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Posts by: Julie Russell

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Four Stages Of Emotions After Receiving My Mesothelioma Diagnosis

It is never an easy thing when your doctor tells you that your biopsy report is abnormal. In order for you to accept your mesothelioma diagnosis, you must go through many stages.

Stage 1: Denial

In the fall of 2007 while watching a Patriot game, my cell phone rang. Did you ever get a phone call and look at the number and say I have no idea who this is but… I need to take this call? It was my colon-rectal surgeon who had just done a bowel resection for diverticulitis. My ovaries and sigmoid colon were removed via a laparoscopy. I was recovering with minimal discomfort. I was almost one-week post-surgery at this time. Why on earth would my surgeon be calling me at 7:30 in the evening???   After 2 minutes of small talk, he states that there is a “little problem” with my pathology report.   “A little problem!!!” I repeat his words. “I don’t understand. I had diverticulitis, this is not a malignant disease.” He then tells me that both my ovaries had abnormal cells that they can’t differentiate. Now I immediately feel that ugly pit in my stomach. This can’t be happening. Denial, yes I don’t want to believe this. My slides were sent to Mass General for a second opinion. I was told it would be about 10 days to get their report. Unless you have been through this yourself, you have no idea how stress, sleepless nights, and anxiety take over your life.

Stage 2: Anger

After my long 10 days of waiting, I call for my report. Doctor is away until end of week; the secretary tells me “No!”.   I try telling the secretary that I need my report but am told I must wait until my surgeon returns as no report is in my chart. I can’t tell you how angry I became, yet there is nothing you can do. Wait…. 4 more days feels like eternity. I don’t want to talk to anybody about it. I have 2 sons who are in there 20s yet why tell them about it when I don’t really know what I am dealing with.   Anger has no limits!

Stage 3: Depression

On Friday afternoon, my dreaded phone call confirms mesothelioma in both ovaries. The pathologist states it is a rare finding and prognosis is guarded.   I’m shocked, sad, and in a fog. “Guarded, guarded,” I repeat the words over and over. I look up the definition. Not good. I refuse to just sit back and let this disease take over.

Stage 4: Acceptance

Well I don’t actually think I ever accepted it but I definitely learned to deal with it. I became my own advocate as no cases of peritoneal meso had been diagnosed at my hospital. I called numerous doctors who dealt with peritoneal mesothelioma. I was not going to let this disease take over my body without a fight. It was a tedious job but it was what I needed to do to feel comfortable with the plan of care I was going to take. It is indeed a rare tumor. I did end up traveling to New York for surgery and chemo.

In conclusion, it’s ok to deny your diagnosis, be angry at the world, and feel depressed. These are all stages we must go through to finally reach our accomplishment.

8 years and cancer Free. Yes!!!


About Julie Russell R.N.

julie-russellJulie Russell is an experienced Registered Nurse who is also a mesothelioma cancer survivor. Julie’s clinical expertise in nursing is in the area of the Cardiac Intervention. She has also been an instructor of Advanced Cardiac Life Support (ACLS) and Basic Life Support (BLS) for many years. Her varied nursing background includes roles as a nursing supervisor, educator and staff nurse.

Diagnosed with peritoneal mesothelioma in 2008, Julie has undergone surgery, chemotherapy, and become an advocate for herself and others. A mesothelioma diagnosis effects the whole family. Her two sons became active in the mesothelioma community as well. She is a passionate advocate for all patients, but peritoneal mesothelioma is a personal cause of hers. She will be a guest blogger for us. Julie will be sharing her personal experiences with peritoneal mesothelioma as she continues to live and work a full life. Since diagnosis, Julie has also become a grandmother. We invite you to follow Julie’s journey and feel free to contact her for any questions or support.

Thoughts From An Eight-Year Mesothelioma Survivor

Well here I am in the summer of 2016, alive and well.   After being diagnosed with peritoneal mesothelioma in 2008, I had abdominal surgery and heated chemo in New York. I also received intraperitoneal chemo via my ports.

First let me begin, yes I am well, working, teaching classes and exercising, all with completely negative Cat Scans.  I must tell you that yes there are some bumps in my 8 year journey.  For me, my major issue after abdominal surgery and that heated chemo is small bowel obstructions.  Ok, now I must be honest I have had my share, but now I think I am a pro at early recognition.  In 2008, I had no idea what to do with a distended abdomen and abdominal pain but go to the E.R.  The treatment is always the same, pain med, cat scan, nasal gastric tube and NPO. (Nothing per oral).  The only problem with the treatment is the placement of that unruly tube.  Down your nose and yes into your stomach to drain everything that can’t pass through the blockage in the small intestines. Why the blockage you might ask??? Well your body after having abdominal surgery and heated chemo forms scar tissue which can pull on the intestines. If it pulls in such a way, the bowel will become narrow. When this happens, it makes it difficult for solid foods to pass, hence the dreaded bowel obstruction.  Well after having 4 obstructions I finally learned that raw vegetables just can’t pass into my narrow small bowel. I can still see the orange drainage in my tube, Carrots, the dreaded vegetable!!!!!!!!! For me they are on my list of Never Eat Raw.  I can proudly say I have learned that by modifying my diet I no longer visit the E.R. with an obstruction. Now, I cook my vegetables and thus they can pass through this narrow intestine. The ups and downs of surgery for this disease can be tiring BUT you will never see me back in any ER with an obstruction. It’s been 3 years for me without any abdominal issues.  It takes time to understand your body but in doing so you too will ease your journey to recovery.


About Julie Russell R.N.

julie-russellJulie Russell is an experienced Registered Nurse who is also a mesothelioma cancer survivor. Julie’s clinical expertise in nursing is in the area of the Cardiac Intervention. She has also been an instructor of Advanced Cardiac Life Support (ACLS) and Basic Life Support (BLS) for many years. Her varied nursing background includes roles as a nursing supervisor, educator and staff nurse.

Diagnosed with peritoneal mesothelioma in 2008, Julie has undergone surgery, chemotherapy, and become an advocate for herself and others. A mesothelioma diagnosis effects the whole family. Her two sons became active in the mesothelioma community as well. She is a passionate advocate for all patients, but peritoneal mesothelioma is a personal cause of hers. She will be a guest blogger for us. Julie will be sharing her personal experiences with peritoneal mesothelioma as she continues to live and work a full life. Since diagnosis, Julie has also become a grandmother. We invite you to follow Julie’s journey and feel free to contact her for any questions or support.

Taking Inspiration from a Peritoneal Mesothelioma Survivor

InspirationWhen diagnosed with mesothelioma or any cancer some of the questions that run through your mind are: Will I ever be able to work again? Will my life ever return to being my own? Is this the end of life as I know it? What does my future look like? A diagnosis of mesothelioma with its survival statistics can be overwhelming for many people.

Sometimes in life you meet people that make a life-long impression on you. Whether it be at school, work, or socially you just don’t forget them. Many years ago at my first nursing job as a R.N., Julie was one of those memorable people. Julie was outgoing, fun, friendly, kind, a role model, a co-worker that you looked forward to working with. We were both R. N’s on a busy surgical floor. The patients all loved her enthusiasm and her wit. After a few years Julie left to get married and move to another state. The grape vine over the years reported that she had two sons.

A few years ago one summer day, I received a call from a friendly nurse inquiring about a nursing position. After talking for about 20 minutes, I disclosed that in addition to the service she was inquiring about we also did another service that we were passionate about: we followed patients that have mesothelioma, a rare disease. The phone went quiet as the nurse on the other end of the phone revealed she had peritoneal mesothelioma. We talked about what the chances are for her to be calling about another position and stumbling on our other services with mesothelioma patients. Continuing our call, she talked about her work experiences. I made the connection when she said her name. “You are tall, blonde, pretty, but what I remember most is you are very funny.” She laughed and said she was still funny. It was Julie!   She had been diagnosed with peritoneal mesothelioma 5 years previously. She had surgery and now was living with mesothelioma. She had returned to work within 4 months of surgery because she wanted to. She now admits this was not such a good idea physically but mentally yes it was a great idea. She had control, she was living her life on her terms. Peritoneal mesothelioma would not define her. She has advocated for herself and for others and is active in the mesothelioma community. As for advice for patients who are diagnosed, “have a positive attitude, listen to your heart, listen to your gut, advocate for yourself, have fun and go out and dance!”

If you are interested in connecting with Julie who is and continues to be an inspiration, reach out to us. Chances are that she will become one of those people that you don’t forget many years later!


About Julie Russell R.N.

julie-russellJulie Russell is an experienced Registered Nurse who is also a mesothelioma cancer survivor. Julie’s clinical expertise in nursing is in the area of the Cardiac Intervention. She has also been an instructor of Advanced Cardiac Life Support (ACLS) and Basic Life Support (BLS) for many years. Her varied nursing background includes roles as a nursing supervisor, educator and staff nurse.

Diagnosed with peritoneal mesothelioma in 2008, Julie has undergone surgery, chemotherapy, and become an advocate for herself and others. A mesothelioma diagnosis effects the whole family. Her two sons became active in the mesothelioma community as well.   She is a passionate advocate for all patients, but peritoneal mesothelioma is a personal cause of hers.  She will be a guest blogger for us. Julie will be sharing her personal experiences with peritoneal mesothelioma as she continues to live and work a full life. Since diagnosis, Julie has also become a grandmother. We invite you to follow Julie’s journey and feel free to contact her for any questions or support.

Think Positive: Advice from an 8 Year Mesothelioma Survivor

Think positive! Yes, those 2 little simple words. Simple words they may be but a difficult thing to do when your pathology report just came back “peritoneal mesothelioma”.

Well let me introduce myself, I am a 64-year-old nurse who was diagnosed with peritoneal mesothelioma in 2008. I had absolutely no clue what this meant, what organ was involved and what my prognosis would be. I should know something about this disease right? I’m a Registered Nurse for 40 years. Wrong. I knew nothing and after contacting many doctors at my hospital I still was in the dark. No cases ever treated or diagnosed at this hospital. “Be positive” I kept hearing from everyone. How do you be positive when you can’t even find information about a disease. Ok I’m trying to be positive. Yes, I am aware of all the positive outcomes if you remain positive. But it’s really hard!!!!

After doing much research I was able to find an oncologist in New York who was very knowledgeable about the disease. He referred me to a surgeon in New York who performed abdominal resection with heated chemotherapy. Actually I didn’t think the surgery was that difficult. I was out of the hospital in 6 days. Chemo via those abdominal ports did knock me down a few times but maintaining a positive attitude does really help. I know it is difficult to be positive when the chips are down but being negative definitely doesn’t help! So here I am 8 years later working in my same cardiac unit, rollerblading weekly, and teach BLS and ACLS classes. Did I get here without any set backs?? I would love to say no it was a walk in the park. BUT now I can hopefully help others by telling how I coped with the ups and downs of my diagnosis. Hopefully you will follow my journey with me.


About Julie Russell R.N.

julie-russellJulie Russell is an experienced Registered Nurse who is also a mesothelioma cancer survivor. Julie’s clinical expertise in nursing is in the area of the Cardiac Intervention. She has also been an instructor of Advanced Cardiac Life Support (ACLS) and Basic Life Support (BLS) for many years. Her varied nursing background includes roles as a nursing supervisor, educator and staff nurse.

Diagnosed with peritoneal mesothelioma in 2008, Julie has undergone surgery, chemotherapy, and become an advocate for herself and others. A mesothelioma diagnosis effects the whole family. Her two sons became active in the mesothelioma community as well. She is a passionate advocate for all patients, but peritoneal mesothelioma is a personal cause of hers. She will be a guest blogger for us. Julie will be sharing her personal experiences with peritoneal mesothelioma as she continues to live and work a full life. Since diagnosis, Julie has also become a grandmother. We invite you to follow Julie’s journey and feel free to contact her for any questions or support.

  • This field is for validation purposes and should be left unchanged.

Your message to us will be held in strict confidence. All requests for information by mesothelioma patients and their family members will be answered within 24 hours. Mesothelioma Treatment and Care Guides are sent to mesothelioma patients and families by overnight delivery.

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