Previous Thread
Next Thread
Print Thread
Page 2 of 2 1 2
Joined: Aug 2016
Posts: 11
Member
Offline
Member

Joined: Aug 2016
Posts: 11
I think most insurance pays (or not) per doc visits, procedures, tests, etc regardless of where they take place, as long as the facility accepts that particular insurance. However, if it's the type of insurance that requires everything be done in a specific network unless they give authorization to go elsewhere (such as a Medicare Advantage plan) you have to be sure that you go to a network facility. And if he has regular Medicare, he may also have a Medicare Supplement which picks up all or part of the 20% of charges Medicare doesn't pay. Can you find out exactly what insurance your dad has? Then you can look online to find out what it covers and where.

Joined: Jun 2007
Posts: 10,507
Likes: 7
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)
Offline
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 10,507
Likes: 7
Call the insurance company or ask your parents if they were sent a directory of in-network physicians and facilities. You can also ask when you make the appointment.


Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
Joined: Aug 2016
Posts: 14
JohnJr Offline OP
Member
OP Offline
Member

Joined: Aug 2016
Posts: 14
Well just to update. We researched and found him a great oncologist with a lot of experience in OC. Hes at a cancer center in our area. He just had an MRI and CT scan this past Friday. He goes for the results on Monday.

His first meeting with the oncologist was a good one. He really likes her and she is very kind and understanding. According to her the spot is less than 2cm and she cannot feel any lymphs in his neck or jaw area enlarged. She said thats a good size that its localized, but said to take that very lighting until we get the results from the MRI/CT back.

For the first time in my life ive seen my dad show emotion. Hes obviously very shaken up. Not so much worrying about himself, but the possibility of leaving his kids behind. So we have been trying to keep him busy with various tasks around the house to keep his mind from going there.

Of course it hasnt been easy at all on me or my mother. We are both pretty nervous wrecks and I havent been sleeping as well as I would like with my mind so heavy.


CareTaker for my dad (John Sr)
Being Treated at Chao Family CCC and UCI
Diagnosed T2 SCC BOT 8/9/2016
Partial Glossectomy w/ Neck Dissection Done 9/22/16
Joined: Aug 2016
Posts: 14
JohnJr Offline OP
Member
OP Offline
Member

Joined: Aug 2016
Posts: 14
Father met with the surgeon this past week to discuss the surgery needed. Hes going to have a partial glossectomy. And he also wants to remove a few questionable lymph nodes in the neck just to be sure. He was told the surgery would take 8-10 hours. We looked at many surgeons and decided on one that came highly recommended for treating many with OC. He tandems with a Vascular surgeon.

Dad is freaked out of the surgery and is worried that by the time the surgery is performed (Approx. 3 weeks from now) that the cancer will spread.

We are trying to keep him bust and reassured its going ot be alright.


CareTaker for my dad (John Sr)
Being Treated at Chao Family CCC and UCI
Diagnosed T2 SCC BOT 8/9/2016
Partial Glossectomy w/ Neck Dissection Done 9/22/16
Joined: Oct 2012
Posts: 1,275
Likes: 7
Assistant Admin
Patient Advocate (1000+ posts)
Offline
Assistant Admin
Patient Advocate (1000+ posts)

Joined: Oct 2012
Posts: 1,275
Likes: 7
It looks like you have a medical team that you like and can trust. That's a good thing.

Can you talk to your dad's surgeon about his fear of the cancer spreading and see if the doctor will give him some reassurance? If you or your dad can be proactive in this way, it will help him through the treatment ahead as he will feel he has some control.


Gloria
She stood in the storm, and when the wind did not blow her way, she adjusted her sails... Elizabeth Edwards

Wife to John,dx 10/2012, BOT, HPV+, T3N2MO, RAD 70 gy,Cisplatinx2 , PEG in Dec 6, 2012, dx dvt in both legs after second chemo session, Apr 03/13 NED, July 2013 met to lungs, Phase 1 immunotherapy trial Jan 18/14 to July/14. Taxol/carboplatin July/14. Esophagus re-opened Oct 14. PEG out April 8, 2015. Phase 2 trial of Selinexor April to July 2015. At peace Jan 15, 2016.
Page 2 of 2 1 2

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,260
EzJim 5,260
Brian Hill 4,916
Newest Members
TZwicker, Mareea, Crzyborgs88, Chevymudnut, Charlsena
13,222 Registered Users
Forum Statistics
Forums23
Topics18,209
Posts197,040
Members13,222
Most Online614
Jul 29th, 2024
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5