Pituitary tumor symptoms: joint, muscle and body aches
Hi. I am new to this. And not sure I'm in the right category. I was diagnosed with a pituitary tumor in November. However, I have been experiencing terrible joint, muscle and body aches for a year now. No doctor knows why and nobody can confirm its from the tumor. I'm frustrated and becoming very hopeless and depressed. Can anyone with a pituitary tumor relate to body pain?
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
I think after the surgeries and they get your hormone levels corrected you will see a big change.
So stay strong even if it's easier said then done, but I've been there, 22 years, and now have p net, fun!!
I am sure your still just as beautiful as can be, remember we are our worse critics. I wish you well and my prayers are out there for you. Take care. If it weren't for my wife I don't know what i'd do..
Anthony
@sturns
Are the numerous tumors in your liver and lymph glands related to the pituitary tumor? What’s the plan for them?
You have been through a lot.
@georgiamartin - It must be difficult to live with that pain for so long and no answers.
Did your Endocrinologist test for all the pituitary hormones?
It seems like a long time to wait so many months for another MRI. What does the Endocrinologist say about that?
@sturns - My daughter also had her surgery at UVA - 11 years ago. Excellent facility. Who was your surgeon? My daughter had Dr. Oldfield- wonderful. Unfortunately , he has passed away.
Yes they are the best , my Dr. was Dr. edward laws and endo was Mary lee Vance, both great and if I had to have a hospital experience it would be there. I also met the man who invented the gamma knife. He looked just like Einstein and came in, sat down like I was his only patient for the day and explained why the GK couldn't be used, because the tumor was to big. But he took the time and he didn't have to. That's what it's about, making the patient calm and informed so they aren't so nervous. Glad she had a good experience to.
I get tested a lot for my hormone levels and they say the Pituitary issue has nothing to do with the NET I have. I disagree, but what do I know. I do know the pain can go off the scale and mentally it feels like my hormones are off but last time I had Blood work everything was good..?? I am being seen by 2 dr.s, one is the Moffitt center and my treatments are from Florida cancer specialist's because the drive to Moffitt is 4 hours one way, but they are the main one because they are one of the top 5 for this type of cancer. My wife had stg. 4 metastatic melanoma and they just wanted to put her on a clinical trial to give her another year or two. The 7 large tumors are gone and that was 7 years ago but the side effects are real bad, but she's here.
@sturns - I’m sorry to hear about your wife’s struggle with her treatments, but the results of the clinical trial she is in are incredible!
The two of you are fighters and you apparently have access to the best cancer care.
I agree that it seems that it is more than a coincidence to have the pituitary problems and NET.
My daughter also had Mary Lee Vance- superb.
Her surgeon said that he tried to get everything but there was a possibility that some cells remained near the carotid artery. He also said that if she needed more surgery it could be done with Gamma knife.
It has been 11+ years and so far all looks good.
She had extreme body pain after surgery but was lucky to find a good pain management doctor where we live. It took time to get rid of it.
Yes, Dr. Vance is awesome, very focused, professional but she does have a caring side as much as she tries to keep it low. Dr. Laws is at Brigand young woman's hospital now or retired but I don't think people like them retire. My artery had tumor still wrapped around it but that was 22 years ago and no issues with it. I never had pain until I had net. and extreme it is. I had so many issues with pain management, so many treat you like a criminal but this, meds, were made for this... So I went to palliative care and they are like gold and i'm going through the VA. They truly are wanting to help me with the pain. It gets to the point where it will take me to my knees. Nothing, no pain , to a ten just like that. Not fun. Good luck for both of you. Thanks for responding, being alone with no outlet to people like us is very lonely. It's as I am the only one and well, i'm not, so thank you for all your reply's. They were/are appreciated.
I phoned my Neuro surgeon 10 days ago and said, "I cannot wait until July for another MRI, I am in continual agony, feel like all my joints are disintegrating, I need help now!!!
So, I have a new appointment for Dec 21. In the meantime I am doing EFT " tap" method for calming the nerves, praying through healing scriptures in the Bible, knowing the Lord Jesus wants me healed and enjoying the life he has given me!!
All blood tests from New GP came back normal!!🤷♀️
feel blessed, have my very own medical team👍 and I'm pushing myself to stand up and be as active as possible for my mental state of mind.
I am still active in my Interior Design business and it helps my mental state of mind to get up and move and create!!!
blessed Christmas, stay hopeful and advocate for yourself everyone!!
Same as my experience, still on the journey with getting the right solution, have to advocate for yourself!!!keep pushing!! Cheering you on