मेंदूच्या कर्करोगाची लक्षणे

It all started with an extreme headache. When I bent down, I felt everything flowing downwards and then flowing backwards. I initially suspected it could be related to asthma, so I consulted a doctor. However, he attributed it to stress and recommended seeing a psychiatrist. Despite this, I was skeptical because I knew stress wasn't the cause.

नंतर माझ्या वडिलांनी न्यूरो फिजिशियनकडे जाण्याचा सल्ला दिला. पण जेव्हा मी न्यूरो फिजिशियनकडे गेलो तेव्हा त्यांनी मला न्यूरोसर्जनकडे पाठवले. म्हणून आम्ही हैदराबादला आलो, न्यूरोसर्जनचा सल्ला घेतला आणि माझा एमआरआय करून घेतला. अहवालांमध्ये, आम्हाला आढळले की ते ए मेंदूचे कर्करोग ट्यूमर, परंतु मला ग्रेड 2 एपेन्डीमोमाचे निदान झाल्याची बातमी माहीत नव्हती.

मेंदूचा कर्करोग उपचार

मला आनंद झाला आणि मी वाट पाहत होतो शस्त्रक्रिया कारण मला वाटले की यामुळे माझी डोकेदुखी थांबू शकते. माझी आईसुद्धा त्याच मानसिकतेने शस्त्रक्रियेसाठी उत्सुक होती.

माझी दृष्टी, माझे हातपाय किंवा चालणे कमी होईल याविषयी डॉक्टरांनी माझ्या आईशी किंवा माझ्याशी नव्हे तर माझ्या भावाशी चर्चा केली होती. हे यापैकी काहीही किंवा सर्व असू शकते, आणि मला त्या वेळी त्यापैकी कोणतीही गोष्ट माहित नव्हती.

साडेचार तासांची ही अत्यंत आक्रमक शस्त्रक्रिया होती. डॉक्टरांनी जवळजवळ 99% काढून टाकले, त्यामुळे माझ्या चेहऱ्याच्या नसा, ऑप्टिकल नसा आणि सर्व काही प्रभावित झाले. माझी दृष्टी, माझी बोलण्याची आणि ऐकण्याची क्षमता गमावली आणि मला चालताही येत नव्हते.

Every day in the hospital was a struggle. I didn't know if I would wake up each morning. I developed pneumonia and had to undergo a tracheostomy. With the tube in place, I couldn't open my mouth or speak for three and a half months. My mother was worried if I would ever regain the ability to speak.

My face was paralyzed; I couldn't move any part of it. I remember my brother asking me to smile, but I couldn't even convey that I was smiling inside because I couldn't move my lips. I couldn't express anything through my facial expressions, and I couldn't even write properly because of my impaired vision.

To make things worse, my creatinine used to shoot up to 6, and doctors were confused about whether to do dialysis or not because I already had a lung infection. So, they didn't take the risk and gave me medicines and increased my water intake. After one week, point by point, the creatinine level started to decrease.

Later, my radiation started. But I had surgery on the backside of my head, and there was a big bulge there. When I laid down for my radiation, I almost lost consciousness, so again the radiation would be canceled and rescheduled for some other day. Every week, doctors used to perform a lumbar puncture before radiation. Even the doctors were worried that too many lumbar punctures could affect my spine, but they had no other choice. That process was harrowing, so every day, I felt like I didn't want to go through with it, but somehow, I managed to complete my radiation.

One day I had a fall, and again, it created a very panic situation because I had undergone surgery and already had a big bump on my head. I was immediately taken for scans and other tests, but fortunately, nothing had gone wrong. Later, I was given physiotherapy sessions where I was taught how to sit on a chair, how to walk forward, backward, and sideways, how to swallow food. I had to relearn everything from scratch and used to ask my parents how to do simple things because I couldn't even remember those things.

पण शेवटी, मला रुग्णालयातून यशस्वीरित्या डिस्चार्ज मिळाला आणि माझी श्वासनलिका काढली गेली.

परत घराच्या दिशेने

घरी आल्यानंतरही मी माझ्या रायल्स ट्यूबवरच होतो. एका वर्षानंतर, मी पाहू शकलो, परंतु मला फक्त अस्पष्ट प्रतिमाच दिसू लागल्या.

My eyes don't move sideways. I developed a squint after surgery, and because of that, I have double vision, even now. I used to bump into doors because I could see two doors, and I could not figure out which one was the original. Because I couldn't see correctly, I lost my balance and used to sway when I was walking or standing.

I underwent eye Surgery in 2015, but it was not successful. I had dry eyes and a dry mouth. I could have lost my corneas because of the dryness, but I used to put eye drops frequently to keep my eyes moist. Because of the dry mouth and absence of saliva, I couldn't eat spicy food; I'd lost a protective layer to my teeth, so they became so brittle that even if I bit a biscuit, my teeth would break off. I underwent 12 root canal treatments, and all my four wisdom teeth were removed.

Every dental procedure was more excruciating than my radiation. I used to cry silently on that dental chair every time. I couldn't even open my mouth. It had to be done in 2-3 sittings as I couldn't stand all that Pain in one sitting. Saliva plays a vital role in our body that no one is aware of or cares about, but I do now.

जेव्हा मला रेडिएशन होते तेव्हा मी माझ्या भुवया आणि केस गमावले होते आणि माझ्या डोक्यावर ठिपके होते. म्हणून, जेव्हा मी माझ्या अपार्टमेंटमध्ये आलो, तेव्हा लोक अक्षरशः माझ्याकडे पाहून घाबरले.

My face had changed completely due to the Surgery. I still don't know how that happened. It took me around three years to accept my face because, by the age of 25, your brain registers how you look. When I look in the mirror, it's not me; it's someone else, and it took me a very long time to accept it. Anyways, I couldn't see correctly, but still, even if I looked in a mirror, I couldn't recognize myself. It used to take a moment to realize that okay, that's me.

मेंदूच्या कर्करोगाच्या सुरुवातीच्या शस्त्रक्रियेमुळे चेहऱ्याचा अर्धांगवायू झाल्यानंतर, माझी एक बाजू सुधारली होती, परंतु दुसरी बाजू अजिबात सुधारली नाही, त्यामुळे माझा चेहरा एका बाजूला मागे पडला होता. डिस्चार्ज केल्यानंतर, द माझ्या चेहऱ्याची फिजिओथेरपी दोन वर्षे चालली. माझ्या मज्जातंतूंना चालना देण्यासाठी ते मला इलेक्ट्रॉनिक उत्तेजन देत असत. ही दुसरी वेदनादायक प्रक्रिया होती.

It took a year for the bulge to go away, and the fluid in my head applied pressure on my optic nerves, causing them to swell. My neuro-ophthalmologist was concerned after looking at the scan reports because the nerves were swollen, and if the pressure increased, I could have lost my eyesight forever. He wanted my neurosurgeon to address the fluid, but my neurosurgeon was hesitant to perform any procedure because it would require placing a stand inside to drain the liquid, which could pose further risks if he needed to open my brain again. He couldn't take the risk of the Surgery and preferred to wait. I was very confused because both options were risky, and I am still waiting for the right time to undergo the Surgery and fully regain my eyesight.

After that, I wasn't happy staying at home with all these thoughts swirling around in my mind, so my brother approached an advertising agency, since that is what I had always wanted to do. He asked them as a favor if I could come to the office for 3-4 hours to boost my morale. They were such wonderful human beings that they agreed. Despite the paralysis, I wasn't able to sit, walk, talk, or even see properly, but still, they decided to let me in, and I am still working with them in the HR department.

I can't do what I want to do, even basic things like playing badminton or running or walking like everyone else. I love playing badminton, but now I can't because I cannot estimate or judge correctly, and it gives me a kind of bumpy feeling in the head and results in a headache. I can't step out on roads because I can't see properly. But I don't want to look at it that way; I am fine, and I am going to do it. I am never going to give up; I am not accepting defeat.

ब्रेन कॅन्सरविरुद्धच्या माझ्या प्रवासातून माझी प्रेरणा

मला माझे कुटुंब, डॉक्टर आणि परिचारिका यांच्याकडून प्रेरणा मिळते. त्यांच्याशिवाय मी काही करू शकलो नसतो. प्रत्येक क्षण, प्रत्येक सेकंद मी होतो आणि अजूनही झगडत आहे, पण कुटुंबाच्या फायद्यासाठी मला हार मानायची नाही. जेव्हा मला मेंदूचा कर्करोग झाल्याचे निदान झाले तेव्हा मी फक्त 25 वर्षांचा होतो - एपेंडेमोमा. माझ्या आयुष्याची अजून बरीच स्वप्ने आणि दृष्टान्त होते. मी माझ्या शिक्षणाचे नियोजन केले. मला एक व्यवसाय करायचा होता, आणि मी माझ्या मित्रांना सांगायचो की वर्तमानपत्र वाचायला सुरुवात करा आणि एक दिवस, तुम्ही नक्कीच माझ्या यशस्वी व्यावसायिक महिला असल्याबद्दल एक लेख वाचाल. एक यशस्वी व्यावसायिक महिला बनणे हे माझे स्वप्न होते.

When I was on a wheelchair or stretcher, I used to look around at people in the hospital, all of my age, smiling, walking, doing everything, and I used to ask myself why I am like this? But now, I need to get over all these. I need to go and chase my dreams. Now, I want to have a happy and healthy life, and I wish that for everyone. Only if you have health, you can do anything. I see people running behind material possessions, but they don't realize that they are doing so, putting their health at risk.

I used to sketch. I love painting, and I do pencil sketching. Even without proper vision, I wanted to do something for my doctor, so I made his sketch. I also used to play the guitar. My brother used to take me out on the hospital campus so that I could spend some time in greenery. All these things used to relax my mind amidst all the chaos. Initially, I was not fond of going to the top floor of the hospital to watch the view, but gradually, that became one of my most favorite parts of the day for which I used to wait for my brother.

ऑफिसला गेल्यावर माझा खूप आत्मविश्वास वाढला. तिथं माझ्यात कोणी भेदभाव करत नाही; प्रत्येकजण मला प्रोत्साहन देतो.

माझे शिकणे

I believe that life doesn't challenge you with things you can't handle. It only gives you whatever you can handle. Many miracles have happened in my life. I have learned to be positive. I don't complain; instead, I count my blessings that I have an amazing family and got a fantastic set of doctors.

I believe that life doesn't challenge you with things you can't handle. It only gives you whatever you can handle. Many miracles have happened in my life. I have learned to be positive. I don't complain; instead, I count my blessings that I have an amazing family and got a fantastic set of doctors.

विभाजन संदेश

कधीही हार मानू नका, नकारात्मक बाजू पाहू नका आणि कधीही निराश होऊ नका. हे तुमचे जीवन आहे; तुम्हाला त्याचा सामना करावा लागेल. कोणालाही तुमच्याबद्दल सहानुभूती दाखवू देऊ नका किंवा तुमच्यासमोर रडू नका कारण ते तुम्हाला कमजोर करेल. स्वतःला डिमोटिव्हेट करू नका आणि तुमच्या कुटुंबालाही डिमोटिव्हेट होऊ देऊ नका. तुम्हाला यातून मिळेल. लाथ मारणे कर्करोग आपल्या शरीराबाहेर.

काळजी घेणारे देखील सकारात्मक असले पाहिजेत. जे लोक फक्त सहानुभूती देण्यासाठी येतात त्यांना कधीही परवानगी देऊ नका, कारण दिवसाच्या शेवटी ते फक्त तुम्ही आणि तुमचे प्रियजन आहात. आपल्या जीवनातील सर्व जंक वगळा.

कीर्तना थ्रिवेदीच्या उपचार प्रवासातील महत्त्वाचे मुद्दे

• हे सर्व अत्यंत डोकेदुखीने सुरू झाले. जेव्हा मी खाली वाकत असे, तेव्हा मला सर्वकाही खालच्या दिशेने वाहते आणि नंतर मागे वाहत असे वाटायचे. मला वाटले की ही काही दम्याशी संबंधित समस्या असू शकते, म्हणून मी डॉक्टरांचा सल्ला घेतला, परंतु त्याला असे वाटले की हे सर्व तणावामुळे आहे. आणखी काही डॉक्टरांशी सल्लामसलत केल्यानंतर, मला ग्रेड 2 एपेंडीमोमाचे निदान झाले.
• माझ्या मेंदूच्या कर्करोगाच्या ट्यूमरसाठी मी रेडिएशन आणि शस्त्रक्रिया केली, परंतु ती शस्त्रक्रिया खूप आक्रमक होती. याचा माझ्या चेहऱ्याच्या मज्जातंतूंवर, ऑप्टिकल नर्व्हवर परिणाम झाला, मला नीट दिसू शकले नाही, मला स्क्विंट विकसित झाले आणि आणखी बरेच दुष्परिणाम झाले.
• शस्त्रक्रियेनंतर माझा चेहरा पूर्णपणे बदलला. मी स्वतःला ओळखूही शकत नाही. माझा चेहरा स्वीकारण्यासाठी मला तीन वर्षे लागली. मला हव्या त्या मूलभूत गोष्टीही मी करू शकलो नाही, पण तक्रार करण्यापेक्षा मी माझे आशीर्वाद मोजणे पसंत करतो. माझ्याकडे आश्चर्यकारक कुटुंब आणि डॉक्टर आहेत; त्यांच्या पाठिंब्याशिवाय मी काहीही करू शकलो नसतो.
• कधीही हार मानू नका, नकारात्मक बाजू पाहू नका आणि कधीही निराश होऊ नका. हे तुमचे जीवन आहे; तुम्हाला त्याचा सामना करावा लागेल. कोणालाही तुमच्याबद्दल सहानुभूती दाखवू देऊ नका किंवा तुमच्यासमोर रडू नका कारण ते तुम्हाला कमजोर करेल. स्वतःला डिमोटिव्हेट करू नका आणि तुमच्या कुटुंबालाही डिमोटिव्हेट होऊ देऊ नका. तुम्हाला यातून मिळेल. आपल्या शरीरातून कर्करोग बाहेर काढा.

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