1-2 capsules 3x daily.
30min before meals.

Bilberry
Boswelia
Comfrey
Chondroitin
Hyaluronic Acid
Hydrolysed Collagen
Hydrangea Root
Raspberry
Resveratrol
White Willow Bark
Wild dagga
Other African Herbs

Not suitable for pregnant woman.
Protect from sunlight.
Store below 25°c.

Our Herbal Arthritis Supplement provides comprehensive support for patients with arthritis, offering a blend of ingredients known for their anti-inflammatory, analgesic, and joint-stabilizing properties.

By targeting inflammation, preserving cartilage integrity, and relieving pain and stiffness, this supplement aims to improve overall joint health and enhance patients’ quality of life. With its multifaceted approach, it represents a promising adjunctive therapy for managing arthritis symptoms effectively.

 

Types of Arthritis:

• Arthritis is a general term used to describe a group of more than 100 different types of joint-related conditions that cause inflammation, pain, stiffness, and swelling in one or more joints. The most common types of arthritis include:

 

Osteoarthritis (OA): This is the most common form of arthritis and often referred to as “wear-and-tear” arthritis. It occurs when the protective cartilage that cushions the ends of your bones wears down over time. Symptoms include joint pain, stiffness, and reduced range of motion.

Rheumatoid Arthritis (RA): RA is an autoimmune disease where the body’s immune system mistakenly attacks the synovium (the lining of the membranes that surround the joints). This can lead to joint damage, pain, swelling, and deformity.

Psoriatic Arthritis: This type of arthritis typically affects individuals with psoriasis, a skin condition. Symptoms include joint pain, swelling, and scaly skin patches.

Ankylosing Spondylitis: This is a type of arthritis that primarily affects the spine and sacroiliac joints. It can cause pain and stiffness in the spine and may lead to fusion of the vertebrae.

Gout: Gout is characterized by the buildup of uric acid crystals in the joints, often in the big toe. It causes sudden, severe pain, redness, and swelling in affected joints.

Juvenile Arthritis: This term encompasses several types of arthritis that affect children. Symptoms can vary but may include joint pain, swelling, and fever.

Lupus-Related Arthritis: Systemic lupus erythematosus (SLE) is an autoimmune disease that can affect various organs, including the joints. Joint pain, swelling, and stiffness are common symptoms.

These different types of arthritis can have varying degrees of severity and affect different joints in the body.

 

What causes Arthritis?

Age: Osteoarthritis, the most prevalent type of arthritis, is strongly correlated with advancing age. The natural aging process leads to wear and tear on the joints, causing progressive degeneration of the articular cartilage. Over time, this can result in joint pain, stiffness, and reduced mobility, particularly in weight-bearing joints such as the knees, hips, and spine.

Genetics: Genetic predisposition plays a significant role in certain types of arthritis, notably rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Specific genetic markers, such as certain human leukocyte antigen (HLA) alleles, have been linked to an increased risk of developing these autoimmune conditions. Family history can be a crucial determinant, as individuals with close relatives affected by RA or AS have a higher likelihood of developing these conditions themselves.

Autoimmune Disorders: Rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and psoriatic arthritis (PsA) are examples of autoimmune disorders characterized by the immune system attacking healthy tissues, including the joints. In RA, immune cells infiltrate the synovium, causing inflammation and cartilage destruction. SLE involves widespread inflammation affecting various organs, including the joints. PsA, a type of arthritis occurring in some individuals with psoriasis, leads to joint inflammation, pain, and swelling.

Joint Injury: Trauma or previous joint injuries, such as fractures or ligament tears, can predispose individuals to post-traumatic osteoarthritis. Joint misalignment resulting from injury can accelerate cartilage degeneration and lead to early-onset osteoarthritis in the affected joint.

Infection: Certain infections can trigger inflammatory arthritis. Lyme disease, caused by the bacterium Borrelia burgdorferi transmitted through tick bites, can result in Lyme arthritis characterized by joint inflammation, particularly in large joints like the knee. Hepatitis C virus (HCV) infection is associated with the development of cryoglobulinemia-associated arthritis, a type of inflammatory arthritis involving the deposition of abnormal proteins in the joints.

Metabolic Disorders: Metabolic abnormalities contribute to the development of crystal-induced arthritis, such as gout and pseudogout. Gout arises from the deposition of monosodium urate crystals in the joints, typically due to elevated serum uric acid levels. Pseudogout, or calcium pyrophosphate deposition disease (CPPD), results from the accumulation of calcium pyrophosphate crystals in the joints, leading to acute arthritis attacks.

Environmental Factors: Environmental factors, including smoking, exposure to air pollution, and occupational hazards, can influence the risk of developing arthritis. Cigarette smoking, for example, has been linked to an increased risk of rheumatoid arthritis and may exacerbate symptoms in affected individuals. Exposure to certain pollutants or chemicals in the workplace may also contribute to the development or worsening of arthritis symptoms.

 

Detailed explanation of how autoimmune diseases can cause different types of arthritis:

Rheumatoid Arthritis (RA): In RA, autoantibodies such as rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibodies target self-antigens, leading to immune complex deposition and activation of inflammatory cascades within the synovium. This results in synovial hyperplasia, infiltration of immune cells such as T lymphocytes, B lymphocytes, and macrophages, and release of pro-inflammatory cytokines like tumor necrosis factor-alpha (TNF-α), interleukin-1 (IL-1), and interleukin-6 (IL-6), perpetuating the inflammatory milieu within the joint. The sustained inflammation triggers osteoclast activation, leading to bone erosion and cartilage destruction, hallmark features of erosive arthritis in RA.

Systemic Lupus Erythematosus (SLE): SLE involves dysregulated B cell function, aberrant T cell activation, and immune complex deposition. Antinuclear antibodies (ANA) and other autoantibodies target self-antigens, leading to immune complex formation and deposition in various tissues, including the synovium. This triggers an inflammatory response characterized by synovial inflammation, infiltration of immune cells, and release of pro-inflammatory cytokines, resulting in joint pain, swelling, and deformities. Additionally, immune complex deposition in small blood vessels can cause vasculitis, contributing to joint pathology in SLE.

Psoriatic Arthritis (PsA): PsA is associated with autoimmune-mediated inflammation against keratinocytes in the skin and synovial tissue. Autoantigens like keratins and filaggrin trigger an immune response, leading to infiltration of immune cells such as T lymphocytes and neutrophils into the synovium. This results in synovitis, characterized by joint pain, swelling, and stiffness. PsA is also associated with enthesitis, inflammation at the sites where tendons or ligaments insert into bone, and dactylitis, inflammation of entire digits.

Osteoarthritis (OA): While not primarily autoimmune, inflammation may play a role in the pathogenesis of OA. Chronic low-grade inflammation, characterized by increased levels of pro-inflammatory cytokines such as interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-α), contributes to cartilage degradation, synovial inflammation, and joint damage in OA. Additionally, autoimmune responses against cartilage-specific antigens may contribute to the progression of OA in some cases.

Ankylosing Spondylitis (AS): AS is a type of spondyloarthropathy characterized by inflammation of the axial skeleton and sacroiliac joints. The exact cause of AS is unknown, but it is believed to involve genetic susceptibility (e.g., HLA-B27), environmental triggers, and dysregulated immune responses. Autoimmune mechanisms, including aberrant T cell activation and production of pro-inflammatory cytokines such as TNF-α and IL-17, contribute to synovial inflammation, enthesitis, and new bone formation in AS.

Juvenile Idiopathic Arthritis (JIA): JIA encompasses several autoimmune-mediated arthritis conditions in children. Each subtype of JIA has distinct immunopathogenic mechanisms. For example, oligoarticular JIA is associated with autoantibodies targeting nuclear antigens, while enthesitis-related JIA is characterized by aberrant immune responses against entheseal tissue. Dysregulated immune responses, including T cell dysfunction and cytokine dysregulation, contribute to synovial inflammation, joint damage, and systemic manifestations in JIA.

 

The impact of Gluten, Dairy and Sugar on Autoimmune arthritis:

1. Gluten’s Impact on Autoimmune Arthritis: In individuals genetically predisposed to autoimmune arthritis, gluten, found in wheat, rye, and barley, can initiate an immune response. This immune reaction involves the release of pro-inflammatory cytokines, primarily interleukin-17 (IL-17), by T-helper 17 (Th17) cells. These cytokines contribute to chronic inflammation and may exacerbate autoimmune arthritis symptoms, such as joint pain and swelling. Gluten sensitivity can disrupt immune tolerance and perpetuate the autoimmune process, making it a potential dietary trigger for arthritis.
2. Dairy’s Influence on Autoimmune Arthritis: Dairy products, specifically those containing casein and lactose, can affect autoimmune arthritis through various mechanisms. In individuals genetically predisposed to autoimmune arthritis, the consumption of dairy can trigger immune responses.
3. Casein and Immune Response: Casein, a protein found in dairy, can provoke immune reactions. In some individuals, particularly those with genetic susceptibility, casein consumption may lead to immune responses that involve pro-inflammatory cytokines, such as interleukin-17 (IL-17), produced by T-helper 17 (Th17) cells. These cytokines contribute to chronic inflammation, which can exacerbate autoimmune arthritis symptoms, including joint inflammation and pain.
4. Lactose and Gut Inflammation: Lactose, the sugar in dairy, can also play a role. Individuals with lactose intolerance may experience gastrointestinal discomfort upon consuming dairy. This discomfort can result from lactose malabsorption and lead to gut inflammation. Prolonged gut inflammation can disrupt the integrity of the intestinal barrier, allowing the entry of gut bacteria and their byproducts into the bloodstream. This, in turn, can trigger an immune response, contributing to systemic inflammation and potentially worsening autoimmune arthritis.
5. Sugar’s Role in Autoimmune Arthritis: Excessive sugar intake can have a detrimental effect on autoimmune arthritis. High sugar consumption has been linked to chronic, low-grade inflammation in the body. It can promote inflammation by several mechanisms, including the formation of advanced glycation end-products (AGEs) and activation of pro-inflammatory pathways. The immune system’s response to these changes can further contribute to the autoimmune process and worsen arthritis symptoms. Managing sugar intake is essential for individuals with autoimmune arthritis, as it can help reduce chronic inflammation and potentially alleviate joint discomfort.

 

In all cases, patients with autoimmune arthritis should consult with healthcare providers and nutritionists to develop personalized dietary strategies, as the impact of gluten, dairy, and sugar can vary among individuals. Dietary modifications should be carefully monitored to ensure patients receive proper nutrition while minimizing potential triggers for autoimmune arthritis.

 

Ingredients which are traditionally used for this disorder
Technical info:

Alpha-Lipoic Acid: Alpha-lipoic acid (ALA) is a potent antioxidant that plays a crucial role in mitigating oxidative stress implicated in arthritis pathogenesis. Its ability to scavenge free radicals and reduce oxidative damage contributes to its anti-inflammatory properties, which are vital for alleviating arthritis symptoms. Moreover, ALA has been shown to modulate inflammatory pathways and decrease the production of pro-inflammatory cytokines, thereby reducing joint inflammation and offering relief from arthritis discomfort.

Beta-Alanine: Beta-alanine is a non-essential amino acid that serves as a precursor to carnosine, a dipeptide abundantly found in muscle tissue. Carnosine plays a vital role in buffering acidic compounds that accumulate during intense physical activity, thereby delaying the onset of muscle fatigue and enhancing exercise performance. In the context of arthritis, beta-alanine supplementation may support joint function by reducing muscle and joint fatigue, improving mobility, and facilitating comfortable movement, which are essential for individuals experiencing arthritis-related limitations.

Bilberry: Bilberry contains potent bioactive compounds, including anthocyanosides and flavonoids, which exhibit strong antioxidant and anti-inflammatory properties. Anthocyanosides have been shown to inhibit collagen degradation and promote collagen biosynthesis, thereby preserving connective tissue integrity essential for joint health. Additionally, flavonoids present in bilberry exert anti-inflammatory effects by modulating inflammatory pathways and reducing the production of pro-inflammatory mediators such as histamine and prostaglandins. These mechanisms contribute to bilberry’s ability to alleviate joint inflammation and pain associated with arthritis.

Boron: Boron is a trace element that plays a crucial role in various physiological processes, including bone metabolism and joint health. It facilitates the metabolism of calcium and vitamin D, essential nutrients for maintaining bone and joint integrity. Boron supplementation has been shown to enhance bone mineral density and reduce the risk of osteoarthritis by promoting cartilage repair and inhibiting cartilage degradation. Moreover, boron exhibits anti-inflammatory properties, which contribute to its ability to alleviate arthritis discomfort and improve joint function.

Boswelia: Boswellic acids, the active constituents of Boswelia, exert potent anti-inflammatory effects by inhibiting the activity of pro-inflammatory enzymes such as 5-lipoxygenase and cyclooxygenase. By blocking the synthesis of leukotrienes and prostaglandins, Boswelia suppresses inflammatory pathways involved in arthritis pathogenesis. Moreover, Boswelia modulates immune responses and reduces the production of pro-inflammatory cytokines, further attenuating joint inflammation and offering relief from arthritis-related symptoms such as pain and swelling.

Chondroitin Sulfate: Chondroitin sulfate is a naturally occurring glycosaminoglycan found in cartilage, bone, and connective tissue. It serves as a structural component of cartilage, providing elasticity and resistance to compression. Chondroitin sulfate exhibits several mechanisms of action beneficial for joint health, including the inhibition of cartilage-degrading enzymes such as matrix metalloproteinases and the promotion of cartilage repair and regeneration. Additionally, chondroitin sulfate has been shown to reduce inflammation and inhibit the production of pro-inflammatory mediators implicated in arthritis pathogenesis.

Conjugated Linoleic Acid (CLA): Conjugated linoleic acid (CLA) is a group of omega-6 fatty acids with potent anti-inflammatory properties. CLA modulates inflammatory pathways by inhibiting the production of pro-inflammatory cytokines such as interleukin-1β (IL-1β) and tumor necrosis factor-alpha (TNF-α). Additionally, CLA promotes cartilage repair and regeneration by stimulating the synthesis of collagen and proteoglycans, essential components of cartilage matrix. These mechanisms contribute to CLA’s ability to mitigate joint inflammation, alleviate arthritis symptoms, and promote overall joint health.

Comfrey: Comfrey contains allantoin, a bioactive compound known for its regenerative properties. Allantoin accelerates tissue repair and wound healing by promoting cell proliferation and extracellular matrix synthesis. In the context of arthritis, comfrey may support joint health by facilitating tissue

regeneration and reducing inflammation associated with joint damage. Additionally, comfrey exhibits analgesic properties, which contribute to its ability to alleviate joint pain and swelling commonly observed in arthritis patients.

Glucosamine Sulfate: Glucosamine sulfate is a naturally occurring amino sugar that serves as a precursor for glycosaminoglycan synthesis, a major component of cartilage matrix. By providing essential building blocks for cartilage repair and regeneration, glucosamine sulfate supports joint health and attenuates arthritis-related symptoms such as pain and stiffness. Moreover, glucosamine sulfate exhibits anti-inflammatory effects by inhibiting the production of pro-inflammatory mediators and modulating inflammatory pathways involved in arthritis pathogenesis.

Glycine: Glycine is a non-essential amino acid with diverse physiological functions, including anti-inflammatory and immunomodulatory effects. Glycine serves as a precursor for glutathione, a potent antioxidant that scavenges free radicals and reduces oxidative stress. Additionally, glycine modulates inflammatory responses by inhibiting the production of pro-inflammatory cytokines and promoting the synthesis of anti-inflammatory mediators. In the context of arthritis, glycine supplementation may attenuate joint inflammation and alleviate arthritis-related symptoms such as pain and swelling.

Hyaluronic Acid: Hyaluronic acid is a glycosaminoglycan found in synovial fluid and cartilage, where it plays a crucial role in joint lubrication and shock absorption. In arthritis, the degradation of hyaluronic acid leads to decreased joint lubrication and increased friction between articular surfaces, resulting in pain and stiffness. Hyaluronic acid supplementation may restore joint lubrication, reduce inflammation, and promote cartilage repair, thereby alleviating arthritis symptoms and improving joint function.

Hydrangea Root: Hydrangea root contains bioactive compounds with anti-inflammatory and immunomodulatory properties, which may be beneficial for individuals with arthritis. Research suggests that hydrangea root inhibits the activity of pro-inflammatory cytokines and modulates immune responses, thereby attenuating joint inflammation and offering relief from arthritis-related symptoms such as pain and swelling. Additionally, hydrangea root may support joint health by promoting tissue repair and regeneration, contributing to improved joint function and mobility.

Hydrolysed Collagen: Hydrolyzed collagen is a bioactive protein derived from collagen-rich sources such as bone and connective tissue. It contains essential amino acids, including glycine, proline, and hydroxyproline, which are crucial for collagen synthesis and tissue repair. Hydrolyzed collagen supplementation may stimulate the production of joint collagen, promoting cartilage repair and regeneration in individuals with arthritis. Moreover, hydrolyzed collagen exhibits anti-inflammatory effects, which contribute to its ability to attenuate joint inflammation and alleviate arthritis-related symptoms such as pain and stiffness.

L-Methionine: L-methionine is an essential amino acid with diverse physiological functions, including anti-inflammatory and analgesic effects. Methionine serves as a precursor for various molecules involved in inflammatory pathways, such as glutathione and S-adenosylmethionine (SAMe). By modulating inflammatory responses and reducing the production of pro-inflammatory mediators, L-methionine may attenuate joint inflammation and alleviate arthritis-related symptoms such as pain and swelling. Additionally, L-methionine supports tissue repair and regeneration, contributing to improved joint health and function.

Magnesium: Magnesium is an essential mineral involved in numerous physiological processes, including bone metabolism and muscle function. In arthritis, magnesium supplementation may alleviate joint discomfort by reducing muscle cramps and promoting muscle relaxation. Moreover, magnesium exhibits anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines and modulating inflammatory pathways involved in arthritis pathogenesis. These mechanisms contribute to magnesium’s ability to attenuate joint inflammation and improve arthritis-related symptoms such as pain and stiffness.

Manganese: Manganese is a trace element with antioxidant properties that play a crucial role in protecting joint tissues from oxidative damage. Moreover, manganese is essential for the synthesis of glycosaminoglycans, collagen, and other components of cartilage matrix, contributing to joint

health and integrity. Manganese supplementation may support cartilage repair and regeneration in individuals with arthritis, thereby alleviating arthritis-related symptoms such as pain and stiffness.

Milk Thistle: Milk thistle contains silymarin, a bioactive flavonoid with potent antioxidant and anti-inflammatory properties. Silymarin scavenges free radicals, reduces oxidative stress, and inhibits inflammatory pathways involved in arthritis pathogenesis. Additionally, milk thistle promotes tissue repair and regeneration by enhancing cell proliferation and extracellular matrix synthesis. These mechanisms contribute to milk thistle’s ability to alleviate joint inflammation and pain associated with arthritis.

MSM (Methylsulfonylmethane): MSM is a naturally occurring organosulfur compound found in plants and animals. It exhibits anti-inflammatory and analgesic properties, which may be beneficial for individuals with arthritis. MSM supplementation has been shown to reduce joint inflammation, alleviate arthritis-related symptoms such as pain and stiffness, and improve overall joint function and mobility. Moreover, MSM promotes tissue repair and regeneration by enhancing collagen synthesis and supporting cartilage health.

Olive Leaf: Olive leaf contains bioactive compounds, including oleuropein and hydroxytyrosol, which exhibit potent antioxidant and anti-inflammatory properties. Oleuropein inhibits inflammatory pathways and reduces the production of pro-inflammatory mediators implicated in arthritis pathogenesis. Additionally, olive leaf modulates immune responses and promotes tissue repair and regeneration, contributing to improved joint health and function. These mechanisms make olive leaf a promising therapeutic agent for alleviating arthritis-related symptoms and supporting joint integrity.

Resveratrol: Resveratrol is a polyphenolic compound found in various plants, including grapes and berries. It exhibits potent antioxidant and anti-inflammatory properties, which may be beneficial for individuals with arthritis. Resveratrol scavenges free radicals, reduces oxidative stress, and inhibits inflammatory pathways involved in arthritis pathogenesis. Additionally, resveratrol promotes tissue repair and regeneration by enhancing cell proliferation and extracellular matrix synthesis. These mechanisms contribute to resveratrol’s ability to alleviate joint inflammation and pain associated with arthritis.

Rosehip: Rosehip contains bioactive compounds, including galactolipids and phenolic compounds, which exhibit potent antioxidant and anti-inflammatory properties. Galactolipids inhibit inflammatory pathways and reduce the production of pro-inflammatory mediators implicated in arthritis pathogenesis. Additionally, rosehip promotes tissue repair and regeneration by enhancing cell proliferation and extracellular matrix synthesis. These mechanisms contribute to rosehip’s ability to alleviate joint inflammation and pain associated with arthritis.

Selenium: Selenium is a trace element with potent antioxidant properties that play a crucial role in protecting joint tissues from oxidative damage. Moreover, selenium modulates immune responses and reduces inflammation by inhibiting the production of pro-inflammatory cytokines and promoting the synthesis of anti-inflammatory mediators. Selenium supplementation may alleviate joint inflammation and oxidative stress associated with arthritis, thereby improving joint health and function.

Vitamin B3 (Niacin): Niacin, also known as vitamin B3, plays a crucial role in various physiological processes, including energy metabolism and DNA repair. In arthritis, niacin exhibits anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines and modulating inflammatory pathways involved in arthritis pathogenesis. Additionally, niacin supports tissue repair and regeneration by enhancing cell proliferation and extracellular matrix synthesis. These mechanisms contribute to niacin’s ability to alleviate joint inflammation and pain associated with arthritis.

Vitamin B5 (Pantothenic Acid): Pantothenic acid, also known as vitamin B5, is essential for energy metabolism and adrenal function. In arthritis, pantothenic acid exhibits anti-inflammatory effects by inhibiting the production of pro-inflammatory mediators and modulating inflammatory pathways involved in arthritis pathogenesis. Additionally, pantothenic acid supports tissue repair and regeneration by enhancing cell proliferation and extracellular matrix synthesis. These mechanisms contribute to pantothenic acid’s ability to alleviate joint inflammation and pain associated with arthritis

Vitamin C: Vitamin C, also known as ascorbic acid, is a water-soluble vitamin with potent antioxidant properties that play a crucial role in protecting joint tissues from oxidative damage. Moreover, vitamin C is essential for collagen synthesis, a process vital for maintaining cartilage integrity and promoting tissue repair and regeneration. Vitamin C supplementation may alleviate joint inflammation and oxidative stress associated with arthritis, thereby improving joint health and function.

White Willow Bark: White willow bark contains salicin, a bioactive compound similar to aspirin (acetylsalicylic acid), which exhibits potent anti-inflammatory and analgesic properties. Salicin inhibits the activity of pro-inflammatory enzymes such as cyclooxygenase (COX), thereby reducing the production of inflammatory mediators such as prostaglandins. Additionally, white willow bark modulates pain perception and transmission, offering relief from arthritis-related symptoms such as pain and swelling. These mechanisms make white willow bark a valuable therapeutic agent for individuals with arthritis.

Wild Dagga: Wild dagga contains bioactive compounds, including leonurine and flavonoids, which exhibit potent anti-inflammatory and analgesic properties. Leonurine inhibits inflammatory pathways and reduces the production of pro-inflammatory mediators implicated in arthritis pathogenesis. Additionally, wild dagga modulates pain perception and transmission, offering relief from arthritis-related symptoms such as pain and swelling. These mechanisms make wild dagga a promising therapeutic agent for alleviating joint inflammation and supporting joint health.