nonprofit site For Grace, devoted to helping women find answers about their chronic pain. More recently, she has channeled her crusade against chronic pain conditions into the political realm, making it a centerpiece of her run for a California state congressional seat in 2006 and in other political efforts to bring more attention to these conditions.

It is a success story that stands in stark relief against the lives of those who are still searching for answers to their agony. Michael Smith, associate professor in psychiatry and behavioral sciences at Johns Hopkins University in Baltimore, says that there are a number of pain conditions for which the origins and exact causes are still unknown.

"We're supposed to be this wonderful medical system that can do anything, that can save lives," Smith says. "But we really don't know enough about pain."

"It is often difficult to come up with a diagnosis for a patient with chronic pain in particular," agrees Dr. Paul Christo, director of the Multidisciplinary Pain Fellowship at the Johns Hopkins School of Medicine. "Sometimes these types of pain do have names, but we still don't understand the exact mechanisms of the pain."

And because chronic pain is often misunderstood, many patients go without the treatment they need. This, in itself is a problem; untreated, chronic pain conditions can actually worsen, recruiting more nerves until the pain spreads throughout the body.

Dr. Doris Cope, director of the Pain Medicine Program at the University of Pittsburgh Medical Center, says that this spread is often ignored -- particularly in the absence of a proper diagnosis.

"Some doctors say, 'Oh, there's nothing wrong with you,'" she says. "Meanwhile there is pain."

Still, patients may find themselves swept into dismissing their conditions as well.

"First of all they begin to doubt it themselves," Cope says. "Secondly, they get the feeling of helplessness and hopelessness. They don't know what's happening."

Worse, for these sufferers chronic pain has not only a physical component but an emotional one as well. As the pain spreads, the same chemical signals involved in depression, anxiety and stress also come into play, commencing a symphony of physical and emotional misery for the chronic pain patient.

"For many people, their pain takes over their entire life. It affects their work life, their family life, their social life," Cope says.

It is a personal tragedy to which Toussaint can attest.

"It destroyed every relationship in my life except for my relationship with my partner, John," she says. "He stood by me, but my entire family left me behind.

"The emotional pain becomes more serious than the physical pain."

Chronic Pain, Depression Closely Linked

Little surprise, then, that chronic pain is regularly tied to depression.

"Imagine that you develop chronic pain and in time you are no longer able to work," Christo says. "That can be very disruptive and lead to a loss of self-esteem and self-worth. At the same time, it can change the nature of your relationship with your family and friends.

"If the patient has lost their sense of self-worth and become depressed, that in turn can lead to social isolation."

Smith agrees. "[Patients] get the feeling that they really can't control the pain; they feel helpless about it... In some cases these patients can go to full-blown clinical depression."

The roots of this depression even appear to transcend emotions alone. On Monday, scientists revealed additional biological clues as to why pain and depression may be so closely linked. A team of researchers led by Irina Strigo of the University of California San Diego compared brain scans of people with depression to those of 15 people who were not depressed while these subjects anticipated or experienced a painful sensation.

What the researchers found was that those with depression showed a higher level of activity in the areas of their brain that processed emotions. Moreover, the regions of the brain that are normally involved in mitigating pain were less active in the depressed subjects -- a hint that chronic pain may have a propensity to feedback on itself.

Toussaint says the depression that accompanied her chronic pain was nearly too much for her to bear.

"I suffered very, very extreme depression," she says. "All of us with pain do. We're being tortured 24/7, we're not believed, and our lives are upside-down.

"I had a plan of suicide -- not because of the physical pain but because everyone I knew had abandoned me."

Fighting the Pain

Fortunately, pain experts say, the majority of those battling mysterious chronic pain can find answers if they search long enough.

"Most pain does have a label," Cope says. "If you can find some general idea of what's causing your pain, you can tailor treatment toward that."

"A lot of people don't realize that there are treatments available," Christo says. "We do have some pretty reasonable treatments for people that can help control the pain and increase quality of life."

As for the best way to access these resources, Christo says pain sufferers can start with a simple Internet search, using their symptoms as search terms.

"What will usually come up is a description of the condition, and sometimes a directory of self-help groups," he says, adding that some support Web sites even have suggestions for doctor referrals.

For those who have found themselves being pinballed from one doctor to the next, finding a multidisciplinary pain management center may be the best step. Here, patients can afford themselves an entire spectrum of care services -- from pain physicians and physical therapists, to psychiatrists trained in helping those with chronic pain come to deal with their conditions.

"Medication, injections, physical therapy and pain psychology all can come together to significantly improve quality of life," Christo says.

For Toussaint, the medicine that worked best was the anti-seizure drug Neurontin. Today, this medication, combined with a physical therapy regimen that incorporates Eastern and Western healing techniques, allows her to control the pain brought about by her condition.

As is the case with some who face chronic pain, Toussaint may live with her condition for the rest of her life. But she says that those who face a similar struggle must take heart that an answer exists for their mysterious pain.

"Know that you're not alone," she says. "Know that you're pain is real. And know that you deserve the dignity of proper diagnosis and treatment."

To visit the For Grace website, click here.

(Copyright ©2008 ABC News Internet Ventures.)
11-05-08 Chicago News abc7chicago.com

Thursday, August 14, 2008

Immunosyn Corporation Files 10-Q

Last update: 11:23 a.m. EDT Aug. 14, 2008
LA JOLLA, Calif., Aug 14, 2008 (BUSINESS WIRE) -- Immunosyn Corporation (IMYN:
immunosyn corp com

Sponsored by:
IMYN 1.70, -0.10, -5.6%) , a biotechnology firm that has obtained exclusive worldwide marketing, sales and distribution rights to the biopharmaceutical SF-1019 from its affiliate Argyll Biotechnologies, LLC, has announced its results for the quarter ending June 30, 2008.

For the quarter ended June 30, 2008, the company incurred $629,884.00 in general and administrative expenses and $15,297.00 in interest expense which was funded from advances by affiliates of $26,527.00, accounts payable of $60,376.00, accrued expenses of ($1,498.00) and services rendered for stock of $529,250. As a result, the company had a Net Loss of $645,181.00 for the second quarter of 2008. During the same period in 2007, the company incurred $71,025.00 in general and administrative expenses, interest expense of $4,810.00 and had a Net Loss of $75,835.00. Immunosyn has had no revenue to date as Argyll Biotechnologies, LLC is still in the process of obtaining governmental and regulatory approval for SF-1019.

"We have continued to significantly control costs this quarter and appreciated the advances from affiliates," noted Stephen Ferrone, Immunosyn's CEO. "In 2008, Argyll Biotechnologies, LLC has reported positive research results for SF-1019 and Immunosyn hopes to add shareholder value by striving for financial efficiency in the execution of its marketing and distribution strategy when approvals for SF-1019 are obtained by Argyll Biotechnologies, LLC," added Ferrone.

Research suggests that SF-1019 has analgesic properties with a perceived ability to substantially reduce the inflammation present in a number of clinical conditions including Multiple Sclerosis (MS), Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), Reflex Sympathetic Dystrophy Syndrome, (RSD or RSDS) and other auto-immune and neurological disorders. A limited proof of concept trial for SF-1019 in Europe has shown positive results in effectively treating diabetic ulcers. Immunosyn went public in January 2007 and its stock began trading on October 26, 2007 on the OTCBB under the symbol "IMYN."

Sponsored by:
IMYN 1.70, -0.10, -5.6%) plans to market and distribute life enhancing therapeutics. Currently, the company has exclusive worldwide rights from its largest shareholder, Argyll Biotechnologies, LLC, to market, sell and distribute SF-1019, a compound that was developed from extensive research into Biological Response Modifiers (BRMs). Argyll Biotechnologies, LLC has initiated the process for regulatory approval of SF-1019 in several countries and preparations for clinical trials are underway in both the US and Europe. Research suggests that SF-1019 has the potential to affect a number of clinical conditions including complications from Diabetic Mellitus such as Diabetic Neuropathy (DN) and diabetic ulcers (DU), auto-immune disorders such as Multiple Sclerosis (MS) and neurological disorders such as Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) and Reflex Sympathetic Dystrophy Syndrome (RSD or RSDS).

The above news release contains forward-looking statements. These statements are based on assumptions that management believes are reasonable based on currently available information, and include statements regarding the intent, belief or current expectations of the Company and its management. Prospective investors are cautioned that any such forward-looking statements are not guarantees of future performance, and are subject to a wide range of business risks, external factors and uncertainties. Actual results may differ materially from those indicated by such forward-looking statements.

For additional information, please consult the Company's most recent public filings and Annual Report on Form 10-KSB for its most recent fiscal year. The Company assumes no obligation to update the information contained in this press release, whether as a result of new information, future events or otherwise.
SOURCE: Immunosyn Corporation

The Blaine Group
Lisa Baker/Devon Blaine
310-360-1499
310-360-1498 (FAX)
blaine@blainegroupinc.com