Reversing Multiple Sclerosis Neuropathy or MS Nerve Damage Using Vitamin B12?

When it comes to Multiple Sclerosis neuropathy or MS nerve damage
is there anything natural or alternative that can help to reverse the
damage to the nerves, or at least reduce the problems with the
nerves functioning?

That is one of the big questions, when it comes to Multiple Sclerosis.

I have been searching for something myself, when it comes to
reversing or at least reducing the peripheral neuropathy or nerve
damage or nerve function problems, which my doctor has told
me for several years that I have had a major problem with,
since I was diagnosed with Multiple Sclerosis.

I am excited to say that I think I found something that is
helping to reduce the nerve function problems in my legs,
feet, hands, and arms in many ways.

What is it that can help??

Vitamin B12 is a natural way to help repair nerve damage...at least
that is what information I found, while doing my own research for me.

I am so excited to let you know about what I am finding
that taking extra of vitamin B12 is helping with, when it
comes to Multiple Sclerosis neuropathy or MS nerve damage.

I'm not totally sure that taking the higher doses of B12 will reverse
the nerve damage totally or the peripheral neuropathy, just yet, since
I have only been taking extra vitamin B12 myself for 2 weeks, but
since I started taking the extra B12, I have already found that my
legs and feet and hands are functioning so much
better than they have for years.

If you are at least curious as to how I have found that taking
the extra B12 is helping me with nerve function, then...

Click on either link to find out more -- Multiple Sclerosis neuropathy or MS nerve damage

If you have found this information to be helpful to you, or if you have anything else that you would like to add, about this topic, leave us your comments and let us know! We would love to hear what you think about this topic!

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B12 and MS: What form of B12 Helps Reverse MS Nerve Damage?

When it comes to B12 and MS, can taking B12 help to reduce or even reverse MS nerve damage?

I am so excited to tell you about what I am finding with taking higher doses of vitamin B12, how it is helping with reducing, or maybe even reversing MS nerve damage and increasing how well my nerves are functioning with Multiple Sclerosis.

I have had several problems with my nerves not functioning as they should because of the more severe effects of Multiple Sclerosis attacks on my body, which taking the higher dosage of vitamin B12 has been helping to reduce.

Taking a higher dose of vitamin B12 has been helping in several ways, but taking the B12 only helps if you take it in certain forms and in combination with B complex.

Click on the link to read more -- B12 and MS

If you have found this information helpful or if you would like to add anything further, leave us your comments! We would love to hear what you think about this topic!

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MS CCSVI: Dr. Hubbard connects Multiple Sclerosis to CCSVI theory

Check out this video about a neurologist's point of view of Multiple Sclerosis and MS CCSVI, after his son is diagnosed with Multiple Sclerosis.

This video discusses another way of doing a "study" for people, diagnosed with Multiple Sclerosis in connecton with the blood flow blockages to the veins in the the neck or the upper chest that has been called chronic cerebrospinal venous insufficiency or CCSVI.

This video discusses another way to classify studies for MS and CCSVI, as data collection, that focuses more on the venous insufficiency rather than the Multiple Sclerosis.

This way of viewing the blood flow blockages appears to allow for legitimate funding for the study, that is being done, while making it possible for more of the costs of testing and having the procedure done to open up blood flow blockages to be covered by insurance, rather than making it so the the MS patients have to cover the cost of the testing and the procedure.

This is the first study that is being conducted in this way with MS patients and the venous blood flow blockages, but there is the potential for this type of study to become a way of doing more studies throughout the USA, making it possible for doctors to collect more data, scientifically, while allowing MS patients to be able to be tested and evaluated for CCSVI, as well as actually having the procedure done too.

Click on the link below to watch the video for more details.

http://www.komonews.com/home/video/106175483.html?tab=video

Interesting, but only available in San Diego, CA area at this point.

Have you heard about this, yet?

Please leave your comments, as to what you think about this video or if you know anything else about this.

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Multiple Sclerosis Bladder Control Problems and MS Bladder Infections

Multiple Sclerosis bladder control problems and MS bladder infections can create many problems for people, diagnosed with Multiple Sclerosis.

MS bladder control problems can include:

* Bladder Not Draining

* Bladder Leaking

* Night time Incontinence

* Stress Incontinence

* More Frequent Bladder Infections

There are alternative and natural ways to help combat bladder infections with MS.

Click on the link to read more -- Multiple Sclerosis bladder

If you have found this information to be helpful or if you would like to add any other comment related to Multiple Sclerosis, please leave us your comments, so that we can better assist you.

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MS Sleep Apnea Pillow To Aid With Full Face CPAP Mask

The MS sleep apnea combination and the use of a continuous positive airway pressue or CPAP mask can take some getting used to.

Although there are many different kinds of CPAP masks and machines on the market, there are 2 main types of CPAP masks.

One covers just the nose and uses a chin strap to keep the mouth closed, so that the person wearing the mask breathes through their mouth, while they sleep.

The second kind covers both the mouth and the nose, so that if the mouth is kept open while you sleep, the CPAP mask still works at helping to keep the airway open, while the person sleeps.

The CPAP mask that cover just the nose is typically tried first, by the sleep clinics to see if it is helpful to the wearer of the mask, but the problem is that if the mouth is not kept closed while you are sleeping, then the CPAP mask is not effective in keeping the airway open during sleep.

The CPAP mask that covers both the nose and the mouth is used for people who sleep with their mouth open while they sleep or for people with allergies, which cause sinus congestion, which can restrict the person from breathing through their nose only while they sleep.

The nose only CPAP mask is easier to keep sealed while moving around while you sleep, especially if you move around while you sleep.

The nose and mouth CPAP mask doesn't seal very well, if you move around more when you sleep.

Because I tend to get more violent leg spasm, because of the effects of Multiple Sclerosis, whenever I try to roll over when I am sleeping, I have trained myself not to roll over while I sleep.

Adding teh MS sleep apnea combo, and sleeping with the sleep apnea mask and machine, and getting comfortable, while you are sleeping becomes even more of a challenge

In spite of the fact that I don't roll over in my sleep, I do tend to move my head from side to side, while I am sleeping.

If you tend to sleep on your side or if you tend to move your head from side to side, while you are sleeping, this can shift the full face mask enough that the mask doesn't seal as it should, or it can blow air in your eyes, which can wake you up many times a night.

There are adjustable straps on the CPAP masks to loosen or tighten to make a better seal with the mask to prevent major leaking to help the mask work better.

One of the problems you can have with tightening the straps is if you make them too tight so that you either get frequent headaches in the morning or you end up with marks on your face from the mask being too tight.

One of the things that I have found, that helps, if you were a full face CPAP mask (the mask that covers the nose and mouth) is to use a CPAP neck pillow.

The neck support CPAP pillow, that I found that works very well at supporting the neck and allowing moving your head from side to side or for sleeping on your side when you sleep with a full face CPAP mask was one I found online.

Once you go to the website for the CPAP neck pillow, scroll to the right of the screen.

If you are interested in finding out more about the CPAP neck pillow or where to purchase one for yourself that I found that works --

Click on the link -- sleep apnea CPAP neck pillow

If sealing the CPAP mask becomes more of a challenge, as far as keeping the positive pressure air from blowing into your eyes, there is a small additional comfort piece of soft plastic or rubber that can be purchased to help reduce this problem.

To find out more about this or to purchase one for yourself --

Click on the link -- CPAP comfort Pad

Click on the link to find out more about -- MS sleep apnea

Note: I do not gain anything from you going to or purchasing from these sites, I merely want to help you who have MS sleep apnea to find ways to reduce the problems, which tend to accompany wearing a CPAP mask, for alleviating the problems often associated with sleep apnea.

If you have found this information to be helpful or if you would like to add anything else, please leave us your comments.

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Reducing Multiple Sclerosis Infections Using MS Diet Changes?

Multiple Sclerosis is known for weakening the immune system, but can using MS diet changes help to greatly reduce the infections, the majority of Multiple Sclerosis patients tend to struggle with?

Alkalizing the pH of the body can help in a big way for reducing the severity and frequency of the majority of infections when it comes to Multiple Sclerosis.

To read more click on the link -- MS diet

We would love to hear from you, please leave us your comments or tell us about your concerns with Multiple Sclerosis!

We are here to help you to find out more about MS and to help you find ways for you to find relief to the effects of Multiple Sclerosis!

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Reducing Spasticy Multiple Sclerosis Can Include As MS Symptom

Spasticity Multiple Sclerosis patients tend to experience can include what is called spasms, tremors, twitching, or tics.

But what is Multiple Sclerosis Spasticity or MS Tremors, MS Spasms or
MS Twitching anyway?

Spasms, tremors, twitching or tics are different names for the uncontrollable movement of the arms, legs, hands or feet, which are often a big problem for the majority of people, who are diagnosed with Multiple Sclerosis each year, in many different countries around the world.

Twitching, spasms or tremors are like a knee jerk reaction, when the doctor hits your knee with a small hammer to test your reflexes, but in the majority of the cases of Multiple Sclerosis the spasticity is more out of control and more random and can occur too frequently.

Spasticity Multiple Sclerosis patients may experience can be mild to severe and can be more frequent or only occur every so often.

The spasticity can be so severe that it can almost throw you on the floor when it happens, if you don't hang on to something.

What can help to reduce the spasticity MS patients can experience?

Click on the link to read more -- spasticity Multiple Sclerosis

We would love to hear if you have found this information helpful to you.

Leave us your comments!

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Dirty Electricity or Electromagnetic Radiation Causes Multiple Sclerosis?

When it comes to what causes Multiple Sclerosis, there is much
speculation, as to its causes.

But, when it comes to studies and researches over the last
several years into the effects of electrical disturbances and
the effects of dirty electricity on Multiple Sclerosis there
are a few reports, which actually appear to verify their
more drastic effects on causing the symptoms of
Multiple Sclerosis to become much worse.

Click on the link below to find out more about how
dirty electricity and other electromagnetic
frequencies can affect Multiple Sclerosis
or be some of the sources for what causes Multiple Sclerosis

We would love hear from you!

Please leave us your comments, questions or concerns.

We want to help you to find more of the information
about Multiple Sclerosis and other related topics.

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MS Grief and MS Stress, After the Loss of A Loved One

When it comes to MS grief, the death of a loved one, relative or even close friend can be very traumatic.

After the initial shock has set in...now what?

Often the death of a relative or someone, who you live with, can mean drastic changes in your living arrangements or in how you are going to survive after the traumatic event itself.

It is tough enough dealing with the stress that the death of a loved one, relative or someone, whom we were close to, can bring but other stresses can also present themselves by the worry and stress that may also follow by you having to move or having to change drastically what you are able to physically do from day to day, which can increase the stress and its effects on actually setting you up for more MS attacks, excitations or relapses.

Stress along can aggravate or even cause more MS attacks or relapses to appear, which can set back your recovery from previous relapses, but to have too many of the typical stressors that can enter our lives to occur way too closes together...

...this can even be more than your body can handle all at once when Multiple Sclerosis is present.

But what can you do to reduce the internal and external stress that you feel, if this is happening to you?

The following tips can help you to minimize the stress and survive the tougher times in life that are closer to a traumatic experience, like the death of a loved one, a relative or close friend.

Tips on surviving MS grief and the stress of your life changing after the death of a loved one can include:

* Admit it yourself and maybe even others around you that you don't like the changes going on in your life, while it happening.

All too often we can either deny how we feel or act like we have to be strong and just accept it.

Just because things sometimes happen to us, which are out of our control, doesn't mean that we have to like it.

* Do what you feel that you need to do for you to get through it all.

Sometimes we need to sort through physical objects or things that belonged to the person that died and that can be a tough job.

This is especially harder to do, if you have a shorter period of time or a deadline that you need to meet by when you need to be done doing this.

But sometimes, just getting it done and working through the grief later can cause us to stress out much less than if we think about every little thing as we have to do it.

* Allow yourself to grieve, when the stress starts to build up to be too much for you to handle.

Crying is a good outlet of our emotions, when the stress becomes too much for us to handle.

Allow yourself some time to think through things...as in re-evaluate where you need to or want to go from here.

The death of someone close to us can make us re-evaluate our lives.

That isn't necessarily a bad thing, but we need to figure out what is really important to us in our lives.

Death has a way of helping to clarify what is important to us in our lives.

* Find a support network, support group or other friends that you can talk to about the feelings that you are going through, who will be supportive and let you "talk it out".

Find an MS support group or a grief counselling group to help you to work through the MS grief.

* Do what you can to help improve your situation in some way.

Sometimes this is easier said than done, but doing something, even if it seems small can help to relieve the internal stress or even the external stress that you are feeling, while going through moving or changing something in your daily life, after the death of a loved one, relative or close friend.

Clean if you need to.

Sort through things if you need to.

Throw things out or give things away if you need to.

Prepare to move if you need to.

Do whatever you need to do for you to get more order back in your life.

* Be thankful for who is still in your life, who is supporting you and helping you through this stressful time for you.

Sometimes, it helps to change your perspective, when you make an effort to be thankful for those who help you through the trying and stressful times in your life.

It may seem difficult at first to be thankful, when you are going through MS grief, but the attitude of gratitude can make all of the difference in you making through the stress, without you suffering more major MS attacks or relapses.

* Don't sit and drive yourself crazy over analyzing things or thinking through things over and over without doing something.

It's okay to think about things...we all need to do this from time to time in our lives, but don't set yourself up for major depression to set in by driving yourself crazy about everything that is stressing you out.

I'm not suggesting not to grieve, for it's part of the healing process, but allowing yourself to focus on becoming upset about everything that is changing in your life after the death of a loved one, relative or close friend will just set you up for more MS relapses or attacks to occur.

When you internalize the stress rather than finding ways to work through it and find ways to go on living life again, this increases the adverse effects on your body by causing your nervous system to short circuit even more than the Multiple Sclerosis can cause by itself.

I'm not suggesting that you forget the person that has died, but to the contrary...

...for the sake of the person that you were close to, who has died, find a way to go on living as a tribute to how much they loved you and how much you loved them.

Your mind has a strong connection to your physical body.

You can use your thoughts and/or your emotions to help guard your body from more harm, because of the effects of MS grief on your body, or you can use focus your thoughts and your feelings for a prolonged period of time in a negative way, which can greatly impact how severe the MS relapses and attacks can become.

We would love to hear what you think!

If you have found this to be helpful or if you have any other comments, leave us your comments.

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Coping With MS Grief, and Stress After Death of Loved One

The added stress from the death of a loved one is tough enough to deal with, when you don't have Multiple Sclerosis added to the mix, but when it comes to MS grief it is so much tougher on your body, since the added stress can cause much more severe MS attacks, if you don't find a way to cope with it.

That means that it is so much more important for you to allow yourself to grieve for a period of time, since that is definitely a needed thing, but then you have to find ways to cope with the grief and the added stressors, to allow yourself to heal from the inside out -- including body, mind, soul, and spirit.

That is one of the things that need to be kept in mind that you allow yourself to heal and grieve as is needed to prevent bottling up your emotions and all of the stress that you feel on the inside.

Because if you do bottle it all up inside, this will make you become much sicker because of the way that Multiple Sclerosis and the effects of stress over stimulate the nervous system and actually cause the nervous system to short circuit.

Death is a part of the circle of life, but the added stress experienced after the death of a loved one is even worse for people, who are diagnosed with Multiple Sclerosis.

If you don't find a way to deal with the stress, the added stress can set you up for a more severe MS attacks.

MS grief can aggravate the symptoms of Multiple Sclerosis and cause them to become much worse.

But what can help with reducing the effects of grief on Multiple Sclerosis, when there is a death in your family or of someone that you were close to emotionally?
Even though there is no easy answer for this one, don't despair about you being able to work through the grief and cope with it for you.

Facing working through grief is something that all of us have to deal with in life, whether we have been diagnosed with Multiple Sclerosis or not, after all death is part of the cycle of life.

There is a time to be born, a time to live and a time to die.

It's part of being human.

It's just that when it comes to Multiple Sclerosis, it's much more vital that you find ways to work through the grieving period without it impacting the Multiple Sclerosis in a way that can set you up for more severe MS attacks or relapses.

Although there is no "one size fits all" answer for dealing with grief, I do think that the tips listed below can help to some degree.

For tips on coping with the stress that grief can cause, which can aggravate MS attacks, if left uncheck...

Click on the link to read more -- MS grief

Leave us your comments, if you found this post helpful or if you would like to add more to the topic of discussion. We would love to hear from you.

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Tips For MS Cooling and Beating Effects of Heat on MS Symptoms

When it comes to MS cooling and the effects of heat on aggravating the symptoms of Multiple Sclerosis, hot weather can become unbearable or even down right dangerous for those of us diagnosed with Multiple Sclerosis.

Finding ways to reduce how overheated you can become with Multiple Sclerosis is vital for reducing the MS symptoms that are aggravated by the effects of heat on your nervous system.

But what can help you with cooling off?

Well...I myself have also been diagnosed with Multiple Sclerosis and when a heat wave strikes (where the temperature outside soars to above 90 degrees Fahrenheit or above 32 degrees Celsius for at least 3 days in a row) --

...then it is very difficult for me too to cool off to reduce the problems that do tend to occur from the effects of heat on aggravating the symptoms of Multiple Sclerosis.

If you don't have a pool or can't get in a pool or you can't drive or for some other reason you can't find something to help you with finding relief to the heat, then what can you do?

What can help you with cooling off with Multiple Sclerosis, when the weather gets too hot for you to handle it?

Click on the link to read more -- MS cooling

If you have found this blog post to be helpful to you, or if you have anything else you would like to add, please leave us you comments, since we would love to hear from you!

Remember -- KEEP COOL, my friends!

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What Is MS and How Does CCSVI Blockages Relate to MS?

What is MS or what is Multiple Sclerosis?

This question is often one of the first questions that is asked, after someone is newly diagnosed with Multiple Sclerosis.

Currently, Multiple Sclerosis or MS is still classified as an autoimmune disorder, where the body becomes confused and attacks itself, as if it is a foreign invader, that it needs to protect itself from.

Multiple Sclerosis is known for attacking the nervous system, especially the spinal cord and/or the brain, which often results in scarring that interferes with the nerves being able to function as they should.

But there was a recent breakthrough discovery announced towards the end of 2009, where Dr. Paolo Zamboni of Ferrara, Italy announced his findings of 2 year study that was conducted with 120 MS patients in Ferraro, Italy.

Dr. Paolo Zamboni, a vascular surgeon, conducted a study, in conjunction with a neurologist, where 120 MS patients were evaluated and found to have at least partial blockages to the veins, which drain the blood away from away from the brain.

Dr. Zamboni's results and conclusions from the study brought up the idea that MS may include a problem with a blockage to the blood flow away from the brain, through partially blocked veins in the neck (jugular veins) or addition veins near the shoulder blades and arm pit regions, which help to drain the blood away from the veins on the side of the neck.

Dr. Paolo Zamboni found that the majority of patients in the 2 year study had blockages of veins in the neck (one or both of the jugular veins, as well as veins that help the jugular veins to drain), which restricted blood flow from leaving the brain as it should.

This resulted in high iron levels in the brains of most of the MS patients and could possibly be contributing to the symptoms of Multiple Sclerosis, which the patients were experiencing.

Dr. Zamboni developed a surgical procedure he called chronic cerebral venous insufficiency or CCSVI, where a thin a catheter was inserted in the blocked veins and after the restriction was removed, the majority of the MS patients that under went the surgical procedure showed improvement.

Other studies have been done in the USA and a few other countries around the world to try to duplicate what Dr. Zamboni did with the patients in his study, but a much lower percentage of patients in the USA were shown to have the blockages. Not all of the MS patients, who underwent the same type of procedure as the patients in Dr. Zamboni's study, showed such remarkable improvements or results at such a high percentage., as the MS patients did, who were in Dr. Paolo Zamboni's study group.

In spite of all of the skepticism that resulted after further studies were performed in the USA and in other countries, which had mixed results that were not easy to draw good conclusions from, the CCSVI surgery seems to have many of the patients, who were found to have the restricted blood flow, who underwent the surgery, similar to the procedure that Dr. Zamboni developed for MS patients, have experienced some improvements in their MS symptoms from removing the restriction to the blood flow leaving the brain.

When it comes down to the studies that were done on MS patients in the USA and the other studies that were done in other countries around the world there are 2 things that should be noted about all of this.

First of all, the overall medical community has not fully accepted Dr. Zamboni's findings or conclusions, based on the results of the MS patients that were in the 2 year study that was conducted in Ferrara, Italy.

Especially when it comes to the majority of doctors in the USA. This breakthrough in MS research hasn't changed the definition as to what medical doctors overall are defining the answer to the question "What is MS?"

Medical doctors, generally in the USA, think of Dr. Zamboni's findings as being very speculative, at best and not proven by rigorous medical standards of double blind placebo studies and the like.

Secondly, the results and conclusions, which Dr. Zamboni received with the study that he participated in with 120 MS patients had an very high percentage of MS patients who had the blockages to blood flow present and had the CCSVI procedure done,

were not able to be duplicated with similar results for the same kind of percentage results of the number MS patients that were found to have the blockages, compared to those who did not have the blockages and with the same or similar percentages of the number of MS patients that under went the procedure that had positive results from having the CCSVI procedure done that helped to reduce their MS symptoms and

But there are doctors scattered about in the USA, who will at least work with you to help evaluate you to help you to find out if you do have the blockages that Dr. Zamboni found in the majority of the patients of the 120 MS patients, that were in the Ferraro, Italy study.

After keeping up on the continuing developments of Dr. Zamboni's continuing work, I think that the blockages that he found in MS patients are at least a consideration for each of us, diagnosed with Multiple Sclerosis, depending on our symptoms of Ms.

Since I was having big problems with passing out or fainting spells, my doctors thought that it was a good idea for me to be evaluated, since this could have been a potential explanation for me passing out so frequently over a period of more than 2 years.

But it was found, after running ultra sound tests, that I didn't appear to have any of the type of blockages that Dr. Zamboni saw in the study he was involved in.

So it still stands, when you ask a doctor "What is MS", that the prevailing theory still is that Multiple Sclerosis is an autoimmune disorder, which appears to be even more of a mystery to doctors across the board.

Multiple Sclerosis attacks the nerves through out the nervous system, as well as the membranes that line certain parts of the body, like the membrane called the Blood Brain Barrier, which surrounds and protects the brain.

MS is known for attacking and causing damage to the spinal cord and/or the brain.

Scarring can result from the MS attacks and depending where the scarring ends up being, this can cause a whole list of symptoms of Multiple Sclerosis.

To learn more, click on the link -- what is MS ?

If you found this information to be helpful, or if you would like to leave any comments, we would be happy to hear what you think.

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Finding Ways To Help Reduce MS Nervous System Effects

Reducing MS nervous system effects can be a challenge, since Multiple Sclerosis is not well understood as to what causes it and what can help to reverse its effects on the nervous system.

Multiple Sclerosis is known to attack the central nervous system and cause damage to either the spinal cord or the brain or both, as well as attack other nerves throughout the body.

Repairing nerves or reversing nerve damage is not very well understood either, but medical research within the last 10 years is finding out more and more that the nerves can be retrained by exercising the muscles that are attached to them.

It is like retraining the nerves and stimulating them at the same time, so that when the exercises are done consistently over a period of time, the nerves are gradually retrain and actually redeveloped, where they were once damage.

Exercise isn't the only thing that can help to regenerate and repair the MS nervous system damage, but exercise along with dietary changes, reducing stress, getting more rest and using other natural and alternative ways to work with the body can help the body to recover more of its abilities to function again, after the effects of the MS attacks have cause damage to different parts of the nervous system.

Natural and alternative ways don't fight against the body, like using prescription drugs do, and they don't result in the side effects that are typically associated with prescription drugs either.

Natural and alternative ways do take some time to work though and they are not a quick fix, but at least, most of the time, they do help more for coaxing the body into healing itself from the effects of Multiple Sclerosis, at least that has been our experience.

Depending on what the effects of Multiple Sclerosis on the nervous system that you are dealing with, not all natural and alternative ways work for every one with MS, since the alternative and natural ways are not cure-alls or anything like that.

But to the favor of natural and alternative ways, more doctors are turning to more complimentary ways of helping their MS patients to find relief to their symptoms of Multiple Sclerosis.

This means that more doctors are considering using natural and/or alternative ways either by themselves or in combination with using the prescription drugs, which are often prescribed for Multiple Sclerosis patients.

As a result, more MS patients are finding relief to more of their symptoms of Multiple Sclerosis, in addition to finding that more of the effects of MS are also beginning to be reversed.

Maybe natural and alternative ways are at least worth considering for reducing the effects of Multiple Sclerosis on your nervous system to help you to find relief from MS.

To read more click on the link -- MS nervous system

If you found this information to be helpful, or if you would like to leave us your comments, we would be happy to have you leave your comments.

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Challenges of Using A CPAP Sleep Mask For Reducing Problems with MS Sleep Apnea

It can be challenging to wear a continuous positive airway pressure sleep apnea masks and machines or CPAP machine for taming the problems associated with MS sleep apnea.

There is more than one type of sleep apnea. Depending on which type of sleep apnea that you have, there are quite a few different kinds of CPAP sleep masks that can be used for reducing the effects of the sleep apnea or for even getting the sleep apnea under control.

When it comes to the CPAP mask and machines, which help the person with sleep apnea to breathe better while they are sleeping, there are many different ways that the masks and machines are made.

But basically the majority of CPAP masks fall into 2 general types of masks.

One type of CPAP mask covers the nose, but not the mouth and the other type is considered a full face mask, where it covers both the nose and the mouth.

When we sleep, breathing through our noses helps us to get more oxygen to our brains and into our blood while we sleep.

Those of us, who tend to breathe more through our mouths, when we are sleeping, tend to have a much lower level of oxygen being supplied to our brains and to the rest of our bodies from the oxygen levels in our blood, which circulates through out our bodies.

The reduced levels of oxygen in our bodies and our brains can greatly reduce the abilities of our brains and our bodies to function as they should normally.

Often the CPAP mask that covers only the nose is tried first, during the overnight CPAP sleep study to see if it helps us to be able to get adequate levels of oxygen while we are sleeping.

At times, the CPAP mask that covers the nose only does not help enough, since if allergies are present or if you tend to breathe through your mouth while sleeping, the full face mask is needed to boost the oxygen levels back to the level that is needed to help your bran and your body to function as they should.

Mouth breathers often have an obstruction in the nose, throat or some other part of the airway or they can have a problem with congestion from allergies, which can prevent them from being able to breathe through their noses only.

If sleep apnea is suspected, an over night sleep study is done with you to determine if sleep apnea is present.

Multiple Sclerosis can set us up for sleep apnea to develop, since MS is known to attack the nervous system and cause many parts of our bodies and our brains not to function as they should.

Once it is determined that sleep apnea is the problem that you are having problems with, another overnight sleep study is done to determine which type of CPAP sleep mask will work for your particular type of sleep apnea.

Sleep apnea is basically where for one reason or another, the person stops breathing temporarily several to many times a night, while they are sleeping.

Most often the breathing problems occur while the person is lying down to sleep, but sleeping while sitting up in a chair can sometimes cause the restricting of the airway too that can cause breathing problems while sleeping.

Difficulties, which can present more problems with MS sleep apnea, while you are trying to get used to sleeping with a CPAP sleep mask can include:

Allergies can cause congestion

Congestion can make it difficult to breathe through your nose.

To use a sleep mask that covers only the nose, you need to be able to sleep with your mouth closed. This can present a problem when allergies are present.

Chin straps can be used to help to keep the mouth closed when using a sleep mask that only covers the nose, but the congestion can cause a problem that can prevent being able to drain the congestion enough for you to be able to breathe through your nose and not your mouth.

We unconsciously breathe through our mouths when we are congested.

Sleep masks do have filters on them, but some only come with 1 filter and some have 2 filters.

The sleep masks with 2 filters work better for those who have allergic reactions, since 1 filter removes dust and other particles from the air and the second one removes molds and other airborne pathogens, which can help reduce allergic reactions while sleeping.

It is best if you can clean up the room that you sleep in to remove as much dust, mold and clutter to minimize clogging the filters on the masks and to help reduce possible allergens in the room that you sleep in.

When it comes to MS sleep apnea, getting used to wearing a CPAP sleep mask when sleeping can be difficult.

Typically, problems encountered when getting used to sleeping with a sleep apnea CPAP mask can include:

* Difficulty getting used to sleeping with the mask on your face

We can unconsciously find it uncomfortable at first, when we first start wearing a CPAP mask to sleep at night to help us to breathe better when we sleep at night, especially if you have never had to wear a mask on your face before..

* Claustrophobia

This is the fear of not being able to breathe with the mask on your face or fear of the feeling of being closed in or too restricted.

This can be more of a problem if you need to wear a full face sleep mask, since there are also ones that just cover the nose and not the mouth.

* Sinus congestion or problems with Allergies

This can make it difficult for you to breathe through your nose when sleeping.

We get much more oxygen to our brains and into our bloodstream, when we breathe through our nose and not through our mouths, while we are sleeping.

But this problem can also make it so that we can't use the type of sleep apnea mask that covers the nose only. This can make it so that we need to use a full face CPAP or sleep mask.

* Difficulty breathing more deeply and more regularly

Sleep apnea already comes with the characteristic where we stop breathing temporarily a few to several times when we are sleeping at night.

This can just add to the sleep apnea problem or it can be a major contributing factor to the sleep apnea problem to start with.

This type of problem with holding your breath is more of a problem where learned responses of holding your breath when you feel under stress can make it where you are not getting enough oxygen to the brain and the rest of the body.

This can be a learned response from past traumatic events in your life, where you tend to hold your breathe more often when you feel stressed out.

Finding ways to relax and de-stress the nervous system can help reduce this problem, as well as learning to breathe more deeply and more regularly.

We can retrain ourselves, while we are awake to help us to learn to breathe more deeply and regularly and then carry this over to helping retrain ourselves to do the deeper breathing, where we slow down our breathing and make it more regular to help relax our nervous system, our bodies and our minds before we go to sleep after we put on the CPAP mask.

At times, we may have difficulties retraining ourselves to breathe more regularly and more deeply while we are wearing a sleep mask, simply because we are so used to our old habits of not breathing regularly like we should be doing.

These and other problems that learning to sleep with a CPAP or sleep apnea mask can be overcome, but it does take some retraining ourselves and with changing our habits from what we did previously and it can often take a few weeks up to 1 or 2 months to get used to sleeping with wearing a CPAP sleep mask.

When sleep apnea is present, especially for more prolonged periods of time (we are talking often we can have sleep apnea problems for years before we are diagnosed), it can take time to convince ourselves that we are actually allowed to be able to get a good night of sleep every night.

This can be part of the problem too with sleep apnea

We need to give ourselves permission for us to be able to work with our bodies to allow them to relax and find sleep to be an enjoyable experience again, instead of us feeling like we are being tortured almost every night.

Getting used to sleeping with a sleep mask or CPAP mask and machine can be a challenge, but I have found that in my case of multiple sclerosis sleep apnea, that sleeping with a CPAP mask does help me most nights with with being able to actually get a very good restful night of sleep each night.

It isn't as intimidating as it may seem at first to get used to sleeping with a sleep apnea CPAP mask.

Although sleeping with a CPAP sleep apnea sleep mask is not necessarily the only solution for your case of sleep apnea to get it under control, it can help a lot with allowing you to finally get a good night sleep.

Sleeping with a CPAP mask may not be the only solution, since sometimes undergoing surgery to correct any physical obstructions, that may be creating much of the problems that contribute to sleep apnea, can sometimes help to correct the sleep apnea, so sleeping with a CPAP mask may not be needed after the surgery.

Going for surgery doesn't always fix the physical obstructions with sleep apnea either, but this may be a consideration, if using a CPAP mask doesn't seem to be helping you to sleep better at night.

If you want to at least consider if surgery can help to correct the problem you are having with sleep apnea, you can get additional opinions by visiting an ear, nose and throat doctor to see if there is a deviated septum, a problem with the tonsils or a problem with the adenoids, which could be contributing to the problem that you are having with sleep apnea.

Click on the link to read more about -- ms sleep apnea

If you find this information to be helpful or if you have any other comments or suggestions, we would be happy for you to leave us a comment.

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What Problems Can The Multiple Sclerosis Symptom of Dropping Things Cause You?

When I started out with a severe case of Multiple Sclerosis 13 years ago, I was having a very difficult time with the Multiple Sclerosis symptom of dropping things.

This made it so that I had to cut out doing every day activities like doing dishes, putting dishes away in the cabinet, stopping using any dishes or glasses that were breakable, since I broke everything I used by dropping it on the ground and shattering it.

It was like I was losing control of my hands.

It took a while of changing lots of things, before I started to recover my abilities to use my hands again to do even daily activities that we can sometimes take for granted that we can do.

The scariest thing about all of the problems that I had with dropping things is that I love kids. I used to help my friends out with babysitting for them and I loved playing with their children.

At the time, I had no children of my own and I remember that at one point I was somewhere around lots of people and someone handed me their 2 month old baby to hold. I hadn't really thought about it at first, since it was about 3 years after I was first diagnosed with Multiple Sclerosis and my friend was talking with someone else and they had walked a few feet away from me and left me holding the baby.

I suddenly was in a panic, when I realized that I couldn't hang onto to the baby for more than a few minutes. All I could think about was that I was going to drop the baby.

I tried desperately to get my friend's attention and when she finally sent her husband over to take the baby away from me, I felt such relief that I hadn't dropped and hurt the baby.

After that, I was not willing to pick up a baby or any child and hold them. That was difficult, since I love children.

What kind of things does this Multiple Sclerosis symptom of dropping things get in the way of you doing, that makes it difficult for you to function from day to day?

I'd really like to hear more from you , as to what you are dealing with because of the effects of Multiple Sclerosis, since you have been diagnosed with Multiple Sclerosis.

Sometimes just discussing the way that Multiple Sclerosis has affected our lives does help us to feel like we are not alone in our struggles with MS.

I'd love to hear from you. Leave us your comments and we can talk about it.

Take comfort in knowing, you are not alone in your struggle with Multiple Sclerosis.

We can learn to help each other to reduce the effects of Multiple Sclerosis on our health.

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Multiple Sclerosis Sleep Apnea and Passing Out

I apologize for my delay in answering any questions e-mailed to me within the last 2 months. I was recently diagnosed with sleep apnea on top of the Multiple Sclerosis that I have been dealing with for 13 years.

On top of this, I have had a severe problem with passing out often and the combination of the 2 has made it very difficult for me to think straight enough for me to write very much or be able to carry on conversation via e-mail, like I typically can do.

My doctors have recently figured out that my adrenal glands are not functioning very well, which is causing my blood pressure to drop to the point where I can pass out for 1 to 3 hours at a time.

I recently received and started using the sleep mask or CPAP machine as it is called (or continuous positive air pressure machine) to help me reduce the problems that I exerience because of sleep apnea and to help me to get more restful sleep at night.

I was also started on a few different medications to help boost the function of my adrenals to help prevent the dizziness and passing out that I have been experiencing all too much over the last 2 to 3 years.

Both the medications and using the sleep apnea CPAP machine have been helping me to start to function better again.

I am working back into the swing of things with providing you with more information on what I have learned about living with Multiple Sclerosis and about what I have found that has helped to reduce the effects of Multiple Sclerosis and other conditions that accompany MS to help you to find relief too!

Helping you, who alsp struggle with Multiple Sclerosis and the other health conditions that can accompany Multiple Sclerosis is my main objective with everything that I do with my website and blog.

But I can't do this alone. I need your feedback to help me to know what information you are searching for to help you to find relief to what you are deling with, when it comes to Multiple Sclerosis.

I don't to just talk about what I have been through, since this may or may not help you to find relief.

Please leave me your comments, or questions as to what you would would like to find out more about when it comes to what you are dealing with because of Multiple Sclerosis.

I just want you to know that I understand how difficult living with Multiple Sclerosis can be and sometimes additional health challenges can also appear, which are not initially related to the Multiple Sclerosis, but that is somehow related to the effects of Multiple Sclerosis on the body, that can sometimes make it difficult for you to function.

Where I can, I describe things from a first hand point of view, since I have been there with much of what I describe that those of us with Multiple Sclerosis can ourselves be struggling with in each of our own cases of Multiple Sclerosis.

Although I myself don't take any of the typically prescribed medications for Multiple Sclerosis, if you find that they do help you, in reducing the struggle that you find yourself in with the symptoms of Multiple Sclerosis, then use them.

But remember that no matter what treatment method or other ways that you use, while working with your doctors, to reduce the effects of Multiple Sclerosis on your body -- remember it's your body.

You know how you react to things and what kind of thing appear to help you, and which do not seem to help you much at all...or may even cause you to become worse instead of doing better.

No matter what ways you use for you, it is always your choice. Don't let anyone else tell you otherwise.

If you would like to learn more about how sleep apnea can affect those of us with MS, click on the link to learn more -- Multiple Sclerosis sleep apnea

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MS Fatigue and Multiple Sclerosis Sleep Problems

Multiple Sclerosis sleep problems or not getting a restful night of sleep on a regular basis can actually contribute to causing the worsening of MS attacks or MS relapses by making the attacks appear more often and become more severe.

Getting adequate rest is very important for those of us with Multiple Sclerosis. When we get adequate rest on a regular basis, this increases our body's own production of stem cells, which help repair damage to the nerves through out the body.

When it come to what can contribute to Multiple Sclerosis sleep problems, there can be several things that can either make the fatigue much worse or can actually be one of the root causes of problems with getting a good night of restful sleep more often when you are struggling with MS.

Sleep disorders are one of the problems that can develop as a result of Multiple Sclerosis attacking and damaging the central nervous system. Going for an overnight sleep study can often get to the bottom of any sleep disorder that has developed, that might be interfering with our bodies going through the normal sleep cycles that our bodies go through when we lie down and sleep.

To read more click on the link -- Multiple Sclerosis Sleep

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Can Multiple Sclerosis Sleep Apnea Contribute To MS Sleep Problems and MS Fatigue?

When it come to Multiple Sclerosis sleep apnea is often a common problem for disrupting sleep than you think!

When it comes to sleep apnea, 10 out of every 100 people have sleep apnea, but a whopping 40% to 50% go undiagnosed for most, if not all of their lives!

This is what is reported for people, who are not diagnosed with Multiple Sclerosis, but when it comes to those of us who have been diagnosed with Multiple Sclerosis, the incident rate of the appearance of sleep apnea increases even more for us.

Click on the link to read more -- Multiple Sclerosis sleep apnea

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MS Stress: : How Does Stress Affect Your Symptoms of Multiple Sclerosis?

When it comes to MS stress is known to play a big part in how severe the Multiple Sclerosis attacks, relapses and exacerbations can become.

Stress can also influence how severe the symptoms of Multiple Sclerosis can become, as well as how long many of the more severe MS symptoms tend to last.

How have you found that stress affects your symptoms of Multiple Sclerosis?

Have you found anything that you would recommend to others with problems with the affects of MS stress that could help them to find relief too to the effects of stress on their symptoms of Multiple Sclerosis?

Leave a comment and let us know about your experiences dealing with MS stress.

We'd love to hear what you think! Leave us a comment to tell us your story.

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MS Tips: Reducing Dry or Cracked Skin Problems With Multiple Sclerosis

MS Tips can be very helpful, when someone with Multiple Sclerosis passes on tips for things that they have found that has helped to reduce one or more of their symptoms of Multiple Sclerosis.

When it comes to Multiple Sclerosis, problems with the skin becoming dry and cracking is all too often a problem, that can set us up for getting even more infections than we would other wise.

Click on the link to read more -- MS tips (for reducing dry or cracked skin)

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MS Tip: Reducing Scrambling Things From MS Brain Function Problems

MS tip for reducing MS brain scrambling:

I was travelling in a car today on a sunny day, as a passenger (someone else was driving) and I tried something as a curiosity to see if it could help to reduce the scrambling that I was having a problem today from the effects of Multiple Sclerosis scrambling my brain and what I tried worked!

Since it helped, I wanted to pass this MS tip on to you, since it doesn't require buying anything or taking supplements or prescription drugs for you to find relief.

It was a very sunny day and as we were travelling down the road, towards the sun, I found that if I put up the visor in the car and let the sun shine on my face as much as possible and enter my eyes (don't look directly at the sun, look from side to side and don't wear sunglasses) that this helped to greatly reduce the scrambling that was going on because of the MS brain function problems that I was experiencing today.

Most people, diagnosed with Multiple Sclerosis, have a problem being low in vitamin D levels and vitamin D has been found to have a protective quality in Multiple Sclerosis to help reduce the number of MS attacks and relapses by preventing them.

Most people with MS tend not to get enough sunlight exposure because of the problem people with Multiple Sclerosis have with over reacting to heat and because of the reduced ability to stand and walk because of the effects of Multiple Sclerosis attacks, which reduces our outdoor activities more most of the time.

Since I found something that helped me to find relief to the MS brain function problems with scrambling things or with dyslexia, I wanted to pass this MS tip on to help you too.

Have a great day!

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MS Brain: Have You Found Yourself Scrambled Because of Multiple Sclerosis?

MS Brain function can be affected by Multiple Sclerosis attacking the brain, resulting in lesions or scarring in the brain. Scrambling words, numbers or concepts can be one of the many problems that can result in many cases of Multiple Sclerosis.

When this happens, this can make it difficult to write, form sentences when you talk or cause everything to be so jumbled up that it can be difficult to carry on a conversation with anyone or understand what other people are saying to you. This is often called dyslexia.

As with most cases of Multiple Sclerosis, we tend to have "good" days and "bad" days. With my case of Multiple Sclerosis, the days that I tend to scramble things or that the dyslexia goes crazy tends to come and go.

Although today is a scrambled day for me, sometimes in spite of the scrambling of my MS brain, I am still able to write some (go figure, since this makes no sense at all).

Okay...it makes a little sense, since the degree of scrambling from the Multiple Sclerosis can be much worse some days so much more than on other days. Some days when the scrambling becomes much worse, I can't do much of anything on those days, except wait until the problem with scrambling everything calms down.

Do you find that with your symptoms of Multiple Sclerosis that you tend to have problems with scrambling words, numbers, concepts or whatever?

What do you do when this happens to you?

I'd really like to know -- please leave me your comments to help me out here, since this is not an easy thing to deal with because of the effects of Multiple Sclerosis.

I look forward to your comments!

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MS Disability: Dealing with Electrical Power Outages with Multiple Sclerosis

Having a MS disability is difficult enough to deal with, but what can help when the power goes out and no electricity is available to help you to function for a period of time?

What do you do then, to help you to function?

Click on the link to read more -- MS disability without electrical power.


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MS Breakthrough: More Medical Information on CCSVI for Your Doctors

The MS breakthrough for the reduced blood flow from the brains of Multiple Sclerosis patients (or CCSVI as it has been called) has people with MS talking up a storm all over the Internet on blogs, forums, message boards, social groups and all over the place.

I also was diagnosed with Multiple Sclerosis and my doctors have been working with me to evaluate me, using ultrasound testing, to determine if I have the reduced blood flow from the brain or in the veins in the upper chest, but my doctors are having a tough time deciding which veins that they need to run the tests for, like Dr. Paolo Zamboni did with the MS patients that he did the study with in Ferrara, Italy.

Just in case you are having this problem too, click on the following link to read more about information that I found that can help you and your doctor in evaluating you for CCSVI -- MS breakthrough more information to help your doctors.

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Stress MS: How Does Stress Affect the Symptoms of Multiple Sclerosis?

Stress MS patients often feel can create a big problem for those of us, who have been diagnosed with Multiple Sclerosis.

The effects of stress can contribute to setting us up for MS attacks, exacerbations and relapses, which can appear much more often and much more severely, than they would if the stress was not present.

Although we can not totally get rid of the stress in our lives, especially when we are dealing with Multiple Sclerosis on a long term basis, we can reduce, minimize or maybe even neutralize the way that we respond to the stress and greatly reduce the way that the effects of stress can have on the symptoms of Multiple Sclerosis.

Click on the link to read more -- Stress MS


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MS Tips: Helpful MS Tip for Helping Reduce Symptoms of Multiple Sclerosis

There are many natural and/or alternative MS tips that can be helpful for reducing the symptoms or even the effects of Multiple Sclerosis, that can be discussed on-line. Some of the tips can be more helpful than others when it comes to reducing the symptoms of Multiple Sclerosis.

Which of the MS tips have helped you the most to find relief to your symptoms of Multiple Sclerosis, that you would like to pass on to other people, who have been diagnosed with Multiple Sclerosis, to help them to find relief too?

Feel free to post your comments, as we are all working together to do what we can to help others who have also been diagnosed with Multiple Sclerosis.

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Multiple Sclerosis News: What Can We Do with the MS News About Blood Flow Problems with MS?

How does the more recent Multiple Sclerosis news apply to those of us with MS?

Does the blood flow problems to the brain or Chronic cerebrospinal venous insufficiency (CCVI) apply to all of us, who have been diagnosed with Multiple Sclerosis?

Can we be tested for this particular problem, to see if this a problem for us, that may be contributing to some degree to our symptoms of Multiple Sclerosis?

Click on the link to read more -- Multiple Sclerosis News

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MS Work: How Can Having Multiple Sclerosis Affect Our Ability to Work?

When it comes to having MS work may or may not be something that we are able to continue doing, based on how mild to severe the effects of Multiple Sclerosis are on our nervous systems.

Multiple Sclerosis can vary from person to person as to how it affects how well we can function from day to day.

Click on the link to read more -- MS work

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MS Food: Is Eating or Drinking Foods containing Caffeine a Good Idea with Multiple Sclerosis?

Some controversies exist, when it comes to discussing MS food selections for helping those of us with Multiple Sclerosis for reducing MS symptoms and increasing the amounts of energy that we have each day.

Is it a good thing for those of us with Multiple Sclerosis to eat or drink foods that contain caffeine?

Click on the link to read more -- MS food

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MS Food: Example of Foods That I Eat To Help Reduce My Multiple Sclerosis Symptoms

I have been asked a few times: What MS food do I eat that helps with reducing my symptoms of Multiple Sclerosis and help me to function better?

I have found that if I include more foods of the following on a more regular basis, that I function better more often and my MS symptoms and MS attacks become less often of a problem.

Click on the link to read more -- MS food

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How Can the Recent MS News Apply to Those of Us with Multiple Sclerosis?

The recent MS news, that was released about the discovery that Dr. Paolo Zamboni found with his MS patients involves restricted blood flow to and/or from the brain. After the restrictions were opened up, these MS patients found relief to their MS symptoms.

How does any of this recent MS news apply to us, who also have been diagnosed with Multiple Sclerosis?

Click on the link to read more -- MS news

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MS Talk About It !!

MS talk about it?

I don't about you, but I find that there are days where I just feel better if I find other people, who have also been diagnosed with Multiple Sclerosis, that I can just talk to about what I am dealing with on a daily basis because of the effects of Multiple Sclerosis on my body.

Don't you feel like that sometimes?

Well...it's your turn!

What is the worst thing that you have found yourself dealing with, since you have been diagnosed with Multiple Sclerosis?

Now's your chance -- Leave us your comments and tell us about it!

Sometimes, just talking about it all can help relieve stress and help you to feel like you are not alone in what you are dealing with because of the effects of Multiple Sclerosis.

So, let me tell you right now...you are not alone!

Somehow, we are all in this together.

Let us know what you are dealing with because of Multiple Sclerosis and we will do what we can to help you to find more information on alternative and natural ways that can help you to find relief too.

Hang in there my friends...until next time...

We wish you the best on your quest to wellness!

The Taming Multiple Sclerosis Team

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MS Fatigue: Can a Virus Contribute to Fatigue in Multiple Sclerosis?

What virus can possibly contribute to the MS fatigue seen in Multiple Sclerosis?

Can anything help to reduce the fatigue, associated with this virus, in addition to helping with reducing the fatigue that is often associated with Multiple Sclerosis?

Click on the link to read more -- MS fatigue

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Reducing MS Fatigue can be a Challenge

Finding ways to reduce MS fatigue can be a challenge, but I have found some ways that can help reduce the effects of the fatigue that is often associated with Multiple Sclerosis.

Click on the link to read more -- MS fatigue

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MS Infection: How Does Having An Infection Affect Symptoms of Multiple Sclerosis?

MS infection: how does having an infection affected those of us diagnosed with Multiple Sclerosis?

Can having an infection aggravate MS symptoms and make them worse?

Click on the link to read more -- MS infection

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MS Breakthrough: A Recent Discovery in Multiple Sclerosis

Have you heard about the recent MS breakthrough, which involves a promising discovery is stirring hope for the estimated 2.3 million people diagnosed with Multiple Sclerosis around the world?

Click on the link to read more -- MS breakthrough

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Multiple Sclerosis Treatment: A Newer Type of Treatment Being Considered for MS?

Since a new development how Multiple Sclerosis recently was announced, this may potentially suggest a new Multiple Sclerosis treatment, that wasn't a consideration previously.

This may also mean that the way that Multiple Sclerosis is approached and the whole notion that of Multiple Sclerosis being a autoimmune disorder (where the body becomes confused in some way where it attacks itself) may change in the future.

Time will tell, but this also has the potential of changing the way that the medical community around the world approaches and treats Multiple Sclerosis in the future.

Click on the link to read more -- Multiple Sclerosis treatment.

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MS News: What's All the Buzz About for Multiple Sclerosis?

Have you heard about the recent MS news that MS patients are talking about and how this discovery is stirring hope for the estimated 2.3 million people, who have been diagnosed with Multiple Sclerosis around the world?

This amazing discovery has the potential of helping thousands of people around the world, who have been diagnosed with Multiple Sclerosis. This breakthrough could possibly even change the way that the medical community around the world views Multiple Sclerosis on both how it is classified and how it is treated.

On November 21st, an amazing breakthrough for the treatment of Multiple Sclerosis (MS) was aired on the news across Canada, that described about a new discovery by Dr. Paolo Zamboni, an Italian vascular surgeon. According to Dr. Zamboni, he found that there is a structural defect that exists in the blood vessels of the MS patients that he treated, which could be causing symptoms of Multiple Sclerosis. This interesting discovery has peaked the curiosity of the medical community around the world.

Click on the link to read more -- MS news

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MS Tip for reducing MS symptoms Resulting After Using Injectable Drugs for Multiple Sclerosis

A MS tip from other people, who have also been diagnosed with Multiple Sclerosis, can often be invaluable with helping us to find better relief to our MS symptoms, because they themselves are also dealing with many of the same or similar MS symptoms as we are experiencing ourselves.

A MS tip was recently passed on to me from someone with Multiple Sclerosis that may help those of you that are using one of the injectable drugs, which are often prescribed for helping to reduce MS symptoms.

We have asked her permission, for us to be able to pass this information on to those of you, who are also currently using one of the injectable drugs to help to manage your Multiple Sclerosis symptoms, in the hopes that it may help those of you, who may also be battling with similar experiences yourself.

Click on the link to read more -- MS tip

If you have any further ms tips that you wish to pass along to others who may also be facing problems with similar MS symptoms, as to what you are experiencing, you can leave a comment on this blog and we will pass the information along to others, also diagnosed with Multiple Sclerosis.

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MS Caregiver: Being a Caregiver with Multiple Sclerosis

Being a caregiver by itself can be a challenge, but being an MS caregiver or a caregive with MS presents so many more challenges than it would otherwise.

An interesting phenomena is occurring around the world, as a larger percentage of people in many more different countries around the world are living longer lives and as the number of people entering later stages of life is increasing as more of the "baby boomer" generation approaches retirement age.

This often means that as more of the aging population develop health conditions that require more assistance for performing every day tasks, such as Alzheimer's, Parkinson, different forms of dementia or cancer, or even Multiple Sclerosis, more and more of the younger generations are finding themselves in more of a care giver role.

Click on the link to read more -- MS Caregiver

If you find any of this information helpful to you, or if you disagree with any of the information included here, leave you comments and let us know what you think!

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Vitamin D MS: Can Increasing Vitamin D Levels Reduce MS Depression?

Vitamin D MS: what can we do for helping to increase vitamin D levels and how can this help to reduce or maybe even eliminate depression in Multiple Sclerosis?

What other benefits are there from increasing vitamin D levels?

Click on the link to read more -- vitamin D ms

If you find any of this information helpful to you, or if you disagree with any of the information included here, leave your comments and let us know what you think!

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MS Flu: Can Anything Help to Curb the Flu with Multiple Sclerosis?

When it come to Multiple Sclerosis, MS flu is very often a big problem. I have found, that with my own case of Multiple Sclerosis, that I can end up with "the flu" much more often throughout the year than any other type of infection, that I tend to get each year.

Another name for the actual main virus, that is often called "the flu" is the Influenza virus. The main problem with "the flu" is that it isn't just one organism, but instead it is actually a group of different forms of the same virus, that are related in one way or the other.

Click on the link to read more -- MS flu

If you find any of this information helpful to you, or if you disagree with any of the information included here, leave your comments and let us know what you think!

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How Can Multiple Sclerosis Insomnia Affect the Memory, While we are Awake?

How can Multiple Sclerosis insomnia affect how well the memory works, during the hours that we are awake?

As more sleep studies are being done to observe the effects of insomnia on the body, the more is being understood about how insomnia affects the ways that our memories can function during the day, while we are actually awake. This effect of insomnia on decreasing the abilities of our memories to work as they should is seen as a much bigger problem for those of us, who have been diagnosed with Multiple Sclerosis.

How does sleep help the memory to work better?

Click on the link to read more -- Multiple Sclerosis insomnia

If you find any of this information helpful to you, or if you disagree with any of the information included here, leave your comments and let us know what you think!

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Multiple Sclerosis Diet: What Diet Changes Can Help?

During the initial healing phase of dealing with Multiple Sclerosis, changes to the Multiple Sclerosis diet is very important for helping to reduce stress on he digestive tract and the nervous system and to aid in speeding up the healing process in the body.

But...what are the Multiple Sclerosis diet changes that we can make that can help to reduce Multiple Sclerosis symptoms or possibly even help to reverse the effects of Multiple Sclerosis on the body?

Click on the link to read more -- Multiple Sclerosis diet

If you find any of this information helpful to you, or if you disagree with any of the information included here, leave your comments and let us know what you think!

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