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Top 10 Search Results for "question dot dot dot that has me a little puzzled"

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Strange Docs
A MyMyelomaTeam Member asked a question 💭

I just had my first follow up after my SCT in November with my local oncologist. He just yelled at me because the nurse didn’t go through my med list one by one. She asked if anything changed. No. I stupidly asked doc if he really felt I should be taking 2400 calcium daily with D3 if my calcium is 10 already. He screamed at me there’s nothing here about your calcium pills. Final answer was ‘ it says you’re taking 200 a day’. No clue why his report said that, but he had no answer for me. He has… read more

A MyMyelomaTeam Member

Agree

I Have Been Diagnosed With Light Chain Multiple Myeloma. My Doctor Will Not Treat Me Now. Has Anyone Had Treatments In The Early Stages?
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

Please dont delay the treatment,better to go for second opinion. Best wishes 🙏

This Question Turned Into A Discussion About MRD-SURE And Curcumin - Will Repost The Original
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

Hello Larry
Other then using Turmeric it is better to take Curcumin, that helps inhibit inflammation to support joint comfort, encourages a healthy immune response, promotes cardiovascular health and… read more

How Many Of You Know That Viagra & Other Male Enhancement Are Known To Be The Cause Of Multiple Mylomia?
A MyMyelomaTeam Member asked a question 💭

Does anyone know if there is a Class Action lawsuit in the works related to Multiple Mylomia, and OTC Male Enhancement supplements which many have been proven to contain generic Viagra?
https://www.drugs.com/sildenafil.html#warnings

A MyMyelomaTeam Member

Well, Ms. Ryan, an interesting question. Causes one to reflect on the joys of living. I've not heard this concern with male enhancement drugs. At my age clinical proof of deleterious effects would not… read more

Who Has Stopped Maintenance Meds Like Revlimid 2 Years After SCT And How Are You Doing
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

I have heard that maintenance chemo is important to hopefully extend remission. I am on the same chemo (darcelex and kyprolis) for maintenence as I took to get me into remission. My doctor shared and… read more

My Wife Has Smoldering Myeloma. Her Oncologist Thinks A Good Measure Of The Progression Of The Disease Is The M-spike. What Is Your Opinion?
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

Best of luck, for the most part we all have to trust the oncologists and hope they are doing their best for each individual case. Hope she feels better soon. Ray

Necrosis Of The Jaw
A MyMyelomaTeam Member asked a question 💭

Hi, just wanted to tell you a little of what I have learned this week. My husband Ed, (was diagnosed with MM in 2016) has Necrosis of the jaw. He was on Zometa for three years. Longer than recommended. He has recently had to have some teeth pulled. They were just crumbling, and his own dentist could not keep up with them. She spoke to a surgeon Ed has seen in the past, who had not wanted to pull any of his teeth, because of the necrosis. The surgeon agreed that they would have to come out… read more

A MyMyelomaTeam Member

That’s what my Oncologist recommended for my teeth also.

Help With Questions To Pose To Doctor At Next Visit.
A MyMyelomaTeam Member asked a question 💭

My husband is being seen by a blood cancer oncologist. He has been diagnosed with MGUS. His Kappa # is 38. Notes in his blood tests say possibly SMM. Many blood numbers/results are not normal. He is currently suffering with major headaches and bone pain in his head. He has little energy. He has neuropathy in both legs/feet. He can't walk a mile without being out of breath. This is so not normal for him.

I am extremely frustrated with his doctor. We go in and the doc says " how are you". My… read more

A MyMyelomaTeam Member

Thank you so much for the information.

How Do I Pay For Revlamid Once I Retire And Go On Medicare?
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

Thanks for that information 👍

This Group Has Been So Helpful & Awesome So Far -- So Many Questions -- Please Forgive Me -- I Have Another Question For You All
A MyMyelomaTeam Member asked a question 💭

I have had bloodwork done (came back) and proteins are high & all points to mutiple myeloma - BUT I can't get into my GP for weeks & waiting for a MRI -- sitting in referral (whether necessary or not) - QUESTION --
should I move forward on my own accord in finding a hemotologist -- seeing if I can get things to move along faster? OR -- I might try another doctor (that has been recommended) outside this town?

HELP -- not sure how to proceed in this situation

Thanks again awesome team!

A MyMyelomaTeam Member

My GP hooked me up with a Hematologist who than got me into Dana-Farber the next week after my tests showed Myeloma