Should Waldentrom's Patients Get Flu Shots?
I had a bone marrow biopsy back in February and was diagnosed with Waldenstrom's. I'm still learning about my cancer and wonder if I should get a flu shot this year. Also, should I get the Covid booster that will be out this fall?
Since WM produces bogus white blood cells that crowd out the good white blood cells that provide immunity, will the shots cause my immune system to produce IgM at an increased rate? Will the shots only speed up the proliferation of IgM rather than build up my immune system?
Thanks in advance.
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
Hi Mike, Contacting Mayo Clinic is easy. Here’s a link to get you started. It will take you to the Mayo Home page where you can follow the cues to request an appointment.
http://mayocl.in/1mtmR63
Mayo Clinic specializes in difficult cases. Their collaborative approach to medicine means that you, with your WM, would not be limited to a hematologist. If you have lung concerns there would be a lung specialist added to your team, etc.. I had a bone marrow transplant and had a fabulous team. But a few complications with my health had 2 neurologists, an allergist, ophthalmologist and liver specialists added to my team. No chest thumping between them! They all worked together to find solutions to restore me to full function. I’m 4 years out and feeling like nothing ever happened. So I may be a little biased but I owe my life to the amazing medical teams at Mayo-Rochester.
So I encourage you to follow through with a request for an appointment. You’ll have the option of choosing Rochester, Jacksonville or Phoenix. Do you live close to any of those cities?
Thanks for the link Lori. Rochester is closest even if it's over 400 miles away. Great opportunity to use all those points I've been accumulating for travel on my credit card. By chance, can you recommend accommodations in Rochester? I won't have a car if I fly, so I need to be close to the hospital.
Hi Mike. Rochester is my home away from home…many months living there for my bone marrow transplant and lots of followups. Most everything you need is within walking distance to Mayo…it’s in the center of the city with quite a few hotels, stores and restaurants connected by the Subway, which is an underground tunnel system. It’s excellent!
Here are some links to accommodations from many of our members… (you can reverse the order from Oldest to Newest with the little oval under the opening paragraph in the lower right corner so you get to the most current comments).
Lodging for Mayo Clinic, Rochester
https://connect.mayoclinic.org/discussion/lodging-for-mayo-clinic-rochester-mn/
~~~~
Rochester Mayo Clinic Concierge Services
— https://www.mayoclinic.org/patient-visitor-guide/minnesota/becoming-a-patient/concierge-travel-services
Map of downtown Rochester Accomodations:
— http://318commons.com/main/wp-content/uploads/2015/03/Dowtown-subway-and-skyway-map.pdf
These will get you started. Don’t hesitate to ask if you have any more questions! To make sure I see your comment please tag me with @loribmt so I get a notification. ☺️
Good luck with your appointment request. You don’t need a referral but I’ve heard it can be helpful. Let me know what you find out, ok?
@mike02041950, Here’s another link that might be of interest to you. It’s a a current discussion for lodging in Rochester.
https://connect.mayoclinic.org/discussion/closest-best-hotel-for-one-night-stay/