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Thyroid cancer...secondary to lymphoma??

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Thyroid Disorders
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damouthy1
Veteran Member
Joined : Sep 2009
Posts : 663
Posted 2/11/2011 8:26 AM (GMT -8)
So I have been having a ton of problems with my thyroid (along with a bunch of other things) I had an uptake scan done 3 months ago due to my levels being out of whack. My TSH is basically nil but my T3 and T4 are in the normal ranges. No nodules present at that time. My doc was thinking Graves (I need to see an endo, but the closet one is 4 hrs away).

In the meantime I am having all sorts of pain everywhere, extreme fatigue, lack of appetite (but havent lost any weight, I gained a bunch in the previous months) and emlarged lymph nodes in my neck, abdomen, under my arms etc. I also have superior vena cave syndrome (my veins are very distended on my upper arms and chest and tons of fluid in my neck and face).

Everyone is thinking probable lymphoma, but I am basically on a watch and wait to see if the lymph nodes continue to grow and multiply. Also my SED rate has been high for 8 months or longer. The only way to dx lymphoma is to biopsy a lymph node (they want them to be over 2cm) I have a couple in my neck that are big enough now.

Anyway, on to my concern. I now have several solid appearing hypoechoic nodules on my thyroid that weren't there before. I am really scared that now I have thyroid cancer too! My reasons being the nodules appeared within 3 months, they appear to be solid and they are hypoechoic. All these things point to cancer.

I am seeing a surgeon on the 26th to see if he wants to biopsy the nodules and or lymph nodes. Any suggestions? I feel like my doc here (I live in a very small town) isn't taking this very serious. She agrees that it is probably lymphoma, but says it can take a long time before it becomes aggressive. We just need  to wait for it to rear it's ugly head, is what she says to me.

So, this has been going on for months and months now and now I am afraid I have thyroid cancer too! I am just so scared and stressed right now. I just don't know what to do. Anyway, thanks for listening. It helps to get it off my chest if nothing else. I hope you all are doing well, take care.

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MIKEL99
Veteran Member
Joined : Feb 2010
Posts : 914
Posted 2/11/2011 9:27 PM (GMT -8)
Hey Shannon , Don't they have a cancer specialty clinic somewhere near you ? If there is I would make the trip , because the advice of ''waiting for it to rear its ugly head '' sounds terrible to me . Catching it early and using preventitive measures seems to be a key if it is indeed what you fear it might be . In any case finding out asap is always as far as I know very important , please check to see if there is a cancer treatment center near you Sweetheart , don't wait . I'll check on you soon . love Mikel
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damouthy1
Veteran Member
Joined : Sep 2009
Posts : 663
Posted 2/12/2011 6:41 AM (GMT -8)
Thanks Mikel, I truly appreciate all the support you give me and my Sis. You are such a great guy! I am going to call the cancer center in Kearney on Monday and see if they can see me. This surgeon keeps rescheduling my appt. I was supposed to see him the 2nd but he keeps putting it off a week (now it's the 23rd, I wrote the 26th but I was confused..lol) Once again hun, thank you for being you! I will keep you posted. Take care.
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Screaming Eagle
Veteran Member
Joined : Sep 2009
Posts : 5005
Posted 2/12/2011 7:18 AM (GMT -8)

    Oh Dear! I did not realize, just how bad a shape you were in! I don't know anything about this type of stuff, but will keep reading your post to see how your doing.

    My wife and I plan on seeing you and that sister of yours this summer. Your not that far away, and we have some land pretty close by that we need to check on.

         Take care, and if there is anything I can do, just let me know. I could be there in 3hrs or so, and tickel you to pieces and make you laugh! smilewinkgrin   

   SE wink

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Mrs. Dani
Veteran Member
Joined : Jun 2009
Posts : 2787
Posted 2/12/2011 8:30 AM (GMT -8)
 

  Dear Shannon,

 

   Well, if I were in your shoes I would get to the nearest University. Or wait for the surgeon. You have to relax as much as you can until you get your biopsy done. Worrying about it now will take a toll on your body as well as your mind. After you get the biopsy done it should take about a week to get the results. It is going to be one heck of a long month for you.

 

    I know you said your appetite was nil... can you transition over to a high protien diet? That is what I do so I can get more "bang for my bite". Peanuts, eggs, tofu, yougart...? It will help to keep your energy up as much as possible. No matter what is going on, once you get the answers, you will need to be ready to fight it! You will need as much energy as you can muster.

 

     Please know you are always in our hearts and prayers. Try hard to take your mind off things. the wait has got to be terrible.

 

*hugg*
   dani

 

p.s. Do you read much? Or have something that could occupy your mind?

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damouthy1
Veteran Member
Joined : Sep 2009
Posts : 663
Posted 2/13/2011 12:35 PM (GMT -8)
Thank you Michael and Dani, I appreciate the heck out of both of you! Thanks for poppin over here and taking the time to read about my drama. I love you guys too! Take care.
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Lymer
Veteran Member
Joined : Sep 2012
Posts : 511
Posted 1/26/2013 12:19 AM (GMT -8)
Hi damouthy1, I realize this an older post, but I'm in a similar situation, in that I have ongoing thyroid issues, and now my rheumatologist suspects Lymphoma.

I've been Dx'ed with: Fibromyalgia, Depression, GERD, IBS, Hypothyroidism, Vit D Def. I also have migraines and anxiety.

I couldn't help but notice we have very similar symptoms, and so when I came across this post and read your story it really hit home with me.

If you're still around on this forum, I would love to hear how you are doing now. I hope by now you've been able to sort things out, and that you are doing well!

Thanks for listening, and I hope to hear from you soon! :)
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jujub
Elite Member
Joined : Mar 2003
Posts : 10424
Posted 1/26/2013 5:34 AM (GMT -8)
Lymer, we haven't seen damouthy1 in this forum for quite a while, but she does post regularly in the Chronic Pain forum. You might give her a shout there. Good luck in finding your answers.
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