Category Archives: Survivor Stories

Kenneth’s Lupus Survivor Story

In the year of 2006 on September 11, at the age of 16, he was diagnosed with a sickness called (S.L.E.) Systemic Lupus Erythematosus, class V Lupus Glomerulonephritis with ‘Kidney Disease’ Nephritic Syndrome. Systemic Lupus affected both of his kidneys which almost killed him. A lot of people don’t live long with this sickness; like his great grandmother (Kenneth was born on his great grandmother’s birthday) – who lived only a couple of month before she passed away. Kenneth still has this sickness today.

In the year of 2006, Kenneth was in the hospital often. He went through a lot of surgeries; the first surgery he had was on his kidneys – The results came back and that’s how he found out that he had Systemic Lupus. This sickness is rarely found in males but it’s a very dangerous illness. Hair loss, swelling of the body [He had some much fluid inside of his body that he couldn’t urinate with taking a water pill], back pain, mouth sores, headaches, low stamina, muscle pain, can’t stand/walk for a long period of time and depression are a few of the side effects that Kenneth had to deal with and is still dealing with. Kenneth is in pain every day of his life but he thanks Jesus for giving him the strength to deal with the pains. Every since Kenneth Weal was diagnosed with Systemic Lupus, it changed his life around in a very positive way and that’s the only good thing that came from this sickness.

Please read his full testimony on http://www.KenWeal.com/HISTORY

Website http://www.KenWeal.com
Facebook URL achaten-suisse.com http://www.facebook.com/KennethWeal
Twitter URL http://www.twitter.com/KennethWeal%20

Andrew’s Lupus Survivor Story

Andrew KuzykI was diagnosed with Lupus after a difficult battle with Renal Cell Carcinoma, requiring my right kidney to be removed. Not many men are stricken with Lupus, which cannot be explained by the medical community. All the unbearable pain, signs and symptoms along the way we’re never collectively considered by anyone, including myself. From Gall Bladder Cancer, Malignant Melanoma, extreme fatigue, organ failure, headaches, memory loss, extremely painful joints, nothing ever added up. That is until a routine blood test confirmed I suffer from the incurable disease, Lupus. Suddenly, I began to experience horrendous joint pain, especially in my knees, hands, and feet. I noticed them swelling up and turning red, while the pain only increased in magnitude. I ignored it for months as I take care of my grandkids and 5 chihuahua rescue dogs. I was simply too busy trying to take care of my family instead of taking time to care for myself. My joint pain has increased and due to my physical and mental decline, I am trying to balance how to deal with these life-changing illnesses. I had a great physician in Arizona, who never dismissed me or my condition. Unfortunately, I lost my home in Arizona, relocated to Georgia to be near my 4 grandkids and now live in a small basement with my chihuahuas. I am in a world of hurt right now from the effects of 6 bouts of cancer, sickness, and Lupus. God gives us the strength we need each day. He has also given me my life, my 4 grandkids, and 5 chihuahua rescues, who help me when times are tough, which seems to be quite often these days. Of course, God has given me the will to keep going, no matter how severe my pain and suffering become. I still feel I am very richly blessed even though life is slipping away. I have been in the workforce since I was 13 years old and never in my worst nightmare thought I’d find myself here like this. I have dealt with multiple bouts of various cancer, Ewings Sarcoma (Bone Tumour) Adenocarcinoma (Gall Bladder Cancer) and was forced to have my right kidney removed due to Renal Cell Carcinoma. Orthopedic surgeons were forced to have my left leg sawed in half to remove a large cancerous bone tumor there, which has now been affected with severe degenerative arthritis and I suffered a serious heart attack. I now require double knee joint replacement surgeries but have no insurance. and severe rheumatoid arthritis. Being affected by Fibromyalgia, extreme depression, shortness of breath, high blood pressure, diabetic peripheral neuropathy, advanced Alzheimer’s disease, coronary artery disease, and now this incurable sickness, Lupus for me is quite overwhelming at best. Lupus is one of the world’s cruelest, most unpredictable and devasting diseases with a brutal impact on the human body. The inflammation and permanent organ damage caused by Lupus has harmed everything from my kidneys, joints, internal organs, heart, and brain. The physical and mental implications can be different from person to person. Many people say to me “you don’t look sick” when there is actually a horrible battle raging within my own body and vital organs. I try my best to avoid negativity at all costs and embrace God’s grace and spirit daily. That being said, The physical pain is now so intense I cannot even roll over in my bed any longer and am definitely losing the battle. Sometimes it means taking a four-hour nap simply because my depleted body says “No More”. I cannot work any longer because of my conditions and the pain is so intense. I cannot afford the medications I need to even attempt to manage it. The list of lifestyle changes seems only to grow longer as time passes by and I realize my time here on Earth is very, very limited. I take pride in my ability to keep my spirits up, even in my darkest hours. God gives me the strength I need each hour and every day…even though Lupus, Melanoma and high blood pressure is destroying my healthy organs, which I have already lost my gall bladder and right kidney to cancer. I’m a Grandfather and a friend much like many others who have been diagnosed and cannot physically or mentally function any longer. I simply push forward. Just a small window into my private life. I would be grateful for any prayers and positive thoughts sent my way. I am still here.

Despite Lupus I …

So often we lupies tell our woeful stories of the devastating effects lupus has had on our lives. And as important as it is for us to be able to discuss the difficulties we  face from our illness, it is just as important to discuss what lupus survivors do with our lives despite lupus. Besides Lupus Awareness Month, this month I celebrated my son’s graduation and acceptance to 10 of the top Philosophy graduate school programs in the country including Marquette, Kent State, Boston University, Boston College and his choice Brandeis. It was the proudest day of my life!  Diagnosed when he was 3 years old, I had been sick as long as he could remember. Estranged from his father is levitra better than viagra the same year, he has been the man of the house and main caregiver since then as well. Partly because my CNS symptoms prevented me from driving and partly because I felt public school was failed to challenge my precocious child, I decided to homeschool my son in 5th grade. My participation in his education magnifies my pride in his success. During the family celebration, my best friend praised my achievement, exclaiming, “Despite Lupus you have raised your son single-handedly seen him graduate college!” This inspired me to start the “Despite Lupus…” twitter campaign in which I shared some of the things I have accomplished in spite of my illness and invite my fellow lupus survivors to do the same. There has been an overwhelming response  from followers tweeting messages about the positive aspects of their lives despite lupus.  Some made me tear up, some made me laugh. But most of all they all inspire hope. So here are a few of my favorite replies along with a live stream below in the hopes that they will inspire you too.

Despite Lupus …

I cannot thank you enough for all of your inspiring tweets! You all have proven that we might have lupus but lupus doesn’t have us. Despite lupus we can still maintain quality in in our lives. I would even say that for us Lupus Survivors each day we wake up is all the more precious. The unpredictability and potential threat of lupus makes us appreciate life even more.

If you have not already please join the conversation on twitter @lupussurvivors and our Facebook page. Please share what you do despite lupus.

Kathleen’s Lupus Survivor Story

lupus survivors imageMy name is Kathleen. I’m living with systemic lupus. I was diagnosed in 2005 with

lupus and have been on Benlysta since 2010. I’m struggling every day with pain, fatigue and worry about my future.
I can’t work anymore because of my disability. But I don’t let it stop me from living my life. I’m into adaptive sports like scuba diving. My insurance has increased 51% in the last two years and it’s been difficult for me on a fixed income . I’m a cancer survivor and I miss driving and I honestly feel that what doesn’t kill me makes me stronger and sometimes I feel like the strongest person in the world. And other days I feel alone and lost. But I have discovered an entire world on Twitter of other cialis effet duree lupus warriors and lupus survivors .
I hope to help raise awareness about Lupus and maybe one day there’ll be a cure. I have no family support but I have a service dog named Iris who helps me everyday.

Jennifer’s Lupus Survivor Story

lupus survivors imageI was 19 and in college when I first heard the word lupus. I wasn’t sure how to act or react as my mother and my sister both sat there with tears in their eyes (both of them are nurses and my grandmother passed away at the age of 43 and my mom is only 19 and they think it was for lupus but no one ever told me that back then), so I wondered why they had tears in their eyes when the doctor came in and said that I might have lupus. I was in college getting my degree and neuroscience and was on my way to medical school. Well as the years passed so did my money flares of lupus they came they when they came they went but being so young I wasn’t going to let them stand in my way and I was able to finish my degree but I could not go on to medical school. Then I met my Husband who is a cancer survivor and we have this instant connection that was deeper and life than anyone could know however our dreams of having a child we’re very slim so we traveled the world and did what we could I focused on my career in medicine and finally went back to school and got my degree in medical forensics and ended up working with a well known pharmaceutical company in clinical trials for breast no varying cancer . All through the while keeping my lupus quiet going to flares again and then going in remission and going to flares and going in remission trying to hide it from everybody as if I was a healthy individual who could take on the world. Then I got the best news of my life, I was pregnant! Sadly I was 35 but no less I was pregnant and into thousand seven I gave birth to a healthy baby girl I named her after my mother and my mother-in-law we combined our names to crate her name. So now I had the life… A great husband, A great career in which I was moving up the corporate ladder her and a beautiful daughter. Then one day it all came to a screaming halt! My lupus and taking a turn for the worst I slowly started breaking bones I broke my spine I started breaking my feet started having us have pins and screws in my bones relentless my greens with vomiting every week,pneumonia every 4 to 6 weeks I was in the hospital and then I ended up in ICU I don’t remember much for those couple weeks and I see you but when I did finally come out of the ICU for hog they had told me that I was bleeding in my lungs.& I had been diagnosed with lung disease called interstitial lung disease and then I went into kidney failure in and started having multiple problems with other organs I’m in a permanent adrenal gland organ failure after many years of being on prednisone I had to have a total hysterectomy at the age of 37 I had to go on long term disability which ended up into permanent disability I lost the career of my dreams I lost my self-esteem I Lost myself worth & I saw the toll it was taking on my very young daughter so I try to hide more and more which just led me to become depressed. I am still fighting in and out of the hospital every 4 to 6 weeks was some visits being better than others. I do most of my suffering in silence and I see the financial toll it has taken on our family, I’ve taken out loans against my retirement funds I’ve taken out personal loans going to put us further into and all I really want is for my daughter to have a normal life and a normal upbringing and a normal mom. I’d spend many nights crying a long suffering inside. I am now 43 years old and feel so lonely however I have finally realized I cannot go through this alone anymore. I am now seeing a therapist who is making me realize that if I’m not here then I cannot be here for my daughter. And she’s not worried about the quality of her mom she’s worried about just having a mom and she’s fine with me being just me and some days I realize that and I love to watch her play outside and catch all the beautiful butterflies we have I called them gods luckiest little gift on Earth. I told her I always loved catching butterflies when I was growing up as a girl and that is something that we can have that is ours and that is special and that is incontinent. I lost so many friends along the way and it first I used to grieve that empty hole in my heart as these are my friends since I had since we were nine but I’ve realized over the last 10 years it is more about your family than it is about your friends. And that just because you’ve been diagnosed with lupus doesn’t mean you have to suffer in silence or suffer alone and you don’t have to go to that deep dark lonely place that chronic pain pulls you into rather spend your good days with your loved ones and for now that is what I do I focus on my beautiful daughter and her little daughter flies.

Denise ‘s Lupus Survivor Story

Hi my name is Denise I have Lupus (SLE) since 2004, I also have Sjogrens, Raynauds, RA, Diabetes, OA, Neuropathy, DDD, Herniated disk in my lower and upper back, I have sleep apnea too. I have thyroid problems and been having seizure symptoms and TIAs since 04 I was in and out of hospitals because of it. I was on Gabapentin for 6 years and my Neurologist said he, would wean me off it because he thought maybe that was why I was having the symptoms of TIAs and Seizures. Well he was right I am so glad I got off that medicine I have not been in the hospital for over a year since being taken off that medicine. I have been in and out of a wheel chair since 2003. Since 2011 I have been back in the wheel chair. I used to dance ballet and Jazz and tap for 20 years. I fought for SSDI it took two in a-half years to get accepted.

In January 2013 I had a Radical Hysterectomy. Because they suspected I had uterine I think of all the changes in my life through the years and some times I feel like it is not my life, some times I wake up in the middle of the night and think this is a nightmare, but it is not, it is my life. I have had to accept it. Writing helps me accept my life as it is.

I wrote my story to let others know that no matter what you have been through, that you can make a good life for yourself. I share about being abused and being a survivor. I share about my sobriety. I stopped drinking in 1995. I share about finding my birth mom. I share about my loving husband. He is such a sweet heart. My husband and I met before I was ill. Are relationship has been wonderful and very hard because of Lupus, I feel our relationship is growing stronger because we both take time for each other and we listen to each other. Lupus https://www.acheterviagrafr24.com/vente-viagra-pharmacie-je/ has taught me to communicate and talk things out better. Communication is important; I have a peace in my life today.

I am a Lupus advocate here on line. I enjoy sharing with others helping others. Life is short so I feel we should enjoy each other’s company and help each other. God brings the right people into our lives for a reason. To read my story. “Thank you God. One Lady’s Journey Within.”

Here is my new blog Where I share poems and more.
The reason I write is because I want to share with others that no matter how bad our life may have been we can have a good life. We are able to live and be happy. I am so glad to be able to share with you. Denise Love

Carlotta’s Lupus Survivor Story

Susie-Leather-Headshot-2-webI am a Lupus survivor for almost 30yrs. Diagnosed in 1985. Since then, I have also developed FM & Raynaud’s. I am also a cancer survivor having lived through Thyroid Cancer as well as Breast Cancer. While I am a survivor, my cross to bear is the fact that my precious daughter did not survive this disease, succumbing to it at the age of 24 in 1999. So, my survival story is more a story of living my life to honor her, to be someone that she is proud of, and, of

most importance, to helping others who suffer from this disease and any other autoimmune disease.

I run an online support group www.wehavelupus.com, where we have been providing support, comfort, information, and understanding to anyone suffering from the 60+ autoimmune diseases. I dedicate many hours to this site, as well as to the sister site on Facebook. Lupus is such a heinous disease and affects each of us differently, my goal is to increase awareness as well as to provide understanding and support.

I pray for a cure, but until then..I pray for pain-free days for each and every one of you!


www.wehavelupus.com

Angie’s Lupus Survivor Story

lupus survivors imageMy name is Angie and in the 90’s I was diagnosed with Lupus. It was actually very fast. I went to my Primary Care Physician three months in a row with the flu and flu like symptoms. He decided to run some tests and on my follow up appointment he sat me down and said, ” all your lab work is great, excellent but you tested positive for Lupus we also did an EEG let’s get it and look at it.” When he came back he told me everything on the http://www.cialispharmaciefr24.com/ou-acheter-cialis-generique/ EEG looked great except my theta waves are hitting while I’m awake. I just looked at him for about a minute let it absorb then told him I’m really glad he didn’t do a pelvic exam because everything else is broken. We both laughed and it took the tension out of the room which was a relief. Then he explained what Lupus was and how it would change my life and I started slowing falling down the rabbit hole. When I finally hit bottom I was confused, scared and felt so relieved to know I was [not] actually crazy there was actually something wrong with me. So my PCP (Primary Care Physician) set me up with a rheumatologist. Mistake. You know what I mean if you have ever been to one before. We are the red headed stepchildren of rheumatology. Especially back then. When I went to the appointment it felt like everything was spinning out of control. The doctor came in asked a few questions but didn’t give me time to answer and didn’t allow me to ask any questions and I had a lot. Then he handed me a script and left. No instructions. No information on side effects. I had no idea what to expect. So I started falling further down the rabbit hole. More like spiraling. Like a good patient I got the scripts filled. Methotrexate, plaquenil and quinacrine. I had no idea what I was getting into. I started taking the medication and here came the rabbit, “Read the directions and directly you will be directed in the right direction.” All I was thinking was It would be so nice if something would make sense for a change. I didn’t need to read the side effects because I had everyone. The medication was worse than the Lupus.

I was working night shift and I always took the methotrexate before I went to bed on Thursday. I had already gone to sleep when the vomiting woke me up. It was so severe I was urinating on myself. I didn’t realize my daughter who was six had stayed home from school because she was sick. She walked into my bedroom and just stood their. In shock. She finally started crying asking mommy what’s wrong with you. At that moment I decided the medication wasn’t worth it. I choose quality over quantity when it came to my life with my children and would make the same the decision again. So I pulled myself out of that rabbit hole and back into the real world. Not realizing what it was doing to my body. Back then most people had never heard of Lupus nor how dangerous and deadly it can be. So I went about my life trying to forget about that rabbit hole. I would have the joint pain and headaches but push through it. The fatigue made daily life extremely difficult but what choice did I have. I had three beautiful babies that depended on me. I went back to my PCP and he wasn’t happy but he gave me a little advice I’ve carried with me. Prednisone, which may make you feel normal again will take years off your life. Stay away from it when you can. I will follow that advice the rest of my life. I am actually one of the lucky ones. Most people go years without knowing what is wrong and by then the buy levitra in india damage is done. I at least had a choice. So this is the beginning of my story and how I have learned to live with Lupus.

I am now trying Benlysta. Having some pretty sever side effects today. But I have faith. It will work. It has to work I have severe CNS Lupus with Dementia, meningitis, encephalitis and ceribritis. So it has to work.

Regina’s Lupus Survivor Story

lupuss urvivors imageI was first diagnosed with lupus in 2010. Although I had 3 positive tests, my doctors insisted that I did NOT have lupus and further tested me for other collegan diseases. I also have RA, OA, Raynauds and Colitis. This came after being mis-diagnosed with MS and Multiple Myeloma; both mimic Lupus. After my doctors mis-diagnosed me, I realized I needed to become my own advocate and find a new rheumatologist and neurologist.That’s when I wanted to become an advocate for other lupus patients. In the beginning of my disease I was really sick and didn’t know how I was going to take care of my then 1 year-old and 3 year-old boys. My husband jumped right into action to help. I found that support from family and friends is key to a chronic disease because depression runs so high with lupus. Today, not only am I a lupus survivor, but I’m a co-founder of a “YOU” Can’t See Lupus online support group (Facebook). I write a blog describing what it’s like to live with lupus on a daily basis along with the daily challenges that come along with the life events. I mentor other lupus patients on how to be their own advocate, where the lupus patients can locate

their resources and how to utilize those resources. It’s my mission to bring daily awareness and educate others on lupus. I reaffirm to myself and others that we will not be defined by our diseases.I have found that if I find one thing that I’m grateful for daily and with a positive attitude my life has been better and will feel better. To me, quality of life is everything. I chooses to feel and look better; “But You Don’t Look Sick” sticks with me and really,, who chooses to look like how they feel, not me! Lupus has taught me a lot during this journey also. I look at life in a different light and don’t take things for granted. For the past 2 years, my dear friend and I have (she’s done it for 3 year but I jumped in the last 2) run the Annual Crystal Lake Lupus Fundraiser. The money we raise benefits the Lupus Foundation of America. We decorate downtown Crystal Lake in purple ribbons, the local stores and community donate baskets and gifts that we make into raffle baskets and we raffle off the items. Last year we raised over $16,000 and this year our goal is $20,000! We don’t stop at May by spreading awareness, for us it’s 365/24/7!


“YOU” Can’t see Lupus Living with LUPUS – A day in the Life