Anybody in the Maryland area?

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Proverbs312b
Proverbs312b Member Posts: 22

Hello ladies,

I was diagnosed with Mets to the lung, liver and several bones back in November. I would really like to speak with a woman with similar diagnosis, who lives locally (near baltimore or DC area). My friends & family are all very sweet & supportive, but it would be nice to know someone who actually is in the same "boat" as I am :)

Thank you for even considering reaching out.

Jessica

Comments

  • Partyoffive
    Partyoffive Member Posts: 188
    edited February 2020

    hi

    I live in pa about 40 min from Baltimore-in fact I go to John Hopkins in Baltimore. I feel the same way my family is great but it’s hard for anyone to understand unless you are living it. Pm me if you want to make plans to meet up.

    Kristin

  • BevJen
    BevJen Member Posts: 2,523
    edited February 2020

    Hi,

    I live in the DC suburbs (Montgomery County) and also am treated up at Hopkins.

    PM and let me know where you are and maybe we can meet up -- also, if you are in Montgomery or Prince Georges County, I have a recommendation for a metastatic breast cancer discussion group that meets one time per month, if you are interested.

  • PugMother
    PugMother Member Posts: 1
    edited February 2020

    I have lurking in this group for five years. I have stage 4 breast cancer which is ER +. I live in Montgomery County, MD and work in Baltimore. I would be very interested in a local group or meetings.

  • Moderators
    Moderators Member Posts: 25,912
    edited February 2020

    Welcome, PugMother! We're so glad you decided to join our community here - connecting with others in your shoes is such an important part of managing what you're going through. We're all here for you!

    The Mods

  • edyste
    edyste Member Posts: 3
    edited February 2020

    I also live in Montgomery county and am being treated at sibley in dc (affiliated with Hopkins).

  • Partyoffive
    Partyoffive Member Posts: 188
    edited February 2020

    if you give me some ideas on where we could meet I’d be happy to try and schedule it. I’m almost 7 years out from a stage 4 de nova diagnosis with innumerable bone mets. I was stable for 6 years on tamoxifen and recently had growth in my bone tumors and have switched to letrozale/100 mg ibrance. So far so good. Let me know preferred days,times and places and let’s see if we can get together.

    Kristin

  • Proverbs312b
    Proverbs312b Member Posts: 22
    edited February 2020

    hello ladies!


    Partyoffive, bevjen, Pugmother & Edyste....thank you all so much for responding & so quickly.

    I will PM y'all now.

    :)

  • CynMD
    CynMD Member Posts: 11
    edited December 2020

    Hi


    I want to join too. Just diagnosed with Bone Met in CT, and possible more after Pet Scan. Need your advice. Lived in Potomac, mary

    Thanks

    Cyn

  • Proverbs312b
    Proverbs312b Member Posts: 22
    edited April 2020

    Hi Cyn, I'm sorry that you have bone mets! Hope it hasn't spread anywhere else! when is your scan scheduled for? I'm new to Mets but will gladly help however I can! Which cancer center do you work with? I go to GBMC (greater baltimore medical center) in towson.

  • CynMD
    CynMD Member Posts: 11
    edited December 2020

    Hi, Proverbs312b

    Thank you for the reply. I had my CT scan last week (3/25/2020) and found bone Mets on my rib and spine. I will have PET scan next week, hope nothing else other than bone Mets. I go to Shady Grove hospital currently. I am looking for good Oncology center nearby for 2nd opinion or switch the doctor.

    Cyn

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