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Multiple Myeloma - MD Anderson's Dr. Robert Orlowski speaks on “Exciting New Drugs and Combinations for Myeloma” or Why survival rates and the life expectancy prognosis for myeloma patients will continue to improve!

4/27/2013

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Dr. Orlwowski was the featured speaker for the April Myeloma Panel broadcast, and his topic was "Exciting New Drugs and Combinations for Myeloma".  He has an excellent bio, works for  the number one cancer hospital in the USA(per US News)and perhaps the world, but he was in front of an extremely talented panel that is very hard to impress.  So what did some of them have to say about his participation?    

Pat Killingsworth said, "  Dr. Orlowski is an exceptional myeloma expert.  I would rank him among the top five in the world."


Nick Van Dyke said, "That was a great call and Dr. Orlowski was fantastic, both in terms of knowledge and in terms of "bedside manner" if you will.  What a great guy!"

Jack Aiello said, "“I’ve seen & heard Dr. Orlowski speak many times and am always impressed by his ability to clearly articulate answers to complex myeloma questions so that patients/caregivers can understand and learn more about our disease.”

I also was very impressed with Dr. Orlowski's depth of understanding of Multiple Myeloma and how skillfully he was able to put it into terms that the panel, patients, and caregivers can understand.   You can listen to a rebroadcast of the entire program is you just CLICK HERE!

If you would like a summary of the presentation and discussion, I have provided a summary of the broadcast in the following paragraphs.  If you would like to follow Dr. Orlowski on Twitter his address is: https://twitter.com/Myeloma_Doc

Combinations for Newly Diagnosed

Dr. Orlowski started his discussion of  "Exciting New Drugs and Combinations for Myeloma" by stating that he was recently at the early April International Myeloma Workshop in Kyoto, Japan and so he had some of the most recent updates on treatments.   He felt the focus was on the use of combination regimens and believed that these combinations were the best way to get to a myeloma cure.

In the low risk patients there were excellent results from two drug combinations such as Vd(Velcade, dex) or Rd(Revlimid, dex) and three drug combinations of VRd(Velcade, Revlimid, dex), and CVd(Cytoxin, Velcade, dex).  All of these work well, but none of these combinations will provide 100% complete response.

Exciting New Combinations for the Newly Diagnosed

KRd or Krypolis, Revlimid, and dexamethasone is a new combination in phase one and two trials in the newly diagnosed setting that has a remarkable almost 100% response rate.  It appears to have a higher CR(complete response) rate or improved quality of response.  The study is being coordinated by the US Cooperative Network and would be a great clinical trial for anyone who is newly diagnosed.  

High Risk Newly Diagnosed Patients Remain a Challenge

For those patients who are considered high risk by either evidence of the 17p deletion based on the FISH test, or have a high risk signature from the 70 gene array panel, the outlook needs to improve.  These patients, who represent 15 to 20% of all patients, have a life expectancy of only 3 years, with the current standard of care VRd(Vecade, Revlimid, dex) Induction, and followed by VRd maintenance.  

An exciting new 4 drug combination includes a new antibody drug Elotuzumab, along with Velcade,Revlimid, and dex, or EVRd.  Elotuzumab is an antibody that attaches to the myeloma cell and tells the immune system where the myeloma is, so the immune system can then target the cancer cells.  This may have fewer side effects because it is a targeted therapy.  The question to answer is whether this 4 drug combination is better than the current VRd standard of care.

Other New or Recently Approved Drugs

Ixazomib is in the same class of drugs as Velcade, however it is an oral  proteasome inhibitor, and does not require a hospital visit for infusion.  A trial using Ixazomib with Revlimid and dex or IRd has shown good results as presented in Kyoto, Japan.  This combination provides a much better quality of life  because the patient can take this oral therapy at home.  

The recent approval of Kyrolis in July of 2012 and Polmalidamide in Feburary of 2013 for use in the Relapse and Refractory(RR) setting has shown a huge benefit to these RR patients.  The most benefit from these drugs appears to be in combination with other drugs.  An MD Anderson led study using KPd(Kyprolis, Polmalidamide, and dex) in the RR setting has shown a response rate of 77% in heavily pretreated patients.   What is great about this combination is that it can be used outside the clinical trial setting by your local hematologist oncologist.   


Another combination that is being evaluated by MD Anderson is the combination of Thalidomid, Relimid, and dex or TRd.  These drugs (TR) are in the same class of drugs, but in combination have shown a response on patients who have progressed on Revlimid.  This is also an all oral regimen and has had a 50 to 60% response rate.   

Daratumumab is another new antibody drug under development.  It binds to a different protein on the myeloma cell and helps the immune system find a good target.  It has had a nice response rate with heavily pretreated myeloma patients.  There will be a large trial coming up which should result in FDA approval.

ARRY 520 is a drug which targets a protein that inhibits myeloma cells from duplicating, and has no potential for neuropathy at all.  ARRY 520(no name chosen as yet), plus Krypolis, and dex or AKd has shown good activity even for patients who have progressed on Velcade, Revlimid, and dex.  This combination will be in test across the country.  


In Summary 

Dr. Orlowski, mentioned that he believes that there are two major spheres of thought, one of which is to use 1 or 2 drugs and save others available for relapse, or use combination of drugs early in the disease as possible(both newly diagnosed and RR) The data in ongoing, however there is a growing number of multiple myeloma specialists  that believe the use of the combinations works better.  Three and four drug combinations are better that two drug combinations.  Although transplant was not mentioned in the doctor's presentation, he indicated later in the Q&A section that his standard of care would be induction(2 to 4 drug), transplant, and then maintenance.  

Q&A Discussion

After the doctor's presentation, he took several questions from the audience.  There were 22 questions entered, which Nick and Jack were kind enough to consolidate into 11, plus we had a few additional questions from the panel members.  Please listen to this discussion if you would like to hear all of what was said, however I will summarize what I felt were some of the most interesting findings.  

Dr. Orlowski felt that tandem transplants may be effective for some patients, but only those that did not get a CR(Complete Response) or the NCR(Near Complete  Response).  In most other cases he felt that in the era of the newer novel agents the induction therapies are now far superior to those used in the pre novel agent era.  He noted there will be a large US trial which will compare induction with VRd(Velcade, Revlimid, and dex) with early transplant, and others that delay transplant to relapse.  Dr. Orlowski feels that the myeloma cells are more sensitive to all drugs at the time of diagnosis when they have not developed any drug resistance.  He would consider induction(2 to 4 drugs), transplant, and maintenance as his standard of care.  

Pat had asked if there has been any trials that put the two antibodies(elotuzumab and daratumumab)  in combination.  Dr. Orlowski thought that would be an excellent idea if used in conjunction with Revlimid.  

MD Anderson, has a myeloma immunotherapy project under a grant from the National Cancer Institute called SPORE.  It has 4 different components as outlined in the abstract found if you CLICK HERE.  The myeloma M protein is isolated prior to treatment and then used as a vaccine which trains the immune system to destroy the myeloma cancer cells.  They plan to use this in conjunction with transplant, and if it works after transplant it may be tried prior to transplant.  Another element of this project is designed to train the patients T cells to attack the patient's myeloma cells.

Concern over being on the placebo side of a clinical trial, and getting substandard care was expressed.  In the context of clinical trials, placebos are usually not used in phase 1 and 2 studies, but only used in phase 3 trials which usually will compare the current best practice standard of care with a placebo, versus the standard of care plus a new drug.  In addition, any patient can opt out of a trial if the patient chooses another course of care.  

The Black Swan initiative is a hot topic and MRD(minimum residual disease) as a measure of response is integral to the program.  Dr. Orlowski provided a history of myeloma disease measurement, and concluded that FISH, 70 gene array, and the 3 different ways of determining MRD are all great tools for use to detect low levels of disease and help determine if more treatment is needed or not.  He believes that 10 to 20% of patients stay in CR for 10 years or greater and they may be cured.

Please listen to the entire broadcast to hear additional Q & A on 1) tests used to determine risk, and ways to use this data to determine treatment 2) the use of Ixazomib, Revlimib, and dex as an all oral maintenance regimen 3) treatment for high risk smoldering myeloma or treating myeloma now in a MGUS state 4) Is IgD myeloma more aggressive 5) GI issues from melphalan and long term maintenance therapy and, 6) body rash from Revlimid use.  

I hope you find value from this exceptional program, and as always may God Bless your Myeloma journey.  Gary Petersen/[email protected]


For more information on mulitple myeloma go to www.myelomasurvival.com or you can follow me on twitter at: https://twitter.com/grpetersen1







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Multiple Myeloma - What you Don't Know Might Just KILL YOU!!!

4/23/2013

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I came across an article by Sharon Begley of Newsweek and it definitely resounded in my mind.  Her article is based on the premise that Care at a top Cancer Center may just save your life, and not knowing this fact might just KILL YOU!  She also makes the case that most cancer centers covet their survival statistics as if they were state secrets, and Sharon is as confused as I to understand why this is the case.  It has taken me nearly two years to get the cooperation of just 10 doctors, and it has been like pulling teeth, with the wonderful exceptions like, Dr Berenson, Dr. Hari, Dr. Barlogie, Dr. Faber, and several more.  

Multiple Myeloma ???

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< What a Myeloma Specialist might say about multiple 
myeloma cancer!!      





I have made similar statements about mulitple myeloma specialists.  That they can provide a life expectancy 3 times greater than the average facility, and have survival rates that are also 3 times greater for 5 years, but as much as 10 times greater for 2 years.  Sharon makes a similar assertion for all cancers that are not widely seen by the typical local oncologist.  This would include most rare incurable cancers, and most stage 4 cancers or those that have metastasized. 

This became very personal to me when a neighbor of mine found out  that his wife had stage 4 colon cancer.   He was told at the local hospital  by their oncologist that she had a 6% chance of surviving 5 years.  I told him about my work with multiple myeloma, and that there is probably a center someplace in the United States that has better rates of survival for stage 4 colon caner.  I did some research on line for him and this is what I had found:

M D. Anderson, Houston, TX -  Dr. Steven A Curley  -  5 year survival with surgery  50%
 
Memorial Sloan Kettering, NY - Dr.Leonard B Saltz, MD  -   5 year survival rate  30%
 
Seattle Cancer Care Alliance - University of Washington Medical Center - 5 year survival of 27%
 
Mayo Clinic, Rochester MN.  -  Dr. Steven Alberts -  5 year survival of  19.2%
 
Northwestern University -  5 year rate of 7%



They will be going to MD Anderson, where the 5 year survival is 8 times greater than the average reported by the American Cancer Society.   Sounds like exactly what I would do, but sometimes you "Don't Know, What You Don't Know!!", and it can KILL YOU.

You can read Sharon's excellent article if you just CLICK HERE!  It is well worth the read!! Thank You Sharon for your excellent work, and hopefully together we can SAVE LIFE!


Best Regards to all my readers and may God Bless your families cancer journey/ Gary Petersen


For more information on multiple myeloma go to www.myelomasurvival.com






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Dr. Robert Orlowski is the Featured Speaker on The Cure Panel Talk Show on April 25 @ 6pm EST

4/15/2013

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***Now that this program has aired you can listen to the rebroadcast of this very patient friendly presentation on "Exciting New Drugs and Combinations for Myeloma" if you CLICK HERE.***
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Fresh from the Myeloma International  Workshop in Kyoto, Japan, Dr. Orlowski will be the featured speaker on the Myeloma Cure Panel Broadcast on April 25 at 6PM EST.  

Dr. Robert Z. Orlowski, MD, PhD is Director of Myeloma, and Professor of Medicine in the Departments of Lymphoma/Myeloma and Experimental Therapeutics, Division of Cancer Medicine, at The University of Texas M.D. Anderson Cancer Center in Houston, Texas. He is board-certified in internal medicine and medical oncology. Dr. Orlowski earned his doctoral degree in molecular biophysics and biochemistry from Yale University and his medical degree from the Yale University School of Medicine. Dr. Orlowski has published numerous book chapters, articles, and abstracts on cancer therapy, with a focus on the molecular pathogenesis of oncologic disease processes and the mechanisms of action of chemotherapeutics. His clinical research efforts focus on the translation of promising laboratory based findings into novel clinical trials for patients with hematologic malignancies. He has published in, and is a reviewer for, several journals,including Blood, Cancer Research, Journal of Clinical Oncology, and the New England Journal of Medicine. He has received several awards, including The Leukemia & Lymphoma Society Scholar in Clinical Research and the Jefferson-Pilot Fellowship in Academic Medicine.



M. D. Anderson is one of the most famous cancer centers in the world, and Dr. Orlowski is one of the worlds most renowned multiple myeloma specialists.  I am sure he will be bringing  back the latest news from the Kyoto meetings.  Please join me and the rest of the Cure Talk Panel where patients will have an opportunity to ask Dr. Orlowski questions that they would like an expect to answer.  You can still sign up for a the few remaining spots that are available if you CLICK HERE!

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Want to improve your Multiple Myeloma Prognosis? Just ask, "What would Mayo do?"

4/10/2013

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For the thousands of patients living all over the world who do not live near a myeloma center of excellence, who's insurance will not approve a center of excellence, or who cannot obtain or afford a second opinion.  What do you do? How can you improve your life expectancy prognosis and survival rate.   First , find a hematologist oncologist., and second tell him or her to just ask, " What would Mayo do?"  Without the assistance of your own multiple myeloma expert, the next best thing would be to follow the cook book set up by some of the best myeloma specialists in the world.  This cook book happens to be the mSmart Program published as a consensus view by the multiple myeloma experts from all  three of the Mayo Clinics in the United States.  Doctors like Dr. Rajkumar, Dr. Kumar, Dr. Chanan-Khan, Dr. Lacy, Dr. Fonseca and many more had a hand in putting this document together.  It is designed  to help patients to understand what care should be given to the myeoma patient and to provide doctors with a plan that will provide excellent care for their myeloma patients.  Care  that usually only a multiple myeloma expert can provide.   Mayo is the only organization that I know of that has put together their standard of care into an understandable form, hoping to provide the doctor who does not have sufficient multiple myeloma experience with the tools to provide a level of care that will provide an above average life expectancy and survival rate.  If a patient reads this information, they will have a better understanding  of what to expect and what questions to ask their doctor.

I make this statement, because Mayo has some of the best 3 and 4  year survival rates in the world, has an excellent reputation, is a myeloma center of excellence, and has the MAYO MYSTIQUE.  I have previously written this about the Mayo survival  results. 

Mayo Clinic, Rochester, MN - The Mayo Clinic Medical Edge Video from July 11, 2011 states that their 3 year survival has improved from 29% to close to 90%.  When compared to the SEER rate of 55.6% you are at least 3* times more likely to survive under their treatment than at the average SEER facility.  A recent analysis of 290 patients using LD or TD induction and delayed or early stem cell transplant reported equal 4 year survival of 82%* vs the SEER 4 year rate of 50%. Link: http://getmadcat.com/video/47064/  An outline of their risk adapted treatment program called mSmart can be found at the attached link: http://msmart.org/newly%20diagnosed%20myeloma.pdf  


So what is this mSmart program.  Two great links that will explain Mayo's  multiple myeloma treatment philosophy are at:


http://www.mayoclinicproceedings.org/article/S0025-6196(13)00077-3/fulltext

http://www.msmart.org/msmart_mar09_002.htm


In a summary, for the newly diagnosed patient, they break the disease into three different disease classifications, High risk, intermediate risk, and low risk, and then provide treatment plans for each risk classification.  They also break the treatments into transplant eligible and ineligible patients.  This usually is age and health related (comorbidities).

Without question this is an option for those who can not be treated at or get a second opinion from centers like  IMBCR, Medical College of Wisconsin, UAMS, Mayo, MD Anderson, Dana Farber, Moffitt, or many other great myeloma centers of excellence.  It would be an excellent tool for those patients who do not have access to these centers of excellence, but still  want treatment that will provide an above average life expectancy and survival rate.  And for the hematologic oncologist that does not have much experience with this very rare disease and is mSmart enough to ask the question "What would Mayo do?"


Best Regards and may God Bless your Myeloma journey/ [email protected]


For more information on myeloma survival and treatment go to www.myelomasurvival.com.
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Dr. Craig Hofmeister, Dr. Jan Moreb, and Dr. Parmeswaran Hari are Multiple Myeloma Heroes providing free second opinions for a patient in Poland,  Kosovo, and Racine, Wisconsin -  Updated 4/10/2013

4/5/2013

2 Comments

 


To help promote Mulitple Myeloma Awareness month I had asked a number of doctors that are excellent multiple myeloma specialists  if they would contribute a second opinion for a patient anywhere in the world who was in need of an experts assistance    Dr Hofmeister of The James at Ohio State University, Dr. Moreb of Shands at the University of Florida, and Dr. Parameswaran  Hari of the Medical College of Wisconsin volunteered to participate.  To me they are not only excellent multiple myeloma specialists, but selfless humanitarians as well.   I had asked patients to provide their situation in writing to the [email protected] and the most compelling would be chosen April 1st.  So what was the outcome.  
___________________________________________________________________________

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Dr. Jan Moreb - Professor Bone Marrow Transplant Program, University of Florida, Department of Medicine


This is letter from Kosovo which was selected, and Dr. Moreb has already started the discussion with Arlinda.


Dear Dr. Moreb,
 
Accidentaly I have seen on the internet the link: http://myelomasurvival.com/1/post/2013/03/multiple-myeloma-awareness-month-and-the-world-renowned-myeloma-specialist-dr-hofmeister-is-providing-a-free-second-opionion.html , where I can be addressed for a second opinon on Multiple Myeloma which recently was the medical diagnosis for my father- 64 years old. We live in Kosovo a new country in South East Europe and with many deficits in the health system.
 
Please, if you are interested I can send you the medical report in English translated for an second opinon on the treatment, options of the treatment, world centers for the treatment and prognosis of this illness.
 
Hope to hear from you soon.
 
Best regards,
 
Arlinda

____________________________________________________________________________


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Dr. Craig Hofmeister - Assistant Professor of Internal Medicine at Ohio State University Medical Center


This is the letter from Poland which was selected, and Dr. Hofmeister has already contacted Edyta.



Dear Doctor Hofmeister,

I am writing this email to you as my uncle Stanislaw has been diagnosed with multiple myeloma.
He is 64 and full of life. He lives in the small village in south east corner of Poland (Rzeszow is the nearest town) where the medical care is really poor and especially in this part of Poland we do not have any good specialists who deal with this illness. 
He is very lovely person. He is my God father and I love him dearly. He is very brave and decided to take this illness as destiny and God's will and accept that he can die soon but I would like to help him and get second opinion about his illness and methods of treatment he should undertake. He is under care of one doctor but I am not sure if the proposed treatment is the best for him and maybe there is more that can be done for him. 
Would you be please so kind to reply to my email so I can send you his full results and what kind of treatment has been offered to him so far.
I would appreciate your reply and your good heart help in this case. 
Please help him.
Many thanks 

Kind regards, 

Edyta Rybak

____________________________________________________________________________

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Dr. Parameswaran Hari- Section Head and Clinical Director, Bone Marrow Transplantation and Associate Professor of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin


This is the letter from a 30 year old with no insurance from Racine, Wisconsin which was selected, and Dr. Parameswaran Hari  has already contacted Nicholas.


Dear Doctor Parmeswaran Hari,

Dr. Hari, please save my life.  I have a wonderful support system and a good job that's fulltime. I never saw this coming. I have been with my girlriendf for 5 years now and we planned on having a long and fun life together.. My life seemed invincible until 1 year ago on a spring night. I was at a friends party and we were all having such a great time. My friend decided to get on his trampoline and so I followed suit. After a few drinks this was obviously not a good idea. My friend jumped off of his trampoline. I did the same only I landed onto my shoulder HARD and It hurt. I put off seeing the doctor for a few days to see if the pain would eventually go away. It's when I was in the shower and heard a pop followed by my cry of pain that I knew something was seriously wrong. My girlfriend and I went to see the doctor. The Doctor took the usual x-rays. He never acted surprised or suspicious at what he saw, why would he? He has seen so many broken bones in his time. It wasn't until he came into the office after I waited and he said he noticed "something interesting was going on in there and he'd like to take a look at it with an MRI. MRI's cost tons of money, especially without insurance. I politely declined as I explained all my finances would be tied up into this injury as it is. After I healed up I was released and back to a normal life.

Everything was going fine with minor pain. On a saturday afternoon our manager had asked us to remove some donor beds (I work in a plasma center) so that a crew could come in to wax the floors that night. I knew I had been feeling pain for a few weeks in my neck/shoulder area so I really didn't want too. I figured it must have been from repetative motions at work. But I did and this decision changed my life dramatically. As my coworker and I lifted a donor bed I felt a sharp pain in my neck. I could barely move my arm as it was so excruciating. I shyly let my manager know I hurt myself. She wanted me to go to Concentra health care the day after but they were closed because it was a sunday. The first available day for concentra clinic to be open I was sent there.  It was there that I met Doctor Krieger.  They took x-rays and began putting me into physical therapy. a day later.  After a few days or so there was very little progress. I was frustrated because I really wanted to get back into swimming but I couldn't even lift my arm to chest level.  I am a big Michael Phelps fan and always joked I was training for the Olympics.  About 4 days later I saw doctor Krieger at Concentra again. to have my x-ray impressions read to me  He walked me into the physical therapy room and had me lift a few weights to test my limits. He then led me into his office and told me I might want to sit down for this. I could tell he was nervous and wasn't sure how he would say what he was about too. I thought to myself right away, "oh crap, because of my past medical issues with my shoulder workers comp won't cover it". I rreally wish that was the issue but as we all know it wasn't. Even as I write this I have tears in my eyes remembering this day like it was just yesterday. He started to read the radiologist's report explaining, "a soft tissue mass was shown with associated destruction of the second left rib". Not understanding this he then said the words I thought Id never hear, "this could be cancer". Tears streamed down my face as I sat back in my chair floored by this horrible news. My whole world was just flipped upside down. My heart sunk. He said he was very sorry and he'd help me as a resource in anyway he could. I left that day with a broken heart and spirit. I only lived 3 blocks away from Concentra and I remember it was the longest coldest winter walk home of my life. I then called work in tears explaining I needed the day off. The second person I called was my girlfriend on her lunch period. She has been my comforter and support in all of this. She was a little stressed but she took the news quite well and I was impressed by her composure. We both kept thinking it may be something to do with my scoliosis or various other possibilities. After a couple of weeks of visiting the Dr. Krieger at Concentra he decided that physical therapy wasn't working due to my underlying medical issues.  He said we would have to end workers comp. because he has to be fair with them.  He let me work with him a few more days.  I wanted to believe that the physical therapy was working but it wasn't.  He wrote me an order for an MRI and sent me to P.D.I. in Franklin.  It was there that I met Dr. Robert G. Wells.  I had a pretty good idea of his credentials because I googled him.  He is a well respected radiologist within the medical community.  He was also one of the nicest gentleman I have ever met and quite possibly saved my life.  I was led to the area where the MRI would be performed.  Never having been in one I can now state that I am not claustrophobic.  After what seemed like forever I was finally done with the MRI scan.  He then decided to do a CT scan.  He confirmed that I had a tumor and clearly explained that it is malignant from what he can see and set a follow up appointment for a core needle biopsy. He did all this knowing I had no insurance but I paid what I could in cash.  I saw Dr. Krieger again and he set up an oder for the needle biopsy with Dr. Wells.  The biopsy was not painful at all and we had a good conversation while he was working away. The core needle biopsy confirmed that I had a cancer called plasmacytoma. When I got the call from Doctor Krieger I actually kind of laughed at the irony because I work at the plasma center.  He said it is an incredibly rare cancer. I walked to his office to pick up my pathologist report.
 
I did everything I could researching this new thing called plasmacytoma.  Hours upon hours on google were spent.  I learnt that it is very slow progressing and is usually delt with by a few zaps of radiation or monitored. I also learnt it is more prominent in males over the age of 55! I also discovered it was not fatal so long as it is treated immediately. After a few days I talked with the doctor at the plasma center and he recommended I go to the Aurora Oncology Clinic right across the parkinglot from Concentra because his friend Doctor Malone worked there. I met doctor Ruggeri because Dr. Malone has been so backed up with patients,  He was a very nice enthusiastic gentleman. He then looked at all the reports forwarded from doctor Robert Wells office.  He explained to me what exactly plasmacytoma was as well as multiple myeloma.  A lot of information I already knew from my research.  After he got the files from Dr. Wells office he began reading a few reports.  It is when he got to the CT scan impressions that left me with another surprise in my lap. This was the first time I had them read to me. He read, "several abnormal leaions in the right clavical, left clavical, right and left second ribs, and the spine were apparent." I knew from research online that this could mean I have multiple myeloma which is considerably more dangerous than plasmacytoma and is fatal. I also knew I was a rare case.  More importantly I knew that there was no cure for this.  

Here I was only 30 looking at cancer that generally is diagnosed in patients over the age of 50. A skeletal survey (20 x-rays or so), a bone marrow biopsy, blood work, and a PET scan were all done. The bone marrow biopsy was considerably more painful than the core needle biopsy but not as bad as people make it out to be. All tests verified that I had multiple myeloma. The good news is that the calcium level in my blood is low and there's no damage to my kidneys. The cancer was caught early enough before ANY apparent damage to my organs has begun. The bad news, as revealed by the CT Scan is that I have abnormal cell activity in both clavicals, my left femur right above the knee, both ribs, and a small hole in my skull right in the center. Talk about a third eye!  Doctor Ruggeri said "it's like I have plasmacytomas in multiple areas".  I didn't understamd if I had multiple myeloma or not.  So he said he would say it is.  I asked how long do I have.  Doctor Ruggeri said he would try to get me 10 years at least. 10 years at the age of 30! That is definitely not enought time! I have so much more I want to do in my life. I want to travel and see so many parts of the world.  Eventually I wanted to go to school and pursue a career. I have so many more books I wanted to read and skills to learn. I want to experience ALL life has to offer and 10 years just isn't enough. I love my girlfriend with all my heart and I want to live with her and marry her, (provided her father gave his blessings). We just moved in together 3 months ago. I want to know what it is like to spend the rest of my life with her but definitley for more than 10 more years. Ever since my diagnosis I have had so many sleepless nights wanting to stay up as late as I could just so my days last longer. It's like when you sleep everything goes by so fast.  I know that if I have any hope of living long enough to see a break through in cancer research then I need the proper care.  I just want to live my life as normal as I can.  I don't want a death sentence at the age of 30.  So can you please help save my life Dr. Hari? 

Best Regards,



Nicholas Avery


__________________________________________________________________________________________________

Dr. Hofmeister, Dr. Moreb,  and Dr. Hari, we at www.myelomasurvival.com thank you for your paticipation, and we thank Edyta,  and Arlinda, for the love and caring that they have shown for their family members  in need.  Nicholas, your letter was so compelling  and moving.    May God Bless your myeloma journey, and we will continue to follow up with Edyta, Arlinda, and Nicholas to see how their myeloma journeys unfold. 


Best Regards and toghether we will SAVE LIFE/ Gary Petersen [email protected]
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    Gary R. Petersen
    [email protected]
    CLICK HERE for my myeloma journey

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