Anyone else have CHEK2 gene mutation? And have had multiple cancers?

Hi! I just came across your post. Feeling a little alone out here. After 8 years cancer free I was just diagnosed with 3rd occurrence of breast cancer AFTER 2 double mastectomies. Possible Factors: Chek2 mutation, hemochromatosis, MTHFR 2 variants, family history of blood clotting, mother had uterine cancer. I’m just at a loss. This is now on chest wall. I live in a small community. Don’t know where to turn to get more guidance. How have you been? I have been super holistic in approach but also had diverticulitis and scared to continue any raw food diet situation

@charlotte8910
Goodness!!
Thank you for sharing! That's a lot. I'm thankful you're doing well now. That's wonderful you were able to figure out what to eat & not.
I too am allergic to certain foods. I have diverticulitis so I have to be very careful what I eat.
Good luck to you.
Thank you again.

@charlotte8910
I eat all organic and prepare everything from scratch.

Alot has changed with me since this original post! I had a new plastic surgeon look at my case with the overfilled implants I had before, that were causing horrific pain! And the Dr that did that surgery would NOT listen to me. I found a new one!
He took those out & put in smaller ones & I've been happy ever since!!💕 I'm still in physical therapy due to chronic pain from fibromyalgia & swelling from 2 breast surgeries.
But now, an ultrasound on my throat AFTER thyroid was removed last year due to cancerous nodule, the current ultrasound has found 2 masses in my throat! Radiologist said both look suspicious.
So my Endocrinologist is referring me to an ENT in southern Missouri. Due to having Medicaid, I'm limited on resources. I think it's unfair that a person like me that has had & continues to have multiple cancers, can't utilize KU cancer center, which isn't far from me, due to my insurance!
My Drs have tried many times to refer me to KU, & each time they reject me due to insurance. How is it that others are in charge of who you see, or what procedures you're allowed to have or not just due to insurance status. I find extremely unfair! Something NEEDS to be done about this!
I'm sure I'm not the only one going through this. I've had friends that have died due to hospitals or Dr's refusing to see them due to insurance reasons. Why!!?? It should NOT be this way! Everyone should be treated fairly & have EVERY opportunity like others are treated. It's people like me that fall through the cracks due to insurance or income status.
Is my life not as important as someone else? Is my family not important enough to want me around longer? Why should they have to suffer because of incompetent & bureaucratic system of unfairness.
I'm just really frustrated with this whole process so just bare with me.
I go today to talk to a Dr that may not be able to help me. Please pray for me through this process. I'm getting emotionally tired.

I'm truly sorry you're having to go through this.
You're in my prayers.

I'm truly sorry about your situation. You'll be in my thoughts & prayers. This journey is hard when you don't know a lot about the mutation. It makes it very difficult to find the right Dr's & to make the right decisions you need to make for yourself.
I just recently had my yearly ultrasound on my throat. After my thyroid cancer,they removed the glad. But now, I have 2 masses in my throat. Trying to find the right Dr to go to for follow up or 2nd opinion has been difficult.
Or that accepts my insurance. That's also been frustrating.
Anyway, good luck on your journey through this! Positive vibes being sent your way!

@judyrapp, that's a lot to handle. Are you in treatment for any of the cancers at the moment?

Yes, I have the CHEK2 mutation as well. I’ve had breast cancer twice, and I have some type of skin cancer removed every 3 months. Both occurrences of breast cancer were accompanied by squamous cell carcinoma or melanoma in the same month. I’ve also been diagnosed with polycythemia, and my latest diagnosis is IGA deficiency.

Did the injection drug do anything for you? Thoughts are with you.

Thank you!
Oh my, I'm sure sorry to hear of your long journey too.
I have PCOS too, which doesn't help any. My OBGYN says I need a hysterectomy, but my body has been through so many surgeries that she doesn't want to do anything right now. But it's definitely on the list of things to get done!
I'm praying that science hurries up & finds a cure for the gene mutation.