#LouGehrigsDisease

[symptomfinder]

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. It is also known as Lou Gehrig's disease, named after the famous baseball player who was diagnosed with ALS in the 1930s. 💪 The symptoms of ALS can vary from person to person, but typically include muscle weakness, stiffness, and twitching. As the disease progresses, individuals may experience difficulty speaking, swallowing, and breathing. 🔍 While the exact cause of ALS is unknown, it is believed to be a combination of genetic and environmental factors. Some cases of ALS are inherited, while others occur spontaneously. Research is ongoing to better understand the underlying mechanisms of the disease. 🧬1. Understanding ALS: Definition and Overview of the DiseaseALS, also known as Lou Gehrig's Disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. It causes muscle weakness, paralysis, and eventually, respiratory failure. There is currently no cure for ALS, and the cause is unknown. Most people with ALS live 2-5 years after diagnosis. ALS affects people of all ages and ethnicities, but it is most commonly diagnosed in people between the ages of 40 and 70. It is slightly more common in men than women. There are two types of ALS: sporadic, which accounts for 90-95% of cases, and familial, which is inherited. Early symptoms of ALS include muscle weakness, twitching, and cramping. As the disease progresses, individuals may experience difficulty speaking, swallowing, and breathing. There is no single test to diagnose ALS, so doctors use a combination of tests to rule out other conditions. Living with ALS can be challenging, but there are resources available to help individuals and their families. Treatment options include medications, physical therapy, and assistive devices. Support groups and counseling can also be beneficial. 2. The Main Symptoms of ALS: Weakness, Muscle Atrophy, and SpasticityALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. The main symptoms of ALS include weakness, muscle atrophy, and spasticity. Weakness: This is the most common symptom of ALS. It usually starts in the hands, feet, or limbs and gradually spreads to other parts of the body. Muscle Atrophy: This is the wasting away of muscle tissue due to the loss of nerve cells that control muscle movement. It leads to weakness and eventually paralysis. Spasticity: This is a condition where muscles become stiff and difficult to move. It can cause muscle spasms, cramps, and pain. Other symptoms of ALS include difficulty speaking, swallowing, and breathing. As the disease progresses, patients may also experience weight loss, fatigue, and cognitive changes. Early diagnosis and treatment can help manage the symptoms of ALS and improve quality of life. There is currently no cure for ALS, but research is ongoing to find effective treatments and a cure. 🧠💪🦶🦵🤕🤔💊🧪🔬🧬👨‍🔬👩‍🔬🧑‍⚕️🏥🌡️📈3. The Causes of ALS: Genetics, Environmental Factors, and LifestyleALS is a complex disease with multiple causes. Genetics plays a role, with about 10% of cases being inherited. Environmental factors, such as exposure to toxins, may also increase the risk of developing ALS. Genetics Environmental factors Lifestyle Lifestyle factors, such as smoking and poor diet, may also contribute to the development of ALS. However, the exact mechanisms by which these factors contribute to ALS are not well understood. Research is ongoing to better understand the causes of ALS and develop effective treatments. Early diagnosis and intervention can improve quality of life for those with ALS. 🔬🧬💊4. Diagnosing ALS: Tests and Examinations to Confirm the DiseaseThere are several tests and examinations that doctors use to confirm a diagnosis of ALS. These include: Electromyography (EMG) to measure muscle activity and detect nerve damage. Nerve conduction studies to evaluate the speed and strength of nerve signals. Blood and urine tests to rule out other conditions with similar symptoms. Magnetic resonance imaging (MRI) to look for other possible causes of symptoms. Doctors may also perform a physical exam to assess muscle strength, reflexes, and coordination. A spinal tap may be done to analyze cerebrospinal fluid for abnormalities. Genetic testing may be recommended for some cases of familial ALS. It's important to note that there is no single test that can definitively diagnose ALS. Rather, a combination of tests and examinations are used to make a diagnosis. It's also important to see a neurologist who specializes in ALS for an accurate diagnosis and appropriate treatment plan. Early diagnosis is crucial for managing symptoms and improving quality of life. If you or a loved one are experiencing symptoms of ALS, don't hesitate to seek medical attention.5. Treatment Options for ALS: Medications, Therapy, and Supportive CareThere are several treatment options for ALS, including medications, therapy, and supportive care. Medications can help manage symptoms and slow the progression of the disease. Physical therapy and speech therapy can improve mobility and communication. Occupational therapy can help with daily activities and assistive devices. Supportive care, such as nutrition and breathing support, can improve quality of life. Riluzole is the only FDA-approved medication for ALS, but other drugs can alleviate symptoms. Respiratory therapy can help with breathing difficulties and prevent respiratory infections. Emotional support and counseling can help patients and caregivers cope with the disease. Alternative treatments, such as acupuncture and herbal supplements, have not been proven effective. Patients should discuss any alternative treatments with their healthcare provider. Clinical trials are ongoing to develop new treatments for ALS. Early diagnosis and treatment can improve outcomes and quality of life. It's important for patients and caregivers to work with a multidisciplinary team to manage ALS. Team members may include neurologists, physical therapists, speech therapists, and social workers. ALS can be a challenging disease, but with the right treatment and support, patients can maintain their independence and quality of life. 💪🏼💜 6. Coping with ALS: Managing Symptoms and Maintaining Quality of LifeLiving with ALS can be challenging, but there are ways to manage symptoms and maintain quality of life. Here are some tips: Stay active: Exercise can help improve muscle strength and flexibility. Use assistive devices: Wheelchairs, communication devices, and other aids can help with daily tasks. Eat well: A balanced diet can help maintain weight and energy levels. Manage breathing: Breathing exercises and equipment can help with respiratory function. Seek support: Join a support group or talk to a therapist to cope with emotional challenges. It's important to communicate with healthcare providers about symptoms and treatment options. Medications, physical therapy, and other interventions can help manage symptoms and improve quality of life. ALS can affect communication, but there are ways to maintain connections with loved ones. Technology, such as video calls and text messaging, can help stay in touch. Living with ALS can be difficult, but it's important to focus on what can be done to improve quality of life. With proper management and support, it's possible to live a fulfilling life with ALS. 💪🏼7. Research and Future Directions: Advances in ALS Treatment and PreventionRecent research has shown promising advances in the treatment and prevention of ALS. Gene therapy has shown potential in slowing down the progression of the disease. Stem cell therapy is being studied as a potential treatment option. Immunotherapy is being explored as a way to boost the immune system and fight off the disease. Prevention strategies are also being developed: Identifying genetic risk factors for ALS can help with early detection and intervention. Lifestyle changes, such as exercise and a healthy diet, may reduce the risk of developing ALS. Environmental factors, such as exposure to toxins, are being studied as potential risk factors for ALS. The future of ALS treatment and prevention looks promising, with ongoing research and clinical trials. New drugs and therapies are being developed and tested. Advancements in technology, such as brain-computer interfaces, may provide new treatment options. Collaboration between researchers, clinicians, and patients is crucial for progress in the field. Overall, there is hope for those affected by ALS, with continued efforts to improve treatment and prevention. 🙌 In conclusion, understanding the symptoms and causes of ALS is crucial for early detection and treatment. Quizlet provides a comprehensive resource for learning about this debilitating disease. 🧠💻 By using Quizlet's interactive flashcards and quizzes, students and medical professionals alike can deepen their knowledge of ALS. 💡📚 Let's continue to raise awareness and support research for ALS. Together, we can make a difference in the lives of those affected by this devastating disease. 🙏💜 https://symptomfinder.com/als-symptoms-and-causes-on-quizlet/?_unique_id=647b54589ca22

[ritaltime]

Understanding Amyotrophic Lateral Sclerosis (ALS): Causes, Symptoms, and Treatment

als #ALSawareness #NeurodegenerativeDiseases #MotorNeuronDisease #LouGehrigsDisease #ALSResearch #ALSsymptoms #ALScauses #ALStreatment #ALSsupport #Neurology #ALSfundraising #FightALS #ALSeducation #ALSprevention #ALSadvocacy #ALSimpact #ALSsurvival #ALStherapy #ALSawarenessmonth #LivingwithALS

[jaxracing]

The 2023 season got off to a good start for me this year: Two third place finishes and one fourth place finish. What a great weekend competing against friends. New personal record of 1.23.2 and I know where that extra second is. Just need the practice. Continued thank you to ProAuto for thier work on the car and Racing for ALS and Altruistic Joe Coffee for their support. The newest contingency for Spec E30, The Gil Barakat Commemorative contingency of $100 and Altruistic Joe Coffee, was awarded to Andrew Agurkis for his sixth place finish during Saturdays race. #coffee #coffeetime #coffeelover #cafe #coffeeshop #coffeeaddict #coffeelovers #coffeegram #Altruisticjoe #als #alsawareness #lougehrigsdisease #amyotrophiclateralsclerosis #endals #racecar #racing #cars #motorsport #car #race #carsofinstagram #carporn #bmw #becauseracecar #m #racecars #speed #trackcar #proautosc https://www.instagram.com/p/Cnkol15Li68/?igshid=NGJjMDIxMWI=

[als-lou-gehrig-disease-awar-blog]

Hope for a cure ALS Lou Gehrig Disease Awareness T-shirt  ---> http://bit.ly/2IqtnsN

Join us in wearing blue and help promote ALS Lou Gehrig Disease awareness in your community.

ALS Lou Gehrig Disease awareness support t-shirt. Purchase this t-shirts and we guarantee it will exceed your highest expectations!

[nakeya52]

Amyotrophic lateral sclerosis notes #lougehrigsdisease #als #mbbs #usmle #medicalmnemonics https://www.instagram.com/p/CNsutPFBE0D/?igshid=w2o3f7r3anxs

[secretasagrado]

Para mí, vos eras única #straighttomyheart #lougehrigsdisease #unattainable #notlikeyou #worse #pleasebaby #enough #compliments #imblushing #luckyme (at Córdoba, Argentina) https://www.instagram.com/p/CJ8pPBih_Et/?igshid=tx8272puok4z

[smoothfunfacts]

Smooth Fun Fact #1114: In 2014, Smooth was twice nominated to participate in the Ice Bucket Challenge, a dare to dump a bucket of cold water over his own head, to promote awareness of amyotrophic lateral sclerosis. (Bonus Fun Fact: Balancing both family and work obligations, Smooth never found the time nor motivation to perform the presumably chilly and uncomfortable act. Extra Bonus Fun Fact: Always one to stump for a worthwhile cause, Smooth feels guilty for not requesting donations for the horribly debilitating disease by creating a 10-second, self-shower, viral video.)

[wholecarenetwork]

HT 2.0: 30 in 30 with Hope Loves Company

[mybookbath]

How do you feel about reading heartbreaking memoirs? You know, the ones that should come with a box of tissues. Dance With Me To The End by Alison Acheson is one of those books. But don’t let that stop you from picking it up. It is a profoundly honest and intensely personal story of a woman who cares for her husband after the devastating terminal diagnosis of ALS. Marty, age 57, was given a preliminary diagnosis of ALS by his family doctor. Seven weeks later, the diagnosis was confirmed by a neurologist. Ten months and ten days later, Marty passed away. Alison, the author of this book, and Marty’s wife of twenty-five years, kept a journal as a way to navigate the overwhelming state of her mind and soul. . . . . . . . . . #alisonacheson #als @alisonacheson #booksandbeans #lougehrigsdisease #cureals #booksandblooms #booksandflowers @touchwooded #pagesandpetals #pinkvibes #booksandcoffee https://www.instagram.com/p/B9hvmZHHSmv/?igshid=81wcoz4yxnjt

[stitchmonkee-blog]

May is ALS Awareness Month. . . Specializing in Cause Awareness Damn It Dolls and Bracelets - handmade with ❤️ for those in need. . Check out other options available in my shop link in my bio . . . . . #lougehrig #alssucks #disease #getalittle #regrann #lougehrigsdisease #stephenhawking #raffleforrafa #osyb #cureals #documentary #osybforals #alssupport #life #oldsoulyoungblood #family #support #alsfoundation #amsterdamcityswim #stitchmonkee #rafflefortreatment #alsawareness #repost #givealittle #icebucketchallenge #love #gofundme #alschallenge #biggerthanmedoc #als (at Solon, Ohio) https://www.instagram.com/p/ByDj6OuhXOX/?igshid=32c22bgemq37

[supportsmallbiz]

🌟Because you are doing your best🌟 . . . #bohobabe #bossbabequotes #bossbaby #cancer #lupus #leukemia #arthritis #widow #aids #lougehrigsdisease #specialneedsparent #mommy #madre #parents #raredisease #uncurabledisease #lymedisease #crohnsdisease #ibs #stressrelief #stressedout #newlywed #newhome #abuelita #grandmas #furbaby #toddler #backpain (at Kansas City, Kansas) https://www.instagram.com/p/Buz-vQzHaAw/?utm_source=ig_tumblr_share&igshid=fmgncld8uiqh

[als-lou-gehrig-disease-awar-blog]

I have so much left to say to you ALS Lou Gehrig Disease Awareness

Join us in wearing blue and help promote ALS Lou Gehrig Disease awareness in your community. 

[stwb]

Jan 30th!! I will be headed up with @chucktreece & @milton.roy for the @therealjaysaun ”Kill Ya Boss” record release party. It’s also an important night bc it’s a fundraiser for our friend Billy who has ALS Make sure you come out Jan 30th and of you can’t make it - hit the go fund me!! #Repost @omertamia ・・・ Our fam in Boston has set up a benefit hip hop show, auction and Go Fund me account for our friend Billy who has recently been diagnosed with Lou Gehrig’s disease...please scroll to the right to see artist flyer and Go Fund me info for Billy...any help is appreciated on his behalf!!! #hiphop #boston #omerta #omertamia #benefit #benefitshow #als #lougehrigsdisease #slaine #jaysaun #bostonhiphop (at Great Scott) https://www.instagram.com/p/BsJBEFBFFfNBIckHT7W2IfY32CFInWG-qTJY2Q0/?utm_source=ig_tumblr_share&igshid=3zjn06dtfkhf

[sitstillshutup]

On Other Sites --ALS Newsletter, Exercise and ALS, Two New Movies About ALS Warriors and Other Resources

On Other Sites –ALS Newsletter, Exercise and ALS, Two New Movies About ALS Warriors and Other Resources

Prof. Stephen Hawking with David Fleming, manager of the Intel Innovation Open Lab in Ireland (center), and Martin Curley, vice president of Intel Labs Europe. credit: Intel Free Press// Wikimedia Commons

For those with ALS, loved ones with ALS, or just interested in knowing more about ALS/MND/Lou Gehrig’s Disease, you will want to check out ALS News Today and subscribe.

The latest installment…

[rjbailey]

Reposted from @parksrecmemes Bragger... *this* in the second box S6:E4 "Doppelgängers" #parksandrec #parksandrecreation #parksandrecmemes #parksandrecbloopers #pawnee #parksnrec #parksandrecedit #nbcparksandrec #parksandrecedits #parksandrecquotes #parksandrecreationmemes #parksandrecrp #parksnrecedit #parksnrecreation #parksnrecmemes #melindacohen #leslieknope #leslieknopequotes #leslieknopeapproved #leslieknopeaffirmations #amypoehlersmartgirls #amypoehler #amypoehlerquotes #amypoehleredit #lougehrig #lougehrigsdisease #diabetes #eagletonian @melinda__c_private @amypoehlersmartgirls- #regrann https://www.instagram.com/p/CHixG1Phq4P/?igshid=x6rjr9vyc8eh

[alslougehrigsdiseaseawareness]

'First Step' Mass. Research Turns Off Key Gene In ALS That Runs In Families | CommonHealth

See on Scoop.it - #ALS AWARENESS #LouGehrigsDisease #PARKINSONS

The method uses small molecules called "micro-RNAs," delivered by a virus into the spinal fluid, to block a gene key in the fatal nerve disease ALS, also known as Lou Gehrig's disease.