Serracor-NK: Reverse the Disease Process

Supplements that can reverse the disease process

Supplements that can reverse the disease process

Serracor-NK is a supplement that you can buy on-line from www.biomediclabs.com . This blend has tremendously improved my Rheumatoid Arthritis. First I noticed not having stiffness at night. Then I noticed getting out of bed and not feeling pain when my feet hit the floor.

Disease activity is in direct correlation to inflammation. If you can decrease inflammation, then you have less disease activity which means less destruction on joints and organs. Side effects from this supplement were only beneficial. It reduces high cholesterol, improves circulatory health, induces viral cleansing and I never expected this one… hair thinning-gone! Expect to have the same amount of hair that you had as a teenager! (Of course, individual results may vary). Perhaps my hair loss was being caused from my body attacking itself. After all, Lupus causes hair loss and even though I was diagnosed with RA, I do get a lot of Lupus-like symptoms. I had thought my hair loss was simply hereditary. I’ve always had great hair but the amount of hair I’d loose in the shower still bothered me. Methotrexate caused me to loose even more but when I stopped Methotrexate I noticed that during a flare, I’d still loose more hair than normal. Now I lose almost no hair at all. It’s amazing! Serracor-NK works by removing excess Fibrin in the body. If your inflammation is not caused by excess Fibrin, then Serracor-NK probably won’t work for you.

“Recent research has shown that fibrin plays a key role in the inflammatory response and development of rheumatoid arthritis.-Wikipedia

For some people, experimenting with a supplement doesn’t sound like a good idea to them. I already felt that the medicines prescribed normally for Rheumatoid Arthritis are experimental, so trying supplements were a natural choice for me. A recent study in WebMD about Biologics shows that though they help with symptoms, they’re not the medical breakthrough doctors and patients were hoping for. Biologics like Enbrel are a very new choice of therapy. There are no guarantees. Although people feel safe taking a drug like Methotrexate because it has been around for a long time, I don’t find this any more consoling. Methotrexate is a drug that yes is widely prescribed by doctors but because it has been tested for so long, it is a fact and not a theory that taking this drug increases chances of cancer, digestive issues, Alzheimer’s and other disconcerting possibilities. It seems likely that at some point, you will suffer from some side effect. From my support group, Daily Strength, I commonly see people who have to temporarily stop taking Methotrexate because their liver enzymes were elevated. What this means is, their liver is getting damaged and they have to stop a medicine that is reducing pain, inflammation and joint damage, putting them behind with their therapy. I have been happily surprised that since starting Serracor-NK, I have not had to deal with a single flare. I feel healthy and can participate in most social events and activities without RA holding me back. Bottom Line: “The findings suggest that RA patients’ medical needs are not being totally met”WebMD

After having been on traditional medications for over a year and then switching over to Low Dose Naltrexone and Serracor-NK, I can honestly say that stiffness, inflammation and quality of life have greatly improved. I do believe that I’m getting increasingly better. This kind of feeling wasn’t happening on Methotrexate and Prednisone. I would go to the gym several times a week and find myself unable to work out as hard. I lost a considerable amount of muscle and since then have been able to improve my exercise routine. If you do decide to try Serracor-NK, make sure you don’t expect miracles right away. Just like immune suppressant drugs, these things take a while. I didn’t really feel a difference until the end of the second month and even then it was a small change. By the third month I was extremely impressed and the fourth month, I felt even better. Unfortunately, you do have to take a lot of pills. That’s the downside….and it sucks. But the alternative is even worse in my opinion. I would much rather take pills everyday, all day long than have to deal with the amount of suffering caused from taking a drug like Methotrexate. For some people, they never experience side effects. I did experience many side effects and I worried constantly about side effects from methotrexate years down the line.

At the height of my RA, I couldn’t even sit up from the couch without a helping hand. Now I can run, lift a full pot of coffee and wake up early in the morning with ease and without the worry of morning stiffness.

If you are looking to avoid the toxicity of chemotherapy drugs, the side effects of corticosteroids, and the expense and issues involved in Biologics, then you have come to the right site. There are so many options out there but coming up with a plan that tailors to your disease and your body can be difficult. Immune suppressive drugs work so well across the board because they don’t have to figure out the problem. They work by suppressing the immune system to a point that the body simply stops reacting. My theory however is that your immune system will eventually try to figure out a way to overcompensate by being suppressed. This is just my theory and I am in no way suggesting that you stop your DMARD. On the other hand, for some people who are looking to find an alternative, I think these are great solutions. What if they really do reverse the disease process? All I can say is, get back to me in 10 years and I’ll let you know. Hopefully I’ll have the answer we all hope for which is yes, you can reverse the disease process if you catch it in time.

In the beginning…….

Sarah Keturah

Sarah Keturah

When I was first diagnosed with Rheumatoid Arthritis over two years ago, I was scared out of my mind. I worried that I would die early, my body would one day be filled with replacement joints, and that my quality of life had just gone downhill 100 fold.

With that, a variety of feelings came flooding in. I didn’t ask “why me?” but I did feel anger towards other people. I felt anger that they didn’t know what I was going through, that they complained about hangnails, colds and headaches and I felt anger that lots of people had advice for me. I also felt sadness of course that the life I once lived was now difficult and painful. And it wasn’t just any kind of pain, it was the kind of pain that had me crying several times a day. It was the kind of pain that made me think that child birth might be a piece of cake. It was the kind of pain that made me wonder how many months of this I could handle, and was my life over? My daily routine now consisted of a plethora of medicines with terrible side effects, some that made me scared I would one day have cancer.

Even before I was diagnosed, I pored through the Internet in search of what was wrong with me. I felt like I was dying. Surely I must be, I thought because my body every day was loosing functions. I could no longer turn my head or brush my teeth with ease. If I fell on the floor, not only would it cause excruciating pain, but I would be at a loss of how to get back up. I remember when RA was first starting, I was in a jewelry store and I had crouched down to look at some jewelry. I lost my balance because my knees were starting to be affected and when I reached the ground, I avoided putting any pressure on my wrists because they couldn’t bend or else they felt like they had just been broken. So here I was, in a public place and in pain, wondering how in the world I was going to get back up. And this was just the beginning, I wasn’t even at my peak of the debilitating stage RA can put you in. It was a couple of months later that sitting up from the couch required a helping hand. I was young and fit and yet my body was deteriorating at an alarming pace, swelling in all of my joints and developing noticeable bumps. Even my shoulder bones were poking out. When I woke up in the morning, it felt like I had smoked packs of cigarettes. My ribs constantly hurt. Sleeping was nearly impossible. My rib pain and other joints caused all positions except for lying facing straight up, too painful to bear. I woke up with every turn and twist. I couldn’t even stand the feeling of a blanket on my toes because the weight of the blanket on those small joints was unbearable. Am I exaggerating? Not in the least!

I had begun a new job, one in the industry and I was leaving my old one. My old job could have possibly started the inflammation process. I had been cutting cardboard for 10 hours a day using an Exacto knife. Hour after hour of constant pressure had turned my fingers into swollen sausages. It may have been just a coincidence, but in my opinion, this job had something to do with the onset of my RA.

In the first weeks of my new job, luckily my hands were able to rest. Not only were my fingers swollen, but they had eczema of some sort all over and I kept them hidden. The eczema was itchy and painful. I kept my illness hidden, thinking each day was my last. When I drove in the car in the morning of L.A. traffic I feared getting in an accident. Was I even capable of turning the steering wheel? My head certainly couldn’t turn easily any more. At night when I left my car, I didn’t even bother looking back and checking my surroundings. I wouldn’t be able to run or fight back. I felt as vulnerable as a newborn baby.

At this time I didn’t even have insurance and I was going to a local clinic. The doctor, who had a difficult time communicating with me, (English wasn’t her first language) finally prescribed Prednisone when I was on my last days of even being able to brush my teeth. Thankfully, this drug turned my life around and I was able to function a little better for some time before I got insurance and started seeing a Rheumatologist.

I began to talk about my disease to those who were close to me because hiding it was stressful and difficult. It’s hard to explain when you’re 30 why you can’t do something if you look perfectly healthy.

I realized soon enough that people just didn’t get it. Even in the very beginning as I became less functional and told my husband that I was looking into support groups on-line and I thought I had either Lupus or RA, his reaction was unhelpful. He didn’t want me to join a support group if I didn’t know what I had. It was as if he could just ignore what was happening and somehow it wouldn’t exist. I’m certain there was a part of him that didn’t believe me and felt I was making this disease manifest.

Time went on and my husband began to finally realize I had a real disease and it wasn’t in my head. I think all of my family “gets” that I have Rheumatoid Arthritis. Unfortunately, unless they read about it thoroughly this disease varies from person to person, so much that even the person going through it doesn’t really know what to expect on a day to day basis.

I imagine that it’s not just Rheumatoid Arthritis that has this type of variety. I think that’s one of the most important aspects of learning about a person’s disease is, is to know that just because you read about it doesn’t mean you truly understand it. Even as part of a support group, I realize that just because I have Rheumatoid Arthritis, doesn’t mean I know what another person is going through.

If you would like to be a contributor, please send your story to: sarahketurah@gentlehugscafe.com

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