The Meyer Cancer Treatment Center at Weill Cornell Medical College offers both professional and personal treatment, and is regarded as one of the top Lymphoma Treatment Centers in the world. Weill Cornell also offers the most cutting edge Clinical Trials and new treatment methods. The doctors of Weill Cornell Cancer Treatment Center are experts in noninvasive and nontoxic Lymphoma treatments, and have revolutionized how Cancer is treated over the last few decades. Connected to New York Presbyterian Hospital, patients seeking treatment at Weill Cornell can be assured that any problems they might encounter throughout the treatment process can be quickly and expertly addressed by doctors outside of Weill Cornell.
My brother faced similar situation and its type 4, he died...its the mistake of doctors who didnt diagnosed properly, They reported Tuberculosis and he ate all those medicines and atlast he was suffering from Hodgkins lymphoma after consulting with another doctor found out. 😢
Its very hard to remembering his last breath, his face and his reaction looking at me was painful after imagining now, Sorry my dear brother, Rest in peace 🙏 😢
Hi! Thanks for posting this. I am confused, it was mentioned that OS (overall survival) was 6.5 months but they also said that 50% get complete remission. I cannot fully understand, is there a chance to have a complete remission with such diagnosis? And live like 5-10-15 years after? Thank you!
Dr. Furman is exactly the kind of doctor he describes he wants to be in this video. He connects with his patients as if they are family -- and respects their input more than many other doctors I've seen. When it came time for me to make treatment decisions, I felt fully informed about my alternatives. He is very knowledgeable and will take the time to make sure you understand.
During the mid-late summer of 1986, I I started to develop some symptoms. It started with a very nagging dry cough, that my mother threatened to send me to a tuberculosis sanitarium. Then I noticed a swelling above my left collarbone, and I also had begun to have a fever of 101 degrees every afternoon , starting at 1:00 pm. I was very tired, and lost my appetite, and maybe about 15 pounds. About 7 years before that, my sister in law had some of the same symptoms, and was diagnosed with Hodgkin’s lymphoma. I figured that’s what I had. I went to a local doctor, who was very nice. He scheduled me for a CT scan and a biopsy at a local hospital . I was sort of prepared that the biopsy would prove to be malignant, and that’s what the surgeon said to me in the recovery room. I went home, and started to make phone calls. My brother called my sister in law’s oncologist, who agreed to see me on Thursday (I later found out he never saw new patients on Thursday, but agreed to see me as a favor to my brother). Another brother drove me to his office in the lower level of a brownstone. Dr. Lacher was wonderful-he outlined exactly what his plans for me might be, after a few more tests. I had another CT scan, a lymphangiogram, a chest x ray, a bone marrow biopsy, and lots of blood taken. He also gave me a prescription for an old arthritis drug called Indocin, which he said would alleviate some of my symptoms , and he told me to come back in a week. At that next appointment, he outlined my treatment for Stage 2B modular sclerosing Hodgkin’s lymphoma. The B means that you’ve experienced symptoms such as fevers, night sweats, etc. My chemo treatment regiment would be TVPP (thiotepa, vincristine, prednisone, procarbizine), and I would have about 8 weeks of radiation treatments in the middle of treatments. All of my chemo treatments were administered in the doctor’s office by the doctor himself . He did have a lab tech who drew your blood, though. There were always other patients to talk to, which was nice, and plenty of sweets, particularly near the holidays. I did experience a premature menopause about midway through the treatment. I was about 34 at the time,. I lost some hair, not all, but it was during radiation and only on the right side behind my ear. When my hair grew back, my hair dresser noticed it was a different texture than the rest of my hair. My last chemotherapy treatment was on 9/28/87. So, I have been a survivor for just over 36 years, and as time has gone by, I look at how my life has changed. I became a teacher in NYC, and was able to retire a few years ago . I have premium free health care,and pretty good drug care when supplemented with Medicare. As patients are becoming long term survivors, they are developing other health problems that may or may not be related to their treatment . I have developed cataracts in both eyes at a relatively early age, probably due to all of the prednisone (steroids) I took during chemotherapy. I also experienced a decrease in thyroid function (hypothyroid) due to the radiation . I take a thyroid hormone pill daily. I experienced premature menopause, and I was probably through with that when I was about 40 or so. No treatment for that. I also developed asthma-the damage is mostly in my bronchial area, which was where the original growth was located. You know, it sounds bad, but all in all, I’ve had a pretty good life over these past 36 years. There have been ups and downs, but I think I’ve managed ok. You can do it too! I would recommend that you bring a notebook and pen to each doctors or clinic visit. If they say something you don’t understand-stop and ask questions. Tell the doctor that you would like to record his/her instructions on your phone. This way you won’t miss any important information. Sorry for this LONG note-I just wanted to let you know that other people have been through this, and that we are carrying the lantern to light the way for those that follow.
I’m going through Hodgkin’s lymphoma currently. I finished radiation in June. I’m going to get A Pet Scan In September to see if I’m cancer free. I’m really nervous seeing this is inspiring!
You speak far too frequently about the story and ignore the important aspect; the symptoms. Saying she had a neck mass, is really immature to clinical diagnostics. Was it a supraclavical node ? Was it a Lima bean sized node in the cervical chain that didn’t go down? Was it the size of a baseball? These are all very important for people who might not be aware of potential cancer symptoms. There are plenty of viruses that keep lymph nodes palpable permanently. But if it’s the size beyond a Lima bean, that’s the concern.
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If you are reading this I was stage 4 non-Hodgkin's diffuse T-cell lymphoma. Obviously I'm alive and well as of this writing. YOU CAN SURVIVE! Does the diagnosis suck? Of course. Do as much body/mind healthy stuff as you can. Stay TF alive! If you have a good support system all the better. I didn't. I had no one. But I intended to live. You must believe in that. It's been over 30 years. Stay free.
I was a patient diagnosed with Peripheral T cell NHL in the year 2014. Location of the infected lymph node was Right Groin, which enlarged to lower abdomen. Peripheral T cell NHL diagnosed after excision biopsy. I got 7 Cycle CHOP and Radiotherapy. In September 2020 a PET-CT Scan done after I notice sever itching problem. PET scan showed an 70x51x70mm sized Anterior Mediastinal Mass with SUV max 11. Thoracic surgeon refused to operate the mass. A core biopsy and histochemistry done. Which shows an Intermediate grade Diffuse large B cell Lymphoma. CD20, BCL6 & MUM1 are positive. BCL2, CD3, CD5 & CD10 Negative. Bone marrow aspiration suggesting "Reactive marrow with myeloid hyperplasia and excess of lymphocytes. Before all these diagnosis I only faced itching problem. First symptom noticed in beginning of August 2019. Last 24-26th October I suddenly faced swallowing face. An echocardiogram of the heart on 27th October showing small amount of fluid buildup around my heart. LDH lifted to 366. My oncologists immediately suggest chemotherapy. The new chemo protocol is R-GCEOP. 1st Cycle started on 27th October and spited into 3 days. Rituximab, Cyclophosphamide, Gemcitabine, Etoposide, Vincristine, prednisone given. After 1st cycle chemo, face swallowing and itching removed significantly. We took part in a research project which involved a two day trip to Florida to the ALS Disease Centre, We had the opportunity to meet with Dr Odia, A highly recommended herbalist with scientific medicine. There is a lot to say about Dr Odia. I began healing herbs from Dr Odia, MD, who specializes in internal and pulmonary herbal medicine at ( Dr Odia Herbalist Home on Facebook). I would encourage anyone to seek a second opinion especially if they’ve been told there’s no hope. It’s also crucial to learn as much as you can about your diagnosis. Seek options. Find out about what’s out there that could help. Contact Dr Odia via: facebook.com/DrOdiathenaturopathic/ WhatsApp +17278553511.. He has a cure for Encephalitis, Herpes and cancer.
I met with Dr. @$#!@$ at CINJ and I was like ... I definitely DON'T want to be treated here. Ended up being treated for Hodgkin's in Hackensack. Not bad. Good luck to Katie. There's something sickening about the smooth professional quality of this video.
Hey things will get easier when it gets harder. Its a blessing to survive as many don't get that chance. I had bulk as well but beat it two months ago constantly fighting fatigue even today. You are important this experience is not a bad part of you its shows how strong you are in bad times. I wish you nothing but glory and luck have a blessed recovery.
@@tomtran270 im one year in remission. I gain all the weight i lost back. My hair is patchy at best but im exercising and eating normally. I guess i got back to normal or "new" normal about 2 weeks after my final treatment. Sorry about being absent, i forgot i commented.
@American Fighter I recently was givin news of possible lymphoma as well, my biopsy is next week. If you have any contact information and would like to talk to someone, let me know.❤️
Turn to Jesus He loves you, He is the healer of the body, And savior of the soul, There is True Hope in Jesus, He is the God of miracles, Acts 2:21 And everyone who calls on the name of the Lord will be saved, Jesus alone saves Trust Him with your salvation Take care
@@jesussaves1827 I am muslim so I don't believe Jesus was God but just a prophet (PBUH). Even if he follows the path of God, which would be great, he should still seek medical treatment.
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Dr. Martin is a doctor you can trust because of his experience and knowledge in this field. He is also a very nice guy. He provides confidence in a treatment plan and thorough knowledge to the patient who is going through a challenging time in his/her life with lymphoma. He is caring and easy to talk to when questions arise. Supporting staff always respond to phone calls from patients when something comes up or there are questions that require same day answering. I recommend this facility and Dr. Martin.
This might sound weird. But I'm going through tests. One said "clinical data: R/O lymphoma. I know my white blood cells r high and keep reproducing. And my lymph nodes r swollen in a few different places. I'm jus curious what that meant I've been researching and apparently I'm not asking the right question. Thank u in advance
Hello Dr Rutherford, My 77 yr old Mom was just diagnosed with PBL last week. We are from San Jose, Ca. Where do we begin to get a second opinion from you? She started her chemo last week to last till end of March and at that point we will find out the results. Right now she has a 16 by 8 cm growth in her stomach. Help please...
+Layla Suarez Hi Layla, We are always willing to work with a referring physician, and we are always available to offer a second opinion in the form of a consultation with one of our specialists like Dr. Rutherford. We frequently work with cancer doctors outside of New York City to help provide expert care. If you wish to make an appointment please call Dr. Rutherford's secretary at 646-962-2064. If you have any additional questions about our practice you can visit our homepage listed below, or contact me via the details I sent you in the direct message. Wishing your mother all the best! weillcornell.org/lymphoma
Weill-Cornell really does have an outstanding lymphoma program, should you ever have the misfortune of needing such a thing. I only wish I didn't live 3 1/2 hours away, but I know they will be there when the time comes. I saw Dr. Furman for a consult 5 years ago, and have to agree with the sentiments of the survivor in this video. This treatment team lives, eats and breathes lymphoma, and they are on mission, with the brainpower and resources to back it up.
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