Chronic Pain members - Welcome, please introduce yourself
Welcome to the new Chronic Pain group.
I’m Kelsey and I’m the moderator of the group. I look forwarding to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Why not take a minute and introduce yourself.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
Hello @amandajro in 2019 I was diagnosed with a pseudo tumor that had formed around a failed hip implant, causing metallosis. The surgeon replaced the metal implant with a nonmetal component, and removed most of the large pseudo tumor. The tumor may have impacted the femoral nerve which causes the pain and neuropathy in my legs. They aren’t really sure.
Hello
I have had migraines since I was 8 years old. The hormonal ones were the worst and I have tried every treatment imaginable. I’m older now and don’t have the classic migraine with the hammer inside your head and extreme sensitivity to light and sound. However, it feels like my head is in a vice-grip, 90% of the time. Has anyone experienced this and, if so, did you ever find a solution?
Thank you
Francine
Yes, Botox and using a device called Cefaly. If it gets really bad, I take a triptan and ibuprofen and it relieves the tightness. The Cefaly device has been extremely helpful!
Hi, my name is Guy from Pa. cannot swallow anything solid at this point due to a lymph node/scar tissue on the outside of my esophagus pressing inward, causing the esophagus to measure roughly 2mm or less. A stricture I believe it’s called. I have a feeding tube which up until 2cweeks ago did not have to use. My thoracic surgeon says the high location of the stricture make to high risk for surgery. My GI Dr. Says that since the lymph node/scar tissue is o vthe outside, inserting a stent would be very uncomfortable and not recommended. My oncologist says my therefore my options are limited and suggested that we revisit chemo tx. I’ve had 35 radiation tx’s and 12 chemo tx’s over the past 12-15 months or so. Those tx’s don’t appear to help my esophagus at all. I’ve have 3 endoscopes in the past 6 months to retrieve food that has lodged in my esophagus. I have a call in to the Mayo. Linic in about 2 hours to discuss my case and if they can help! Originally diagnosed with colon cancer in 2008. Had over a dozen surgeries thus far, highlights being removing 2 ribs, some intestines, half my right lung, piece of my left lung, etc. That’s my recent medical hx in a nut shell.
My dream is to eat normally again, as soon as is humanly possible. I was and am a foodie!
Hello Guy @warden45, Welcome to Connect. It's hard to imagine how difficult your journey has been trying to get back to eating like it was before your treatments started. There is another discussion which you might find helpful where other members have similar problems eating.
Esophageal problem: food gets stuck, swallowing issues: https://connect.mayoclinic.org/discussion/esophageal-problem/
You mentioned that you have a call into Mayo 2 hours or so ago to discuss if they can help you. Have they called back? Wondering if you have any new information.
Hi John, they did call me earlier. It was more of a get my personal info and what did I really want to do. They asked if I want a pre-visit call prior to actually going to the Clinic, if that was warranted. I agreed to that, hoping the GI/Thorasic Dr./rep will have something good to say. After that, depending on what’s offered, would be a trip to the Clinic itself!
Hi Guy,
Did you have esophageal cancer? If yes, I invite you to join the discussions in the Esophageal Cancer group here: https://connect.mayoclinic.org/group/esophageal-cancer/
You may also be interested in virtually attending this patient conference hosted by Mayo Clinic on July 31, 2021.
- Gastroesophageal Cancer Education Symposium https://connect.mayoclinic.org/event/gastroesophageal-cancer-education-symposium/
Hi Colleen, I do not have esophageal cancer, but colon cancer that has metasasized over the years. The mass/lymph node/scar tissue is the colon cancer, apparently!
It sounds very uncomfortable, Warden. If you'd like, you can connect with others in the Colorectal Cancer group: https://connect.mayoclinic.org/group/colorectal-cancer/
I also think you'll find the discussions in the Esophageal group regarding feeding tubes to be useful.
Hi, my name is Joyce C. I had colorectal surgery several years ago and continue to have sporadic pain in the abdomen and rectal area, as well as the feeling of pressure in the rectal area.