#multiple sclerosis symptoms

[getyoungersblog]

Discover a Life Without MS: The Power of Natural Healing

Multiple Sclerosis (MS) is a challenging and often debilitating autoimmune disease that affects the central nervous system, leading to a wide range of physical and cognitive symptoms. Conventional treatment options often focus on managing symptoms through medication, which can sometimes lead to side effects. As a result, many people are turning to alternative and natural methods to help manage their condition. The "Natural Multiple Sclerosis Treatment System" is one such approach that has gained attention for its holistic and natural methods of addressing MS. This review will explore what this system entails, how it works, and its potential benefits for those living with MS.

See More about "Natural Multiple Sclerosis Treatment System" Here!

What is the "Natural Multiple Sclerosis Treatment System"?

The "Natural Multiple Sclerosis Treatment System” is a comprehensive program designed to help individuals manage and potentially reverse the symptoms of Multiple Sclerosis (MS) using natural methods. This system focuses on a holistic approach, which includes dietary changes, lifestyle adjustments, and natural supplements to address the root causes of MS. Unlike conventional treatments that often rely on medications with side effects, this program emphasizes natural ways to boost the immune system, reduce inflammation, and enhance overall health, aiming to improve the quality of life for those living with MS.

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

About the Author

Dr. Gary M. Levin, a well-known health expert and advocate for natural treatments, authors the program. Gary has extensive experience in researching and developing alternative health solutions, especially for chronic illnesses. His work is grounded in a thorough understanding of natural medicine and holistic health principles. With a deep passion for helping individuals regain control of their health, Gary has dedicated years to studying MS and developing this comprehensive treatment system.

How does it Work?

The "Natural Multiple Sclerosis Treatment System" works by targeting the underlying causes of MS rather than just alleviating its symptoms. The program involves several key components:

Dietary Changes: It emphasizes eliminating processed foods, sugars, and potential allergens while incorporating nutrient-dense, anti-inflammatory foods that support immune function.

Detoxification: The system includes natural Detox methods to help eliminate toxins from the body, which can contribute to MS symptoms.

Natural Supplements: It recommends specific vitamins, minerals, and herbs known to boost neurological health and immune system function.

Lifestyle Adjustments: Suggestions include stress management techniques, adequate sleep, and regular physical activity, all of which play a crucial role in managing MS.

Mind-Body Techniques: The program also highlights the importance of a positive mindset and practices such as meditation to reduce stress and improve mental well-being.

Benefits of the "Natural Multiple Sclerosis Treatment System"

Holistic Approach: It addresses the whole body and mind, rather than just focusing on symptom relief.

Natural and Safe: Relies on natural ingredients and methods, minimizing the risk of side effects.

Improved Quality of Life: Aims to reduce fatigue, pain, and other debilitating symptoms associated with MS.

Empowerment: Provides users with the knowledge and tools to take control of their health.

Potential for Symptom Reversal: By targeting root causes, there is a possibility for long-term relief and improvement in overall health.

Pros

Natural Treatment: Focuses on natural remedies, which are generally safer and without adverse side effects compared to pharmaceutical options.

Comprehensive Program: Covers diet, Detox, supplementation, and lifestyle changes for a complete approach to managing MS.

Educational: Provides in-depth knowledge about MS, its causes, and ways to manage it effectively.

Customizable: The program can be adapted to fit individual needs and preferences.

Cons

Only available on official website

Conclusion

The "Natural Multiple Sclerosis Treatment System" offers a promising alternative for individuals seeking natural ways to manage their MS symptoms and improve their overall health. Authored by Dr. Gary M. Levin, a respected figure in natural health, this program emphasizes a holistic approach that includes diet, detoxification, supplements, and lifestyle changes. While it requires commitment and is not a guaranteed cure, its focus on addressing the root causes of MS rather than merely masking symptoms makes it an appealing option for those looking to take a proactive role in their health. For anyone open to exploring natural and comprehensive methods of managing MS, this program could be a valuable resource.

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

[ayushprana0]

Recognizing Multiple Sclerosis symptoms is the first step towards effective management. Ayush Prana, the world's only Ayurvedic MS specialty clinic, has expertly treated over 2000 MS patients globally. Our approach combines accurate diagnosis with scientifically proven Ayurvedic therapies. Learn about MS symptoms and our unique treatments at https://ayushprana.in/.

[alisamart]

Everything you need to know about multiple sclerosis

Multiple sclerosis (MS) is a  nerve disease that can affect the brain and spinal cord and also affects the central nervous system (CNS).In Multiple sclerosis, By mistake the immune system attacks the protective covering of nerve fibers called myelin. Myelin helps simplify the smooth and speedy transmission of nerve signals. When it becomes damaged or destroyed, communication between the brain and…

[missionwalk]

Multiple sclerosis is a chronic autoimmune disorder that affects the central nervous system, including the brain, spinal cord, and optic nerves. Symptoms of MS can vary widely and may include muscle weakness, difficulty with coordination and balance, problems with vision, and cognitive impairment. Treatment for MS, including occupational therapy, physical therapy, and speech therapy, can help individuals with MS manage their symptoms and improve their quality of life.

[jackalope78]

I would like more words for tired. Cause I'm not tired, sleep wouldn't make me feel better and I'm not sure I COULD sleep. Weary has a spiritual connotation that doesn't quite work. Exhausted is too much (and implies the solution is sleep, which as we've discussed isn't it). I'm just... tired. Low energy. Can't do anything but sit on the couch and pet my cat, because everything else takes up energy I just don't have. But it's not tired in the way most people think. So I need a new word.

[skirtsncornbread]

I'm 90% sure I'm going to be diagnosed with MS by the specialist I was referred to and I'm just supposed to be chilling in the meantime like

[snufsnifs]

i knew i was getting sick before i actually showed any symptoma bc my pinky & ring finger started tingling

dem MS spidey senses ey. not much good tbh but they try

[queerlyloud]

Yall, medical trauma is wild as hell. My PCP asked me the basic MS diagnostic questions at our appointment on Thursday after I told her about the pain in my spine that woke me up out of a sleep induced by tizanidine AND meclizine. Like I should have been dead to the world for 8-10 hours, but the pain was so bad it woke me from that heavy a sleep and was so intense that I was in too much shock to move for more than 2 minutes after I woke up. Literally paralyzed by the pain.

Anyway, I told her about that and about how even though I told the neurologist I was referred to that, he only had an MRI done on my head, neck, and upper vertebrae , with absolutely none done of my middle or lower spine, despite those being my primary pain centers. So my PCP immediately booked me for x-rays of my spine so that a full spine MRI would be approved by my shitty work insurance.

I have every single symptom of PPMS, all I need is for an MRI to catch lesions on my spine so they can do the tap and identify the inflammation in my spine that shows up in every single blood work I've had done in the past 5 years.

I might finally get my diagnosis.

But instead of being excited and happy, my brain is instead choosing to have me pre-experience the depression I will feel if they don't spot any lesions on the MRI.

Fml 🙃

[royalwhumpness]

Multiple Sclerosis update:

Just got my MRI yesterday (on a Sunday).

Question for the MSers - How long after your MRI did your neurologist contact you?

I have an appt scheduled with him in September 😫. I’m hoping that if it’s serious he’ll call me sooner. I know something is wrong with me but I’m so scared that the MRI will be inconclusive or that the neuro will be nonchalant, even though he’s an MS specialist.

My symptoms I’ll post below the “read more”.

Black spot in center of vision in my left eye that I thought for sure was a floater. I had honestly forgotten about it because I didn’t think it was serious - annoying… but not serious. My partner asked me just the other day if it was still there and I noticed that no, it wasn’t.

Severe double vision, almost quad vision suddenly one morning with severe dizziness and vertigo. Double vision is now intermittent whenever I am dizzy.

Severe vertigo comes and goes. Sometimes I can’t look up or down or else I’ll fall.

Dizziness is very common, I feel like I’m drunk.

Just had my first random Charlie horse pain in my left leg.

I learned at the neurologist that the left half of my body is much more numb than my right side. I was so shocked. He touched my face and I could barely feel my left side.

Tingling in limbs and hands and feet

Muscle spasms, tightness and weakness. Sometimes it makes me walk weird (need a cane and even a wheelchair at times), and sometimes I fall.

Frequent urination

The week of the attack I had severe constipation. I’m talking almost a full week = no doodoo

Excruciating migraines, even worse than the migraines I’ve had pre-attack.

Extreme fatigue, and I’ve had this for a while now, before even knowing something was wrong. I just thought I was lazy, honestly. I have to go for many hours naps in the middle of the day.

Drop foot was experienced for the first time yesterday

Joint pain

Eye pain

General aches and pains

I experience what I feel like is the “Ms hug”. My chest hurts so much like there’s pressure.

Horrible aching abdomen twitches/cramps.

My left arm went paralyzed for an hour.

I’m sure there are more. Some of these experiences are brief or they last the whole day. I had experienced a few of these symptoms very minor before the attack I had a few weeks ago. When I had the attack, I thought I was going to die. My partner thought he was watching me die. Now they’re still there but a lot less severe, but they still impact my day. Some days I can walk just fine, and some I need a cane. There are even moments where I need the wheelchair we bought. We bought a wheelchair because we thought I’d never be able to walk again.

[amitshahneuro]

What are the common symptoms of Multiple Sclerosis ?

Common symptoms of multiple sclerosis (MS) include:

Fatigue: Overwhelming fatigue that doesn't improve with rest is a common early symptom.

Numbness or Tingling: Many people with MS experience numbness or tingling in various parts of the body.

Muscle Weakness: Weakness in the limbs, often on one side of the body, can occur.

Coordination Problems: Difficulty with coordination and balance may result in stumbling or difficulty walking.

Vision Problems: Blurred vision, double vision, or eye pain can be early signs of MS.

Spasticity: Muscle stiffness and spasms can be quite uncomfortable.

Cognitive Changes: Problems with memory, attention, and problem-solving can occur.

Bladder and Bowel Issues: MS can affect control over urination and bowel movements.

Pain: Chronic pain, such as nerve pain or muscle pain, can be present.

Heat Sensitivity: Many people with MS find that their symptoms worsen in hot weather or after exercise.

Depression and Mood Changes: Emotional changes, including depression and mood swings, can be part of MS.

Speech and Swallowing Difficulties: MS can affect the muscles used for speech and swallowing.

Tremors: Some individuals with MS may experience tremors, which are involuntary shaking movements.

It's important to note that MS symptoms can vary widely between individuals, and not everyone will experience all of these symptoms. Additionally, symptoms can come and go or worsen over time, which is why early diagnosis and treatment are crucial. If you suspect you have MS or are experiencing these symptoms, consult a healthcare provider for an accurate diagnosis and appropriate management.

It's essential to consult with Dr. Amit Shah, a healthcare professional or Neurologist in Mumbai practicing at Dr. Amit Shah Neurology Clinic for a proper diagnosis and individualized care.

[u2hearts]

I’m writing a blog

I keep meaning to write. I have every intention. Then at the end of the day, I realize I didn’t write again. Normally I actually write my blog the day before but since WordPress had an update, I schedule the blog but it never posts. I finally got annoyed and stopped writing the day before and then stopped writing on the day. So here I am. I would love to say so much has happened since I last…

[jamiesonwolf]

The Lessons I've Learned

The little yellow magnet that started it all. Ten years ago, my life changed not once, but twice. The first time it changed, I had no control over what happened, and it ripped over my body like a storm. The second time it changed, I was the one in control, standing in the middle of that storm against the onslaught of my body. I was diagnosed with multiple sclerosis ten years ago in April of…

[ayushprana0]

Recognizing Multiple Sclerosis symptoms is the first step towards effective management. Ayush Prana, the world's only Ayurvedic MS specialty clinic, has expertly treated over 2000 MS patients globally. Our approach combines accurate diagnosis with scientifically proven Ayurvedic therapies. Learn about MS symptoms and our unique treatments at https://ayushprana.in/.

[adozentothedawn]

A Beginner's Guide to Receiving Cortisone Infusions

So, I am looking for a way to deal with my first flare up treatment and since I don't even really have something to vent about or some deep thoughts or even just depression to voice, I might as well make it educational. Do keep in mind these are my personal experiences from my very first treatment cycle, which I am 3 days (of 5) in.

Most people seem to have trouble sleeping on Cortisone therapy and your treatment professionals (be that nurses or doctors) will likely also assume that. I myself got a prescription for rather strong sleeping pills under the order to only take them if really necessary because they can be addictive. That said, my personal experience was that Cortisone made me honestly more tired rather than restless. When I brought this up with the nurse she seemed surprised but not alarmed, so that is probably not a symptom of anything more drastic than me just being a sleepy bitch.

It is very normal to get a weird taste in your mouth during the infusion, which may also linger for a few more hours. In my experience it's thankfully pretty easy to cover with better tastes though, so I suggest taking along some gum or other easy to eat snacks. If you don't have anything along you can usually at least ask for some water to wash it out for a bit.

You will get stabbed. Multiple times. The professionals might also seriously ask you if you want to do one (Anti-Thrombose) yourself. They will not be mad if you don't and they only ask that cause some people are just used to doing those injections themselves, either cause they already had these treatments multiple times or deal with something similar like diabetes. They will also likely ask you the opposite multiple times to make sure you won't faint at the sight of a needle.

You will bruise where you were stabbed. You will also have very annoying and sticky glue lines on your arm when you take the plaster off. Either ask them the next the day to help you with that or get some rubbing alcohol on your own.

When they stick a thick bandaid on the stabbing spot press on it for a few minutes. You will regret not doing it cause it will bleed like hell and look really scary if you notice only a while later. It probably won't be actually scary but it will be very bloody.

Take some entertainment with you that you can use one handed. One of your hands will be mostly unusable. If necessary you can move it, but it needs to lie low so no holding your phone in front of your face with it for example.

You likely can't predict where they will stab you and if it's for multiple days they will stab you into different spots. Especially if you're like me and have really shitty veins. Common spots are elbows and upper wrists. They might have to try multiple times or even call a local specialist over. This is not cause you're in danger or cause they're mean, your veins are just very subtle and they want to avoid hurting you more than they have to.

The cortisone will likely have influence on your eating habits but it might have different directions. I've actually had positive reactions to that cause my appetite was absolute shit recently (which might be related to a lover side effect from my permanent meds, that will be tested in a week) but after the cortison treatments I've had much less issues with nausea and lacking appetite. I've heard the opposite as well though, so keep an eye on it.

[jackalope78]

Coming to the acceptance that I cannot do the things I used to do easily is HARD. Fuck yes, it's a trauma.

I think that it's really important for people to realize that being disabled is traumatic. genuinely. your body and brain feel like they are breaking down and wrong. you are in constant heavy stress from stuff like chronic pain. most disabled people i know have a somewhat regular emotional break down from the trauma of it all. and we are expected to just smile through it by society, to not be in the way, to not be an issue.

[jackalope78]

My hands are not good today. They're numb, clumsy, uncooerative, and they hurt. Despite that I sewed three buttons back onto two of my dresses, and I would like to celebrate my acomplishment by boasting about it. Because it was HARD, and I did it anyway.