Support Meetings, Webinars and Partner Events

Attend a meeting to connect with others and obtain support and vital resources.

Click on a meeting to learn more and register

March 2026
Mon
Tue
Wed
Thu
Fri
Sat
Sun
23
24
25
26
27
28
1
2
3
4
BRCA1, BRCA2 & PALB2 Mutations

8:00pm EST

5
LGBTQIA+

8:00pm EST

6
7
8
9
10
Men

8:00pm EDT

11
ATM, BARD1, BRIP1, CHEK2, RAD51C & RAD51D Mutations

8:00pm EDT

12
13
14
15
16
17
18
Lynch Syndrome Mutations

8:00pm EDT

19
20
21
22
23
APC, CDH1, CDKN2A, PTEN, TP53 & Other Rare Mutations

8:00pm EDT

24
Previvors

8:00pm EDT

25
26
Hereditary Cancer Live Update

2:00pm EDT

Breast Cancer Survivors, Thrivers & People in Treatment

8:00pm EDT

27
28
29
30
31
1
2
3
4
5
BRCA1, BRCA2 & PALB2 Mutations

Wednesday, March 4th

|

8:00pm EST

LGBTQIA+

Thursday, March 5th

|

8:00pm EST

Men

Tuesday, March 10th

|

8:00pm EDT

ATM, BARD1, BRIP1, CHEK2, RAD51C & RAD51D Mutations

Wednesday, March 11th

|

8:00pm EDT

Lynch Syndrome Mutations

Wednesday, March 18th

|

8:00pm EDT

APC, CDH1, CDKN2A, PTEN, TP53 & Other Rare Mutations

Monday, March 23rd

|

8:00pm EDT

Previvors

Tuesday, March 24th

|

8:00pm EDT

Breast Cancer Survivors, Thrivers & People in Treatment

Thursday, March 26th

|

8:00pm EDT

Hereditary Cancer Live Update

Thursday, March 26th

|

2:00pm EDT


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Partner Events

Triage Cancer : Steps to Navigate Common Insurance Hurdles

Educational Event
March 24, 2026
10:00 AM - 11:30 AM Pacific Time

SHARE Cancer Support : Getting Our Fair SHARE

Educational Event
March 25, 2026
9:00 AM - 4:00 PM Eastern Time

Local Pennsylvania Leaders

Karin Roseman (Philadelphia)

Karin Roseman (Philadelphia)
Email

Shannon Ewing (Pittsburgh)

Shannon Ewing (Pittsburgh)
Email

Nicole Deckard, MS, CGC (Geisinger Genomic Medicine Institute)

Nicole Deckard, MS, CGC (Geisinger Genomic Medicine Institute)
Email


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Watch video to learn more

FORCE offers 14 unique community support meetings on Zoom, making it easy to find the group that’s just right for you. These groups are a safe space to connect with others, ask questions and share your concerns with peers, volunteers and genetic counselors. You can attend meetings by either your gene mutation, the community you identify with or by surgery.