Wednesday 27 January 2021

completing My Latent TB treatment

 



My check up date was supposed to be in May 2020 but thanks to covid Pandemic  I was unable to visit the hospital

So had to take opinion from the doctor over phone/virtual.Was asked to continue the medicines.But my knee pain was too much to bear.So he made some changes in my medicine

However even the new medicine gave me sever knee pain.But my other symptoms were not bad as at the start  of treatment which was particularly tough

I continued the medicines and finally in October I could visit the doctor.I went through a pet scan as it would be helpful for my post cancer check up also.

My doctor was happy with the progress and finally I could stop the medicines after almost a year long treatment

Have to go for my Neck sonography in April 2021 but till then it is good bye to all medicines...

I am back to my routine of writing,blogging and painting and living my life to the fullest

 

Wednesday 8 January 2020

MY tryst with Latent TB


July 2019

My pet scans and sonography of the neck continues and the reports were consistent showing the lump in my neck but no change in dimension
I retired from my job in December 2018.Now post retirement I have taken up to follow my long desired hobbies and passion like painting and other crafts. I am able to spend a lot of time with my old friends and catch up on some truly lovely memories.
I go for regular walks,more regular with my yoga and I must say that the pain in my joints ,my cramps are far better .But mouth and tongue problems such as sores and pain still continue.
Also at times I experience nerve and muscle problems such as numbness and tingling which may take some more time to go away
I also try and counsel cancer patients and try and help them in my own way.

So it truly keeps me away from any negative thoughts.
Cancer changes you in the sense that your priorities change.You learn what is important .You learn to do what makes you truly happy.Had cancer not happened probably I would have taken a 2 year extension in my work place.But with all this experience i truly needed a break at least for a year to do the things that i have always wanted to do.
Coming to my  scan done in June 2019,it  showed a slight change in the size of the lump.So was immediately asked to do a biopsy.
Again days of tension .worry and prayers.But luckily cancer was ruled out.How ever I was asked to see a pulmonary specialist.
I was put through a host of blood tests .Non of the blood tests showed anything alarming or any infection.So was asked to go through a skin test to detect TB bacteria.
This test showed that I could be suffering a latent TB infection.
People with latent TB infection do not have symptoms, and they cannot spread TB bacteria to others. However, if latent TB bacteria become active in the body and multiply, the person will go from having latent TB infection to being sick with TB disease. So For this reason, I was told that i have to be treated to prevent from developing  TB disease.
Thus began my tryst with Latent TB infection and the treatment.
I was immediately started on the tablets.RCIN 600,PYZINE 750,COMBUTOL 1000, AND BENADON 40
Though the doctor warmed me about few side effects I dint think it would be really bad..But after 5 days of taking the medicines I was having
Severe nausea and vomiting, stomach pain as well as never ending immense body and joint pain .The drugs really made me feel miserable and threatened to take my liver function and along with that my sanity
When the symptoms dint seem to go away and started getting worse  I had to be admitted to an hospital where it was diagnosed that I was suffering from drug induced Hepatitis.
It was a bad phase .It was then that I realised that Drug-induced liver injury is a common complication of tuberculosis treatment.Also it is quite common to have TB post lymphoma .
After a few days at the hospital I was discharged once my liver functions were almost back to normal.
I had developed a pervasive fear and a hatred for the TB drugs because of the severe side effects.
I was wanting to stop treatment but  that was not a choice that I had .
Subsequently I had a detailed talk with my doctor and  made certain changes to my TB drugs and their combination,dosage etc.He also introduced the drugs in a phased out manner so that he would know which one was causing me maximum side effects.
By then my drug resistant report was received and I was found to be resistant to one drug
so changes were made to my medication.I however developed unbearable leg pain .
So this again involved some changes .After many  changes ,though  the side effects are  manageable now but still it was not easy the last few months..Now after 6 month of taking these medicines ,my system has perhaps got used to the drugs and side effects have gone except that it has left me with a permanent knee pain and burning under my feet
I have to go for my sonography of the neck this month to see the progress
I am also not sure how many more days my drugs will continue .But I was told that it is usually 6 to 9 months.I have already completed 6 months of this treatment.
So hoping to hear a positive response from my doc soon.


An year post treatment

penned on November 2017

My pet scan report done in October 2017, after 1 year of completing Chemo is not cancer free all clear Scan. Some lumps are visible in my neck  area .But as per my doctor it is not a cause for concern. At the same time it cannot be ignored and has to be monitored every three months.So my scans and sonographies will continue 
As per my doc the lump may go by itself and as far as there is no change in the size of the lump there is nothing to worry.

If there is any change in dimension of the lump then perhaps it will be a different story. So I go through sonography of the neck and my pet scans as and when my doctor tells me to do which is almost once in 3 months. I have almost become a permanent visitor of Hinduja hospital. So I still have to listen to the clinking and clanking of CT machines a
At times i feel that   a Damocles sword is hanging over my neck but I can’t be always worrying and thinking as to when it will fall.

I know it's not the end of the road for this stupid cancer journey. I'm not ignoring the facts.

So I continue going about my routine and believe in living my life to the fullest

 which gave me no time to think about myself or my problems.

Cancer has a way of making you look at each day as “special.” There is no time to hold grudges, and you begin to look at the “Big Picture.” Things that used to bother you, no longer matter as much.
I continue with my regular tests and checkups as I go through life.
My advice to cancer survivors is that though you may be worried about your cancer coming back or possible late effects of treatment that can develop months or years later try not to get stressed thinking about this constantly.Take a deep breath and relax.
This is the first move you can make when panic hits you. There will be endless ideas, advice,some medical knowledge slung your way. Your deep breath will help you navigate the noise. Breathe and listen. Your breath has the enormous power to reduce stress.Learn yoga and do regular pranayam.
Try to take regular walks,get out of the house and commit to some form of exercise.It need not be with any fancy equipment.Your body needs to move and stay strong during and after treatment.Drink fresh vegetable juice.Juices are nutrient dense, hydrating and truly energizing
wrangle your stress.AS it is cancer treatment has taken a toll on the body 
So  manage the stress  so it doesn’t  disrupt your sleep and create more illness .Here again yoga is a great stress buster.Put your mind in creative hobbies.Last but not the least sleep well.



Tuesday 7 January 2020

life post treatment

Penned on November 2016




My life post treatment

 Though my treatment ended in July 2016 I was asked to undergo regular tests and check up in periodic intervals.
My first petscan post treatment was in October 2016 .This report seems more or less ok and i feel blessed 

Cancer is often described as a journey that starts at diagnosis. So true this is.During treatment, you at times feel that your life is on hold. After the treatment ends, it is tough to resume normal activities immediately. You tend to feel a bit lost.
Sometimes survivors expect life to return to what it was before the cancer diagnosis or treatment. But for many , it isn’t that simple and easy. The reality is much more complicated  both emotionally and physically. For some it may take quite some time to be back to absolute normal and for some they have to accept the “new normal.
Cancer certainly changes you as a person in more ways than one. Even though we may start to look normal and feel normal physically, it certainly feels different at least at emotional level.
Each person who has fought and survived cancer feels differently once the treatment ends.
Most people tend to re-evaluate and change their values, goals, priorities and outlook on life.
·        Some survivors feel a sense of loss for “the person they once were… or the way life used to be for them and they miss certain things which they are not able to do post treatment.
·        Some people are absolutely happy that they have survived and count their blessings
·        Some continue to wallow in self-pity talking about the changes,the travails of treatment.
·         Some want to return to their previous routine  at the earliest.

How you feel and cope up with life after…will largely depend on the type of cancer treatment that you have had, your basic nature as a person and your mental strength.
Cancer treatment in most cases will certainly leave long term side effects like fatigue, continuous cramps, pain etc.
In my case fatigue continues and i have  severe pain in my legs. I still suffer from severe cramps at times. My eyesight has been affected .My tongue burns even at slightest of hot food. My teeth have become super sensitive.
But yes my meditation, yoga, regular exercise and certain change in my eating habits has helped me to a great extent in dealing with these problems and i  am sure that these post treatment side effects  too will completely  disappear with continuous yoga and exercise. Even if it doesn’t it’s no big deal.
The chemo after effect is truly enormous and not easy to deal with but it is certainly possible to have a new normal where you can be healthy and happy
I always feel that i am blessed I live in a place where medical facilities are available and I am able to afford them. Though I must say Cancer treatment drains you physically emotionally and financially.
Blessed to be surrounded by many many well wishers and fantastic friends.
Yes it does worry me at times when I have any pain,discomfort etc and for a short while my mind tends to be negative.But I try and shake off that negativity and get back to my routine.Its is good that i have a job which keeps me busy


Monday 29 January 2018

My cancer journey

This was written by me july 2016 when I finished my 6th Chemo

About myself-I am a 56 year old working woman happily married with one son




What this write up is about


This write up is about my cancer journey.I am certainly not a good writer .But I have just penned my experience and my emotional state during this phase.If it can help people I would only be too happy.I want people to be more aware about their body and give at most priority to health 


My cancer was totally asymptomatic but cancer is a very silent disease so knowing your body and being aware of your body is very important. Even a little change could possibly be something that’s happening


The scariest part of cancer is the unknown, but we can fight the unknown. More than anything we have to change our view that “cancer is a death sentence.”


Phase leading up to the diagnosis


While I am penning this I have just completed my 6th chemo cycle. I may have a long way to go before I complete the full treatment but I am glad that I have gone through 6 cycles with grit and positivity.
My Cancer diagnosis happened almost by accident. It was 14thFeb and I was getting all set to leave for Srilanka with my friends a week later.
It was a Sunday, Valentine’s day. I was having a slight discomfort in my back and had a little vomiting. I blamed the vomiting on my previous day’s snacks which I had at a mall and left it at that. By afternoon the pain in the back increased which made me reach out to my family Doctor. He prescribed some medicines which made me feel better. I went to work next day but by afternoon the pain cropped up again. I was having constipation. Doctor suggested a sonography to rule out any gall bladder related issue.

So I went for a sonography on 16th. The sonography technician was not very happy with the results and suggested a CT scan for better clarity. She did not spell out the problem. I have always enjoyed peak Health for all the 55 years, and had an active life style. I have never been ill or taken many risks where my health was concerned. So I was not too sure what to make out of the results and was a bit worried but never believed it could be something serious
So I went for a CT scan on the same day. For CT scan you are asked to drink a bottle full of a coloured liquid tasting weird and then you lie down on a narrow table, and lay your hands above your head. The table slides into the "doughnut hole." You have to lie still when the scanning process is on They inject a dye through an IV, and it just feels warm, as it moves through the body.

I didn’t go to see the doctor with the report perhaps out of fear of having to hear some bad news. My hubby collected the report and went to see my family doctor. Family doctor suggested that it could be cancer and I may have to undergo a uterus operation urgently.
Me, my hubby and my son were all dumbfounded on hearing the news as this was certainly totally, unexpected. I felt swamped because Cancer has such scary connotations. Me and my hubby both broke down and it was our son who managed to pacify us.
Our next step was to plan for the operation and also to visit a top oncologist for a proper line of treatment. Based on the suggestion of my company CFO, we decided to see a top oncologist, Dr. Sachin Almel, in Hinduja.

With the help of my brother in law, we were lucky to get an appointment for the very next day. Next day me and my hubby and my sister in law went to see the oncologist.When we spoke to him he suggested that we repeat the test and also do some additional tests at Hinduja, so that the diagnosis was perfect. This sounded ok.

So I went through a Biopsy wherein the test was conducted after administering anesthesia. The room had quite a few people and the procedure took about 30 minutes. They had to take several samples. Luckily it was not as scary as I thought it would be.
I also went through a pet scan after 2 days.A Positron Emission Tomography(PET) scan is an imaging test that allows the doctor to check for disease in your body .The purpose of a PET scan is to identify areas of high metabolic activity .Cancer causes high metabolic activity.

For the PET scan ,I had to be on empty stomach.We reached the hospital at around 9 Am.the process is very similar to CT scan.you are asked to drink a bottle of liquid and then they take you for scan to a room.You need to lie quietly without moving or talking.During the process an injection is also given which suddenly makes your body warm.When all the necessary images have been recorded ,you just slide out of the machine.They ask you to wait and in case they have any doubts about any image they may redo the scanning for few more minutes

We were told that the reports should be available after 5 days.The days when we awaited the results must have been the most anxious days of our life, filled with dread, fear and at the same time hoping against hope that the earlier diagnosis would be wrong.

Feb 26th, a day that will be etched in my memory. When we went to collect the report and visit the oncologist, I was shattered when he confirmed that I was suffering from Lymphoma- Cancer of the Lymphatic glands.
From the time he pronounced the "C" word ,i honestly dint hear much of what eh was saying 
Somehow, I gathered my strength and knocked myself back to my senses. May be my fears were a bit eased when doctor said that it is treatable.The Doctor suggested that I need to go through 6 chemo therapy sessions each with a gap of 21 days with the first chemo to start immediately. He ruled out the need for any immediate surgery which was some relief.

When we hear the three earth shattering words “You have Cancer “our world turns upside down. That moment and those words are the dividing line between life before cancer and life after cancer.

Cancer- the dreaded “C” word is almost always equated with death and that makes this disease most scary. The very name of Cancer pushes the entire family into a state of gloom and mourning.

Despite the ground-breaking medical advancements that have been made in cancer treatment, cancer still remains a scary disease to accept emotionally, because it is still so commonly associated with lot of suffering, and the possibility of death. So many questions start to crop up in your mind as to what kind of cancer do I have? How much has it spread? Can my cancer be treated? What is the chance that my cancer can be cured? Etc.

For the next few days we continued to be in state of shock, not knowing what to do, how to react.
Perhaps my hubby was more hit than me. It was more of disbelief followed by shock. With my health record and my life style I should have been the last candidate for this disease. I had shown no symptoms at all. It was absolutely asymptomatic cancer. So it was truly difficult for us to accept this dreaded reality.

All through this it was my son who remained calm and positive and gave me the much needed strength & confidence. He was a pillar of strength and took the whole thing philosophically and with a lot of positivity.

When my colleagues got to hear of this they were shell shocked and there was utter disbelief in their minds.many did not know how to react and some of them broke down.

Soon I realized I should accept and come to terms with the fact and have to move forward with strength and I realised that that being in a depressed stage or being in self-pity will not take me anywhere. I realised that I could not control the disease but had the choice to control my reactions. I had the choice to impact my thought process.I decided to fight Cancer with grace, dignity and a positive attitude.
We all know at same level that life is finite. But somehow we never think of it as frequently or as concretely as after the diagnosis of cancer.


I recognized mortality in a way I had never done before.

More than wondering if I would survive the disease and the treatment, I was worried if I would be the same person as before, would there be any permanent threat to my way of life, would there be any permanent damages etc.
To keep the things moving in the right direction, we immediately appointed a yoga teacher to come home every day. I knew yoga and had been practicing on and off. But to be regular and focused, I knew I needed someone to come home and make me do it every day. So the practice of doing yoga and meditation started immediately.

Suggestions for others

At first, you need some time to adjust to the fact that you have cancer. It is emotionally a very hard time. But don’t let the panic button hit you and take you on a downward spiral.
And be practical and understand that this can happen to anyone. This has not happened because you have done something wrong to your body.Your emotional state can make it harder to take in and understand and collate all the medical information shared by the doctor. Grieving, feeling sadness, fear, anger, or going through crying spells – is a common reaction to learning you have cancer.But these feelings should not last for a long time and you need to snap out of such feelings.

Never once let go of your positive attitude because that is half the battle won. Be positive because that is the greatest weapon you have.At the same time don’t be ignorant and say that there is nothing wrong. There are so many people making an effort to make you come out of the dreaded disease. So it is important to follow your doctor’s instruction well.

It’s up to you to decide if and when you want to discuss your cancer diagnosis with friends and relatives. You need not go out of the way to inform everyone but it is better to be frank with people who are close to you .Keeping cancer a secret can lead to more stress at a time when you need the support of others. So reach out to close people and discuss. It is not an illness that you need to be ashamed of.
Cancer treatment can be very expensive and many many unexpected financial burdens can arise as a result of a cancer diagnosis. Take into account the cost of treatment, medicines, traveling for treatment etc. and be prepared. If you are a friend of a cancer patient, allow the patient some space to reconcile to the shock of the diagnosis. Do some small act of kindness .Stay in touch but accept the fact that they may not always be in a mood to talk or share their feelings. Respect their feelings.
People dealing with cancer may wish to talk about it at times, but they do not want the focus to be on their cancer all the time.

All cancer patients should be prepared for physical changes. Cancer treatment methods like surgery, chemotherapy and radiation can bring about many changes in your body including complete loss of hair. Surgery may cause scarring and disfigurement.



The Treatment Phase

Chemotherapy did bring with it a lot of fear and the experiences of other people that I had read on the net were shocking .But I had to tell myself that I will face it bravely.

My first chemo was scheduled for March 1st at 12.30 pm. I had an early lunch and post lunch, I reached the hospital well in time. I was taken to the chemo room. I was told that, I would have to go through bone marrow test before starting chemo. I was given a local anesthesia, as bone marrow aspiration, in particular, can cause brief, but sharp, pain. I was fully awake during the procedure, but the aspiration site was numbed to reduce pain.The area where the doctor would insert the needle is marked and cleaned. The bone marrow fluid (aspirate) and tissue sample (biopsy) were collected from the top ridge of the back of a hipbone. Then that place was bandaged and I was told to wear the bandage and keep it dry for 24 hours.The process was painful in spite of anesthesia, as the needle goes into the bone to collect the marrow sample.

After the Bone marrow test, the first test dose of chemo was administered to check for any allergic reactions. I did react to the medicine and had rashes all over my face. So anti allergens were given and once the rashes subsided, chemo was started. The entire process of injecting the chemo medicine through IV lasted for 8 hours. Since it was well past 12 o’clock in the night, I had to stay put at the hospital and to be discharged the next day.

My chemo reaction started the very next day. Though I had done a lot of research on the net, I really didn’t know what to expect. In chemo, there is no one-size-fits-all story. Each one’s experience in different and each one has a different story to tell.I suffered from nausea, metallic taste in the month, severe mouth ulcer and constipation. The constipation led to very severe Cramps in my stomach.
The cramps became worse after the 7th day. Finally on the 10th day after chemo, it was so unbearable that I was just holding my stomach and sitting up all the time.I had applied my own logic that this too was just a chemo reaction and that it would go away. Hence I did not mention the severity of the pain to my hubby. My son was away in Kashmir. Finally On 11th day I could take it no more and had to be rushed to the hospital. I had to be rushed to the emergency ward on a wheel chair.The doctors conducted some tests and we were told that I was having neutropenia where the WBC counts drop drastically. Because of this I had contracted stomach infection.

Later I learnt that some level of neutropenia occurs in about half of the people with cancer who are receiving chemotherapy. It is a common side effect of chemo therapy .Mine was worse as my count dropped very drastically. When neutrophil levels begin to drop it depends on the type or dose of chemotherapy. Neutrophil counts generally start to drop about a week after each round of chemo. The count then starts to rise again as the bone marrow resumes normal production of neutrophils.

I truly wish my doctor had pre warned me or at least given me some idea about this and that I had been told about neutropenia. I would have been better prepared for it and would not have delayed getting admitted to the hospital.

I was hospitalised for 6 days and was administered antibiotics and injection to boost the blood count. The injections were given on the stomach. While in the hospital, I was almost quarantined and no visitors were allowed because you are most likely to catch infections.After the discharge form the hospital, I slowly limped back to near normalcy and got back to having a little bit of energy. 

The chemo had robbed me of my sleep and gifted me with extreme fatigue. Chemo fatigue or Chemo lethargy drains you emotionally, mentally and physically. It is tiredness which cannot be explained. You are too tired to feel tired.

I was unable to eat normal food as I had metal taste in my mouth and nausea. But since I had to have energy for next chemo, I used to eat whatever and whenever I could.After 21 days, it was time for my second chemo. The reaction to the second chemo was more or less the same. Mouth ulcer, loss of appetite and more fatigue.

This time again on the 8th day after chemo, I had abdominal cramps. I was devoid of all energy and had no strength to even stand. Since we had a fair idea from the first chemo experience, we rushed to the hospital the next day. It was the usual story. I was again hospitalised for 5 days and was discharged after the WBC Count started returning to normal.

My third chemo was no different. The only saving grace was that we were well prepared and the minute I felt weak, I got myself admitted to the hospital. In fact this time the doctor had given a booster dose before chemo to avoid neutropenia but to no avail. Every time the count would drop around the 8th day, and would start returning to normal only around the 17th day. Those 10 days were truly tough.

With each chemo though, my side reactions like mouth ulcer, nausea was slightly better but my fatigue got worse because of the cumulative chemo effect. The lethargy was frightening. Just the idea of having to walk a few steps made me scared. Many things we take for granted became difficult or impossible for me to manage on my own. From having a shower, handling utensils, to getting dressed, I had to depend on someone’s help.

I am not an individual who is easily brought to tears or feel depressed over difficult situations in my life. However watching my life turn from that of a super active independent person to depending on people for the smallest and simplest of activities in less than 2 months was very tough to digest but I accepted this phase and carried on. When I was admitted to the hospital after the 4th chemo for neutropenia, I had to be given blood transfusion as my hemoglobin count had hit rock bottom.
I started to develop severe flatulence and developed bladder control issues. Bladder incontinence can be very embarrassing and tough to manage.

After my 4th chemo, a pet scan was again done to check the progress .The prognosis was good and the doctor was happy with the report.My 5th and 6th chemo produced the same reactions. Both the times it involved blood transfusion and injections to boost the blood count and all types of antibiotics. My fatigue had gone from bad to worse. I felt drained of all energy. In addition, I developed severe joint pain and extreme sensitivity of teeth. This caused unbearable pain in my teeth whenever I would bite anything especially sweet or anything even moderately cold.

Whenever I suffered from this neutropenia problem, I would rush to the emergency ward of Hinduja hospital. But it was a huge task to get a room in Hinduja. So invariably I would be in emergency ward for more than 6 or 7 hours. As luck would have it, there would be no bed in the emergency ward also and I would have to sit on a wheelchair for hours and hours with an IV on my arm. This was truly a very painful process.

At the end of 6 chemo's, I have lost count of the number of injections that I have taken. They number at least 70 . I don’t remember how many times I have been pricked for blood test. I don’t remember how many times I have had an IV for pushing antibiotics, chemo medicines. I do not know when my energy level will be back to normal. I have no idea as to when my joint pain would go, when my teeth sensitivity and pain would reduce, when I will have my complete strength back or when my hair would grow back. But I am truly thankful that I am alive and I am thankful that I can walk, talk, eat & laugh.

My suggestions for others


If you are a working professional, take time away from work. Health should be the main priority at this point. Be prepared for physical changes
Chemo therapy can have many upsetting side reactions which may include affecting the bowel movements , bowel and bladder incontinence, body pain, fatigue, and sensory changes.
It is important to follow a proper diet. Choose a healthy diet consisting of a variety of food. There may be days when you have no appetite or you may not be in a mood to eat anything. But make it a point to eat small meals. It is very necessary to have lots of fluid intake so that the body can rid itself of waste and toxins.You have to ensure that you get adequate rest in order to help manage the mental stress and fatigue which may result due to treatment.

Chemo therapy can make you very very susceptible to infections. So it is essential to maintain high levels of hygiene.Maintaining a healthy life style is very important and this also improves the energy level.
It is important to do something that you enjoy. Exercise helps the mind and body to be active. You may not have the energy to exercise every day but it is important to know that even if you are experiencing fatigue, even light exercise can help you feel better. Yoga and meditation and other relaxation methods can help to a great extent.

Don’t feel embarrassed to seek help. Chemo fatigue can make you incapable of doing even the smallest task on your own. So accept the fact that you may be dependable on others for help and seek help when needed. Please don’t shy away from seeking any type of help. Please don’t hesitate to speak up your problems.
Encourage your family to accept help if it's needed. Cancer diagnosis affects the entire family and adds a great deal of stress, especially to the closest family members.Above all, stay positive and cheerful and never give up hope at any point of time.

If you are a care giver to a cancer patient, ensure that you get adequate rest, sleep and try to stay away from tension. You need to be in your best of mental and physical health in order to help the patient

Post-treatment Phase

My chemo journey was truly tough but manageable. My yoga practice and meditation on days when I had the strength, made it better to cope. My inner strength helped me to pull through these six cycles.

I have been a voracious reader and this habit of mine helped me a great deal and during this period I must have read not less than 30 books including fiction, non-fiction, and spiritual.

More than anything I had a great support system at home. My hubby & my son were the greatest support & strength. My hubby had to do a lot of running around, had to forgo sleep on many nights. He was mentally & physically tired. My son was always there to cheer me, motivate me & keep me in good humour. I know it was incredibly tough for both of them but never once did they complain.
I was extremely lucky that I have a fantastic network of friends and colleagues. My colleagues were wonderful and they met with me regularly to ensure work worries didn’t hinder my recovery. My company was most supportive and granted me long leave .

My family and friends were so attentive and concerned and so kind during that time. The whole process of learning that so many people were there for me when I was at my most vulnerable self was so very emotional.
I went through the entire treatment with as much positivity as I could as I believe that attitude really shapes everything. Never once did I allow myself to go into self-pity. Infact I stopped thinking about my illness as something very critical.

I had lost all my hair on my head, my eye brows, and my eye lashes. I truly looked strange something like an alien. But every time l looked into the mirror, I looked at what I had and not what I lost. I learnt to make fun of my looks.
I took one day at a time. Every day I remembered my blessings as a mantra and thanked God for all the blessings. I was fortunate that I could afford the treatment, fortunate that I had a great medical team to take care of me. I was immensely blessed and lucky to have a great support system. I was lucky to have such great friends and so many well-wishers. The illness was critical but atleast I had contracted this illness at a time when my son was grown up. My hubby and my son could devote time for me.

Most of all I had the prayers, blessings & good wishes of so many countless people. I don’t even remember the count of people who have prayed for my recovery.I am immensely thankful to each and every one who has been a part of this journey in one way or other.
Life after chemo is different. The body has been through an enormous assault & recovery is truly time taking. You can’t just just bounce back. Chemo changes your life in many ways & that lasts well after the chemo is over.

But with regular routine exercise and rest, I am sure things will be much better.
Having this disease has changed me in some ways. I was always a person who valued time and who cherished memories. After cancer, I value time much more. Cancer has made me re-examine my life choices and has motivated me to make life style changes. My priorities have shifted and I will have more of ‘ME TIME’. I want to learn many new skills, travel more and enjoy each day of my life and celebrate life.


Suggestions

Once the treatment is over you may be in remission stage or may be completely cured but it is certain that you will undergo a whole set of emotions. Please know that there is no right or wrong way to feel. Evey cancer survivor’s experience is different ,will be different – it all depends on your personality, personal circumstances, the type of cancer, the type of treatment and the type of support system you have had. It is an emotional journey

Infact at times you will be scared to be happy in case the cancer comes back. This thought is very natural. But don’t live in a constant fear. Fear can keep you focussed on the past. Take each day as it comes. Don’t expect life to be 100% normal immediately. It will take time. But try and start the normal routine.
Let us accept that Life is unpredictable. It is a reality that none of us will live for ever. Disease or no disease, I could be gone tomorrow and this is true for all of us .None of us know what life has in store for us.
So cancer or no cancer, live life with no regrets. Learn from mistakes. Don’t wish for any change or to have anything differently. Everything in life happens for a reason and it has got us where we are today. Enjoy life and all that it has to offer. Enjoy your family, friends your job, enjoy nature, go places. Do what makes you happy. Our life today is a gift. The present where we must live in. past is gone and future is a dream.
Believe me, each one of us has the inner strength courage and determination to face any challenges in life. We just need to tap our mind, tweak our attitude and look at every thing with a positive thought. We can fear something but that fear should not define us.
It is so rightly said “You never know how strong you are until being strong is the only choice you have.”
With regard to diet try to follow a healthy diet and keep your body alkaline .It is said that cancer cells are more active in an acidic body.Eat lot of raw vegetables and fresh fruits. Try to include nuts in your daily diet

Most of all keep your mind active and positive

PS:- After 7 months of being away from work, I resumed my duties as a cancer survivor. Here I should take a minute to speak about my first day at work after cancer. The welcome I got from my colleagues was so overwhelming. It was truly a humbling experience. The specially decorated cabin, the welcome signs in the office, the standing ovation when I entered were truly touching and moved me to tears.

The emotions and feelings cannot be expressed in words. I could feel the genuine love and warmth of each and every one present in the office.Certainly my days at the office are not like before. I do get tired mentally and physically. I do feel like quitting my job and staying at home.
There is numbness in the hands and feet due to injured nerves. My joints still ache a lot.Recovering from cancer treatment isn't just about your body — it's also about healing your mind.
I am also waiting for my final test and the results. I do not know what the reports will tell.Even after a clean report, there is always a fear of cancer recurrence. It is a long long journey.
Today I am not be where I want to be, but I am certainly not where I used to be.

I have started doing regular exercise, changed my diet; my eating pattern. I have learnt reiki and have completed my second level.

I heal myself through reiki and try and stick to my yoga practice at least 3 days a week.Perhaps this illness has made me slightly more spiritual, I enjoy meditation. I want to be more creative and take up painting when my health permits.

For the present, rather than worrying about things that are beyond my control, I want to use my energy to focus on wellness and what I can do now to stay as healthy as possible, stay cheerful and celebrate life.