When trying to understand the complexities of migraine disease, it's crucial to explore the intricate relationship between the trigeminocervical complex (TCC), the trigeminal and occipital nerves, and how they contribute to migraine pain. This new blog post aims to demystify this connection, providing insights into the mechanisms behind #migraine and potential avenues for relief. Read more: https://lnkd.in/gtac7Cdr
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Imagine waking up each day with the unpredictability of a storm brewing within your own body. This is the reality for many individuals living with Behçet’s Disease, a rare, chronic condition that manifests through inflammation in various parts of the body. The journey to understand and cope with this disease is marked by emotional highs and lows, scientific breakthroughs, and personal triumphs. #arthritis #osteoarthritis #osteoarthritistreatment #osteoarthritissupport #osteoarthritiscare #osteoarthritisawareness
The Root Causes of Behçet’s Disease: - | Arthriticare
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CONDITION SPOTLIGHT: Multiple Sclerosis Around 1 million people in the United States have received a diagnosis of multiple sclerosis. With promising results from extensive research, HBOT shows the potential to slow down symptom progression and enhance the quality of life for those battling this autoimmune disease. Read our latest blog below to learn how HBOT can help mitigate MS symptoms: #MultipleSclerosis #HBOTBenefits #HBOT
Hyperbaric oxygen therapy for Multiple Sclerosis: Learn the benefits | Hyperbaric Healing Treatment Center
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Ophthopedia Update:Discordant dry eye disease and chronic pain: A systematic review and meta-analysis: To evaluate the relative contributions of objective and subjective indicators of dry eye disease (DED) in individuals with chronic pain conditions compared with controls. #eye #Ophthalmology #CLAE
Discordant dry eye disease and chronic pain: A systematic review and meta-analysis
contactlensjournal.com
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Interested in gaining insights on arthritis? Read this article below by Medical News Today for all you need to know about it's causes, types, symptoms and treatment.
Arthritis: Causes, types, and treatments
medicalnewstoday.com
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𝗘𝘅𝗽𝗹𝗼𝗿𝗶𝗻𝗴 𝗠𝗮𝗿𝗸𝗲𝘁 𝗜𝗻𝘀𝗶𝗴𝗵𝘁𝘀: Acute Kidney Injury (AKI) Curious about the latest advancements in the field of Acute Kidney Injury (AKI)? Look no further! Wissen Research brings you an in-depth report that sheds light on every aspect of this disease, highlighting: #MarketInsights #ProductAnalysis #CompetitiveAnalysis #PatentAnalysis #ClinicalTrials #Treatment #OpportunityAnalysis #MarketForecast For detailed report: https://lnkd.in/gt_R7kcK Request customized report: https://lnkd.in/d6q8Q-5a #marketresearch #marketreport #marketforecast #askforcustomization #wissenresearch #marketinsights #AcuteKidneyInjury #AKI
Acute Kidney Injury : Market Insight 2024-2034 - Wissen Research
wissenresearch.com
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A look at one of the first trials of rapamycin to directly target aging, for gum disease. Rapamycin may slow aging. Here's one way the drug will be tested https://lnkd.in/ex4EqH6S
Rapamycin may slow aging. Here's one way the drug will be tested
npr.org
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FABRY DISEASE is a rare genetic disorder characterized by the body's inability to break down a particular type of fat called globotriaosylceramide, due to a deficiency in the enzyme alpha-galactosidase-A. This lipid accumulation leads to blockages within blood vessels, causing a variety of symptoms and complications that affect multiple body systems. A classic hallmark of Fabry disease is episodes of severe pain in the hands and feet (acroparesthesias), which may be triggered by environmental factors like heat or exercise. The eyes can be affected, with corneal deposits known as cornea verticillata occurring, but these usually do not impact vision. Cardiovascular issues, such as heart enlargement and irregular rhythms, can arise. Furthermore, kidney dysfunction can progress to renal failure, necessitating dialysis or transplantation for some patients. Those with Fabry disease may also experience gastrointestinal problems, reduced sweating (hypohidrosis), skin lesions called angiokeratomas, and a susceptibility to fever. Vascular complications like stroke or heart attack can occur due to the blockage in blood vessels from the lipid buildup. Enzyme replacement therapy (ERT) is currently the main treatment for managing symptoms and preventing the progression of organ damage in Fabry disease. An oral medication, migalastat, is available for certain individuals with specific genetic mutations. Pain management and supportive treatments, along with medications like anti-platelet agents to prevent stroke and antihypertensives to manage kidney complications, are essential components of care for Fabry patients. 1. Genetic Disorder 2. Alpha-Galactosidase-A 3. Globotriaosylceramide 4. Acroparesthesias 5. Enzyme Deficiency 6. Cornea Verticillata 7. Angiokeratomas 8. Hypohidrosis 9. Enzyme Replacement Therapy 10. Migalastat Treatment 11. Organ Damage Prevention
FABRY DISEASE Uncovered: A Comprehensive Guide
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This cohort study characterizes the presentation, causes, treatment, and disease course of erythema nodosum, as well as identifies associations with chronicity and recurrence. https://ja.ma/48oT3yE
Clinical Characteristics of Erythema Nodosum and Associations With Chronicity and Recurrence
jamanetwork.com
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𝐌𝐲𝐬𝐭𝐞𝐫𝐲 𝐨𝐟 𝐀𝐥𝐤𝐚𝐩𝐭𝐨𝐧𝐮𝐫𝐢𝐚: 𝐀 𝐑𝐚𝐫𝐞 𝐆𝐞𝐧𝐞𝐭𝐢𝐜 𝐃𝐢𝐬𝐨𝐫𝐝𝐞𝐫 Imagine having a condition where your urine turns as dark as black tea and everyday movements are painful due to stiff, aching joints. This is the reality for those living with Alkaptonuria, a rare genetic disorder affecting only 1 in 250,000 to 1 million people globally. 🌍 Despite its rarity, there's new hope on the horizon! Here’s what you should know: 𝐑𝐞𝐜𝐞𝐧𝐭 𝐁𝐫𝐞𝐚𝐤𝐭𝐡𝐫𝐨𝐮𝐠𝐡𝐬: ➡ Promising Research: A recent study in the Journal of Inherited Metabolic Disease has highlighted the effectiveness of nitisinone, a drug that targets the enzyme responsible for the buildup of homogentisic acid, the main cause of Alkaptonuria's symptoms. ➡ Ongoing Clinical Trials: Researchers at the University of Liverpool are currently testing nitisinone to better understand its safety and benefits for Alkaptonuria patients. These advancements are offering a glimmer of hope to those affected. 𝐖𝐡𝐚𝐭 𝐢𝐬 𝐀𝐥𝐤𝐚𝐩𝐭𝐨𝐧𝐮𝐫𝐢𝐚? It's a genetic disorder caused by a deficiency of the enzyme homogentisate 1,2-dioxygenase, which is crucial for breaking down the amino acid tyrosine. The deficiency leads to a buildup of homogentisic acid in the body, resulting in symptoms like: ☑ Dark urine that turns black upon standing ☑ Joint pain and stiffness ☑ Limited mobility 🚶♂️ ☑ Deformity of joints and spine ☑ Potential organ dysfunction, including cardiac issues like aortic stenosis 𝐌𝐚𝐧𝐚𝐠𝐞𝐦𝐞𝐧𝐭 𝐚𝐧𝐝 𝐏𝐨𝐭𝐞𝐧𝐭𝐢𝐚𝐥 𝐓𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭𝐬: While there’s currently no cure, early diagnosis and proactive management are key. This can help prevent severe joint deformities and organ damage. Nitisinone is showing promise as a potential treatment, alongside options like physical therapy, pain management, and surgery to repair damaged joints. Raising awareness is crucial for conditions like Alkaptonuria, where early detection can make a world of difference. Let's share knowledge, support research, and bring hope to those living with this rare genetic disorder. 👉 Watch my latest YouTube video to learn more about Alkaptonuria and its latest research breakthroughs. https://lnkd.in/gj5BCu3c LinkedIn LinkedIn News THE ALKAPTONURIA SOCIETY LTD Genetic & Rare Diseases Insights Indian Council of Medical Research (ICMR) AIIMS (All India Institute of Medical Sciences, New Delhi) World Health Organization Centers for Disease Control and Prevention YouTube #alkaptonuria #publichealth #rarediseases #geneticdisorders #healthcareawareness #share #cfbr #youtubevideo
The Black Urine Disease: Alkaptonuria
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🔬 Understanding your health is crucial in managing autoimmune diseases. The Arthritis Wellness #2 Blood Test Panel provides a detailed assessment of your immune system, helping diagnose and monitor rheumatoid arthritis and other related conditions. Discover the benefits of comprehensive testing with Walk-In Lab in our new article about the Wellness #2 blood test! 🌟 https://lnkd.in/gkvj2Z2m #HealthyLiving #AutoimmuneAwareness #BloodTests #WalkInLab
What is the Arthritis Wellness Blood Test? - Walkin Lab
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