He was given 10mg of Sevedol at 2:00 PM—just a single dose—and now he’s back to tossing and turning in agony. The nurses are refusing to administer anything else, and to make matters worse, there isn't even an attending physician on the floor to consult. We are honestly at a loss here. It is nothing short of disgraceful; it feels like we've been dragged back to the 18th century, forced to watch someone suffer through unbearable pain when the tools to help him are right there. A total disgrace. He’s currently in the neurosurgery ward over at Mayo Clinic.
God bless you all, I called in yesterday regarding my husband, who is fighting lung cancer. We just got his latest results back today—it's spread to his bones. The pain he's in is simply unbearable. The doctors are pushing Sevedol tablets instead of letting us use the Duragesic patches... I can't help but wonder if they're making a mistake. Has anyone here dealt with this? Is one actually a better option than the other when things get this bad? electricgardener14
Hello, My husband is currently dealing with a hospital-acquired infection from MRSA following the removal of a brain metastasis—it’s just one thing after another, really—and he’s on a regimen of Vancomycin combined with another antibiotic. Because of this setback, his follow-up chemotherapy had to be postponed. Now, the illness has progressed, and he is in absolutely excruciating pain. They have him on Tramadol, various NSAIDs, and things like Ketorolac, but honestly, none of it seems to be touching the pain. Given the specific antibiotics he is being treated with, is there any possibility of moving him to a more potent pain management combination? electricgardener14
Greetings to everyone, I am reaching out because I’m looking for some insight regarding a hospital-acquired infection caused by Escherichia coli. My husband has been battling this for two weeks now—following surgery to address brain metastases—but we aren't seeing any progress; his fever simply refuses to break. The doctors have already cycled through three different antibiotics, yet nothing seems to be touching it. I would truly appreciate hearing about any experiences you might have had... any ideas on how to finally get rid of this damn thing. Best regards, electricgardener14
Angela Wright said:Oh, that's fantastic news! I'm so glad things worked out for you. Regarding housing, you might be able to find something at the university dorms after July 15th once final exams wrap up—that’s usually the cheapest bet. There's also The Beverly Hills Hotel, which offers some affordable options too. Maybe try posting on the Washington, D.C. forum to ask about cheap rentals; someone might have a private room available while the students are away. Do you happen to know the exact diagnosis?
We don't have a definitive diagnosis just yet—though, frankly, I expect we will get answers much faster here than back in my hometown. For the moment, they have managed to stabilize his pain medication quite well, so his spirits have lifted significantly—he even seems to enjoy the hospital food (chicken and dumplings). I will give that idea of posting on the Washington, D.C. forum a shot, so let's touch base later. P.S. I was informed today that the ventilator in San Francisco broke down again (the one from unit 48). Good grief... it makes you wonder how much our lives depend on such fragile machinery.
Dear fellow forum members, I want to extend my sincere thanks to everyone who advised me to move my husband from our home in San Francisco to the hospital in a Small town, USA. We were received with such incredible kindness—if only politeness were a form of medicine, my husband would be perfectly healthy by now. He is under the care of Dr. Charles; does anyone here happen to know him? I’m curious if he is considered a top-tier specialist. On another note, I would be so grateful if any lung cancer patients—or perhaps their family members—could reach out so we might exchange experiences. I am particularly interested in knowing what the quality of life is actually like during the treatment process (chemo, radiation, etc.). Is the patient constantly bedridden, or is there at least some semblance of a normal life maintained? Also, a quick practical question: does anyone have leads on affordable lodging in Washington, D.C.? I start my vacation next week and I fully intend to stay close to my husband—even though he insists he’s finally enjoying some peace and quiet away from my constant "nagging." A huge thank you to Unknown for the offer of a place to stay, but I really need something a bit more long-term, though I will certainly reach out once I arrive in Washington, D.C. Warm regards to you all, and may we all find our way back to health.
Greetings to everyone on this forum, My husband was recently diagnosed with lung cancer while we were in San Francisco. They’re still debating the specific type, and frankly, the radiation equipment they’re using there looks like it belongs in a museum—sixty-year-old tech, at best. I have serious doubts about the diagnostic accuracy and the treatment methods available here in San Francisco... and when you're dealing with something this devastating—not to mention we have four children who desperately need their father present for as long as possible—you can't afford to gamble. I am reaching out to anyone with a kind heart to ask for recommendations or any advice you might have; please, if you know something, speak up as soon as you can. Would it be wise to move him to a Small town, USA to seek better care, and is that even legally feasible without having some sort of high-level connection? Is it possible to incorporate alternative medicine—something like the Brojsov therapy—after he finishes his rounds of chemo and radiation? Also, is there any way to get a hold of a phone from Bread or Ivanicapeca? Please, help me if you can. My thanks to you all. electricgardener14
Dear fellow members, I am reaching out to Angela Wright and anyone else who might be able to offer some guidance. My spouse was recently diagnosed with lung cancer here at the Mayo Clinic—they confirmed it via cytological puncture. The current plan is to move straight into radiation and chemotherapy, which feels incredibly rushed since they haven't even pinpointed the specific type of tumor yet. To make matters worse, the equipment they intend to use for radiation looks like it belongs in a museum from the 1950s. On top of all this, the medical staff isn't offering even a shred of hope regarding a cure, and here in San Francisco, there aren't any support groups or organizations available to help patients and their families navigate this nightmare. So, I have a few questions—do you think it would be wiser to transfer him to Washington, D.C.? Does anyone know if lung cancer treatment tends to be more successful abroad? Furthermore, does anyone have experience with alternative therapies—specifically the Numbers method—and can such treatments be used alongside pain medication? He is currently suffering from excruciating pain. Please, if you could respond quickly, I would appreciate it; we are at a crossroads and need to decide our next move immediately. Best regards, and thank you in advance. electricgardener14