May
30

Coping With Multiple Sclerosis Pain

Posted by admin Comments (0)

Not too much is talked about in relation to the pain suffers of this disease experience. Here is a good bit of information about that.

Article by Mike Selvon

When most people think of multiple sclerosis, they think of a disease that causes symptoms of weakness and motor problems – not pain. However, the vast majority of sufferers report various degrees of multiple sclerosis pain.

The National Multiple Sclerosis Society reports that almost half of all people with MS are troubled by chronic pain. In this article, we’ll examine medicines and techniques that people with multiple sclerosis can use to ease their discomfort.

MS pain can affect several areas of the body at a time and get worse or better for no apparent reason. Because MS attacks the body’s central nervous system, messages from the brain can become skewed.

With MS, the nerves are too active and send pain signals without reason. There are different types of MS pain. Acute MS pain can come on suddenly and disappear just as quickly. While intense, these attacks are usually brief in duration.

Trigeminal neuralgia or “tic doloureux” is a stabbing pain in the face that can be brought on by facial movements like chewing, yawning, sneezing, or washing your face. People with MS typically confuse it with dental pain.

Most people can get sudden attacks of pain that can be triggered by touch, chewing, or even brushing the teeth. Lhermitte’s sign is a brief, stabbing, electric-shock-like sensation that runs from the back of the head down the spine, brought on by bending the neck forward.

Some MS pain can be chronic. Spasticity can lead to muscle cramps, tight and aching joints, and back or musculoskeletal pain. These chronic pain syndromes can often be relieved by anti-inflammatory drugs, massage and physical therapy.

For the most part, however, MS pain can’t be effectively treated with aspirin, ibuprofen, or other common over the counter pain reliever medications or treatments. In many cases, the treatment of choice is one of a range of anticonvulsant medications, such as Neurontin and Tegretol.

The side effects of these drugs can also include low blood pressure, possible seizures and dry mouth. They can also cause some weight gain.

Some patients, however, still haven’t found the right drug and the right dosage to control their multiple sclerosis pain. Scientists involved in MS research are currently examining the possibility of using Botox as a painkiller. The anti-wrinkle injections have shown promise in helping to control some types of MS pain by temporarily paralyzing a nerve or muscle.

This method has already been used by some MS clinics to manage spasticity and bladder problems. The biggest drawback is that Botox can only be injected into a limited area.

Finding a treatment for multiple sclerosis related pain can involve some trial and error. Patients should remember that they must be active in the process. If patients follow a proper diet, exercise regularly and monitor their symptoms, then doctors can prescribe a treatment regimen that will relieve the multiple sclerosis pain and help them to live a normal life.

About the Author

Enrich your knowledge further about the multiple sclerosis pain from Mike Selvon portal. We appreciate your feedback at our muscular dystrophy blog where a free gift awaits you.

Related Multiple Sclerosis Society Articles

May
30

What Is Multiple sclerosis

Posted by admin Comments (0)

Here is an informative discussion explaining multiple sclerosis.

Article by Groshan Fabiola

Multiple sclerosis is a rather unknown disease, because it does not affect many people. However, multiple sclerosis is a very hard medical condition. The reason is because when you suffer from multiple sclerosis, the patches of myelin or the fibres of your nerves are damaged. Multiple sclerosis affects the nerves of your eyes, spinal cord or brain.

This disease, multiple sclerosis actually refers to the number of sclerosis areas that are a result of the demyelination of your nerves. Multiple sclerosis affects young adults, with ages between twenty up to fourty years old. Multiple sclerosis affects more women then men. The number of women affected by multiple sclerosis is actually twice of the number of men that suffer from multiple sclerosis. In multiple sclerosis, there are periods of flare- ups and periods of remission. Actually the first type of multiple sclerosis is called relapsing- remitting. However, this is only the beginning of multiple sclerosis. In time, this condition gets even worse. The second stage of multiple sclerosis is second progressive. The third type of multiple sclerosis is first progressive. For the first two multiple sclerosis types, there are drugs that can change the course of the disease, multiple sclerosis.

Multiple sclerosis presents a mistery that people have not been able to solve yet. What causes multiple sclerosis is still unknown. One of the explanation that doctors have given us is that multiple sclerosis may be caused by a virus. Another theory is that an antigen, of unknown origin is the cause of multiple sclerosis. What this antigen or virus do is to make your body attack its own tissues. Then, the auto immune system starts to fight against its own cells, causing inflammation and the distruction of the myelin patch and nerve fibres. This is what happens when you have multiple sclerosis. Genetics is thought to be another probable cause for multiple sclerosis. If someone in your family has had multiple sclerosis, you are more at risk of developing multiple sclerosis then others. Another cause for the development of multiple sclerosis is thought to be the environment. It appears that the first 16 years of your life are very important for multiple sclerosis. If you have lived in a temperate climate, chances are that you will develop multiple sclerosis. On the other hand, if you have lived in a tropical climate, that lowers the risk of having multiple sclerosis.

About the Author

We recommend you clicking this site http://www.multiple-sclerosis-center.com for more multiple sclerosis subjects like multiple sclerosis information or multiple sclerosis diagnosis

May
28

MS Diagnosis, Medical Management, and Rehabilitation Treatise

Posted by admin Comments (3)

Get the medical information you need to understand multiple sclerosis, how it is diagnosed, how it is managed, and what rehabilitation measures are recommended.

Multiple Sclerosis: Diagnosis, Medical Management, and Rehabilitation

Contents: History; Pathology and Pathophysiology; Risk Factors and Theories of Causation; Diagnosis, Signs and Symptoms, and Classification; Treatment; Symptom Management and Rehabilitation; Societal Issues; Multiple Sclerosis in the Community.

List Price: $ 195.00

Price: [wpramaprice asin="1888799358"]

[wprebay kw="multiple+sclerosis+diagnosis" num="0" ebcat="-1"] [wprebay kw="multiple+sclerosis+diagnosis" num="1" ebcat="-1"]

More Multiple Sclerosis Diagnosis Products

May
27

Questions And Answers On Multiple Sclerosis And Treatment

Posted by admin Comments (0)

Shelley asks…

Multiple Sclerosis … What treatment “Alternatives” have you tried?

….and were they recommended by other sufferers or carers?
Dahlia, I heard that too. For obvious reasons many people avoid it but for some it does help with pain relief.
0726 Sorry, can’t comprhend the name but ..HI. Thanks for your research and detailed input. Much appreciated.
Jo..Swimming I know helps strengthen the muscles, good obvious and safe choice. Vitamin D and oily fish? Can you say why please?
Raymond.. Hey there. First, I wouldn’t laugh at anyones attempts to improve their condition and your medicines are the kind of alternative therapy I need to learn more about. In what way do they help?
hey yorkie..thanks for your input (?) but if you dont know any MS sufferers, then obviously you cant answer the question… and by the looks of it, you didn’t read it either.
OK, I’m going to put this to vote…and rather than vote for your own answer…I’d like you to actually read other’s comments and vote for their viability PLEASE…there could be comments/ suggestions here that you may not have tried yourself, thtat’s really the essence of the question…TO HELP.

Thank you all.

admin answers:

Heard that smoking certain stuff helps to relax and ease any pain…
It is not legal though…

Ken asks…

which doctor is the best for the treatment of {multiple sclerosis }plz send me the name and contect number?

admin answers:

Where are you looking for a doctor…I could tell you about my doctor, who is wonderful. Try and ask a doctor or nurse who they would see…or wouldn’t!

Powered by Yahoo! Answers

May
27

Questions And Answers On Quality Of Life With Multiple Sclerosis

Posted by admin Comments (0)

Shelley asks…

Stem Cell Survey…….?

I need this info. for a research paper for my class. I would appreciate it if you could take a couple minutes to do it. Thank you!

Stem cells are a unique type of cells that can specialize into just about any type of cell in the body resulting in a huge potential in the medical world. They can be found in places in the body like in bone marrow (called adult stem cells) or obtained through the destruction of an embryo (called embryonic stem cells). Note: Embryonic stem cells are able to specialize into a wider variety of cells than in adult stem cells resulting in a wider potential of cures for diseases and conditions.

1. Are you male or female?

2. What is your age?

3. How much do you agree with the following statements? Note: Answer strongly disagree, disagree, neutral, agree or strongly agree to the following,

a)It is ethical to use embryonic stem cells for medical purposes.

b)Just because we never seen any cures, doesn’t mean we should give up on stem cell research.

c)I believe that stem cell procedures used today can improve the quality of life of others.

4. Do you believe that stem cell research will eventually lead to a cure of serious medical conditions such as Parkinson’s, Diabetes and Multiple Sclerosis?

5. Do you think that the government should fund stem cell research?

6. Do you think it would be more beneficial to study adult stem cells rather than embryonic stem
cells?

7. Is the potential benefit of embryonic stem cell research worth the embryo that we are sacrificing?

admin answers:

M60
a) strongly agree
b)strongly disagree
c) sronngly agree
4 yes
5 yes
6 no
7 yes

Wayne asks…

Does this man deserve to go to jail?

WINNIPEG – A medical marijuana crusader with multiple sclerosis says he will likely die in prison now that a Winnipeg jury has found him guilty of selling pot to clients across Canada who suffer from chronic pain or terminal illnesses. “I’m ashamed to be a Canadian,” Grant Krieger, 53, said Wednesday after a jury found him guilty of trafficking.

The Calgary resident said the verdict shows how little the country cares for the sick and dying and represents a wasted opportunity to make a statement. “They had a chance to change the law,” he said. “It’s a victimless crime they’ve convicted me of. Now they’re gonna kill me when they put me in jail.” Krieger admitted he broke the law but was seeking to be acquitted on sympathetic grounds.

Krieger – who runs the Grant W. Krieger Cannabis Research Foundation of Canada – has been battling progressive MS since 1978 and says his only relief comes from smoking and ingesting cannabis. He admits selling pot to dozens of people across Canada but insisted there is a major difference between him and a garden-variety drug dealer.

Krieger said his many customers suffer from chronic pain, disease and even terminal illness and have come to him looking to improve their quality of life. Krieger testified in his own defence earlier this week about how his disease had driven him to the point of attempting at suicide before he started using marijuana. “Without it, I wouldn’t be standing here before you today,” he told jurors. “I’d be in a wheelchair or dead right now.”

http://cannabisculture.com/articles/5299.html

admin answers:

It’s an abomination! It should be considered a medical necessity for individuals with chronic pain or terminal illness, (as are pain medications,) it IS a victimless crime, and it should be legalized! All citizens should be outraged, not just the ill and suffering!

There but for the grace of God….

Powered by Yahoo! Answers

May
26

Questions And Answers On Multiple Sclerosis Depression Anxiety

Posted by admin Comments (0)

Mike asks…

Sigh….Anxiety/Depression medication question…celexa…paxil?

So, im going to keep the story short, im having major anxiety issues, last 3 years, tough to leave the house, fear of nausea and panic attacks.

took Celexa for 4 mo’s , it literally did nothing for me….i felt the exact same…..the only thing that i noticed was i started to get minor insomnia…..

i quit taking that crap. it was 10 mg for 1.5 mo’s , then 20mg for 3 ish.

i was off meds for about last 3 months and im starting to get depressed and i’m lashing out at my dad constantly (he’s disabled and has a diseaes, multiple sclerosis), and yes of course, i definately see the error of my ways, it makes me cry at times because i yelled at him and he doesn’t deserve it.

anyways i hav more stress at the moment than any point in my life, i went from 3 years of not leaving the house and bad anxiety and nausea constantly, to moving to CA all of a sudden cuz my grama Ruby died, and now i have to clear this house out, sell it, road trip with my disabled father in 2 vehicles, buy a house in idaho, then finally get back to my own life and dreams (working for a year or 2 saving every single penny eanred (living with parent of course) and buying a vehicle, moving to mexico where i lived for 3 years.

so my life was horrible but i still had my dream, now even the dream is being put on hold for longer, because of all this extra responsibility, the worst part is….everything above mentioned, must be done by me and only me, no one else is here but my dad and he is in a wheelchair.

point is, i went to the DR today, and he perscribed me Paxil, i think 10mg for the first week and bumping it to 20mg so i can “be where i need to be at very quickly” says the DR. i guess he understands to some extent how much im going through (even though he didnt let me tell him everything, he was rushing it seemed)

so….i hear Paxil is the most sedating SSRI, which is awesome, because i didnt get a chance to tell him “i need something that sedates me enough to not have constant panic / nausea(thoughts?) but still enough to function…..work/school? i was thinking of a delivery job llike for pizza hut for a job. i could be alone most of my day and not have too much interactiopn except at doorways, which i could handle. is this stuff going to make me a zombie driver? :(

anyone know differences between celexa and paxil?? celexa didnt make me feel any different or anything at all….nothing. like it was a sugar pill or something. (minus the insomnia part)

admin answers:

Antidepressants function no better than a placebo in most patients, research shows. For each new drug, the drug companies would run a dozen studies to get two showing their drugs were a little better than placebo and submit those studies to the FDA. The other 10 studies wouldn’t get published, and they showed the drugs didn’t help depression or even made it worse. Furthermore, antidepressants are well known to cause manic episodes in people who have undiagnosed bipolar, possibly forever worsening the course of the illness. There is no way to know if you have bipolar or unipolar depression until you get mania the first time. Antidepressants may be worsening the course of depression also, in the LONG TERM (see “Anatomy of an Epidemic” by Robert Whitaker). Even the Abilify ad points out that antidepressants don’t work – that drug company wants you to take a much more toxic antipsychotic that will shave years off your life, because supposedly only 1/3 get better on antidepressants. Their own studies show that many more people must discontinue abilify due to akasthisia than get any benefit from the drug. Besides that, if you are an adult, you should know that most antidepressants will destroy your sex life, and in rare cases, it can be permanent. Most people won’t stay on the drugs long term because of this side effect, but then many people discontinuing the drugs get severe withdrawal symptoms that are much worse than the original depression and/or anxiety.

People will jump up and down and swear that they do help – Lots of “research” papers show that the meds work, but almost all are written by psychiatrists who are paid by drug companies to say that, and they must sign an agreement to not publicize any bad study results before they get their research grants, just in case they should get an attack of conscience (this is true of all corporate medication research). Patients often respond to placebo effect, or naturally cycle out of their illness, and there is no way an individual or their doctor could know if the drug helped them or not– that is why studies are required.

I;ll give you my anxiety tips – try these, and if they don’t work, consider seeing a therapist. Also, are you SURE that there is no one you can ask for help with all this stuff you have to do? Are you SURE??? Is there any spare cash at all to hire some short term help?

Generic anxiety tips (print them out):

Try turning the heat up in the house or dressing more warmly. It is hard to feel anxiety when you are too warm Hot baths work, and at work/school, you can try running hot water over your hands.

Avoid caffeine; it increases anxiety. Also, some cold remedies & other drugs can cause anxiety. Look for the “agitation in children” warning on the box. Adults can get problems too. For me, antidepressants caused agitation and panic attacks, and that is listed as a common side effect. Birth control, blood pressure, acne and sleeping pills & others often cause depression.

Try meditation tapes like progressive muscle relaxation or guided imagery. Try The Anxiety and Phobia Workbook; check the library. There are guided imageries in there, you could make a recording or get a friend to do it. I read mine into the computer using a program called Audacity (free) and digitally altered my voice so it doesn’t bug me. Free 15 minute guided imagery download at healthjourneys.com.

Go out with friends, and if you don’t have any, find a club to join and MAKE yourself go until you actually look forward to it. A little laughing helps reduce anxiety.

Exercise at least 1/2 hour a day, and anytime you feel really hyper or depressed. Exercise is a great mood stabilizer and cuts down on anxiety, research shows. Don’t do it a couple hours before bed, though, or you will be too hyped up.

Here are “sleep hygiene” tips. Go to bed and get up about the same time each day, even weekends. Don’t use your bedroom to watch TV and read and use the computer -just use the room as a bedroom Don’t do stuff that pumps you up right before bed, like exercising and using the computer. Wind down, instead – take a bath ? The light from the computer screen or TV wakes you up if you use them right before bed. Make the bedroom really dark, cover up the clock, even. Use a noise generator (makes wave sounds etc.) to cover up disturbing sounds. Try soundsleeping.com for free relaxing sounds downloads. Avoid caffeine in the afternoon and evening.

Put colorful happy things around the house, and let the sun in. Make a list of things that make you happy. Part of my list: A basket full of fluffy kittens, bread fresh from the oven, Fireworks popping on a warm summer evening, The first fireflies of the season, the scent of Jergen’s cherry almond lotion, The crisp sound of a saltine cracker breaking, fresh sheets on the bed, flicking a topwater plug out onto the still surface of a summer lake, etc. Use all your senses and read that list when you are breaking down. I also use familiar scents, like Jergens lotion, or vanilla or cloves. Scent can be comforting.

Work on time management if overwhelmed. Cut back on other responsibilities temporarily so you can spend more restorative time with friends and family. Ask for help. If there are people or situations that stress you , identify them and reduce them as much as possible.

Learn to breathe. Put your hand on your belly. Now breathe deep, and feel your belly move up in down. That is the right way to breathe. You are probably breathing up in your chest area, and that makes you more anxious. Now breathe slowly. Do a mantra in your head innnnnnnnnnn ouuuuuuuuuuut innnnnnnnnnnn ouuuuuuuuuuuuuuuuuut slowly breathing. Focus on whatever 2 words you want as you breathe slowly.

Look at an object, and observe everything about it for 5 minutes, then stretch that to 10, then 15 min as your gain experience. That’s a form of meditation.

Finally, are you catastrophising, always thinking of the WORST thing that could happen? Try to catch yourself doing this, then change your thinking to, what is the MOST LIKELY thing to happen – hardly ever is the worst going to happen. You can’t die of a panic attack, either.

Cognitive Behavioral therapy is the most effective kind of counseling. Try free computerized CBT at moodgym.anu.edu.au. Computerized therapy appears to be almost as effective as counseling, research shows.

All the best!!

Rachel asks…

Been diagnosed with bipolar, ocd, depression, etc…?

Over the years of my life I’ve been diagnosed with bipolar, severe ocd, severe hypochondria, depression, social anxiety disorder, & generalized anxiety disorder. I’ve also noticed that a lot of the time I have trouble understanding other people’s directions/I always seem to be confused by what should be the easiest task. I don’t really understand how to count money either. Do you think my mental problems can have an effect on my learning abilities? I’ve heard that there’s a link between bipolar and multiple sclerosis. Is that true? Also, do you think being diagnosed with all these disorders makes me crazy or just misunderstood? Thanks.

admin answers:

I’m sure mental problems have effects on learning abilities that is why in school people with mental issues are given, or at least should be given, the option of getting extra help when needed and are protected under the US Disability Act

Also consider that medications you might have been prescribed for these illnesses/disorders can also have side effects such as confusion and memory loss. One of the medications i took years ago gave me memory loss problems and it took me two years to get back to normal after stopping them.

I’m not sure if there is a link between bp and ms but recent studies have said so.

I don’t think crazy or misunderstood describes you. I think that it just shows that the psychological profession is always changing, definitions are always changing, and different doctors see things/analyze things differently. Don’t label yourself.

Powered by Yahoo! Answers

May
26

Questions And Answers On Health Multiple Sclerosis Symptoms

Posted by admin Comments (0)

Lynn asks…

Is it true that people with multiple sclerosis end up bed ridden? Is there a way to tame MS?

I am really praying that someday a cure will be found for multiple sclerosis.No one should have to suffer like this. Is it true that anyone with multiple sclerosis ends up bed ridden later? Isn’t there a way to tame symptoms?
There was this lady on Discovery Health Channel who says she has MS and that she saw how women are confined to wheelchairs, so she said she started working out and body building to combat MS and she is still walking 10 years later! and her MS is barely noticeable. Is it true that working out and running and walking will help people with MS to maintain mobility and combat having to be confined to a wheelchair or bed? This lady said she does this and this has helped.
I know another lady who has had MS for over 30 years and she can still do for herself.She is in a wheelchair but she can still do for herself and she stands too.
Why are some women with MS bedridden?Why are some MS sufferers lucky to escape becoming bedridden?Are there diff. types of MS?
I know MS occurs because the myelin sheath deteriorates from the nerve endings.Is it true that anyone with MS will eventually end up bedridden? Will working out and body building like that woman does combat MS symptoms?I notice that she is still walking and doing for herself 10 years later.She said she is determined not to be confined to a wheelchair like other MS sufferers so she started body building and she jogs/runs everyday.

admin answers:

Yes, there are different types of MS:

Benign
Relapsing-Remitting (most common form)
Secondary-Progressive (many cases of relapsing-remitting MS turn into this form after a number of years)
Primary-Progressive

The majority of MS sufferers do not end up bedridden. Studies have shown that 20 years after diagnosis, only approx. 15% MS-sufferers will be using a wheel-chair.

MS is a very individual disease, some people may have very few and mild attacks, others may have many severe attacks. Some may not have attacks, but grow steadily worse. Symptoms depend on what part of the brain and spine is damaged.

When a person is diagnosed with MS, no-one can tell him or her what the future is going to look like, what the symptoms might be and how the MS will affect his or her life. It’s a bit like crossing a road blindfolded and wearing earplugs, only the cars will not stop and you have no idea whether you’re walking on a low traffic or high traffic road.

Cindy asks…

Can Multiple sclerosis cause high blood pressure?

I’m 42 in good health, however the past month i was suddenly dx with high blood pressure. Along with that i was experiencing a warm sensation in my left calf and on the left side of my face including my lips, but only on the left side of my lips. My dr did an ultrasoud of my calf which was normal. I had a stress test doen which was also normal. Since my symptoms of the warm senstation (does not feel warm to the tough only feels warm inside) were only one sided my dr said that she would need to rule out Multiple sclerosis. Any thoughts? Thanks.

admin answers:

No, multiple sclerosis does not normally cause high blood pressure. I don’t know if your sensory disturbances are related to your sudden high blood pressure or if the two are completely unrelated, but it is not uncommon to start ruling out MS when someone has sesory disturbances. In the vast majority of cases it turns out not to be MS, though, but usually something relatively harmless.

Powered by Yahoo! Answers

May
26

Questions And Answers On What Is Multiple Sclerosis Symptoms Caused

Posted by admin Comments (0)

Nancy asks…

Are there any alternative to injections for Multiple Sclerosis?

I am newly diagnised with this disease. I hit my head really hard and suffered a concusion so I demanded and MRI to make sure the there was no internal damage caused. They found lesions on my brain and diagnosed me with MS. This was more than what I bargained for. I have no symptoms at all but they are sure I have it because Kaisers Neurology dept claims to be the best. They are having me research the meds to chose the one I will marry. I am 29 with 2 young children and I am total freaked out. Can I do something other than inject myself with one of the therapies that are offered. Has anyone had any success with naturally healing your MS. Please help!

admin answers:

All doctors claim to be great. No doctor brags about being slipshod or just plain mediocre. Identifying a lesion that is indicative of multiple sclerosis should be done at an MS Clinic where the neurologists specialize in it. Lots of people are born with lesions or develop lesions from migraines or other diseases and conditions. Having lesions does not mean that you have MS. I do not know of any reputable doctor who would diagnose MS on the basis of one MRI with lesions. I can’t think of anything less professional. I don’t think Kaiser even has an MS clinic. MS is diagnosed on the basis of having two attacks of MS separated by a designated amount of time as well as one or more MRIs and at least several other tests to rule out lyme and devic’s disease and MANY others. How anybody can come up with a diagnosis of MS when you haven’t had an MS attack is beyond comprehension. You need to contact the MS society and find a clinic with neurologists who specialize in MS and then get there. Three of the medications for MS are actually a dose of mild chemotherapy (the interferons) The only other medication that is on the market is Copaxone.There is absolutely no cure for MS, natural or otherwise. You need a second opinion before you do anything.

Bob asks…

Multiple Sclerosis (or any other nervous system disease) questions?

Alright, I started having sinus problems in December 2008, which everyone just thought was just an ear infection. But after 6 months to a year later, we found out that it was a sinus infection (which is still present now, actually). So, around the time the ear/sinus infection started, I began to have a lot of symptoms similar to M.S. I began twitching, especially when I lay down to go to sleep, tremoring/tingling feelings in the back of my head, arms, legs, stomach, neck…basically all over. I’ve also been feeling like I’ve been having some speech problems, but no one else seems to notice it, or if they have they haven’t said anything. So, I don’t know if I’m really having speech problems or if its just because I’ve been nervous lately. So, I’m really wondering what are the MAJOR symptoms of M.S. and how to determine if that’s the cause of if my sinus infection could be the root to the problem. A lot of the symptoms of M.S. are very similar to a lot of other problems and I’m just really confused and scared at this point.

admin answers:

Symptoms
Symptoms vary, because the location and severity of each attack can be different. Episodes can last for days, weeks, or months. These episodes alternate with periods of reduced or no symptoms (remissions).

Fever, hot baths, sun exposure, and stress can trigger or worsen attacks.

It is common for the disease to return (relapse). However, the disease may continue to get worse without periods of remission.

Because nerves in any part of the brain or spinal cord may be damaged, patients with multiple sclerosis can have symptoms in many parts of the body.

Muscle symptoms:

•Loss of balance
•Muscle spasms
•Numbness or abnormal sensation in any area
•Problems moving arms or legs
•Problems walking
•Problems with coordination and making small movements
•Tremor in one or more arms or legs
•Weakness in one or more arms or legs
Bowel and bladder symptoms:

•Constipation and stool leakage
•Difficulty beginning to urinate
•Frequent need to urinate
•Strong urge to urinate
•Urine leakage (incontinence)
Eye symptoms:

•Double vision
•Eye discomfort
•Uncontrollable rapid eye movements
•Vision loss (usually affects one eye at a time)
Numbness, tingling, or pain

•Facial pain
•Painful muscle spasms
•Tingling, crawling, or burning feeling in the arms and legs
Other brain and nerve symptoms:

•Decreased attention span, poor judgment, and memory loss
•Diffulty reasoning and solving problems
•Depression or feelings of sadness
•Dizziness and balance problems
•Hearing loss
Sexual symptoms:

•Problems with erections
•Problems with vaginal lubrication
Speech and swallowing symptoms:

•Slurred or difficult-to-understand speech
•Trouble chewing and swallowing
Fatigue is a common and bothersome symptoms as MS progresses. It is often worse in the late afternoon.

Powered by Yahoo! Answers

May
26

Questions And Answers On What Is Multiple Sclerosis Yahoo

Posted by admin Comments (0)

David asks…

what does Multiple Sclerosis feels like?

Hi yahoo im only 19
I have a question for u guys about Multiple Sclerosis.
well I have tightness feeling on my face around and just a little headache ones a day ( just normal headaches but different pain each day )

i like to know what are the symptoms of MS and is it really painful ? and Causes
and do u think i have MS ?

admin answers:

Hi Jisu, There are more than fifty symptoms that someone with MS can potentially get. MS can affect the emotions, perception, cognition and physical movement. I have had this disease for twenty years. There is no such thing as a classic case of MS or a particular way of feeling if you have this disease although many of us experience exhaustion, tingling and numbness. Beyond that the disease varies tremendously from person to person. Some people experience pain and others have no pain at all. No one knows what causes MS and there is no cure.

May I suggest that you go to the National Multiple Sclerosis Society website at http://www.nmss.org
The website is superior to any other. Hope that you do not have MS. The very best of luck to you.

Lisa asks…

DISABILITY and what is the law concerning multiple sclerosis and parkinson desease?

I had been diagnosed with multiple sclerosis 4 years ago and recently I had been diagnose with Parkinson disease on top of the other. I also have major depression concerning my health. The state of Nevada is saying that I do not have a disability.I have been denied twice concerning this issue. Is this true since I can hardly walk and use a chair and have trouble with my arms and hands. I constantly drop items and fall down alot. I wish that I could work, also my advocate will not return my calls. Can someone give me their personal advice. Please fill free to coment me as I need to know the outcome. Thank- You
Elrod
elrodmiller@yahoo.com

admin answers:

Elrod,
It is a difficult process. The fact is, It is easier for a drug addict or an alcoholic to receive SSDI than a person with MS.Part of the problem is that most of the MS symptoms are “invisible” I know that every person with MS has heard at one time “you look ok to me”
I know only one person with MS that was approved the first time..
She hired an attorney that specialized in disability claims, her Dr carefully documented all of her issues and she was lucky..
Good Luck and hang in there

Powered by Yahoo! Answers

May
26

Questions And Answers On Multiple Sclerosis And Treatment

Posted by admin Comments (0)

Paul asks…

multiple sclerosis, is the treatment a cover up?

Does the thought that the treatment does not need expensive drugs or operations, and that all the research money would disappear, keep sufferers from CCSVI treatment.?

admin answers:

Immunotherapy is an immune modulating therapy that may help to slow down the disease or reduce the frequency of relapses. Steroids can help to reduce the severity of attacks. Antidepressants may be used to improve behavioral symptoms such as depression and mood swings. Medications can be prescribed to reduce urinary problems, and to minimize muscle spasticity.

Complementary treatments may be used together with conventional medicine or as an alternative. However, home treatment of MS is not recommended. Should you decide to explore alternatives to conventional medicine, consult a qualified homeopath that would be able to monitor your progress and ensure that you are receiving the correct treatment.

Herbal remedies for MS would typically include ingredients that would address symptoms which are most troublesome for the individual.

Some commonly recommended herbs include Avena sativa (nerve tonic), Lavendula angustifolia and Melissa officinalis and Passiflora incarnata (stress and anxiety), St John’s Wort (depression and nerve tonic), as well as various herbs for bladder problems, constipation and general inflammation. Biochemic tissue salts can be helpful as a safe anti-inflammatory and antispasmodic and to relieve cramps, improve circulation and support nervous system health.

You may get more info here http://www.healthherbsandnutrition.com/remedies/m/multiplesclerosis.htm

Kylee asks…

Multiple sclerosis Treatments Best & Worse Or Alternatives?

I was just diagnosed wit MS about a week and a half ago and I am nervous having to choose which treatment to use I have read on them but the side effects and the injecting process scare me?

admin answers:

I’m a nurse with MS. I spent a great deal of time talking with my doctor and reviewing the literature to decide which drug was best. Copaxone is a shot everyday but no flu-like symptoms. Because I have two very active children (2 and 4), along with still working part-time, I chose Copaxone so as not to have flu-symptoms.

Copaxone is an expensive drug, but my insurance covers it, so I pay $15/mo. This includes the meds prepackaged in their syringes and the alcohol wipes. You can get an autoinjector free from them, makes it a little easier to psych yourself up to do the shot (I can give a shot to anyone but am a complete baby about doing it to myself). They’ll also give you a child proof container free if you need it (holds 1 mo. Supply)

There are days I don’t want to “shoot up”, and in all honesty I skip a day about once a month, a small reprieve. But I know I will get through it, even if I don’t get used to it. A big incentive for me choosing Copaxone was having 2 preschoolers. I don’t want to have a detrimental flair and not be able to care for them.

I was at an MS symposium in March, as far as any oral meds for MS there are a few, but they are still a few years down the line. There are 3 in Phase II Trials (to evaluate the effectiveness of the drug for a particular disease and to determine common short-term side effects and risks). There are 3 in Phase III Trials (to evaluate the overall benefit-risk relationship of the drug and provide a basis for physician labeling).

And some alternative drug info…
Low dose naltrexone (LDN) just finished a Phase III clinical trial for use in MS last Nov. But articles were already coming out 2 mos. Before that saying more clinical trials are still needed for use in MS.

There are several clinical trials at various stages studying antibiotic therapy and MS.

Reports published in 2006/2007 showed initial benefits with Sativex (cannabis). However, reports published in April from the latest trials showed Sativex was no more effective in treating MS pain than a placebo given to half the patients. It has been approved for use in Canada and is still development in Europe and the US.

Here is a general info link:

http://www.medicinenet.com/multiple_sclerosis/article.htm

An alternative therapy link:

http://www.medicinenet.com/alternative_therapy_for_multiple_sclerosis/article.htm

The National MS Society:

http://www.nationalmssociety.org/index.aspx

And lastly, I also like the “MS for Dummies” book. For me MS was the devil I knew what with my mom having it. But the book was a good reference for my husband. Plus there were tips I hadn’t heard of or thought about.

Powered by Yahoo! Answers