Susan MacDonald
Susan MacDonald is a 62 year-old general manager of a senior citizen's
condominium association. She worked full-time and enjoyed tennis, golf
and driving up and down the California coast with her husband, Geri, a
retired Navy machinist and now an assistant director of mechanical trades
and operations for a large plant.
Susan also enjoyed taking long walks for her health and enjoyment. In early
May 2001, she noticed that walking was more difficult, and her breathing
was becoming labored more easily than before. She was also experiencing
chronic headaches. On May 3, she consulted with her primary physician
in Downey, California. He thought she might be suffering from a small
bronchial infection and suggested she start aerobics. He took a chest
film, but Susan never heard back from him regarding the results.
Susan's shortness of breath and fatigue continued. On September 13,
at the urging of her daughter, Laurie, she underwent an imaging test.
The results of the test indicated abnormalities in the right thoracic
cavity. The imaging test was placed on a disc, which was given to her
with instructions to consult with her physician immediately.
FROM BAD TO WORSE
Susan returned with the disc to her primary physician the next day. He
listened to her complaints and her concern that he never gave her the
results of her May 3 chest film. He asked Susan if he could retain the
disc over the weekend for examination. Susan consented. Her physician
then retrieved the chest film that had been taken May 3 and admitted misplacing
it. The misplaced chest film clearly showed the beginning of fluid accumulation
at the base of Susan's right lung. Her doctor offered to refer her
for a CT scan, saying he would schedule the scan urgently and would direct
his nurse to secure an appointment for Susan's scan by the end of
the week. The MacDonalds did not hear from the physician by late Friday
and began calling the doctor to obtain the appointment. By the end of
the following week, he finally scheduled the test in Los Angeles.
On September 15, Susan's breathing problems drastically worsened. Laurie
insisted she find emergency treatment, and the family rushed to the Emergency
Room University of California Irvine (UCI) Medical Center in Orange. An
ER physician immediately ordered chest films, a CT scan, an EKG, blood
tests, and other diagnostic workups. He attempted a thoracentesis, but
he could not withdraw any fluid as it was too thick. Susan was under observation
for nine hours.
Geri and Susan MacDonald
The ER physician informed Susan and her family that he wanted to admit
her to the hospital immediately; however, Susan's HMO inexplicably
would not authorize the hospitalization, and the MacDonalds reluctantly
decided to seek treatment within their HMO's plan and authorized hospital.
The ER doctor agreed to release Susan only if she first agreed to seek
further hospitalization elsewhere immediately. At the same time they were
fighting against a possibly serious illness, the MacDonalds were also
marshalling their resources to persuade their own insurance company to
perform their contractual and moral obligations.
On September 17, Susan presented to Downey Hospital. Laurie had called
Susan's primary physician to inform him that they were proceeding
to Downey; she gave him the option of meeting them there or authorizing
Susan's admittance. He agreed to neither and asserted to Laurie that
she and her family were overreacting. After more than six hours of testing
and waiting at the Emergency Room of Downey Hospital, the physician there
informed them that Susan's primary care physician had refused to admit
Susan and expressed his wish that she go to his office the next morning.
The next day, Susan again consulted with her physician in his office. He
advised that he was still trying to schedule a CT scan. Laurie, who had
been compelled to leave her employment to look after her mother and assist
her in finding treatment, called the physician's office every day,
to ensure that the CT scan took place, that the results went to the right
place, and that her mother received a referral to a pulmonologist.
Susan underwent the CT scan on September 19. With a good deal of self-assertive
effort, Susan was seen on September 23 by a Lakewood, California, pulmonologist
to whom her insurance group had referred her. The pulmonologist reviewed
the CT scan and additional chest films, including the original taken in
May. He determined that there was a pleural effusion covering half of
Susan's right lung and that it had grown substantially since May.
The pulmonologist scheduled and performed a bronchoscopy on September 25
at Downey Hospital. He was unable to biopsy any tissue. He also performed
a thoracentesis, withdrawing approximately 200 ccs of yellowish, mucous-colored
fluid. Cytological tests upon the fluid were negative for malignancy.
Not convinced by the cytological tests that Susan was healthy, the pulmonologist
recommended a thoracotomy with biopsy. As he did so, he also advised the
MacDonalds he would have to refer them (again, more delay) and asked that
they wait another two weeks for the results of another chest film.
Frustrated to the breaking point by the constraints of their HMO, the MacDonalds
chose to switch treatment groups within their HMO. They would have to
begin with a fresh consultation with a new primary physician with a new
group of doctors and hospitals. They would also have to wait for two weeks;
however, they hoped the temporary setback would soon push them further
ahead than if they did nothing. On November 1, Susan met with her new
primary care physician who, understanding the gravity of her situation,
referred her to a new pulmonologist.
A FRESH START
Susan met with the new pulmonologist on Nov 7. He ordered a new CT scan;
on November 13, the results of the scan showed that Susan's effusion
as expected was growing, and her right lung's breathing capacity was
steadily diminishing. Susan's pulmonologist advised surgery, but as
Susan's HMO would not permit such a procedure for several weeks, he
advised her to present to the Emergency Room of Hoag Hospital in Newport
Beach that same day.
Susan's pulmonologist met with her at Hoag that day and brought in
a thoracic surgeon to perform a thoracotomy, pleural stripping and a biopsy
procedure on November 15. The surgeon made two incisions beneath the right
armpit and harvested tissue for pathological testing. He then insufflated
talc to adhere the lung to the chest wall and prevent the recurrence of
pleural effusions. He inserted a tube for drainage, which would not be
removed for several days. Intraoperative frozen section analysis confirmed
that Susan had a malignancy of unknown type. Susan's surgeon told
the MacDonalds immediately after the surgery that Susan had lung cancer.
Geri and Susan with their five children and six grandchildren
Susan was assigned an oncologist, who on November 21, visited with her
in the hospital and advised her that the pathology department had pinpointed
the diagnosis as malignant mesothelioma, epithelioid type. He wished to
insert a porto-catheter for administration of chemotherapy immediately,
but Susan declined, feeling that she needed more information. Susan was
discharged from Hoag the same night, the night before Thanksgiving.
A FAMILY FIGHTS BACK
With the support of Geri and the help of Laurie, Susan began investigating
treatment options available to her. Everywhere she turned, she found a
lack of information and a glut of misinformation. Reluctant to endure
the traditional and taxing rigors of chemotherapy with no guarantee of
meaningful results, she researched the possibility of ALIMTA trials at
the CTRC in San Antonio, Texas. Besides pharmaceutical methods of attacking
the disease, the family researched new treatments, clinical trials and
any surgical options offered to treat mesothelioma. She researched and
reviewed all information about Dr. David Sugarbaker at Brigham and Women's
Hospital in Boston, Massachusetts, and his extra-pleural pneumonectomy
(EPP) with heated intracavitary chemotherapy wash.
Despite the merits of these programs, it was the pleurectomy / decortication
(P/D) procedure performed by Dr. Robert Cameron of UCLA that caught her
attention. Both the EPP and the P/D are radical procedures; however, Susan
preferred to keep both of her lungs and felt that she would be more physically
suited to undergo and recover from the P/D.
At Susan's request, her oncologist referred her to Dr. Cameron. She
was immediately pleased with his "patient-oriented" attitude.
She felt comfortable. "I don't want a cheerleader with all the
rah-rah stuff, I just want a capable and honest doctor who will help me
fight for my life." After spending an hour-and-a-half consultation
with Dr. Cameron, during which she learned about the statistics surrounding
her disease and the P/D procedure and her eligibility for the procedure,
she felt a mild sense of relief that her treatment was finally moving
ahead. Susan is scheduled for surgery in the next month; she will have
time to recover, and then she will focus on her next treatment option
to win the fight against this disease.
COMPASSION AND RESILIENCE
Despite steeling herself for her upcoming surgery, Susan evinces true concern
for other patients out there facing the same predicament. She and Geri
have been side-by-side since they were children and married 43 years with
five healthy grown children and six grandchildren. They feel fortunate
to have one another and their family. They have supported each other and
worked to make a recalcitrant system work for them. They faced an HMO
that would not grant their requests, a doctor who lost a crucial part
of her file, and nurses irritated that a united family would dare to enter
the doctor's office together and bother to ask so many questions,
instead of letting the doctor speak. Susan thinks about the people she
knows in the association she runs and others like them -- most of them
elderly, some of them without families -- trying to get medical care and
the answers they need. With those considerations in mind, she says with
despair: "God help them, they haven't got a chance."
She adds: "I was unfortunate enough to have been in the first medical
group and very fortunate to have switched into the new group and to have
had this new group of doctors respond so quickly and so effectively on
my behalf. I was also fortunate enough to have a family member who can
devote all her time to working on my medical issues daily and another
daughter who can stay with me continuously for support and care."
At the same time, she resents the asbestos-producing companies that put
profit over people, and exposed her to asbestos through her husband's
clothing, a career machinist in the Navy. She and Geri were planning to
begin building a home in Maine this summer, near one of their daughters,
and enjoy their retirement. With the onset of Susan's illness, they
have had to put their retirement on hold. Susan is the rock of her family,
a dedicated wife and mother who devoted her life and beautiful spirit
to her husband and children. She is dearly loved and respected. Susan
continues: "I'm only 62. We had great plans, and I was so excited
about the future. I am young, and young at heart."
Susan MacDonald plans to live. She is a resilient and strong woman who
intends to fight back against this disease and win. She is rallying in
her own fight against mesothelioma. She has the fortitude, and her family
will do anything to ensure her success in this fight. Together, they are
seeking treatment and believing in prayers and the blessings of God to
get them through this ordeal. They remain positive and hold on to hope.
We will keep you posted on the progress of this beautiful and compassionate
woman and her family.
*** POSTED JANUARY 15, 2002 ***
An Update -- 9/16/02
The following is a medical update from Susan's daughter Laura on September 16, 2002.
On January 15, Dr. Cameron performed the surgery at the UCLA Medical Center.
The surgery lasted six and a half hours and Mom was hospitalized for eight days.
Upon her return home, my sister, Diane, who was visiting from Maine since
November 2001 stayed with her and handled her 24 hour care. She had pain
in the incision areas and was discharged from the hospital with one drainage
tube inserted in the right lung. The first few weeks home the pain was severe.
She underwent breathing therapy to increase the strength of her lungs.
Her initial ability to move around and perform day to day function was poor.
By the middle of March she had healed enough for her to begin the eight
weeks of radiation which took place five days a week at Hoag Hospital.
She suffered some side effects, including nausea but was given an anti-nausea
prescription that she took an hour before her treatments. Mom suffered
only minor skin irritation and burns and her over all health slowly improved.
At the end of May she met with Dr. Cameron for her first evaluation. A
CT Scan was taken as well as several blood tests. Dr. Cameron reviewed
the results and informed that the right lung showed no signs of the cancer.
Mom was encourged to continue exercising in hopes of increasing her breathing strength.
With the care that our family wanted to provide, the decision was made
that my Dad would take early retirement in June and that my parents would
sell their home in Cypress and move in with me Laurie in Villa Park, California
which they did on July 12.
By August, Mom started suffering severe back pain near the incision areas.
She started seeing a physical therapist a few times a week which seemed
to help somewhat but the pain continued.
At the end of August, due to the constant pain, another CT scan was taken
with additional blood work. Dr. Cameron reviewed the tests which did not
reveal a clear cause of the pain. The plan was to continue recovery, exercise
and therapy treatment.
By September the pain had moved to right below the diaphragm on the right
side of the body. Mom stated that this new pain was more intense then
the back pain. Dr. Cameron ordered the administration of Interferon on
a low dosage that Mom self-injects. She will begin the interferon treatments
on September 16.
Today, my Mom is still struggling to perform general housework on a day-to-day
basis. She is walking but only a very short distance each day. Even one
block can be difficult to do before her breathing becomes labored
Some days her overall strength is better and on those days she is more
active and able to do some shopping, maybe walk down to sit on the beach,
go out to dinner or perform some minor exercising. On her bad days she
is in a lot of pain in the back and front area on the right side. She
continues with the physical therapy and has increased her pain medication.
The family takes turns massaging the painful areas and applies hot and
cold compressor throughout the day and evening.
My Mom has been such an incredible fighter and has shown remarkable courage
in getting through all of these things in such a short period of time,
less then a year. She has shown character in her ability to hear and accept
her diagnosis and continue to fight back with a positive outlook for the
future. She is maintaining her eating habits and overall weight which
is critical and is showing progress each and every day.
My parents had previously purchased 14 acres in Maine, with hopes of retiring
there and building a home. However, due to the mesothelioma treatments,
they now just travel to Maine to visit.
We cannot Dr. Cameron enough. We were blessed with a doctor like Dr. Cameron
who is a young, focused, honest and brilliant surgeon who is dedicating
so much of his career into treating and researching a cure for mesothelioma.
An Update -- 10/22/02
The following is a medical update from Susan's daughter Laura on October 20, 2002.
October 20, 2002
My Mother had a second evaluation by Dr. Cameron completed this month.
This November will mark the one year time period from the date of diagnosis
and she has come along way in that 12 month period and is now showing
remarkable leaps in the overall recovery process.
She started the Interferon Injections on September 16, 2002 without side-effects
and the process is relatively easy to inject. She also opted to start
physical exercising under the care and direction of a personal trainer
that she sees 2-3 times a week. This treatment combined with the physical
therapist 2 times a week as proved to be a remarkable routine and the
improvement has been excellent. She only dedicates about 6 hours a week
to the routine but she is more active now, breathing much easier and is
gaining back her old strength again. She is able to take walks in moderate
time frames, do some shopping, and once again visit the beaches and enjoy
small walks and dining that she so loved to do before that dreaded diagnosis
in November of 2001.
The pain is only moderate now and is only occurring at times when she has
done strenuous movement that day so the pain in the incision areas and
the diaphragm is moderate to rare at this time. She has eliminated the
need for prescription pain killers and is now only taking an over-the-counter
pain reliever as needed. Of course, with the control of the pain, then
the mental attitude has also greatly improved and there is more joy in
day to day living.
They have also found their new home a mile from mine that is absolutely
beautiful and what they have always wanted to own. They will be moving
into it sometime in December and they are excited now to shop for their
furnishings and other needed items to complete the home in time for Christmas
this year. We plan a very special Holiday again this year with all the
family members again flying in from out of state and this Holiday will
be even more special as she is in remission and much healthier of course
then she was at this same time last year when we faced the diagnosis and
the upcoming surgeries and the fear of what would happen and how things
would turn out.
Her weight is strong and she has even gained a few pounds which is showing
her marked improvement. Her immune system is incredible and her blood
work is excellent. She looks beautiful and there is no outward signs of
illness in her appearance at all.
As a family and her personal thoughts are that she can beat this cancer
and that they are making huge strides in the treatment of Mesothelioma
and we are in close contact with Dr. Cameron at UCLA and other remarkable
people assisting in, donating to or dedicating their time to helping with
the treatment and cure of this disease. It is hopeful and promising at
this time with all the new information that is becoming available.
I am specifically dedicating my time to assist where needed in the race
for the treatment and cure of the disease. I am in contact with other
patients other then my Mother and keep contact with their symptoms and
progress as well. The small group of patients that we know of, some of
whom were under Dr. Cameron's care and others under Dr. Sugarbaker's
care are also doing quite well at this time. Some are only at the 6-8
month mark since treatment but others are at the 1 year or 1-1/2 years
from their dates of treatment and still not showing signs of reoccurrence.
This is uplifting and offers so much encouragement to others.
I know that the course of treatment of this disease is up to each individual
patient and their families. However, it is our strong belief that with
the doctors currently treating Mesothelioma, as in our case, Dr. Cameron,
the treatment is worth every bit of time it takes to go through it and
recover. The terms used to describe it to us initially was hideous, horrible,
difficult etc. We found that the surgery was no more intense than any
other major surgery and that the recovery and aftercare was relatively
along the same lines. We would describe it as major surgery but not hideous
in any way. My mother actually looked better after the removal of the
tumorous tissues then before and yes, there was some days of intense pain
but for the most part the pain was manageable and the recovery time was
approximately 3-4 weeks for an almost full recovery from it. We cannot
praise Dr. Robert Cameron enough for the brilliance and knowledge he has
in the treatment of this disease. We still marvel at his abilities and
his attitude in treatment.
Her incisions have healed well, some of them are almost completely gone,
just small white lines at this point. Again there was some struggle in
the aftercare issues but this was finally conquered by trial and error
in what to do and what not to do and we are seeing the success of that now.
I am thankful and I thank God as we have seen the presence of him throughout
this ordeal and know that we have had divine intervention to have been
so fortunate. So many wonderful things have come from such a terrible
situation. We have met wonderful people, we have had so many people help
us that we did not even know, we have had some of the best doctors in
the world, we have had wonderful and loving support from family and friends.
We have also had wonderful opportunities present themselves that forever
have changed the course of all our lives in a very positive way. I think
that is important to share. It renewed my faith in God, in people and
in the remarkable courage of people when faced with diversity of this
magnitude. It made my stresses in life (the little things) pale in comparison
and I realize how lucky we all are in the big scale of life.
I would like to continue to keep everyone posted on her progress as it
is wonderful and exciting and positive.
We have met several people in our area that have recently been diagnosed
with Mesothelioma through various medical facilities and were told that
nothing could be done for them. These patients went home facing the possibility
of short-term life with no hope. There is much work to be done in spending
the word that there is treatment out there that is very promising that
offers relief from the pain, the chance to prolong your life and the possibility
and hope for a cure. These patients finally stumbled onto the information
that is offered through
MARFand other critical websites and from word of mouth more and more people
are spending the word and referrals to Dr. Cameron at UCLA and Dr. Sugarbaker
in Boston. We are dedicated in assisting in spending this information
to the public and to other medical facilities who are not up-to-date and
aware of all the treatment options available today to fight Mesothelioma.
The key point would be to seek immediate treatment with these doctors,
never give up hope and continue to involve yourself in the fight.
Laurie MacDonald
An Update -- 6/22/04
Family Group Photo at Christmas 2003
Sue and Scooter on Mother's Day 2004
Sue and her Granddaughter Monica in 2003
Prepared by: Laurie MacDonald-Treiber (Daughter)
I thought it was important to share that is has been
32 months since my Mom's diagnosis of Mesothelioma (November 2001). It
seems so long ago that we were informed that she had this rare and incurable
cancer. We have also been fortunate that things turned out as well as
they have for her.
The original prognosis was 12-16 months to live and treatment was originally
described to us as experimental and not a cure which is true. Most people
we conferred with described the treatment as hideous and worse than the
cancer itself. This proved not to be the case for her. It was not as severe
as that description. Yes, it was difficult. The treatments were not a
cure and she went through several months of pain and several more months
of radiation treatment but we felt in her case that the aftermath of the
surgery was worth the recovery that she has experienced since. We realize
that each person will have different results and different outcomes and
we know that my Mom is one of the few fortunate ones that had such positive results.
Since October 2002 her health has markedly improved overall. Both she and
my Dad are retired and are enjoying the leisure time they now have to
relax a bit and enjoy life. After various trial and error we have determined
that my Mom responded extremely well to:
- A good overall diet (it is critical that the patient maintain weight)
- Working with both a physical therapists initially and then;
- A Personal Trainer on a regular basis each week. Her overall stamina, breathing,
energy and state of mind improved. Exercise for her has been a critical
key to overall well-being
- Avoiding Stressors as much as possible
- Continuous support - she has a very strong family support system
Her symptoms at this time are mild with some breathing difficulty only
after over-exerting or in certain weather conditions which are both frustrating
and at times scary for her.
The pain in the back and around the front rib cage is mild and manageable.
She uses caution when exercising muscles in this area to avoid any damage
to the muscle or bones.
She has not had to use any pain killers or other medication for well over
a year now. She continues to do follow up testing and evaluations with
Dr. Robert Cameron at UCLA every 3 months. Occasionally she still battles
sleeplessness and will take a sleeping aid but that too has improved over time.
She has extensive blood tests done and a CT/PET Scan done for his review
through Hoag Hospital. I am in touch with Dr. Cameron on a regular basis
and I contact him with any irregularities or issues immediately so that
he is apprised of her condition at all times. She was on a low dosage
of interferon for approximately 10 months. Her blood tests on the 11
th month showed a low white blood cell count which is to low so she was taken
off the interferon and proceeded to have her blood tested every 2 weeks
for 8-10 weeks to see if the problem was the interferon usage.
With repeated testing over a 3-4 month period of time her blood count came
up but was still not within the normal range. She is continuing to be
monitored regularly and may need to seek additional treatment to help
assist her white blood cells. Overall she is not feeling anything but
minor symptoms from this problem and some fatigue. However, it has been
recommended that she go back to daily injections of the interferon but
is unable to do so until her cell count is normal. It is also possible
that the interferon usage could have caused the drop in the white cells
as a large majority of patients using interferon could suffer this particular
side effect.
We thought at Christmas 2001 that we may never have an opportunity to experience
Christmas 2002 and we have had the joy of 3 Christmas's since the
dreaded words from Dr. Zusman, "You have a rare lung cancer called
Mesothelioma and it is terminal". We have had some very difficult
times mostly during the initial diagnosis, treatment and than follow-up
treatments (radiation) and recovery. We have also had some of the most
wonderful times during 2002, 2003 and now moving into 2004 in which my
Mom has felt good, looked wonderful and was not in pain.
We have learned so much about Mesothelioma over the course of this journey
and we continue to learn every day. As a family and as individuals, my
Mom's illness has changed all of our lives.. The old saying "life
is to short" became our reality and we truly understood the real
meaning of those words and have all adjusted our lives to live it. We
have met wonderful and caring people who have offered so much support
and we have seen so many miracles that its been a truly spiritual experience
that is difficult to explain in words. We have also had our struggles.
It is a difficult thing-learning to live with incurable cancer. It is
hard to adjust for both the patient and the people who love them. It is
hard not to worry or project out the future at times and it is hard to
fully accept it but you continue to have hope. We take it one day at a
time and our thankful for each day. My Mom continues to be a GREAT mom
who even in an illness this serious is still the one teaching all of us
the importance of life and the courage it takes to truly live it. She
really is remarkable in facing this devastating situation in her life.
Laurie
An Update -- 3/13/07
Five years after her pleurectomy with decortication surgery with Dr. Robert
Cameron and five and a half years after being diagnosed with mesothelioma,
Sue MacDonald and her family recognize they have been blessed. Sue was
originally given a fourteen month prognosis provided she recovered well
from the surgery and the follow-up radiation and interferon therapies.
In March 2007, she has made it 63 months past surgery, but more importantly,
she is not just alive, she is living.
While Sue's health limits her ability to do some activities, she doesn't
hesitate to shop, go to the grocery store, or take walks on the beach
with her family. Sue works out with a personal trainer twice a week for
about an hour and a half, working with weights and limbering up her upper
body. For a portion of that time she walks on a treadmill, as well and
works on breathing exercises, too. Once every two to three weeks, especially
when the humidity gets bad, Sue's breathing becomes too labored and
she has to use one of the small oxygen bottles the family keeps around
the house.
Gerri recalls how the whole thing started over five years ago when Sue
quit smoking and began to exercise at her doctor's bequest. Soon after
that, she noticed she was short of breath and coughing much more than
what a "smoker's cough" would be. After weeks of doctor
visits, Sue was diagnosed with mesothelioma. That's when Laurie, their
oldest daughter, began her research online and found three specialists
across the nation, including Dr. Cameron, was also luckily, close to home.
Beginning on day 1, Laurie chronicled all of the research she conducted,
specialists' opinions, doctor visits, tests results, and Sue's
health in a binder. The MacDonalds still have every piece of paper that
Laurie catalogued, neatly organized into three large binders, each eight
inches across. Gerri says that Sue would not be here if it weren't
for Laurie who became the expert on mesothelioma, arranged the medical
visits, and oversaw every phase of treatment. He believes they have been
blessed by God who has given Sue this time to spend with family, blessed
by Laurie's diligence, and blessed by Dr. Cameron's superb medical
treatment.
Every four months, Sue has a CT/PET scan to monitor the cancer which has
been completely clear for years now. She continues to see Dr. Cameron
for follow ups as appropriate. "Sue's the one that holds everyone
together. She didn't go sit in the chair and say it was all over five
years ago," says Gerri, and "that's why she is here today."
An Update -- 10/13/09
Since the initial surgery performed by Dr. Cameron at UCLA, and Radiation
performed at Hoag Hospital (year 2002), my mother has been doing fairly
well. About a year ago she had tumors that declared themselves and about
8 months ago underwent chemotherapy treatments, series of 6 treatments
and was able to effectively shrink the tumors. However, chemo proved to
be very toxic to her which became apparent by the 3rd treatment and she
was given Neulasta, an engineered protein that stimulates bone marrow
and induces the production of white blood cells.
This was effective in controlling this problem. She also experienced a
serious reduction in the red blood cells and had to get platelet transfusions
to correct it. Because the chemo was so toxic to her she has experienced
low immunities. She suffered "bell palsey" and through acupuncture
was successful in overcoming it. She had "shingles" shortly
after that which required additional medical treatment but healed from
that in a few weeks.
Within a year of the initial surgery in Jan. 2002 she began working out
with a personal trainer several times a week and is continuing this routine
to-date. This has been enormously beneficial for her in building up strength,
keeping her mind and body active and strong. She has always maintained
overall good health and is in great physical shape especially considering
the surgeries and treatments.
In September 2009, she underwent "cryotherapy" treatment (1x
only so far) to freeze the tumor and the results are pending until the
end of October. This was an outpatient treatment, took several hours to
perform and several hours of rest and observation.
She has done remarkably well throughout and continues to be strong physically
and mentally. She looks great and mostly feels well.
We have been remarkably blessed!
I will keep you updated as additional information on "outcome"
becomes available.
Laurie
An Update -- 3/8/10
I believe the last update on my Mom was she was schedule to undergo "Cryotherapy"
treatment through UCLA. In September 2009, she underwent "cryotherapy"
treatment (1x only so far) to freeze the tumor and the results were pending.
This was an outpatient treatment, took several hours to perform and several
hours of rest and observation.
We received the results on its success in February 2009 and the one tumor
they addressed with this procedure was successful. It eliminated that
tumor. Since "mesotheloima" is not curable the medical plan
of attack is to regularly monitor her and to use the "cryotherapy"
to shrink or eliminate any tumors that enlarge. She will see Dr. Cameron
again in June 2010. She feels great, is maintaining her overall health
and weight and continues to regularly see Dr. Cameron which is critical.
As she has from the onset of this disease, she works out regularly with
a personal trainer. She continues to do this twice a week for an 1-1/2
hour each session. This routine has helped her a great deal both in stamina
and strength. She eats regularly and very balanced meals. She has a sleep
routine and gets great sleep each night and is otherwise active. She is
somewhat restricted in heavy lifting, carrying, walking long distances
or for any length of time due to shortness of breath at times but overall
it is quite a gift to all of us that she has responded so well to all
treatment and has recovered so well from each procedure. Dr. Cameron and
his team and any referrals he has given to us have worked out so well.
He is very talented and we have 100% trust in his expertise. I can only
say again and again what a God Send that we found him.
I personally have had calls from various people (through referral) that
have been diagnosed with mesothelioma who have not faired as well. It
is such a tragedy. However, the last two patients I was speaking with
(just this past year) had other medical conditions prior to this diagnosis
that hindered their ability to undergo some of the meso treatments recommended
and therefore opted out for just doing chemotherapy which was not as effective
on its own. One of the two patients, upon their initial diagnosis was
immediately given radiation which was not a good thing to do which also
hindered their ability for more effective treatment. I can only hope that
the more educated the public becomes on this disease, the more people
being diagnosed with this cancer, will do their research and due diligence
before moving forward in treatment. This is so critical to trying to achieve
a positive outcome. Roger Worthington's site was the most comprehensive
and detailed site I found after 1000 of hours of research and their guidance
and information was what directed us to the best possible treatment and
to Dr. Cameron. I can not say enough about my good fortune in finding
that site and his team to help and direct me. They helped me so much to
take a overwhelming and chaotic situation and make sense of it.
I will keep you posted when she has the next treatment - this will greatly
depend on the growth of any unseen tumors in the future. As for now, we
all just continued to be thankful for the blessings bestowed upon us and
for my Mother's continued good results and health.
Sincerely
Laurie MacDonald-Treiber
Daughter to Susan MacDonald
* * * Susan passed away on Janury 14, 2013 ***