MIDDLE-AGED WOMEN 40-60ish
Comments
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Valjean...it is great to see see you here again! Sounds like you had a wonderful time with the grandkids. How I envy you! Glad you were able to get away.
Eph...I was diagnosed with Diabetes last April. I was good for awhile, but I go back and forth. It is really difficult. I did lose about 20 pounds in three months and have not gained it back. It is a daily struggle though. I have not really lost any weight in months, but have not gained so that is good. I have never liked Barbie (the DOLL). Not my role model that is for sure.
Barbe1958....hey, I read your post a few pages back. Not trying to harm myself, just have to get used to how this whole LE thing works. This week my husband painted our bathroom and I was not allowed to paint. I was bummed, but I did clean brushes and buckets and rollers. Plus kept his coffee cup filled throughtout the day! So I did my part just not as active. I am getting more comfortable with the exercises now. They really do help. I will find out next week if I need to get fitted for a sleeve.
I hope everyone had a wonderful Friday. Cheers to all!
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Good Morning Ladies, I have yet another question.. I am flying to visit my sister next week. My Rad onco wants me fitted for a sleeve for when I start rads, I was wondering if anyone has flown without? I do not have any issues with LE so far, but the my onco stated she wants to be sure I do not have any issues.
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Lory, I would see if you can get referred to a LE therapist now. My LE therapist said wear the seeve when participating in triggering actions I.e. Exercise, flying, etc as a precaution (I don't have LE but my RO referred me to get a sleeve for during rads too especially since she zapped the axillary and supraclavicular nodes).
At least this way you'll be sure to get good advice on it. -
Dianarose,
Hi there. I'm new to this group, but your posting jumped out at me. By the way - your fear is not childish at all. Before I had my lumpectomies I tried to see if there was some way I could avoid being put to sleep. (There wasn't). I can handle pain, I can live with being bald, but I absolutely couldn't handle the idea of being put under. It just doesn't make any sense to me, and no amount of Xanax or red wine could make me feel otherwise. But I read somewhere on these discussion boards about Guided Meditation CD's that could lead to a more successful surgery. I was skeptical, but desperate. In the operating room I was a blubbering mess, and I woke up in the recovery room still panicked and frightened.
I ordered 'Successful Surgery' by Belleruth Naparstek. For two weeks I listened to it in the morning, and before I went to sleep. I'm not a great candidate for meditation because I have a very short attention span, and even in yoga class, I'm always thinking about chicken, or cheese, or where I may go on vacation. But I made myself listen to these CDs and learned some good lessons. Ultimately I learned to stay calmer. And to trust. And to feel supported rather than lonely when entering the operating room.
On Wednesday I had a second (smaller) operation and there was a big difference. I still took an Atavin,( because who wouldn't?) And I was still nervous. But I wasn't panicked, and didn't resist being put under like the first time. I was more able to go with it, and I woke up feeling relatively calm. For me, it was a gigantic step.
If this interests you, you can google Belleruth and listen to samples of her meditation. There are also other CDs available by other Doctors and helath practitioners with the intention of a calm and relaxing surgery. Please feel free to contact me if you'd like suggestions.
Janet
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I have my referral in, and an appt scheduled for when I get back from AZ. I figured I would be ok. 1 1/2 hr flight.. no carryon to deal with. I will also be doing my manual stuff during the flight to keep it moving.
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Welcome Janet_M! My BS said he felt he could do a "better job" if I was under general anesthesia. Isn't that a clever way to get me to go under? Actually, I did have an excisional biopsy (which is a non-cancer-y lumpectomy, no different) about 15 years ago and I stayed totally awake. Just had local anesthetic. I think a lot of the procedures could be done with just a local, but then you would have to listen to the small talk your surgery team makes throughout the procedure. Believe me, it is boring enough to MAKE you go to sleep.
I can tell you right now that with those thoughts during yoga class, you will fit in just fine with this group. I think about cheese a lot too.
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Hi, Ladies, I want to jump in here as I saw the issues with the Potassium pills. DH had cardiac issues and was on a slew of meds.......his potassium was like a big alka seltzer that dissolved in water. He is some info. Best to check with the doc about chewing them or splitting them in half. Some have to be swallowed whole to act appropriately. (see the last sentence in what I copied and pasted). Gag. I can barely swallow those big fish oil pills. My Best, Sue
How should this medicine be used?
Potassium comes in oral liquid, powder, granules, effervescent tablets, regular tablets, extended-release (long-acting) tablets, and extended-release capsules. It usually is taken two to four times a day, with or immediately after meals. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take potassium exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
Take all forms of potassium with a full glass of water or fruit juice.
Add the liquid to water. Dissolve the powder, granules, or effervescent tablets in cold water or fruit juice according to the manufacturer's directions or the directions on your prescription label; mix the drug well just before you take it. Cold liquids help mask the unpleasant taste.
Swallow extended-release tablets and capsules whole. Do not chew them or dissolve them in your mouth.
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Janet-thanks for the info. My doctor too gave me some Atavin to take prior too. I was thinking about it today and for me I think it's feeling a lack of control. I keep thinking about possibly going to visit my daughter and granddaughters in NC afterwards. She is pregant or she would come here. She just found out she is having another girl. That will make 5 granddaughters. No boys yet.
Elimar- I was awake for my 1st lumpectomy and it didn't bother me at all. I had a male nurse who talked to me the whole time. The doc never said a word, just did his thing. I was only in recovery for about an hour and went home. I think the doctors are more comfortable if we aren't awake.
All I did was eat at work today. The chef made some wonderful things and I thought I should try a little of everything before we sold it to the public. Must be PMS on it's way.

PMS- Pretty Mean Shi*.
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Okay BS just called and my PBMX scheduled for April 10th
and she sayd I have to go April 9th to radiology for nuclear medicine . I dont understand what that is , Can anyone please tell me what that is .. I guess becuase Of my last time in surgery was Feb 7th she said my pre op will just be a telephone interview ... anyway I am feeling scared now .. Maybe becuause It is now a reality ... anyway feeling sick to my stomach now .. -
could they be doing a sentinel biopsy? before your pbmx
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Juliet , she said she will be doing that with the surgery ..
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they inject a nuclear tracer prior to surgery so the node lights up, so that could be why you are going to nuc med the day before.
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Thanks Juliet now it all makes perfect sence .. such a blessing to have you all here

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Lisamarie - I agree with Juliet - it sounds like you will have the tracer dye injected the day before. I had that done the morning of surgery. You are going to do great. Better wear something with lots of pockets - I believe there will be one heck of a pocket party that day.
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I agree with all of the above. I had mine the day of surgery, but I've heard of others who had it the day before. Different places, different protocols. We're all here for you!
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Lisamarie, I had the nuclear dye injected the day before, just like you. Takes hardly any time at all and then you're on your way.
Dianarose, I have 3 grandSONS and am waiting for a pink one!!! Funny, that we want to experience the other sex, but I had a boy then a girl and it was perfect!
Sue, funny it mentions the bad taste of potassium. In my previous post, I mentioned how the nurses gathered around my bed in the ICU to watch me swallow the dose they gave me. Wasn't that bad, but I didn't get a chaser of orange juice!!
Janet, I actually like going under. Every single person in that room is looking after me. I feel very, very safe. You did great with your CD!! I bet every time it will get easier as you build trust.
Janis, and other ladies who get sleeves: I asked my LE PT if I got a sleeve, wouldn't I need the hand cover too (gauntlet?) as wouldn't the sleeve push fluid into my arm? She said yes, but hadn't offered it in the beginning....made me wary. I didn't get any wraps. And I did fly successfully. My LE is truncal and managed by massage techniques that I learned from my PT.
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I had the dye instead of nuclear and they did it after I was under so no help here but I am sure you will do fine.
I have not flown in quiet awhile but I am hope that next year we can make a trip to Seattle to see my kids. I guess I need to get a sleeve just to be on the safe side. So far I have not had any LE but I guess you never know
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Flying with or without sleeve - my LE therapist explained to me (long after I was dx'd with LE) that if you are showing no symptoms or high risk, the sleeve alone should be fine for precautionary care when flying because your lymphatic system is working okay, and the sleeve just helps keep it that way. Once dx'd or showing symptoms or at high risk of LE, very very bad to wear only sleeve because yes, it will tend to "pocket" in the hand if no gauntlet is present.
To anyone already wearing garments, I wear a great combo sleeve/gauntlet, one piece, that is so much more comfortable than separate sleeve and gauntlet. My LE is not lower arm/hand ... so I don't need major compression around the wrist area. If anyone interested, just PM me and I'll give more info.
Again, I'm so many pages back that I just read the current page. If I missed any major news, please pardon me for not commenting. Know that I'm in every pocket when needed, even if I didn't know I was needed
I have a routine I say each morning when saying some prayers on the train which includes asking God to put me in the pockets of my BCO sisters who need it.Love and hugs
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i'm supposed to fly up to DC to see my son and while i don't think i have LE, i wonder. he only took 2 nodes and i haven't had any symptoms i don't think. it's funny that i'm not sure. i feel so pushed to be symptom-free that i ignore more pains and stuff. at any rate, should i get a sleeve for flying just in case? i'm confused.
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YaYa, that's how we all felt hon...confused on top of confused. Having even one node taken puts you at risk of LE. No symptoms are good, wonderful
Talk to your ONC and ask for a recommendation to an LE therapist. Not any therapist, an LE therapist. Then ask her/him about their thoughts on flying without or without a sleeve. More than likely, you'll be measured for a sleeve to wear as a precautionary measure while flying. I'd be happy to give lots more info about LE and possible precautionary measures if you're intersted. Just PM me 
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Hi everyone! I'm new to this forum group and look forward to participating. Best wishes and lots of love!

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Welcome Seasiren, the ladies here are all wonderful, I think you will really enjoy the group and they have a bunch of knowledge and Love ..
Hugs
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Siren, welcome! Good to have you on board.
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Thanks, everybody! I just realized that your profile has a biography section on it...I put my story together, and I look forward to reading some of yours! Best wishes

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welcome seasiren this is a great group of ladies here
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Hi you young middies you, Now that I am "in" my 60's I truly feel that way. Anyway, I am just stopping by to tell you that your fearless leader, Elimar, is fine and well, but having computer problems. The problem is the router and a new one is supposed to arrive this week. She also put me in charge of the mystery pic!!! No, I am just kidding about that one, but it's always been my dream to win it sometime.
I read the posts on this page and will comment on a few.:
I also think the scariest part of surgery is being put to sleep.....not so much that I am afraid on not waking up because I always have, but I don't know knowing I am there, but totally gone and have no control over what is being done to me. It is really difficult to stop smoking LisaMarie and you are doing a great job of it.....I smoked for years, look back now and wonder why, but I did and I quit many times.....then one day I just decided OK this is it, and it was. I had to stop coffee for awhile, going to the bars and having a drink, anything I associated my habit with and then one day I realized the craving was gone and TaDah, I was no longer a smoker. I am thankful I am not one of those people who lecture everyone else when I quit and I still have a few friends who smoke, but I am very glad I quit. Not only is is asking for another problem (that's what my onco told me I was doing), it is very expensive.
When I took lasix, I took potattium with it. Once mine was too high and an onco nurse yelled at me when I told her I was taking it and I told her it was a RX I got from my GP and only took it when I was doing lasix.
I wear a lymphedema sleeve that I was fitted for whenever I fly,.... wear it when I am doing yard work or other physical activity that exercises my arm and I have never had any problems with it. I have the hand gauntlet, but normally do not wear that. Once in a pinch when I could not find my sleeve, I wore a rubber stocking on my arm with the foot cut out. I think any sort of compression works. All, I know is that I don't want to get it because I know it can be painful.
Like your name Seasiren.....is there a story behind that? You will like this thread....many of my favorite people are on here.
Well, I am going to move on now, just did not want you to wonder where Elimar is. My neighborhood is so quiet this morning, that I am wondering if everyone forgot to move their clocks forward. Have a good one. Marybe
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Welcome Siren, all these ladies are so helpful.
Marybe- I keep lookin at how many nodes that docs have taken from everyone and it scares me. Why did you bs take so many if the first few were clean?
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Marybe thanks for letting us know about Elimar. I was beginning to wonder about her and thought gee whe must have a really good book she is reading.
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Diana, Who knows why they did what they did on me, but remember it was back in 1990 that I had my mastectomy. They took out 19 and all were clear and thanks to that even though I do not have lymphedema (maybe I do, but it's not in my arm, but under it), I have a pouch under my armpit that is almost like a breast itself. The PS was going to fix it when I had the exchange to a implant from TE, but he did not and I never raised a squawk about it so that is how it still is today. I had never even heard about that sentinal node biopsy until women on here talked about it, so I don't even know if they checked that on me. I think the root of my whole problem and the fact I had recurrent mets many years later, was that I had NO treatment....no tamoxifen, no chemo, no anything and again this was because it was 1990 and they have learned a heck of a lot since then. I don't know if this answers your concerns, but try not to worry....chances are if you did a round of chemo after or did tamox or something as a preventative, you will be just fine. I was young and stupid and just figured I was over and done with it and was happy when they said no treatment....today I would look at it differently and would have gone for another opinion. I have local friends with BC and they only had a few nodes removed and they are doing just fine.
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Marybe- I have a friend who had her sugery 8 yrs ago and they were still taking all of the nodes then, well at least here in Maine. My lumpectomy is scheduled for Thursday. I really wanted to go to NY and have my surgery by a doc who uses laser, but just found out he doesn't take my insurance and it could be 2-8k for the surgery and I don't have the money to pay up front. I am so bummed out.
After surgery I am going to have my dam ovaries surpressed. At 51 I still get my period every 23 days and it's time to shut them down. My MO wants me to take tamoxifen, but I am still reserved about it.
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