Im going for my 1st TURPT July 25th. Im grateful for this information because I like to have my eyes wide open. I live mostly alone with my dog. My bf is an OTR Truck driver and is gone for weeks at a time.
Thank you, this is very informative. In discovering I had breast cancer it was discovered I have B-cell Non Hodgkins Lymphoma, my Oncologist said it’s slow growing. The day before my double mastectomy 2-1/2 weeks ago I met with my Oncologist and he told me I’m. Stage 4 as it’s in my bone marrow. I haven’t had any symptoms. I’m just so surprised by all of the cancers ( 3 types in my breasts) and now NHL. I’ve always been super healthy and active. I’m a young 72.I’ll see my Oncologist again in 3 days and receive results of the breast cancer pathology report and have blood drawn again. I’m so thankful for a wonderful Medical team!
I am now 2 years post surgery for this cancer,it has been a hard 2 years but now back to exercising daily ,swimming , cycling etc. Life a mostly back to normal for a 70 year old , and every day is a blessing.
Yep, it was caught early so very grateful to all involved who helped me get through the last 2 years, surgeon's, nurses , friends and family etc,life is great .
@irmaaviles2076 Stage 2- 3 , lucky ? enough to have fairly urgent surgery , part of esophagus , stomach and some lymphnodes gone but living reasonably normally apart from some digestion issues as no stomach left to speak of. Supposedly cancer free so blessed with life really.
I have had neither esophageal cancer nor Barrett's. My ENT found that stomach acid was burning my vocal cords, which can advance to Barrett's if left untreated. The reason I scheduled an exam with my ENT is that, while singing along with the radio in the car, I noticed I could not hit my top-most octave. So if you present in this way, have it checked.
This doesn’t surprise me. Doctors or scientists don’t know what causes the majority of diseases very sad and very upsetting!! We need cures not just a bandage!!!!!
Thank you. I'm an esophgel cancer survivor that was given 6 months to live. That was February 23 2016. The same surgery and challenges you had, I had and still have. "By His Stripes, I Am Healed." Thank you for sharing your story.
Hi, can you pls help. My grandmother is 80+ and she is suffering from advanced uterine cancer. In last few days her urine output is reduced and bowel movements are once in a week , legs and face has swollen and she developed bed sores also. Also there is a puss kind of fluid while urination. Dr has told that no treatment will work now , take care of her. I can see things are getting worse but can you help what can we expect in coming days . Some people says with these symptoms she has less than a month. Pls help
Fantastic overview of the didease and its characteristics and treatment etc. Clear, concise, methodical and easy to understand. This is the best video ive seen on the subject. Thanks so much.
Hello..my husband was diagnosed with this cancer just a week ago..symptoms are difficulty in eating..about to do chemo rad in two weeks... did u undergo surgery? Can you tell me how was your battle in dealing with this kind of cancer...are you okay now? Thankyou..
@@carmieingalla6978 Ongoing, but I am positive, luckily I have a great principal at the primary/elementary school I work at. I'm working 2 days a week in the library. 13 months on from surgery, I am eating normal meals but smaller size portions. My endurance and stamina levels are still low - i need a nanna nap in the afternoon. I have stage 4 now. its in my lymph noded but I refuse to let this beast beat me. I was having immunotherapy and it was working well until the cancer mutated and evaded the immunotherapy. Not to worry, they have me on a new treatment and I'm hopeful we can beat this thing atleast subdue or keep it under control.
I’m quite sure this is great content,but tinkly Liberace piano music in the background is so horrifying …this ain’t ed Sullivan on Sunday night….I’m out….
I have watched a lot of videos on lymphomas and this is a nice clear summary of the basics - thanks! (And it has not essentially dated even though ten years old!).
No mention of more than 50% cure rate with radiation when lymphoma is found early. Learned the hard way. Always get second opinion on biopsies when there is discrepancy between aspiration result and biopsy, or anything else that is off. Do not trust your primary care doctor who deceives you that everything is ok.
Si hay un Doctor por excelencia gue cura todas enfermedades nuestro senor Jesucristo es la respuesta el sigue sanando fe en el y Busguelos de todo corazon para gue el no libres de todo mal
I was suffering from non hondkingson lymphoma in 2007 . Surgery was done On left shoulder joint to remove cancer tissue. Then I refused to chemotherapy & radiation. So I started anti hiv drugs efenavir , didanosine, lamivudine with My son's 5ml iv blood transfusion to me with ayurvedic medicines arogyavardhini vati, kanchanar guggul Jwarnashak vati , ras manikya bhasm Udaramrut vati giloy ghan vati , hirak bhasm still nows I am alive With o
Recieved this diagnosis yesterday. I was on Azathioprine for 25 yrs for Autoimmune Hepatitis. They stopped that med 6 months ago after 65 Squameous Cell skin cancers removed. I believe this drug is why I have NHL. Unsure of where to go from here. Waiting to hear from Oncologist/Hematologist office.
I seem to be between a rock and a hard place as the saying goes. The reason being, I have had a multitude of tests completed and others scheduled and my problems are many. It all started out late last year, 2021, when my symptoms first began. I was diagnosed with Kappa IgM MGUS. Okay I thought, now what? As more and more tests were done, I was thoroughly surprised to find out my MGUS was progressing towards becoming full blown cancer. Since I’m classified as being rare (many rare health issues) it caught me off guard when it was determined that I was headed towards a diagnosis of Waldenstrom Macroglobulemia. Then it was determined that my WM was progressing directly from my IgM MGUS, a very rare occurrence. Okay, now what, I wondered out loud in front of my Oncologist/Hematologist. It didn’t take long for my body to answer the question with a seizure that felt like it was trying to kill me it was so violent(don’t remember it), just the excruciating pain in my head since the episode. That was April 26th. I just saw my Neurologist yesterday and I’m in line for a battery of tests. You name it, my PCP, Neurologist and Oncologist ordered everything since the after effects of the seizure has left my memory a wreck, the pain a level 10, vision bad, confusion, balance, I may as well sleep on the floor. I’m getting 3 different CT Scans, an MRI, and 6 different blood draws to start the festivities. Oh yeah, I almost forgot, my sister had 2 brain tumors, the second one killed her. A nasty rare star fish shaped one called Anaplastic Astrocytoma. It killed her at only 39yo. I’m 78yo, with a heart defect that’s 1 in a million. I just told my Oncologist, cancer isn’t going to kill me because my heart will since it’s so messed up I have an expensive loop heart recorder emplaned in my chest and monitored 24/7. So others who think life sucks, I have this quote on the wall of my bedroom. “I cried because I had no shoes, until I met a man who had no feet!” Remember, things can always be worse.
@@lisavollaro Sorry to hear but I feel it’s better to know, in order to prepare for the outcome. There are many videos on You Tube pertaining to NHL & WM. I highly recommend you check them out because there has been advances in both conditions. As for me, my saga doesn’t seem to have a conclusion other than death. In January 11th, 2023, I had DNA Sequencing done and got the results March 15th. It was an eye opening experience finding out how limited DNA testing is and lacking in knowledge. With the 3 gene defects they found, I was able to track down 10, yep 10 conditions inside me. No wonder I feel like a freak of nature. Out of the 10, 7 can literally kill me, great news huh. But as I said, it’s better to know and my funeral and headstone are paid for. At least now I know why I was born this way and sickly since I was conceived. With all the defects, you’d think my doctors would have discovered them after 80 years. I found out I have Multiple Sclerosis for one thing, I’m also the proud owner of a gene that has a genetic marker for blood cancer. Specifically Leukemia and Lymphomas, I guess that’s a surprise to my Oncologist/ Hematologist. They kept saying I was going to get Multiple Myeloma because my one older brother died from it. I hope the best for you. WM is an indolent cancer, meaning a slow grower, at least that’s in your favor. Good luck.
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@@ololubebenitah6134 he was having problems seeing dizzy that never went away seizure lost his appetite didn't want to eat and drink felt cold severe headache neck pain couldn't walk without help couldn't talk delirious sleeping a lot mood swings angry
What does it mean if your lymphocytes are over 6000? They started at just under 5000 and by 3rd test they’re about 6200. Reasons for checking was a positive ANA and suspect Lupus. My legs ankles knees all joints Achilles heel hurt like hell. It very hard to walk. I thought lukiemia was high in the 16,000 and up not 6000.
