Escape Negativity!

state_of_emergencyThe world has become a constant state of anger and negativity! It is almost impossible to turn on the television and not be shown another act of violence or another type of anger. So many lives are affected every day by these horrendous acts. Anywhere from school shootings, to ludicrous talk from the White House, to an incredible amount of police brutality, to the lack of ethics in corporate American, it seems never-ending! There has to be something that can be done to stop the outrageous behaviors that have become the new norm.

Personally, I do my absolute best to hold onto the positive aspects of life. I do believe that even in the darkest times we encounter in our lives, there is a bright side somewhere even if it is well hidden. If we surrender to all this negativity surrounding us, we are not any better than those stirring up the pessimism. We do have the ability within us to rise above all the hate and show love for others!

It is possible that I am wrong, but I think the amount of hate in this world has increasedholding-on-to-anger-is-like-grasping-a-hot-coal-with-intent-of-throwing-if-at-someone-else drastically over the last 14 months or so. Politics with family and friends has always been a sensitive subject and probably always will be that way. Everyone wants to believe in who they vote into any political position and will not listen to reason when the facts are proven, over and over again. I think it is safe to say that no one really wants to admit they were wrong and were blindly convinced someone would make positive changes. It does not matter what side we are on, not many politicians are very honest. They all say what they believe people want to hear and will force that person to support them through anything! Who wants to believe that anyone in a powerful position would destroy something that could be truly wonderful? I think that money and greed can influence people to do things that ordinarily they would never think of doing. For me, there is absolutely no amount of money that would make me think it is okay to destroy anyone’s life!

When I was younger I thought that the United States was a great country to live in because we were free and safe. But, now that I am older and a little wiser I am questioning this a lot more! How are we free and safe when we have someone constantly making what were allies angry and making others that could be considered dangerous hostile? In order to create harmony, there must be logic and common sense! I have thought for a long time now that logical behavior and common sense were long-lost, which is pretty unfortunate.

I know that this entire post was absolutely nothing to do with any chronic illnesses or issues that come with illnesses, but these thoughts are pretty important in the big picture. There is way too much hate encompassing people around the world right now! No hateWhen we should be evolving, but it seems as though we are devolving! I have my thoughts on where it is stemming from, but there could be a lot more involved that I am just not aware of. I do not know how to make changes in massive amounts, all I know to do is always treat those I encounter with respect and dignity!

How do y’all feel about the state of the world right now? Do you believe there are positive or negative things occurring daily? How are you personally handling the issues that you view on the television or see in person? I am going to be honest, I was a little worried about sharing this post because I do not want to offend anyone reading. I am just really tired of hearing about all of the hate and violence that is constantly going on. I am and always have been a very compassionate person, but that just seems to be unusual in the world today.

I hope y’all had a great week and I hope you are looking forward to your weekend! I am so glad we finally made it to the weekend because this has been an incredibly long week and I wish the weekend would be just as long as the week felt! I really appreciate you reading my rant today and I would love to hear your comments! I will of course respond to you as quickly as I can! I hope you have a very lovely evening and a fantastic weekend! I am always sending y’all lots of love and comfort!

Love 2

Always, Alyssa

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Time Change Headaches!

edwardrmurrow1After we set the clocks ahead an hour on Sunday, my schedule seems drastically off kilter! Of course I did change all the clocks in the house ahead a hour, but at the same time I seem to have set my dates in my mind ahead an entire day! I thought Monday was Tuesday and I have thought all day that today was Wednesday! It is not a good feeling to realize what the day actually is and that there is still another day of the week. Hopefully my mind will adjust and actually know what day of the week it is! How are y’all adjusting to the time change? I hope y’all are adjusting better than I have so far! I think it is a little harder getting up in the morning and driving to work in the dark, but I guess on the plus side it does stay light out longer! It is always good to find the positive in every situation!

Crazy question for y’all! Those of you that have Multiple Sclerosis, has anyone ever told you that there is no correlation between MS and headaches? I ask because my current specialist has said just that. I had gone to her about the massive amount of headaches I suffer from and she said it does not have anything to do with my MS. I am sorry to say, but it is a quick and easy Google search to find out there is a relationship between the ms and headachestwo. It may not be an extremely common side effect, but Migraines are twice as common is those with MS that those without. Logically thinking if someone has a decent amount of lesions on their brain, how would that not contribute to headaches? I mean the brain has some intruders present that are not welcomed! Most people who I know that live with Multiple Sclerosis do battle with headaches of some sort. I think it is probably a good time to start looking for another specialist that I am a little more comfortable with. It is very important to have trust in your doctor and her comment made me lose trust in her!

The craziest thing happened to me today at work. One of my co-workers, that was not so pleasant while I was on medical leave, told me she was glad that I was back at work. All I could say was thank you and that I have been back working for a while now. She also decided to talk to me about an illness she was recently diagnosed with that make you lose your hair. As she spoke and told me about how depressed she had been, I did my best to try to motivate her to think positive. I told her that in a way she was lucky Kind wordbecause she has very thick hair and you were not able to see the bald spots she told me about. She even talked to me about the treatments she had to endure and at the same time praised me with how well I had the pain I deal with. It is crazy how it takes someone being diagnosed with an illness before they can have a heart for what another goes through. Even though I did have some ill feelings towards her because of how not compassionate she was towards me when I was struggling, I did feel it was best to try to be supportive and understanding of what she was going through. 

How are y’all feeling today? I hope your week is going well and you are staying as positive as you can. Y’all know that positive thoughts will in time bring positive things to your life! I sincerely appreciate you visiting my site today and I would love to hear your thoughts! I do respond to all comments as quickly as I can! I hope you have a nice and relaxing evening! As always I am sending y’all lots of love and comfort!

Love 2

Always, Alyssa

 

Different types of Multiple Sclerosis

types_of_ms_chart_largeAs y’all already know, Multiple Sclerosis is a very unpredictable and for some debilitating illness of the Central Nervous System. With MS, the immune system eats away at the protective covering of the nerves. MS disrupts the flow of information within the brain and between the brain and body. Multiple Sclerosis does not discriminate and can attack anyone no matter race or gender, but it is diagnosed 2 to 3 times more often in women than men. Multiple Sclerosis does affect each person differently, so no single person even if they have the same type of MS will experience the same exact symptoms. With that said I would like to take this moment to give a description of the four different types of Multiple Sclerosis.

Relapsing-Remitting Multiple Sclerosis, (RRMS) is by far the most common form. This type is 80-85% the initial diagnosis of MS cases.  RRMS involves clear episodes of inflammatory activity and well-defined attacks of new or recurrent symptoms. The patient will typically experience partial or even full recovery between the episodes. Symptoms do vary between each individual, but some well know traits are: tingling and numbness, visual loss or changes in one or both eyes, fatigue, weakness and balance problems. It is important to know what your baseline is on all these issues so you can communicate any changes with your specialist.

Primary-Progressive Multiple Sclerosis, (PPMS) is another type that is less common. Ms_progression_types.svgThis type is composed of only 10-15% of all MS cases.  With PPMS neurological functions are impaired and become more significant as the disease progresses. Patients will experience occasional plateaus in the progression, but symptoms can also worsen with no relapse between them. There is less damage done to the brain with PPMS, but more damage done to the spinal cord. Symptoms that can come along with PPMS are problems walking, stiff legs and trouble with balance. Like I have already said, it is so important to know what your baseline is with anything to do with your health, so when there are changes you are able to communicate those changes with your specialist.

Secondary-Progressive Multiple Sclerosis, (SPMS) is actually the next stage of Multiple Sclerosis. I have already shared with y’all that I was diagnosed with Multiple Sclerosis when I was only 19 years old, so this year will make 19 years for me. Time flies because it feels like it was just yesterday when my specialist flipped my world upside down telling me I had this illness. Reports indicate that 50% of those with RRMS will develop SPMS within 10 years and 90% will develop in 25 years. SPMS is similar to RRMS, but may or may not involve the occasional relapse. Symptoms with this progressively worsen and may include bowel and bladder problems, weakness and coordination issues, stiff and tightness in legs, fatigue, depression and problems thinking.

MS SymptomsProgressive-Relapsing Multiple Sclerosis, (PRMS) is progressive from the beginning.  With PRMS there will be clear and acute relapses with and without recovery from the damages. The illness will continue to progress between relapses. Symptoms that are associated with PRMS are muscle spasm, weak muscles, chronic pain, vision changes, dizziness and decreased bladder functions.

All those years ago when I was first diagnosed I did a lot of research on Multiple Sclerosis. Now it was a long time ago, but I do not remember reading that RRMS can possibly progress into SPMS in a matter of time. Sadly it was not until recently I learned that I did not know everything I should have. It was not completely my doctor’s fault for not sharing this with me, it was mine for not learning and or remembering this information. Talk about being a little shocked when I found out it does not necessarily matter if I take the medication I am supposed to in order to slow the progression down. This illness has a mind of its own and can progress no matter how hard you fight it. Maybe that sounds a little negative, but I guess the truth is reality is not always positive. 

I know many of you already have a lot of knowledge regarding Multiple Sclerosis, but I have a goal to raise awareness for everyone! This is an illness that crept its way into so many lives, completely uninvited and just will not go away. I want to believe that fight for a curesomeday there will be a cure and our lives will improve drastically. I look forward to the day that I am not dealing with massive amounts of pain, headaches, numbness, that annoying tingling feeling and vision issues. Until that day comes though, I will continue to live my life and enjoy it as much as possible. I will continue to do my best to help and motivate others that are struggling with illnesses and other issues in life. I want to be able to bring positivity into the lives of others to combat the world of so much negativity. I would love to believe it only takes one person to change another person’s  life!

I hope y’all are enjoying your weekend and feeling well! Again the weekend went by pretty fast, but I was able to get my hair done and some cleaning done in my house, which was a fantastic feeling! It is so helpful being able to take short breaks in between cleaning the house because if I didn’t, it would make me feel absolutely horrible with additional pain!

Thank you for visiting my site today! As always I would love to hear your comments on what I have shared. Being able to read your comments and respond builds a great and supportive network that we all need. I hope the rest of your Sunday goes very well and you are able to rest up for the week ahead! Sending y’all much love and comfort!!

Love 2

 

Always, Alyssa

Spring Forward!

Spring FowardWell it is that time of year again! We get to have a little time confusion by turning the clocks ahead one hour! How fantastic, we get to lose an hour of sleep, but we do get an hour  more of daylight! I guess the good out weighs the bad in this situation because we get one additional hour of sunlight and natural Vitamin D is good for all of us!! I just wanted to remind y’all of this so your time won’t be too far off! I hope y’all enjoy the rest of your evening! Sending y’all love and comfort as well as the correct time:)!

Love 2

Always, Alyssa

Live and Love Life!

2-quote-about-no-matter-how-impossible-unattainable-or-unim-image-background-imageIt may seem that happiness is an unattainable goal in life and that it is only meant for the selected lucky few. Happiness is a state of mind that is not necessarily chosen or ignored, but is sought-after and fought for. When faced with an unbearable and powerless situation it is so much easier to just give up and suppress our desires to excel. It sometimes takes more energy to succeed and far less energy to fail ourselves. Life can be so darn complicated and it may become hard to see the bright side of any given situation, but there is one!

I have always held onto something my grandfather said to me a long time ago, “There is always someone going through something worse than you are in life.” I still do find this to be valuable and very wise information and would never really question anything he had said to me because of how much respect I had for him. But at the same time, how can you really judge what situation is worse in life for anyone? Everyone deals with their troubles in different ways and have their own views on the level of hardships. Is there any comparison in what I live with daily and what someone else with another chronic illness battles? Is my pain any less of a struggle than someone with other pain issues? I think itlife-is-short-time-is-fast-no-replay-no-rewind-25882738 is all in the perspective of the one living with that struggle. I mean think about a person that was just diagnosed with incurable cancer. They have to deal with chemotherapy and so many other decisions, but they do their best to handle that situation the best they possibly can. Or even someone who has already been dealing with Multiple Sclerosis goes to the doctor for an update and is told their illness has progressed from Relapsing-Remitting MS to Secondary-Progressive MS, they have to adjust their mindset in life. Of course these situations are never easy and anyone would go through a vast amount of different emotions, but they do it! Life does not end or allow you to pause it when you are faced with an illness of any kind, you just are required to continue living the best way you can.

We are all supposed to find ways to cope with the life we were given and there is not a rewind or reset button available. Mistakes are inevitable, but we all must learn from our mistakes and carry on with a new outlook on life! We acknowledge what mistakes have perfectly imperfectbeen made, grieve what has been done and lost, set a game plan for moving forward, learn from what has taken place and move on with strength and determination for our future. I believe all of our mistakes made empower us to become even better than we were before. They build our character to be more enlightened and be able to see the bigger picture. We are all just perfectly imperfect humans with the knowledge of what was learned throughout our lives! If we just give up because we failed once in life, we are missing out on all the great things life will offer us!

Our lives are sometimes like a dance. Sometimes we might have our toes stepped on, but dance in the rainsometimes it will be a beautiful piece of work. There may be new and difficult moves to conquer and perform, but over time we will learn to be graceful and almost flawless. It takes determination to learn all the different dances involved in life, but it will end up being something we are incredibly proud of! 

I hope y’all are having a nice and relaxing weekend! I know the weather where I am has been chilly and there is a constant threat of rain which is never very enjoyable, however I am doing what I can to just enjoy the days away from work! I even treated myself to getting my hair trimmed today. It had been a long time since taking care of my hair and it was a wonderful feeling! I am able to relate to my hairdresser’s thought process, which is always great! I like being around people who are down to earth and just very real with their thoughts. It is not so fun being around people that have a fake demeanor because you are always playing a guessing game about what is actually sincere or deceitful! I hope y’all are feeling well and getting the rest you deserve! I appreciate you stopping by my site today and really look forward to any comments you may have, I promise to respond as quickly as I can! As always I am sending y’all lots of love and comfort!!

Love 2

Always, Alyssa

 

Continued headaches and pain!

happy-friday-eve-walking-into-work-like-i-own-the-placeHappy Friday Eve Y’all! I hope you have had a good week and are ready for the much-needed weekend! It seems to have been a long week and I even missed a day of work due to my headaches and pain. I have no answers, only speculation as to what causes my headaches and or pain. As y’all already know, I do not like to give into these issues because it does not ever help and I prefer to push myself further. 

I always lean towards blaming the weather for any pain issues I have and the weather really has been all over the place. It was only last week when it was sunny and warm, but now this week has had a terrible chill in the air and vast amounts of rain. My body does not handle when there is a bitterness in the air because I tend to become very stiff. Then when you add the rain to the mix, I feel every pain possible and more.  Even though I am so thankful for the weekend, it is supposed to rain all weekend. Luckily I will be able to combat the chilly rainy weather by staying inside and under a warm blanket all weekend! 

Stress is a very obvious pain trigger for me. I am pretty sure all of you reading this know how much stress intensifies pain and headaches. I am working on controlling my stress forgive ourselvesbetter. It sounds crazy, but I am the type of person that will stress about being stressed and wonder what I am doing wrong! I think that one way to reduce and manage stress is to set boundaries in life, which I am working on! It is important to recognize that the only thing in life that you are able to control is yourself and you are not able to control other’s behaviors. You are able to control your own reactions and actions, but have absolutely no control on the conduct of another person. We are all have experience with forgiving others, but sometimes forget to forgive ourselves!

Thank y’all for stopping by my site today and your comments are always welcomed! I will respond to all comments as soon as I can and really enjoy the communications! I hope y’all are feeling well and have a relaxing evening! Always look on the bright side of things, we made it through another week and the weekend is almost here! As always I am sending you lots of love and comfort! 

Love 2

Always, Alyssa

 

 

Common Triggers for an MS Flare Ups

TriggersGood evening Y’all! I am carrying on with MS Awareness Month sharing more information with you about the illness. Have you even analyzed what was going on in your life when you had a MS Flare Up? In a way I guess I have, but still never made any changes to what was going on in my life. I know it will not be any fun and might be a little painful thinking back to your most recent flare up, but what was going on at that moment in your life? I will tell you that the major flare up I had this past October was completely and 100% due to stress. Below are some very common triggers for an MS flare up.

 1. Stress:

         a. Emotional stress can lead to a very common MS symptom, depression.

         b. Stress can lead to additional fatigue and confusion, probably from lack of sleep.

    2. Fatigue:

       a. Sleep is very important for everyone, but it is vital for those with MS.

       b. Most people with MS have a lower reserve for energy, so small tasks can be           exhausting.

    3. Infection:

        a. Infections cause about 1/3 of all flares up.

        b. Due to reduced bladder functions in some MS patients, Urinary Tract Infections are very common, which in turn can cause a flare up. 

        c. Even a slight cold or the flu can initiate a flare up. This makes it very important to seek medical attention at the first indicator of a cold or the flu so you can get in front of the ailment before things get worse. 

     4. Heat:

        a. Increased body temperatures, whether due to the weather or having a fever.

        b. Symptoms, like tingling and numbness tend to be more intense during the summer because of the outside temperatures. It is important to stay in the air conditioning as much as possible or try things like cooling vests.

Flare UpNot all MS flare ups are going to need to be treated with steroids. Lord knows, for any of you that have had to be on them they are miserable. Even though I know steroids help shorten the flare up, I will do just about anything to avoid them! Typically issues like tingling, fatigue and mental fogginess will go away on their own, especially once the trigger has been eliminated. Unfortunately there are more severe MS symptoms that can affect mobility and vision that will require a short course of steroids. Each person does need to learn what triggers the various symptoms that take place during a flare up. Sometimes it is easy to acknowledge what your triggers are, but an entirely different situation addressing those known triggers.

Do you know what triggers any flare ups you have had in the past? Do you think there was a way to avoid this flare up if any behaviors had been altered? I do believe if I could learn to manage my stress a little better, I could possibly avoid many flare ups in the future. I can acknowledge what my triggers are, but I have a problem making changes with the issue, which is normally stress. This is not a good excuse for not making changes, but it is in my nature to worry about people I care about and feel an overwhelming need to help them through their problem or problems. I always want to fix whatever issue or issues my loved one are experiencing. Even though logically I do know that I am not able to fix everyone mselse’s issues, but should really focus more on my own life I do still try. This does not fix whatever my loved one is going through, but just causes me so many more issues with my health and an increase in my pain. 

I want to thank y’all for visiting my site today. As always, your comments are very welcomed and I will respond to you as quickly as I possibly can. I know this information is probably well know already, but I hope that it reminded you to be mindful of your own health and try to know what could be possible triggers for you. This information about flares and triggers is not just isolated to MS, but can also carry onto other illnesses. All illnesses can have triggers that cause that illness to rear their ugly heads. I hope y’all have a nice and relaxing evening. As always, I am sending you lots of love and comfort!

Love 2

Always, Alyssa

 

Healthy Anger v.s Unhealthy Anger!

healthy-and-unhealthy-angerDid y’all know there is a difference between healthy anger and unhealthy anger? I honestly had no idea there was a difference. I do not like confrontation at all and I will try to avoid it at all costs. I guess you can say that I just bottle up my emotions even though I know that is not a good way to live.  I try so hard to ignore what I am really feeling, thinking that if I ignore it those emotions will just go away, but they do not! Avoiding confrontation has never been a successful method!

Anger alerts us that we need to protect ourselves. It is an alert that we are not being treated correctly and something in our life is not working out the best way it can and should! Anger is an awareness tool that shines light on an injustice and provides insight to make necessary changes. We should never dismiss the anger that we are feeling, but we should investigate our feelings and make imperative changes and then let it go. Adults-and-Anger-What-Causes-AngerLetting go is never easy, but if we are able to acknowledge and address the pain we are feeling, the next step is to just release those negative feelings and move on with our lives! If we continue to stifle our emotions we may miss an opportunity to make some real positive changes in life and that would be a disgrace to ourselves and we would probably regret not taking the chance we were given for a beneficial change!

Unhealthy anger does not do us any good either. This type of anger can cause emotional and physical issues, but can also have a terrible impact on those around us as well. Anger can suffocate a person that is only trying to avoid the initial confrontation, but the issues are still present until they are dealt with. Unhealthy anger is continuously fed, masks_of_anger_revisited and held onto, but the issue or issues are never addressed. This allows for anger to just pile up and you will feel like you are going to explode. I think the best way to explain it is, have you ever taken an unopened bottle of soda and shaken it vigorously? What happens when you open that bottle? Whatever type of soda you just shook up will explode all over the place.

My soda analogy is what can happen when someone allows for the anger to just stay inside their heart and mind, not address the problem and let it go! Whatever you are angry with will not just magically disappear and improve without talking about it. bottle-explosionCommunication is so incredibly important as it will allow us to learn from the mistakes made in life and make proper changes. Change can be scary, but it can be a good thing as well.

Anger can happen with anyone, not just a loved one or co-worker, it can occur when we drive to work and someone cuts us off. That one small incident with the bad drive sets presence to our mood for the day! With the situation with the bad driver, you are not really able to confront them and get the negative emotion out in the open, so what do you do? I guess you just have to expect for others on the road to not be as cautious and careful as you are and chalk it up to another day on the road! In situations like that I know the initial reaction might be to use some unpleasant sign language, but that does not fix the issue and will not teach anyone how to drive. I can honestly say that it is not easy to let things like this go, but at the same time is not worth our mental time and allowing it to ruin our day!

How many times has your significant other made you so angry that you wanted to angescream? Has anyone in your family ever done something so outrageous that it caused resentment and frustration to the point you were not able to speak to them for a little while?  It is perfectly normal to get angry, especially with family because you know more about them behind the scenes. I think family anger is a lot more painful than most anger because it is so much closer to your heart. I think anger with our family tends to be more intense because we normally have higher expectations for them than just the normal run of the mill person we communicate with. We hold our family to higher standards so we expect so much out of them. Sometimes I wonder if it is just better to keep our expectations low so we are never disappointed, but when something great happens we can savor that moment! 

Life can be extremely difficult and we are all going to face some kind of disagreement angry kittythroughout out lives. It is okay to be angry, but it is also very important to address what you are angry about. If you allow angry to fester and never address the problem, it will only hinder your own happiness. 

I hope y’all had a great Monday! As always I do appreciate you visiting my site today and your comments are very welcomed! I promise to respond to all comments as quickly as I can and look forward to the conversation! I hope y’all have a very relaxing and pleasant evening! Sending you lots of love and comfort!

Love 2

Always, Alyssa

Multiple Sclerosis Awareness

Awareness_buttonThe Multiple Sclerosis Association of America (MSAA) recognizes March as Multiple Sclerosis Awareness Month, so I would like to share some valuable information about this illness with y’all. Many of you already have a decent amount of knowledge on this illness because either you are living with it or know someone who is, so some of this information you are already aware of! Preliminary results from the National Multiple Sclerosis Society reported nearly 1 million people in the United States live with Multiple Sclerosis and 2.3 million worldwide. This seems like a massive amount of people living with this illness worldwide with no cure, yet. I would ask why, with so many fundraisers to find a cure for this illness, why there has not been one found yet, but I think it is pretty obvious what the reason is. You might disagree with me and that is okay, but the drug companies would lose so much money if a cure was released and the greed takes control with that!  I might be wrong about this and it is just hard to find a cure for a debilitating illness, but it would be really great if there could be as it would help so many worldwide.fight for a cure

Multiple Sclerosis is a very unpredictable and sometimes debilitating disease of the central nervous system. This disrupts the flow of information within the brain and between the brain and body. MS is typically diagnosed between the ages of 20-50 and diagnosed 2-3 times more often in women than men. Symptoms do range from numbness and tingling to blindness and paralysis and the severity of symptoms differs drastically between each person.MS Awareness

In 1868 the famous neurologist, Jean-Martin Charcot, lectured on features of Multiple Sclerosis and actually gave it the name. Jean-Martin Charcot was a French scientist, instructor and physician who was the claimed founder of modern neurology. Throughout the 1800’s and 1900’s many other therapists/physicians tried without any success in the treatment of MS. These therapists/physicians created and tested what to me sounds like some very dangerous treatments. One of these dangerous ideas was something called Deadly Nightshade. Deadly Nightshade was a plant with poisonous fruit, arsenic, mercury and injection of malaria parasites. This sounds more like a death sentence than a treatment for the illness. 

It was not until 1951 when steroids started being used to treat relapses in MS patients. Steroids are used to reduce the severity and duration of the relapse. They do not have long-term effects on the disease, but are just used as a short-term fix like a band-aid that just assists the issue. For those of you that have been on steroids, you already know they are not any fun at all. I know when I have been on steroids they make me extremely irritable, exhausted and I have literally no appetite. I think normally steroids increase appetites, but they do the exact opposite for me. I guess I am a little abnormal! Even though steroids have some horrible side effects, they do seem to make the relapse a little shorter.

The first drug that was proven to be effective for a long-term treatment of Multiple Sclerosis was approved in 1993. Since 1993, there have been 15 long-term treatments approved for MS. The 15 approved disease modifying medications include injection, infusion and oral. These disease modifying medications are meant to slow the March is MS Awareness monthprogression of the disease and delay any disability, but unfortunately is not a cure.

In all honesty, I had no idea that this illness had been around since the 1800’s. When I was first diagnosed, I knew hardly anything about the disease. I only knew one person that had MS and granted she was older than me, but she was disabled. I had this overwhelming fear that I would end up in a wheelchair like her. But, it has been almost 18 years and I am still walking just fine. I do experience terrible amounts of pain, numbness and tingling, but at least I have not lost my ability to walk and look like I am perfectly fine. During the times my pain is extremely high is when my motto is “Fake it til you make it!”

For those of you that have been following my blog, you already know I tried numerous different disease modifying medications until I found the one that has been working well for me. I guess back in 1993 when the medications were being released there were far fewer choices for a person to choose from, which must have made things a little easier. Now with so many to choose from you must do your research and test for yourself what works. It is okay to start a medication and find it does not work well with your body chemistry and switch to something else. It is however very important to find one that will work for you so you can have a little better control of the disease. There are a couple of websites that I would encourage y’all to check out as it has a lot of important information MS Warriorabout MS, https://www.nationalmssociety.org/ and https://mymsaa.org/ .

I hope y’all have had an amazing weekend. The weather sure has changed here in the south towards more of a spring like time. It is crazy considering it is technically still winter until March 20th, but I can not complain. It was so warm in February which does make me a little worry about what summer is going to be like. I mean seriously, it was 80 at the end of February, so what are the temperatures going to be in July? 

Thank y’all for stopping by my site today. I hope the information I have given was valuable and interesting. I spent a lot of time researching Multiple Sclerosis when I was first diagnosed, but over the past few days I did a little more reading and what I discovered was so interesting. I hope you enjoy the rest of your Sunday and I hope you are prepared for the new week to start. Truthfully, I am never completely prepared for a new week because the weekend is so short, I always feel like I did not get anything accomplished, if only the weekends were longer! I look forward to any comments you may have about this post today and I will respond to you as quickly as I can! As always I am sending y’all lots of love and comfort!

Love 2

Always, Alyssa

 

 

Months of Awareness!

Awareness 1

Each month recognizes a different illness or cause. Most months actually acknowledge several as there are so many various illnesses that affect people all around the world. 

January is National Blood Donor Awareness.

February is American Heart Health Month.

March, MSAA, Multiple Sclerosis Association of America recognizes as Multiple Sclerosis Awareness Month.

April is National Parkinson’s and Autism Month.

May is National American Stroke and Mental Health Month.

June, National Safety Month.

July is National Cleft and Craniofacial Awareness and Prevention Month.

August is National Immunization Awareness Month.

September is Pain Awareness and also National Sickle Cell Awareness Month. September is also National Alcoholic and Drug Addiction Recovery Month.

October is both National Breast Cancer and Domestic Violence Month.

November is National Alzheimer’s Disease and Family Caregiver Month.

December 1st is World AIDS Day.

I find it astonishing how many different illnesses or causes are acknowledged during the course of a year. Throughout the rest of this year, I would like to talk a little about each month’s awareness that is recognized because I think it will give all of us a little more knowledge on the subject. Now like I stated, there are multiple different acknowledgements so I probably can not touch on all of them each month, but I will choose the most either closest to my heart or not as well-known. 

I hope y’all had a great day today! I do not know about you, but I am SO happy tomorrow is Friday! It has been a very long week filled with many headaches and other pains. IFriday Eve hope that next week is going to be a better week with a lot less pain and stress. Of course as y’all already know, I do believe that a positive mind will bring much happiness and good days in the future. So I will continue to always stay positive because there is no room for negativity in my life! 

Thank y’all for stopping by today! Please let me know what you think of my plan for the rest of this year to talk about each awareness month! I always love hearing your feedback because your comments are so very interesting and helpful! I hope y’all have a great and relaxing evening. As always, I am sending you lots of love, comfort and warmth to those of you dealing with snow!

Love 2

Always, Alyssa