Posted on: Dec 1, 2011 02:16 AM
southcentral, wi
Joined: Jan 2011
Posts: 2,623
thefuzzylemon wrote:
So here I am. Out of active treatment. Found out that looking forward to "it getting easier" and "getting back to a "normal" hasn't happened. Instead, I discovered that the journey only began - that I will forever fight this disease, my mental health continues to be challenged and making "changes" to avoid reoccurance just makes me feel like Cancer gets to control my quality...screwed up, right?
So, here it is...Fuzzy's Romp Room. I'm so ready to drop F Bombs and smack stupid people for the insensitive crap that they say and do. I'm sick of medications "getting me through." I have had just about enough of people on the other side who just don't get it, yet feel they need to say something to make a cancer patient "feel better about themselves" or whatever that reasoning is...
I'm hoping that this thread will just give a place to be 100% open. I do love to write, and I do love all of my sisters here. I do not want to offend anyone, ever. I just need to let it out...feel free to do the same. I thought by opening up my own thread, it would keep me from offending anyone else on thread's that they have built. I'm just such a friggin' mess and I need some help to get it together ...
Fuzzy's Romp Room comes complete with padded walls, restrictive clothing/accessories (for the really bad days) and an endless supply of love to all of ya all. Believe it or not, I do have tons of love and forgiveness in my heart ... it's just my head that's a wreck.
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
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SpecialK
Tampa, FL
Joined: Feb 2011
Posts: 5,732
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Dec 1, 2011 03:09 AM SpecialK wrote:
fuzzy - I will be your first poster! FWIW - I think ditching the "getting you through" meds can be a positive step for those who are ready, not putting up with insensitive crap is GREAT, the need of some to say something when they don't get it is totally annoying, and feeling what you really feel and not trying to rearrange it to make others feel better is GOOD! Making changes as we go forward from this point to try to avoid recurrence is just as much of a crapshoot as who gets BC to begin with. If you don't want to do, or if you feel like it is controlling you, don't do it yet. Learning to live fully while in fear is a tough row to hoe. I am in the boat with you..... I have no real answers, other than you can only live in the moment you are in.
DCIS/IDC ON RT, ADH/ALH ON LFT, NS BMX 11/1/10 AND 12/6/10 TCHX6 (2/17/11-6/2/11) Herceptin until 2012
Diagnosis: 9/27/2010, IDC, 2cm, Stage IIb, Grade 3, 2/14 nodes, ER+/PR+, HER2+
leaf
Joined: Dec 2005
Posts: 8,104
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Dec 1, 2011 03:14 AM leaf wrote:
Fuzzy, I love it! I'm all for 100% open. Glad you have the padded walls. I know you have tons of love and forgiveness in your heart - you wouldn't start this thread unless you did.
I remember long ago, long before I had any semi-concerning health problems (I only have classical LCIS), I went to the doc for my physical exam, and I wanted to check with her about a pain in my foot. I told her I wasn't sure if it was all in my head. She replied, "If your foot hurts, your pain is in your foot, not your head." That made me feel better, even if it was minor. It took lots of years for me to start to learn my head and my body are connected. I'm still working on that.
If you're going through hell, keep going-Winston Churchill
thefuzzylem
southcentral, wi
Joined: Jan 2011
Posts: 2,623
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Dec 1, 2011 03:17 AM thefuzzylemon wrote:
Oh thanks sweetie!! Its just so true. This is what we have...this moment. I need to live by my truth and it just seems to get pushed around. These boards have always been my special place-right from the start.
Just read about my DD (youngest) from internet posts. Here's another reality bitch...but she's got a foul mouth and loves Coors. Just adds to my world. How many battles can I handle...more importantly, handle well.
Our closest family and friends don't get it....bummer....
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
thefuzzylem
southcentral, wi
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Posts: 2,623
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Dec 1, 2011 03:18 AM, edited Dec 1, 2011 03:18 AM
by thefuzzylemon
Leaf....i love that! If your foot hurts, it hurts....:)
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
sheila888-â
Westchester County, NY
Joined: Jul 2009
Posts: 23,737
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Dec 1, 2011 03:22 AM sheila888-♥ wrote:
Hey fuzzy....Thanks for your thread.
Welcome back sister.
I will contribute after my DR appointment.
♥
Sheila♥
Diagnosis: 4/8/2005, IDC, 1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2+
thefuzzylem
southcentral, wi
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Posts: 2,623
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Dec 1, 2011 03:35 AM thefuzzylemon wrote:
<3><3><3>
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
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Dec 1, 2011 07:34 AM, edited Dec 1, 2011 07:35 AM
by bellydancer
Does this room also include gaint soft form paddles....remeber those from the 80's pysch-therapy : )
"I must do something" always solves more problems than "Something must be done." ~Author Unknown
sheila888-â
Westchester County, NY
Joined: Jul 2009
Posts: 23,737
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Dec 1, 2011 08:54 AM sheila888-♥ wrote:
Today was MH day for me. It went well and feeling better than yesterday.
My depression is not related to BC I had it long before my DX...actually the diagnosis shocked my brain I think because for almost one year didn't have a depressive episode.
Then I had my last radiation and it sinked in that I have BC.
To be continued..........................
Hugs to all of you.
Sheila♥
Diagnosis: 4/8/2005, IDC, 1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2+
thefuzzylem
southcentral, wi
Joined: Jan 2011
Posts: 2,623
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Dec 1, 2011 09:12 AM thefuzzylemon wrote:
Bellydancer....rooms of all themes here!!! I'm a 70's disco sort of chick so my straight jacket is tie dyed!
Sheila....I'm all ears whenever you need me. I've heard a million times how "cancer" doesn't discriminate...I'm thinking depression is the same.
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
sheila888-â
Westchester County, NY
Joined: Jul 2009
Posts: 23,737
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Dec 1, 2011 10:00 AM sheila888-♥ wrote:

I know this has nothing to do with the thread........
But it was too cute
Sheila♥
Diagnosis: 4/8/2005, IDC, 1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2+
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Dec 1, 2011 10:14 AM Moderators wrote:
thefuzzylemon, LOVE what you've done with the room. It was so bland and non-existent before, and you've brought it to life with humor and support and what look like...beanbag chairs?
Judith and the Mods
catbill
Prior Lake, MN
Joined: Nov 2010
Posts: 325
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Dec 1, 2011 10:24 AM catbill wrote:
Fuzzy,
I love the room, but being a 70's rock chick myself, I'd like to donate a few lava lamps. I always found them calming and rather soothing.
Sheila-I love the adorable picture.
Diagnosis: 9/29/2010, IDC, 1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2-
barbe1958
Alliston, ON
Joined: Nov 2008
Posts: 17,434
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Dec 1, 2011 12:16 PM barbe1958 wrote:
Glad y'all found me in my rubber room!!!! I'll break through the wall and join you in the fuzzy room. The noise coming from there got my attention....
Sometimes you're the fork, sometimes you're the road.
thefuzzylem
southcentral, wi
Joined: Jan 2011
Posts: 2,623
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Dec 1, 2011 12:39 PM, edited Dec 1, 2011 12:39 PM
by thefuzzylemon
Mods - You're always welcome at Fuzzy's Place ;) Glad you like the decor ... it's called "comfort with hints of blood, sweat and tears". Its a hot new trend this year 
Sheila - LOVE the pic! I wuv animals. I joined the National Humane Society just a few weeks ago!
Cat- Let's put those lava lamps in the "over 21 wing" ... oh yes, I remember them to be calming as well ...
Barbe - Whoot whoot!! When the house is a rockin', you know we're involved!!! LOL
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
Ang7
VA
Joined: Jul 2009
Posts: 1,216
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Dec 1, 2011 12:45 PM Ang7 wrote:
Fuzzy~
I am liking the vibes in this room. No animosity amongst the rompers...
Peace.
Diagnosis: 5/25/2009, IDC, 2cm, Stage IIa, Grade 2, 1/4 nodes, ER-/PR-, HER2+
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Dec 1, 2011 12:46 PM christine47 wrote:
love it!!! I will be back, keep the door open and the lights on.
Diagnosis: 11/11/2010, IDC, 1cm, Stage IIa, Grade 2, 1/17 nodes, ER+/PR+, HER2-
Makratz
Boston
Joined: Sep 2008
Posts: 12,523
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Dec 1, 2011 12:52 PM Makratz wrote:
Fuzzy!! Very well said. I know you speak for me! I do need a rubber room. It's co nice that that room is filled with all my friends. I hope you find relief here, knowing that your not alone in the way you feel, things youa re going through. I know you always put a smile on my face, I hope we can put a smile on yours.
XOXO
Linda...♥♥♥ Never, never, never give up ~ Winston Churchill
thefuzzylem
southcentral, wi
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Dec 1, 2011 12:53 PM thefuzzylemon wrote:
Christine - we'll keep the lights on fer ya
, ... the beer on ice, the pigs in a blanket, the red carpet rolled out and fresh flowers on the table ...
Random issue...why oh why do I want to get in the truck and drive to another part of the country? I need a break...a long, long break ....
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
thefuzzylem
southcentral, wi
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Dec 1, 2011 12:56 PM thefuzzylemon wrote:
MAK!!!!! Oh so awesome!!! I just really didn't want to get anyone's nose outta joint by ... well, being myself I guess. Just so happens that what's going on in my world and I wouldn't have been able to handle it if my sisters became irritated with me ... so, Fuzzy's Romp Room was born...
XOXOXOXOXOXOXOXO
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
sheila888-â
Westchester County, NY
Joined: Jul 2009
Posts: 23,737
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Dec 1, 2011 12:56 PM sheila888-♥ wrote:
I desperately need a sound proof rubber room i need to scream and say few words to NBC for cutting the last 5 minutes of Rockefeller Tree Lighting because the show went over 5 minutes.
I was really waiting for the tree.
Thank You
OK I'm ready for the room.
Sheila♥
Diagnosis: 4/8/2005, IDC, 1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2+
thefuzzylem
southcentral, wi
Joined: Jan 2011
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Dec 1, 2011 12:58 PM thefuzzylemon wrote:
WTH??? Why would they even televise it if they were not going to show it??? Hmmm...maybe I should drive to New York....a girl can only dream...:)
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
Makratz
Boston
Joined: Sep 2008
Posts: 12,523
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Dec 1, 2011 12:59 PM Makratz wrote:
Well, it's a HUGE success Fuzzy!! I think I will wrap myself in bubble wrap and have some fun in the rubber room!
Linda...♥♥♥ Never, never, never give up ~ Winston Churchill
thefuzzylem
southcentral, wi
Joined: Jan 2011
Posts: 2,623
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Dec 1, 2011 01:02 PM thefuzzylemon wrote:
OMG...game time! It could be like human bumper cars. Aw crap...I'm going to have to get a helmet. Better make it Tie Dyed to match the jacket...
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
sheila888-â
Westchester County, NY
Joined: Jul 2009
Posts: 23,737
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Dec 1, 2011 01:02 PM sheila888-♥ wrote:
Linda ?????

Sheila♥
Diagnosis: 4/8/2005, IDC, 1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2+
Makratz
Boston
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Posts: 12,523
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Dec 1, 2011 01:04 PM Makratz wrote:
A foil helmet? I think I still have mine.
Sheila??? I'll PM you!
Linda...♥♥♥ Never, never, never give up ~ Winston Churchill
thefuzzylem
southcentral, wi
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Dec 1, 2011 01:06 PM thefuzzylemon wrote:
Incase you need to find me, I'm, wearing blue...

thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
Makratz
Boston
Joined: Sep 2008
Posts: 12,523
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Dec 1, 2011 01:07 PM Makratz wrote:

I'll be wearing the bubble wrap!
Linda...♥♥♥ Never, never, never give up ~ Winston Churchill
thefuzzylem
southcentral, wi
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Dec 1, 2011 01:08 PM thefuzzylemon wrote:
And...I'll be in this room ...

thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
thefuzzylem
southcentral, wi
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Dec 1, 2011 01:08 PM thefuzzylemon wrote:
I'm searching for 70's bubble wrap...LOL
thefuzzylemon
Diagnosis: 1/20/2011, 2cm, Stage IIIc, 14/15 nodes, ER+/PR+, HER2-
Makratz
Boston
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Dec 1, 2011 01:10 PM Makratz wrote:
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Bubble wrap Jr. this past Halloween!
Linda...♥♥♥ Never, never, never give up ~ Winston Churchill