What’s next: Seeking advice on how to navigate diagnosis appointments?
Hi there! I’ve been posting recently and Thank god I asked about the test and raised my concerns. Before Mayo, I’m flying to MD Anderson tomorrow. Ironically the only thing that anyone took seriously was the mircoandenoma but now it does seem like something is a fowl in my small bowel. Anything I can do to lower serotonin now to keep myself safe? Ok to take pancreatitis enzymes? Or supplements not to take? It’s crazy that this all started with one cortisol test that I ordered for myself in November when I had sudden weight loss…
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
@rickclem - in December I was hypoglycemic at night. So I’d wake up sweating and sometimes the monitor would dip below 70- not to bad. However, while I’ve been seeking a diagnosis my lasting glucose has been rising.
You will learn a lot with your Mayo doctor and it should move quickly. Gallium 68 Pet Scans are used to diagnose / identify Neuroendocrine Tumors (if that is what you / your Mayo doctor is suspecting based on your symptoms/ tests). They provide great detail. Biopsy could potentially follow if something identified.
Mayo has very experienced NeT specialists, which I assume they would refer you to, if you are not scheduled to see one already. Seeing the correct specialist is the most important key.
Some NETs can secrete insulin causing low or volatile glucose levels (can be different than carcinoid NETs). I’m in no way suggesting this could be cause of your low glucose. However, since this is a NET chat support site, I thought I would mention it. They have different blood tests to determine this. If your glucose is often low, particularly in morning (fasting), it’s worth asking your doctor about.
@rickclem thanks- yes, I will definitely ask- I tried a couple times to let Mayo know about my recent labs and forewarn them that I may need GI/NET evaluation as it originally seemed like a pituitary issue and Cushing but I’ve muscle wasting in my legs and arms. They said wait for internal medicine- I just pray it’s not a long term around time. It’s harder to get out of bed in the morning. I have a young son and I am calmer now and more patient but I every day thst goes by without a diagnosis is one more day that things can get worse. Only 5 months ago I was a go getting mom taking my son on play dates and keeping everyone on schedule and now it’s all fallen apart. I just hope and try to have faith that things can get better, but the reality is still that I need action on my case. So I have to give my battle to God and faith in the timing-but it’s a struggle.
Hello @rickclem and welcome to Mayo Clinic Connect. I appreciate your contributions to our NET discussion. You sound knowledgeable. Are you a NETs patient as well?
I look forward to getting to know you. Could you share about your journey with NETs as you are comfortable doing so?
Hello. My wife is a PNET patient at Mayo Rochester - I am her caregiver / advocate. I will follow up and share.
Hang in there. Im hoping you will get some some help.
@phoebeghostwriter
I'm really excited for you and others in our NET group to attend the Carcinoid Cancer Foundation's Meet the Expert on Thursday, Feb. 17, from noon to 1 p.m. EST. The reason for my excitement is that Mayo Clinic's Dr. Halfdanarson will be speaking. Many of you who have been treated at Mayo for NETs have undoubtedly met with Dr. Halfdanarson. He is an excellent speaker and well trained in NETs. This will be both a Facebook Live presentation as well as available on Youtube for those not connected with Facebook. Here is the link for more information,
https://www.facebook.com/Carcinoid/photos/a.434139689226/10159025786344227/
@remi @jhilbish @cvb @lenorahaston @captain1950 @khauert @tomewilson @alphanumeric @gulzar @megansims @netpatient @kate12345 @amd12 @tatteesmom3 @elm60
I'm really excited for you and others in our NET group to attend the Carcinoid Cancer Foundation's Meet the Expert on Thursday, Feb. 17, from noon to 1 p.m. EST. The reason for my excitement is that Mayo Clinic's Dr. Halfdanarson will be speaking. Many of you who have been treated at Mayo for NETs have undoubtedly met with Dr. Halfdanarson. He is an excellent speaker and well trained in NETs. This will be both a Facebook Live presentation as well as available on Youtube for those not connected with Facebook. Here is the link for more information,
https://www.facebook.com/Carcinoid/photos/a.434139689226/10159025786344227/
Hi Teresa! I am very excited to see this CFF Luncheon with the Experts! Dr Thor is one of the top NET Specialists in the country! I encourage everyone to to attend!
I appreciate those encouraging words, @elm60. Was he your doctor?