National Cheese Fondue Day is Sunday, April 11th, 2010.
Matt and Ruby Soik, the new owners who bought our restaurant in January, are hosting Cheese for Charity to benefit the National Multiple Sclerosis Society in my honor. They will donate $10.00 for every cheese fondue purchased to the MS Society. If you would like to join us you may want to call ahead for reservations at 816-931-6358. Join us and have a fun time showing your support towards great steps in understanding MS. Our family will be there 3:00-5:00 or there abouts and would love to see/meet you! Karen
Sunday, April 11th, 2010 ALL DAY LONG Cheese for Charity The Melting Pot 450 Ward Parkway Kansas City, MO 64112 for reservations, 816-931-6358
Fortunate cookies can have some good advice. Call it strange but I began keeping every fortune I got years ago to remind me of the things that are important. The message always seems to come at the appropriate time.
Kylie (10) mentioned this morning that she wanted to be an Olympic athlete so of course Layla (4) had to pipe in too. I almost wet myself after she yelled, "I want to be a professional bath tub washer!"
As the program comes to an end, I am sad. These amazing people are a large part of my daily life and even though they have given me the skills to be successful moving forward on my own with Multiple Sclerosis, I will very much miss their company along the way. I need them each to know that their support and friendships have affected my life on a deeper level. So, how do I expect to thank these people who have truly changed my future and asked for absolutely nothing in return? Words, cards, flowers, even homemade baked goods all seem insufficient in these final moments. I pay it forward by helping someone else. I am confident that this is exactly what they would all want me to do.
To Flourish! Magazine, Sheridan, Mika, Rebecca and Shawnee Mission Medical Center,
Thank you for creating this opportunity. It has been a phenomenal experience and you have started many doors opening for future opportunities. I am living a healthier, stronger life today because of your admirable generosity.
To Gary, Leslie, Mary Lynn, Rennie, Barb, Dr.Foos, Lauren, Julie, Sunlight Day Spa and Travel Concepts…Thank you. Each one of you has given me priceless gifts that I will never forget and can’t wait to share with others in my life.
The seven months before the Transformation program started, I was doing my best to hold it together but it is terrifying being diagnosed with a chronic illness. I was very sick and had some moments that I wish the kids had not witnessed. Needless to say, this has been a highly emotional process for me and that obviously affected our entire family. In our time together, Rennie has helped me to “be prepared” mentally to accept a chronic illness into my life. She has opened my mind to positive ways of dealing with the anger, panic and anxiety that come with each new attack. She has been an incredible mentor to get to know my story and guide me along the way. I have learned a lot about myself and Rennies friendship has been a huge piece of my success.
While I am mentally prepared to fight MS, it is just as important to combat this complex disease with physical strength too. Progress in the gym has been phenomenal. I have gained body strength surprisingly quickly. For the first time in my life, I have muscle definition. The spasms at the base of my neck that were leaving my left arm and face paralyzed have stopped completely. The neurologist says I am officially cleared to stay off the anti seizure meds. I am so relieved. The gym shoes are permanently out of the closet. Several months ago, I was dragging my legs behind me and I couldn’t do stairs without Andy’s shoulder to lean on. I have graduated from an exhausting fifteen minute warm up to an easy 5 mile run. Clearly my body is stronger, healthier and ready to fight after this eight week boot camp with Sergeant Gary.
The medications commonly recommended for Multiple Sclerosis are extremely over the top expensive and fortunately without health insurance I could not immediately follow that more conventional path of treatment. I will be the first to admit that I do not know exactly what this disease will do to my body with or without the recommended medications…BUT NEITHER DOES ANY DOCTOR ON THIS PLANET SO FAR…What I do know is that I have felt pretty darn good without the traditional medications and have experienced overall positive progress. I think sometimes we easily resign to taking medications without giving a holistic approach even a thought. It’s really too bad. I am encouraged however by the large number of people that I have met with stories to share about their own experiences fighting and even eliminating disease with nothing more than a major overhaul of their lifestyle habits. It was “luck” in my case that a close friend who is a doctor in Oregon has a father living with MS and a sister who is a nutritionalist. It was recommended that I read the book, “The MS Recovery Diet” by Ann Sawyer and Judith Bachrach. The book was fascinating to me and it made good sense. I decided that this MS diet was my path to healing for now. When I realized that winning this Transformation would give me personal time with an experienced Dietitian, I was ecstatic. Barb helped me gain strength in my mind and body thru her expert knowledge on diet, nutrition, vitamins and supplements. She taught me how to decode labels and interpret nutritional facts. We shared recipes and information about new allergy free products on the market. What Barb does is give people a strong chance at healing the body through healthy refueling. I admire her work and I feel strongly that my path is leading towards helping people understand how important it is to take stock in how our diet can affect the health of our bodies.
My husband and I have decided it would be best for us to stick with Dr.Foos as our family doctor and my overall health advisor. I feel very secure knowing that she is joining my team of health care providers and at the perfect time. We are a good match and I am blessed that this Transformation led me to her. She has been so kind to have provided the blood testing that I desperately wanted to determine possible food allergies and vitamin deficiencies. I would not have been able to put money into specialty testing right now just to ease my mind. I am extremely thankful. Dr.Foos is accepting of my choice to not take the DMT treatments and she is already communicating with my neurologist in order to understand her piece of my total health care plan. After months of doctor after doctor, I feel a huge weight lifting off my shoulders being united with Dr.Foos.
I also urge everyone to strongly consider the importance of dedicating time to take care of your mind and spirit. I have found that undeniably rest and relaxation are just as important to healing my body as diet and nutrition. I personally recommend a visit to a Sunlight Day Spa. They provide a beautiful serene environment and a variety of relaxing services. I really don’t think which service you choose is so important. Your soul will thank you anyway for taking the time to be alone, breathe deeply and repair through relaxation. I was spoiled by this transformation program and spent one day every week with Lauren alternating treatments between signature facials and Microderm abrasion. My skin is literally glowing and it certainly doesn’t hurt to feel younger.
Being diagnosed with Multiple Sclerosis so far has been something like being a virgin rider on an uncontrollable rollercoaster. There are so many ups, downs, and loop de loops that you never know what to expect. I have to live by the Boy Scout motto to be prepared. It is some darn good advice when your body can literally stop working with no red flag warnings required. It takes some time to get used to having no control and there are certainly still moments I find myself desperately searching for the chicken exit. I have made amazing progress in this Transformation program. It has been such an unbelievable blessing to have had this health care team by my side through early diagnoses. I truly do not know where I would be today or in the future without the support of this program, my family and friends. In just a few weeks with this incredible Team, I have transformed from an anxious newly diagnosed patient to a strong woman on a healthful track.
Sorry for the long hiatus. Andy and I went to a friends wedding and I promised myself that I would leave everything behind and focus on my husband. We had a great trip and we needed it! I am not however in a good mood since we returned to this Kansas City weather. Does anyone else feel like they are living in a black and white photograph? I need this dreary winter to be over. Ugg.
No worries ladies. All the personal emails are just as wonderful!! Thank you all so very much for supporting me on this journey. I have a really amazing group of friends and I am thankful for that. For those of you who have asked, yes, I will continue to blog after the Transformation is technically over. Karen
Thank you for the kind words, support and positive energy. I really enjoy reading everyone's comments and I am truely touched by how many of you are taking the time to check up on our family. Please, please don't be shy. Writting is very theraputic for me, but my relationships with all of you are what I build strength from each day.
Make sure your hubby knows that you would like to spend some time getting pampered at Sunlight Day Spa for Valentine's Day. Ask for Lauren Smith, my esthetician, if you want Kansas City'sbestfacial. Plenty of other services are available from massage to sauna therapy. There are special discounts and packages for couples too.
Make sure you let the spa know that Karen sent you!!!
Sunlight Day Spa 7373 West 107th Street (Metcalf and I-435) OP, KS 66212
I can’t count how many times I have heard the phrase, “You’re so lucky” but in the case of luck, the bad also comes with the good. People who are not “lucky” never consider that truth while accusing others of being lucky in a jealous sort of manner. At the age of 12, I won $100.00 from a McDonald’s pull and play game on the side of a super sized Dr.Pepper. Several years ago, I took my last $20.00 to the casino and won $1250.00 with one Hail Mary quarter in a slot machine on the way out the door. Those times I can maybe chalk up as being lucky. Last year…my husband lost his job, an elderly lady totaled our car with Kylie and Andy in it, we couldn’t get the kids healthy ever it seemed and Andy landed in the hospital twice. Then in June I was diagnosed with Multiple Sclerosis just after losing our health insurance coverage we had carried for years. What luck!
Yes I’m being sarcastic but the part that confuses me is how often people accuse me of being lucky in relation to experiences that have little to do with luck. An old friend contacted me after stumbling onto a Flourish magazine in her doctor’s office waiting area. She left a wonderful message of encouragement at my home number and her final words were, “Congratulations. You always were the lucky one.” Stop right there. We are all super heroes with super powers. We are all capable of creating opportunities for ourselves in this life. If I had not taken the time to write up my story and apply for this amazing transformation, I would not be experiencing it now. It’s as simple as that. Flourish kindly created the opportunity for me and I just gave the universe a push in my direction and created an opportunity to win. Guess what folks there is no secret. Lucky people are just not afraid to put themselves out there and see what life gives back. We should all just go for it way more often than we do. If we fail we still learn from our experiences and are better for trying.
If you don’t believe you have the power here’s another story for you. I have a great woman in my life named Tracy and she had never been on a cruise before. She really, really wanted to take one but didn’t have the means to go on her own. What she did have was her belief in her own power. Through a process of creative visualization, she just knew an opportunity to take a cruise would come into her life. She very consciously spent extra time each day thinking about her swimming suit, warm beaches and tan skin. Tracy is a corporate meeting planner and she and an assistant had been working their ***** off to put together a VIP event for the boss and all his big wig clients. In the end, the event was phenomenally successful and the boss came away with several profitable clients. As the boss was thanking her, Tracy got her opportunity and let’s all note here that she took it. She half jokingly suggested that instead of her normal bonus, the boss treat her and her assistant to a cruise this year. He basically laughed in her face and she left the room. She was sitting at her desk a few hours later when the boss stopped by, placed his credit card on the desk and said, “Book your cruise Tracy you deserve it.”
It’s a darn shame that more people do not take advantage of their super powers. Call it the use of creative visualization, the concept of ask and you shall receive, praying or talking to God, invoking the power of positive thinking. Whatever you like but it’s obvious to me, it works. You truly get the positive energy you put out right back at you. Let me ask you this. How is your current perspective working for you? If you can honestly say it’s not, then change your perspective. Try a different approach. Live with a positive outlook and don’t be surprised when it leads you somewhere wonderful. Believe in living by loving life, create your own opportunities and let the force be with you.
MS is widely believed to be an autoimmune disease in which a person’s own defensive cells are mistakenly attacking their body. In Multiple Sclerosis, those attacks are specifically directed at the myelin or protective covering that surrounds nerve fibers in thebrain and spinal cord. When the damage to the protective covering happens, damages are commonly replaced by scars of hard tissues. Sometimes the actual nerve fibers are even severed permanently. Signalstravelling these damaged pathways get lost when they cannot get through. Ultimately the damage causes miscommunications which lead to a long list of MS symptoms. Some common symptoms include altered sensations like numbness and tingling, disabling fatigue, depression, sudden or spastic muscle weakness, loss of coordination, chronic pain and visual impairments. Don’t forget the slurred speech, loss of sexual function, short term memory problems and cognitive dysfunctions too. And oh, advanced symptoms of the disease can even include the inability to swallow or control breathing and issues with incontinence. It’s not pretty but it’s our reality. As I begin my MS journey, I know it’s simple. I have to stay strong and fight to stay off the path to disability. For me, that means eating a truly healthful diet, keeping my body active with exercise, getting lots of extra rest and not over committing due to guilt. I am self medicating with nutrition, exercise and peace of mind. It’s quite a workout but I believe in it to my core. I will be one old, old woman cruising around KC in my pimped out Hoveround. So how does a healthy diet relate to this chronic illness?Well, however much you don’t want to admit it, we really are what we eat. Most MS diet concepts are built on the idea that certain foods are allergens and will cause inflammation and trigger the confused immune cells to attack the body. The diet is believed to stop the disease process by eliminating the trigger foods and replacing those fuels with ones that promote repair, help the body restore and ultimately recover.
Every hour someoneis newly diagnosed with Multiple Sclerosis and yet most questions I ask in the neurologist office are answered with an apologetic “we just don’t know yet.” Approximately 400,000 Americans have MS; about 2.1 million people worldwide, 2/3 of who are women. It is a very complex disease, being an autoimmune disease, a neurodegenerative disease and a vascular disease. There are many theories about the Who, What, Where, When and Why processes of Multiple Sclerosis but the truth is researchers are still looking for a causeand a cure. All I can hope for is to raise some awareness about thisunpredictable disease.
Seriously. I LOVE the Pulminary Club. Most likely they have NO clue how much more entertaining my workouts are when they are in the gym. This morning's topic of discussion was sex and your air tank. Thanks for the smiles!
Monday, January 18th, 2010 I finally found some energy today after fighting some serious MS fatigue this weekend. I literally slept for the last three days of my life.
4:30: Had an appointment with Dr.Foos. We discussed the weekend fatigue, pain management again and belly dancing. I am going to have to check out this Shimmy show on Fit TV. Michael, the nicest front desk guy ever, helped me with the name of the man in the blood lab with the needle skills. His name is Abraham and you bet he will get a note of appreciation from me soon.
And…my best friend Aimee had a baby girl this morning. Matt, Aimee and Braiden welcome into this wonderful world Reese Mariah Kern. Congratulations!!
Tuesday, January 19th, 2010
10:00am: Trained with Gary in the gym. We are working hard to make me stronger, keep each other motivated and get me in shape for a bikini in Mexico! Let's not be shy, buttocks are very important. Thanks to Gary’s strength building program, I have noticed a significant decrease in the reoccurring spasms effecting my neck and shoulders. Phew, no anti-seizure meds for me!
11:15am: Rennie always gets an earful but she listens like a big sister and always has some great advice. I find myself referring back to our conversations often and I am a little freaked out that our sessions are coming to a close soon. She has helped me to deal with everything from being diagnosed to parenting a 4 year old child.I am thankful for her wise perspective and that she is sharing it with me.
12:15pm: Took an autographed Maxine poster (My dad is the creator of Hallmark's Maxine) to a completely un expecting lady who works in Balance and Vestibular Therapy. I kept noticing her Maxine water cooler as I passed her office on my way to the locker room. Thought she might be a fan and it felt really good to brighten a stranger's day. The plus is that she is no longer a stranger and now I can say hello to Vicki as I pass her door.
I had to burn some time until my appointment with Barb so I went to the Library and got two books: The Sensitive Gourmet, Imaginative Cooking without Dairy, Wheat or Gluten by Antoinette Savill and More From the Gluten-Free Gourmet by Bette Hagman. I will let you know if there are any great culinary discoveries to share after I read them.
2:00: Shared the books with Barb, discussed my horribly fatigued weekend and why I desperately need to start a food dairy. We also had a great conversation about inpatient nutrition, hospital menus and educating newly diagnosed patients about the effects of diet on disease. I have some very strong feelings about the importance of this subject and get a deep feeling that this is the direction my path is leading...
I am sitting at the library (in between appointments at the hospital today) trying to figure out how to manage all my daily tasks and have more free time to write. As a matter of fact, I would love to figure out how to make a living out of writing.
I have been meaning to mention a wonderful facility available to people with chronic illness in Kansas City. It is called Turning Point, The Center for Hope and Healing. They offer free programs for participants including Yoga, Tai Chi, Nutrition Programs, Meal planning, Cancer support groups, Wellness and Relaxation, Families Affected by Illness, Teen Chat, Medical Play...on and on. You get the idea. I went to a program on MS and Nurtition and it was fantastic. Great place. They need our support and donations are always accepted.
Turning Point 8900 State Line Road, Suite 240 Shawnee Mission, KS
A new year. Thank goodness. Let's all pray for a peaceful 2010. Saturday I had my first microderm abrasion with Lauren at the spa. I had immediate results with no irritation so that was great. I look younger already. Yesterday (Monday) I meet with Dr.Foos and got my results back from the blood tests. Both Dr.Foos and Barb (the dietician) were impressed with my cholesterol being so good. Too bad we don't have those numbers from four months and 40 pounds ago...that would have been interesting. They ran a food allergy test for several items none of which came back with a positive. That is good but suprising. The thought is that I may have more food sensitivity then an actual allergy to those items. My vitamin D level was slightly low so I will work to bring that up in the next few months. Everything else looked great! I had a rough day yesterday with a massive headache and lots of leg pain. I still get panicky when symptoms appear in fear that I am about to have another major attack. Thank goodness when I woke up today I felt good. This morning I arrived early to the gym and did an extra 30 minutes on the eliptical for cardio. Gary is pushing me to increase my weight on the machines and I am actually impressed with how much I can handle. Gary says I am getting strong. Watch out! Rennie and I focused on some relaxation techniques today which I have definately needed recently. That was great however I lost feeling in my left arm as we were doing it. This is a daily occurance lately which if it continues will require anti seizure meds. I do not want to start treating every symptom that comes along or I might be a walking pharmacy in the end. Luckily the nuerologist agrees. Barb and I discussed the test results and supplements today also. She hooked me up with the KC Chapter of the Celiac Sprue Association. (gluten free people) I am still working on getting you updated on a simple definition of MS, why I choose not to be on the DMT treatments and what I am doing with diet and nutrition. I think I'll add some photos too so check back soon! Karen
So last night my mom and I were happily shopping at Macy's together when from out of the next dressing room came..."OMG!!" Seriously? When did people start talking in Chat Acronyms?...And she was alone to top it off!
Every girl deserves a day at the spa and when it comes to complete relaxation the place in Kansas City to do that is Sunlight Day Spa. I know I sound like a commercial but it was really that wonderful. The facility is gorgeous and immediately calming. I was hooked the minute Lauren handed me a warm robe, wrap and slippers. Then there was a lovely foot soak with rose petals and a glass of cucumber water; and all this just to fill out paperwork! The plan at the spa is to focus on my skin so the actual facial involved a toasty bed in a dark room with relaxing music, lots of massage and general bliss. Thank you Lauren and the ladies at Sunlight Day Spa! I am counting the days until next week.
A few nights ago I fell asleep with a smile on my face. It is an amazing blessed feeling. I think that anyone facing a lifetime of chronic illness goes through different cycles of emotions. For me it started with panic and an anxious fear of the unknown. Fear turned into relief once I received the diagnoses. Then I thought I was Wonder Woman and could handle this all by myself so as not to be a burden on Andy and my family. Reality sank in along with some pretty intense depression and frustration. Finally the acceptance; I would need help along the way and that was ok. I was able to give myself permission to let go of the impossible expectations I held about being the perfect mother and wife. That was very hard and wonderful all at once. I thank God daily for my patient husband and my incredible mother who got me through the toughest days. But the truth is that being diagnosed with Multiple Sclerosis is nothing short of a blessing. I was on a fast paced track skipping over the most important moments in our lives. I have lived and appreciated more life in the past 7 months then I have in the last 7 years. I have loved deeper and laughed honestly. As Rennie would say, I happily write my name in the dust on the table instead of obsessing over cleaning it.Dust can wait. Children, family and relationships cannot. I have found focus for my life and realized what is most important. All thanks to MS.
Before I began the Transformation program, I was feeling anxious and tired. It has been a long exhausting year and I was nervous about if I would meet the team’s expectations for a successful transformation. I quickly realized my fears were silly; ridiculous really. Everyone on The Team is warm and welcoming. It is their natural generosity to support my needs that got me where I am today. I am happy to say that I feel strong and ready to fight this disease…and The Team and I are really just getting started! What an amazing gift.
I start the program each week with Gary (my personal trainer) in the gym. We discussed the need to build up strength in my neck, shoulders and legs to combat the damage the lesions in those areas have already caused and help my body to heal quickly after the next major attack. Gary introduced me to the gym equipment and has given me a general plan for my future workouts. Leslie, Gary's manager, was kind enough to provide me with an extended membership and 24 hour access to the facility. They could not make this any easier. Last time with Gary in the gym we worked on leg strength training, back end firming and how to fall safely. I am having problems with my coordination and have recently taken some big spills. That was a key lesson.
After my workouts with Gary, I spill my guts to Rennie (my health and wellness coach). I feel incredible leaving the hospital after a great physical and mental workout. Rennie has an amazing way of welcoming you in and just talking. It seems very natural to speak openly with her about my life. I did not anticipate how much I needed Rennie or how much I would enjoy my time with her.
Dr.Foos, my family physician, did a general checkup and we talked about what test were run at the hospital in May and what we still needed. She was able to put my mind at ease about medications for pain management which was a big deal. Dr.Foos ordered some labs and they drew blood to test my cholesterol, vitamin D levels and food allergies. I should have taken the time to learn the name of the man who drew my blood because he is the first person in months with a needle who actually hit the correct spot the first time. Bless you kind sir.
I was excited to meet Barb Marsh, my dietician. I needed to know what this drastic diet change had done to my body. I had a general idea what vitamins and supplements my body needed but had no clue in what amounts. I know I am eating well to eliminate any food allergy triggers for MS but I have not been great about eating enough of the healing foods. Barb said she almost had a heart attack when I started listing the foods I am not eating…no gluten, no dairy, no soy, no sugar, no legumes and so on…the Paleo or Vegan diet with the exception of some lean meats and proteins. All fresh, nothing processed. Andy, the girls and I enjoy visiting City Market and cooking together as much as possible. I think by the end of our time together Barb was impressed by my determination to be as healthy as possible. She will be a great resource for my future health plans.
I saw my neurologist and she was very pleased with my positive progress since our last meeting in September. I made sure she knew that progress was due to this program and the team’s support. Thank you to Flourish! Magazine and The Team once again. I appreciate your individual talents and generosity. You are truly a blessing in my life. Thank you for giving me the knowledge and skills to be healthy, educated and confident through my battle with MS. I am looking forward to our next few weeks together. Karen
What an amazing experience. I am having a hard time putting into words how grateful I really am. I started the program on Monday last week with Gary (my personal trainer) in the gym. He introduced me to all the shoulder and upper body equiptment and gave me a general plan for my workouts. I went back on Thursday and worked out on my own. Leslie, Gary's manager, was kind enough to provide me with an extended membership and 24 hour access to the facility. After my Monday workout with Gary, I spilled my guts to Rennie (my health and wellness coach). That was a great experience for me and I felt incredible leaving the hospital that day. Yesterday I met for the first time with Dr.Foos, my family physician, and she was likewise wonderful. Dr.Foos did a general checkup and we talked about what test were already run at the hospital in May and what labs we still needed to run. She was able to put my mind at ease about taking medication for pain management which was a big deal to me. This morning I met again with Gary in the gym and worked on leg strength training, back end firming and how to fall safely. I am having some major problems with my coordination and have recently taken some big spills so that was a key lesson. Rennie met me after my workout and we dove into more conversation about my process of dealing with all of this emotionally. I honestly did not anticipate how much I needed Rennie or how much I would enjoy my time with her. Tomorrow I will be having my first meeting with my dietitian, Barb Marsh. I am very excited for this meeting because I am looking forward to getting a plan together for what vitamins and supplements my body needs. I know I am eating extremely well to eliminate any food allergy triggers for MS but I have not been great about eating enough of the healing foods. Barb will be a great resource for my future health plans. That brings us to Thursday which I think I may have off. Happy Birthday Dad!! Friday morning is my follow up appointment with Dr.Foos and Friday afternoon I see my neurologist again. Friday is also Layla's 4th birthday. Happy Birthday Layla! I want to thank Flourish! Magazine and the team once again. I appreciate their individual talents and generosity. They are all truely a blessing in my life.
Thank you to everyone who has already read and emailed me about the blog. It really is theraputic to know we have an amazing group of friends surrounding our family. If you would like to post a comment to my blog, you will need to sign up as a member. I promise they won't send you a bunch of junk. I really would encourage you to post comments if you are comfortable doing so- I think it makes the blog more personal and certainly more interesting. Thanks again for all the incredible emails in the last two days! Karen
It was late March just after Spring Break this year when everything started to happen. My husband Andy and I had taken our two girls to Omaha, Nebraska to visit friends. I remember my first “that’s strange” moment happened as we were standing at the zoo by the seal exhibit staring up the hill at the elephants. It just seemed like it was miles and miles away. I felt completely exhausted in a way I had never felt before. It seemed a little strange and I whined about having to walk so far but went along anyway. When we went back to the hotel that evening, we went down to the pool. I enjoyed the hot tub only for a few minutes before I started to feel like I could pass out. Looking back now and knowing all the disease triggers, I realize that I never should have gotten into that hot tub. It may have been just the thing the disease in my body needed to wage its first major attack. It’s a long story so I’ll give you the next months on fast forward…We got home and a few days later I was cleaning the house and my right leg started to go numb. I mentioned it to Andy and we decided I must have pulled a muscle in my back. I went back to cleaning and did not make much of it. The next morning both legs were numb from toe to tummy. I was immediately concerned but didn’t want to overreact either. (At this point you should know that my husband lost his job in January and due to a series of other events, we have no health insurance.) The first doctor, an old school dinosaur by the way, ran some tests. His diagnoses went something like this. You hurt your back. It’s nothing major. Just go home and take these pain killers. If it isn’t any better in a few days we should do some x rays on your back. I let a few painful, anxious days go by before the numbness started to grow up into my abdomen and rib cage. Andy took me for x rays at the chiropractor. After reviewing my x rays and other tests, the chiropractor says there is nothing major going on but there are a few areas of miss alignment that could be causing the issues with numbness. I chose to move forward with his treatment plan thinking doctor number one was right and it was just my back. I think for the first few weeks of treatment the chiropractor must have thought I was crazy. I had never been hurt enough to take me out of commission and I had no idea how to deal with it. I reported every little change just in case. After a few weeks, there was only slow progress with the legs and numbness.I started to get anxious again and decided I needed another opinion. Doctor number three asked a bunch of questions and ran minimal tests to confirm it was just my back. She then gave me a muscle relaxer and a strong anti-inflammatory drug.I went back to my chiropractor and continued treatment.Some time passed and the numbness started to release my body and eventually my legs.I was actually very chipper the morning of the day that I landed in the ER. My legs were recovering and I felt almost normal again. I strutted into the chiropractor’s office and announced my happy news. I could run a marathon today and I would be almost 100% if my eye wasn’t driving me crazy the past couple days. (There was a strange blind-blurry spot in my right eye.) Since the eyes were not his specialty and I think at this point he had a sneaking suspicion this was not just my back, the chiropractor sent me to an eye center to have more tests. I failed the field of vision test miserably in my right eye and before I knew it was off to the ER with the diagnosis of a brain tumor.(I would like to say this. If you are a doctor, please do not tell a patient they have a brain tumor while they sit in your office all alone. They might need some support to hear that news. Thanks, Karen)
Andy took me to the ER and my dad met us there. It wasn’t long before I was strapped into the MRI but it seemed like forever before the ER doctor came back with any results. The good news was it was NOT a brain tumor. I felt relieved. The bad news was that it was most likely Multiple Sclerosis. I was in the hospital for a few days. I held it together through 3 different MRI’s, a spinal tap that went bad and resulted in a blood patch that went bad and resulted in my first experience with the thoughts that I might die. There were also seven days of high dose steroids and two miss scheduled neurologists. I was not well informed about the effects of high dose steroids on your body and emotions. I lost quite a bit of hair and I cried a lot. Waking up in the morning alone in a hospital bed was the worst. I was thankful though that maybe I was getting closer to some real answers.
Meanwhile at the homestead…Andy is at home with two kids and a garage sale we had been planning to raise some extra money for our trip to Disney World in four days…Yes, Disney World in four days. With a couple valium for the plane ride and my Neurologists encouragement, I did make it to Disney World. I was feeling great pumped up on all those steroids until I hit the steroid drop off effects standing in the middle of Epcot. That was fun. It was in the end just what we all needed. An incredible once in a lifetime vacation and a great place to relax with the whole family after the crazy twist our lives had just taken.
What I ‘m working on sharing next…What is Multiple Sclerosis, why I chose not to be on the DMT treatments for the first year, what I am doing with diet and nutrition, why I entered the contest and my first days in the program.
I feel the need to start with this…I am not a doctor or a nurse; nor I am medically trained in way, shape or form. Everything I mention or suggest in my journals is information gathered from speaking to doctors and nurses, research and reading on the internet, in magazines, books and talking with other people living with Multiple Sclerosis. When I was diagnosed, my immediate reaction was to learn as much as I could about this mysterious disease and figure out how that applied to my situation. Knowledge is power in my mind. I am happy to share my story with you and everything I feel is working for me. Please share with others affected by chronic disease keeping in mind I am not a medical professional and you should always check with your trained health care providers before trying anything new in your health care plans…
It must have been a tough decision. I know there are plenty of well deserving candidates out there struggling with life in one way or another. Sheridan called early the morning of October 30th to let me know the news. I had been selected for this amazing life transformation journey and for the next eight weeks will be blessed with the knowledge of a professional health care team from Shawnee Mission Medical Center. I will also be treated at Sunlight Day Spa and rewarded with a four night luxury stay at Secrets Resort in Mexico. I cried. I am thankful, overwhelmed, humbled, honored and most of all hopeful. This opportunity can only bring positive changes at a crucial time in my diagnosis. Please join me on this journey. I promise to be honest and open; sharing the story as it happens. My hopes are that we can all learn together more about Multiple Sclerosis, what it is to live with a chronic illness, to deal emotionally with a diagnosis and what happens when we choose to treat illness with exercise, diet and nutrition instead of drugs. Away we go...Karen