#lupus blogger

[getyoungersblog]

Dr. Gary M. Levin - Natural Lupus Treatment System: A Holistic Approach to Lupus Management

The Natural Lupus Treatment System, developed by Dr. Gary Levin, is a comprehensive package designed to provide a natural and holistic approach to managing lupus and other autoimmune diseases. Lupus is a chronic condition that can affect various parts of the body, and while its cause remains unknown, it is believed to be an autoimmune disorder.

See More about "Natural Lupus Treatment System" Here!

Program Components

The Natural Lupus Treatment System comprises the following components:

Step-by-Step Guide: A comprehensive guide that outlines lifestyle changes to live with lupus without symptoms or pain. It covers healthy food choices, identifies trigger foods, and provides guidance on correct exercise.

Supplement Guide: A detailed supplement guide featuring essential nutrients needed for treating lupus naturally.

Exercise Guide: A guide that assists in regaining fitness safely and swiftly.

E-Book: An informative e-book providing in-depth information about lupus, its causes, and natural treatments.

Audio Course: An audio course offering additional insights into lupus and tips for symptom management.

Bonus Guide: Additional information on preventing the onset of lupus and other autoimmune diseases.

Click Here to Download PDF "Natural Lupus Treatment System" eBook by Dr. Gary M. Levin!

Key Elements Covered

The Natural Lupus Treatment System addresses the following aspects:

Dietary Changes: Guidance on making healthy food choices and identifying foods that may trigger lupus flare-ups.

Supplementation: Information on essential nutrients to support lupus treatment.

Exercise Regimen: A structured exercise program to enhance overall fitness.

Understanding Lupus: In-depth knowledge about the disease, its causes, and natural treatment options.

Benefits of the Natural Lupus Treatment System

Ease of Understanding: The program is designed to be easily understood, even by beginners, with the author explaining concepts in simple terms.

Affordability: Practical advice that doesn't incur significant costs, making it accessible to a wide audience.

Herbal Remedies: Inclusion of cost-effective herbal remedies known for their effectiveness in treating lupus naturally.

Comprehensive Information: The program provides detailed insights into lupus, empowering individuals to understand the disease's causes and treatment options.

Reduced Inflammation: Strategies to reduce inflammation in the body, alleviating painful symptoms associated with lupus.

Working Mechanism

The Natural Lupus Treatment System employs a combination of dietary changes, supplementation, and lifestyle modifications to address underlying factors contributing to lupus. This includes addressing inflammation, oxidative stress, and leaky gut syndrome, aiming to treat the root causes of the condition.

Effectiveness

The program has been reported as effective in managing lupus symptoms, providing relief from pain and inflammation. Users have praised its ability to address lupus comprehensively, going beyond symptom management to tackle underlying issues.

Who Can Benefit

The Natural Lupus Treatment System is suitable for individuals diagnosed with lupus, those suspecting lupus, family members of lupus patients, and individuals working with lupus patients. The program is designed to cater to a broad audience, offering valuable insights and guidance.

Accessing the Program

Access to the Natural Lupus Treatment System is exclusively through the official website. The program is not available in physical stores or on external online platforms. Interested individuals can initiate a free trial through the official website.

Conclusion

The Natural Lupus Treatment System by Dr. Gary Levin emerges as a viable option for those seeking a natural and holistic approach to managing lupus. With its emphasis on education, dietary changes, and overall well-being, the program aims to empower individuals to proactively address lupus symptoms and improve their quality of life. Positive reviews and a money-back guarantee further support its credibility as a potential resource for those dealing with lupus.

Click Here to Download eBook "Natural Lupus Treatment System" PDF by Dr. Gary M. Levin!

[windysjourney]

Unraveling The Mysteries of Autoimmune Diseases

In the intricate tapestry of the human body, the immune system stands as a vigilant guardian, defending against invading pathogens and maintaining overall health. However, in some cases, this defender turns against its own host, giving rise to a category

In the intricate tapestry of the human body, the immune system stands as a vigilant guardian, defending against invading pathogens and maintaining overall health. However, in some cases, this defender turns against its own host, giving rise to a category of diseases known as autoimmune diseases. This blog post aims to unravel the complexities of autoimmune diseases, exploring their causes,…

[the-four-humors]

Also, like, being able to explain the metaphor (or demonstrate with something on hand, like... idk, pens) can often help people better understand, like... energy levels in general. I forced my family to read the original blog post and it helped get them to respect my boundaries wrt activities.

It's... not a big task to explain a metaphor.

i dont think spoons is a very good metaphor and i genuinely dont understand why it caught on

[whatthefibromyalgia]

Dear Followers

I have been thinking about starting a side blog to do most of my actual journaling on. Today I decided I would rather keep it all here. Why start a side blog or keep it all split? It is all part of me and who I am. As an OG tumblr users I want to stay the way I have always been. Transparent and open here. I am not just a kink blogger or adult blogger. I am a human with very real thoughts and feelings outside of the kink catagory. Why not just be me here and now and in the moment?

I have currently been struggling mentally and emotionally with my health and all that comes with it. It still angers me to feel like a year and half ago I really felt like I had found that place in life where everything is calm and you just sit back and marvel at how far you have come and then suddenly without warning you walk out your front door and your entire would changes. Yes, angry is a familiar feeling as of late.

June 30th 2022 I had emergency surgery to have my cervical spine fused and bone grafts placed. This is due to me having a very narrow spinal canal and my spinal fluid and blood flow to my brain was cut off. At this time I also learned that I have Rheumatoid arthritis, Osteoarthritis along with Degenerative disc disease, SLE Lupus, Sjogrens Syndrom. there are a list of other things that go along with all this but I will spare you the long version. I went from being the rock of the family who never stops to being told not to even lift things. All of this will progress and blah blah...Because of it all I am feeling alone and lonely. There are days I feel like I am watching everyone I love live life and I am counting down the days or wondering how many decent days I will have left in me. I no longer know where I fit in the kink world. I still feel submissive but also most days I am so angry I don't feel like I belong anywhere anymore.. Nothing at all seems fair.. Eccentric Submissive

[gohnnyjuitar]

Can I get a #3, a #9, a #14 and a #20 of the Oc ask for a Romulus and Colbat combo? Ich tausche mit Ihnen im Voraus Kekse.

my partner is learning german and they were thrilled to be able to translate this for me dfjkhgd

Cobalt would love to share a cookie (Romulus is like a feral kitten and has to be coaxed out of the gutter however)

3. How would they describe love?

answered here for Romulus! :)

As for Cobalt, love is difficult for him to describe. It's confusing. It's something that comes naturally to him but it's scary. How can something feel so freeing and exciting but also so demanding and claustrophobic? He sees his younger brother with his wife and his family and he knows that's what love is supposed to be. He almost had that with his childhood best friend once they had grown up a little, but where Mercedes wanted to settle down, Cobalt wanted the freedom to roam. He was too young and there was still so much to see, he explained. He loved her dearly but he loved the idea of the world, too.

9. Do they think they’d make a good parent, regardless of whether they want kids or not?

Romulus fears becoming his father. What if having a kid flips a switch and turns him cruel and distant, just like Lupus? It was the only example he ever had so what if he gets it wrong? So, no, Romulus thinks he would make a poor excuse for a parent.

Cobalt thinks kids are great; they're funny, they're creative, they're brutally honest in the most innocent way. He absolutely adores his nieces and nephew and loves being the cool uncle. However, he can't see himself having kids; it's a responsibility he doesn't want to have. He does think that, maybe, he'd make a cool dad, but he'll never find out and he's okay with that.

14. What smells or tastes do you associate with them?

Romulus gets the obligatory leather and motor oil smell 90% of my ocs have, since he actually works on and maintains a motorcycle. Under all that, the sagebrush that thrives in the Mojave.

For Cobalt, it's fresh pine mountain air and the slight smell of smoke that lingers for the briefest of moments after firing his bow. Also, potentially, burnt hair whenever Dyna's explosive arrows don't work like they should.

20. Would they make vines if they could?

Despite probably having great e-boy potential, Romulus wouldn't really care to make them.

Cobalt, however, is a massive social butterfly and would eat that shit up. In modern aus he's a travel blogger and loves the attention social media gets him. He would love to make stupid little vines.

ask meme :)

[anumberofhobbies]

Recently after a crash I kept thinking how I hoped I could get back to where I was before the crash. My mind kept going over and over my current, more limited state and everything I was able to do before that I could not do now. "Would I get those things back?”, I kept thinking. I’m sure you have all felt this and gone through this after a crash. It’s really scary because you don’t know what will happen. But as I reflected on that thought process I realized that ME/CFS/Long Covid is not a series of steady states that suddenly switch from one to another. We aren’t in a steady "crash state" and then a steady "baseline state" and back and forth. I can’t hope to just revert back to where I was. In fact, where I was before the crash was not consistent, every day, even every hour was different. So what I was hoping to return to was pretty elusive. We can’t expect our bodies to act like machines that go from one program to another.

And, we now bring you some related content just posted by a disability blogger here on Tumblr,

What is a Dynamic Disability? A dynamic disability might not be a term you hear often, but it perfectly captures the essence of living with a condition that fluctuates often. Unlike static disabilities, which have a consistent impact, dynamic disabilities ebb and flow, bringing periods of stability and times of significant struggle. For example, multiple sclerosis can cause symptoms that range from mild fatigue to severe mobility issues. Lupus might have flare-ups causing joint pain, skin rashes, and fatigue that can disappear and reappear without warning. Chronic pain conditions can mean some days are manageable, while others are overwhelming. The Unpredictable Struggles We Face Living with a dynamic disability means facing a unique set of challenges that can be tricky for others to understand. The unpredictability of our conditions makes planning a real challenge. We might feel fine when we make plans, but our symptoms might have other ideas when the day arrives. This unpredictability can also affect our work life, making it difficult to maintain a steady job when our abilities change day to day. There’s also the challenge of misunderstanding. People might see us on a good day and not understand why we can’t do the same things on a bad day. They might think we’re exaggerating or being inconsistent, but the reality is that our conditions are the ones being inconsistent. This misunderstanding can lead to feelings of isolation and frustration. Educating those around us about the nature of dynamic disabilities can help bridge this gap, but it’s an ongoing process.

[monkeywiki]

my fellow lupus symptomatic bloggers. unite

[treadmilltreats]

The connection between mind and body

I have often talked about how stress and fear affect your health. How when you're stressed your body reacts to it and you become sick over what you are afraid of or are stressing over. There is research out there about this. This is not just something I pulled out of the sky, this is real.

It also says how your attitude can affect your sickness if you have no hope if you believe you will never get well if you say over and over that you're sick then what you put out will come back to you.

I remember when I was with my ex. I ate right, I exercised every day, and I should have been healthy yet I felt sick every day. I had headaches, my body ached, and I caught every cold and bug known to man. I got vertigo, and I always felt like crap, why? Because I was so unhappy, so stressed, so miserable that it manifested into sickness. Since I have been divorced I have been sick twice and both times were when I let stress control my feelings. How is that for a correlation between mind and body?

I have some dear friends. They all have terrible diseases that they battle each day.

MS, Crons, Schermdoma, Heart issues, back problems, Lupus, and some have it all rolled into one, yet every day when I talk to them, they are grateful to be here. They are positive and happy, they have an incredible outlook on life. They never talk about how bad it is for them, only how great life is, even though I know how much pain they are in. I can't imagine how bad the medicine they must take every day is, the doctor visits and tests they must endure, yet the world would never know as they never focus on that just the positive.

These strong and brave women know the connection between having a positive attitude and their diseases even though they know these diseases will never go away. They have chosen to focus all their energy on healing themselves and being a role model. They lived their lives being grateful, living and loving every morning they are given.

These strong, beautiful women teach me to never take my health for granted. To live in the moment and that they are not their illness, they are positive women who just happen to have one.

So today my friends realize that what you put out there affects your life, your body, and your soul, that even if you have a disease it doesn't have you, how you feel every day is up to you. You choose how you feel, look at my friends who are the most positive women I know and look up to, and know you too can do anything.

"Be the change you want to see"

@TreadmillTreats

"Be the change you want to see"

@Treadmilltreats

"And just when the caterpillar thought his life over...he turned into a beautiful butterfly"

**Now released my latest book**

The Blessing in Disguise.... revealed

https://www.amazon.com/Blessing-Disguise-Revealed-story-faith/dp/1074340493/ref=sr_1_19?keywords=the+blessing+in+disguise&qid=1561392004&s=books&sr=1-19

***Now available***

My 1st book The blessing in Disguise

Selling on my website:

Http://www.treadmilltreats.com

And on Amazon.com

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[stickthelanding]

I'm excited to announce that I have a new blog on blogger. It's called Stick the landing. It will be about my life with chronic illness. I have been diagnosed with APS and systemic lupus.

https://www.anotherillness.blogspot.com

[rogha]

well there was a blogger called christine miserandino who recounted in ‘how to i explain to my friend who has asked me what it’s like to have lupus. I need some kind of spendable token representation as a visual aid to represent how limited my capacity is compared to her’s. there’s a bunch of spoons in this college dining hall(?) so I’ll use those.’ in a personal essay on her blog and it caught on from there. I don’t think she thought it would catch on.

the crazy thing about spoon theory is they could have chosen anything at all in the world for their little metaphor and they still went with the one that sounds stupid as fuck

[desroundtree]

The Perfection of Time

Sometimes I guess I really don't know where to begin. This is one of those times. I jumped back in with my first post yesterday and it felt good to write. To let it out for me but also to let you know it’s ok if you have those same kinds of feelings. All of your shit is valid - good and bad.

So much has happened and not happened it feels ridiculous to rehash it all, or to put myself through the emotions that come with that. I will be concise when I say a lot of things have changed in my life. Some of those changes have shocked me and shaken me. Others have grounded me and showed me who, and what, I really am. Most have showed the world that I am not to be fucked with. It is clear that my peace has become my priority. And my silence can become deafening.

I have opinions and addressing them has always been easy for me. This is my space, and in my space I am free to move as I wish. I am working to make myself feel like a lot more of the world is my space - learning to take it up  and not be apologetic for it - and to demand what I need, when I need it. This hasn't been easy. It is still very much a work in progress. With Covid and my illness, the very idea of taking up physical space scares me to death. But there have been, and will be, more steps toward demanding freedom others around me don't seem to want to share. It's odd to feel like the world has become a place where your existence is not only dismissed, but completely ignored. Then to realize that that feeling and those behaviors are closer to home than you think. 

Gaslighting can come from anyone, and I have learned that even those that should be sympathetic, lose that touch when they’re inconvenienced.

Life was hard in the moments when I lacked concentration, when I couldn't figure things out, when words made no sense in a sphere where they once did. I was scared. I am scared. But I realized that’s something that’s not going to go away but I can learn not to operate from that place.

I am an outspoken supporter of therapy, and mental health treatment - whatever that may be or look like to you. In the time that I’ve been gone, I struggled through medicine after medicine, and spoke to therapist after therapist. I stopped sleeping enough to even constitute what any person would really call rest. My Lupus flared because the stress, sadness and overall nothingness of it made it impossible to stay healthy. I was in a constant state of irritability and it went from bad to worse, with no good to be found on the scale. I struggled with what I felt like was the selfishness of it all. I struggled to feel loved when it is obvious I am.

I can’t imagine what the world would be like if I wasn’t.

But still it was hard. It is hard. Every fucking day. 

It has been a really rough go. 

But in this time I have also made plans, secured ways, made moves. Silently. The way most moves should be made. Not in this day and age it seems. I have plotted. I have been angry enough to push. I have taken care of everything and everyone, so much so that I have forgotten to take care of myself. I have checked my ego at the door, and have really tried to learn and understand the way I work and what I require to exist within my space. 

Yes, require. 

My energy is important to me, too important almost, and I share it reluctantly at best. I have learned because time is a teacher. People say it heals but sometimes I’m not sure. I think it teaches you that there are some things that you might not heal from. And that’s ok too. 

I will leave you with this, we aren’t meant to be perfect. Even if perfection is what we are taught to strive for. Perfect is what you make it. It’s whatever lights you up. Time taught me that we end up working so hard toward something so unattainable that we forget that right now is as perfect as it’s going to be. 

[windysjourney]

Unraveling The Mysteries of Autoimmune Diseases

In the intricate tapestry of the human body, the immune system stands as a vigilant guardian, defending against invading pathogens and maintaining overall health. However, in some cases, this defender turns against its own host, giving rise to a category

In the intricate tapestry of the human body, the immune system stands as a vigilant guardian, defending against invading pathogens and maintaining overall health. However, in some cases, this defender turns against its own host, giving rise to a category of diseases known as autoimmune diseases. This blog post aims to unravel the complexities of autoimmune diseases, exploring their causes,…

[femology]

[wolfsheart-blog]

Wolf 🐺 by C. R. Sams

[lilaclupie]

About Myself...

Hello, thanks for visiting :3

I'm a 27 year old Sagittarius from New York, and I have Systemic Lupus Erythematosus (SLE) or Lupus for short. I was diagnosed last year, and since then I've been learning how to cope and live with this disease. I keep finding myself wanting to write about my journey, whether to vent or to just help myself work through the hardships. So here I am! I'm an open book so feel free to message or ask me anything, even if just to vent or say hello.

~A little about Lupus~

Lupus is an autoimmune disease where your immune system is overactive and attacks your own body. It can be wildly different for each individual. For me the main symptoms are extreme fatigue, joint pain, skin sensitivity and brain fog. Thankfully it hasn't affected my organs as of yet. If you'd like to know more, feel free to ask me anything or just visit lupus.org 💟

[mylupusdiary]

So , there are so many chronic illness patients suffering from anemia and iron deficiency, some are under treatment and some don't even know they have deficiency of any sort ... This vlog will guide you through... Iron deficiency! Watch, like 👍, subscribe and share it if you find it worth! https://youtu.be/kVv143hXJ1c #immunitynme #indianblogger #GastroparesisWarrior #youtubechannelsubscribe #instagood #celiacsucks #irondeficiency #anemia #celiacwarrior #lupuswarrior #lupus #glutenfreediet #covid_19 #lifeofapatient #livinglifeontheedge #lupie #systematiclupus #immunitynme #influencer #blogger #vlogger #mylupusdiary #youtuber #YouTubechannel https://www.instagram.com/p/CRqosEKlXSj/?utm_medium=tumblr