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So sorry you are going thru this. Hopefully it is not what you fear the most.
I can honestly say I have never heard a lump described exactly that way before. The 'sticker' thing and itch puzzles me.
If I were you I would start with your primary physician. Even the group where you are juggled between who ever is on call. One of them can order a mammo or just send you on to a specialist whom is who you would want to see anyway. But as always we have to go thru red tape to get there. I just feel that these doctors could hopefully see you sooner than the OBGYN group.Honestly, I would go for who can see you the quickest. The less time you spend worrying the better. It could be a lot of things but I do understand the worry and I would not put it off. I would not wait until after the cycle even tho that can affect our breast. I waited and then wished I had not. The wait did not benfit me at all. So please get it checked. And try not to worry.
Let us know, we are here for you.
Blessings.... PatView Thread

The pelvic muscle prollapse can be caused by lack of hormones...re:hormone blocker meds
The lack of hormones weaken the pelvic muscle walls.Among a million other things it can do to us. I am dealing with that but the pain in my joints and muscles and the fatique is really ticking me off. I am walking with a cane right now. I twisted my knee a few weeks ago and it just will not get well.
I just have not been a happy camper for a good while now.
I will be happy to let you know what ever I find out
Blessings.... Pat.View Thread


(¯`"665´¯) ."665."022*¨`*"66B."665
´*.¸."022´ "665 "665 HAPPY ANNIVERSARY!
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View Thread

Yes,it has been a long time. I do continue to come here often and read but have little energy most of the time to post. I did post here and I also posted on the so called doctor that refuses heavy wt women for treatment. ggrrrrr.....
I hope you are well also my dear friend.
Blessings....PatView Thread

To answer tjbethel....no I have never been told to avoid anyone or anything while on Arimidex, and believe me one of my doctors{radiation) would have told me this....he is a bundle of knowledge and waste no time at sharing it. I adore him!
Jenna.....yes, I have had all of those side effects and many more. I too, can get up and do any small chore and sit down with the hot sweats for no reason.ug! But that is the least on my side effects.......the bone and muscle pain is massive.....the joints are totally miserable and every joint I have hurts with every movement I make. I have extreme fatique to the point that I now do very little because I am just to tired to move and it just flat hurts so bad. I have gained an enormous amount of weight which I feel is from the pill AND from little activity. I feel trapped there. My hair is thinning........I get sick easy......I am mauseated......often have constipation.......insomnia........and the newest, that I diagnosed myself from extensive research.....PELVIC MUSCLE PROLAPSE. From my front to my back. EVERYTHING in that area gives me pure havoc. I do believe this is due to weight gain,constipation and lack of hormones, which we all know effects our entire body. But this condition I feel is a domino effect from the Arimidex.
So.....in other words I am absolutely miserable! I have an appt with my doctors in 2 weeks and intend to discuss all of this with them. Thing is.....I do not want to change to the meds that could have negative effects on female organs sense I still have all of mine. re:uterine cancer etc; So what can I do. I have been on Arimidex for 2 1/2 years and I feel like I am 100 years old.What will it be like in 2 1/2 more years. I can do very little that I use to due to body pain and fatique. I am nearing home bound. And will this be reversible later on? Pushing thru it is not even any where near a big enough statement.
Blessings.....PatView Thread

May I ask if you are experiencing any side effects from the Arimidex? I too have been on it 2 1/2 years and could write a book on side effects IF I had the energy.
Thanks,PatView Thread

Blessings..."020
Pat~Sadblossom
..
View Thread

Stay cool as possible at all times. Apply ice packs as needed,you get so much relief from the icepacks. Place them anywhere you itch. The colder/coler you stay the less you will itch.
Go braless and wear soft cotton t shirts and/or even night shirts at home,anything that does not rub or cause friction. Wear loose thin clothing.
Apply ordinary kitchen cooking corn starch straight from the box like it were bath powder to all areas that itch. There is a line of routine that worked best for me.............apply ice packs, when ice melted apply corn starch then reapply ice packs.Store corn starch in the freezer for added cool comfort.
Do NOT bathe/shower in very warm water. The cooler the better.Do NOT rub skin while bathing. Just blot on lightly sudsy water and rinse off well with clear water. Blot dry DO NOT RUB OR SCRATCH. If you MUST touch that area and can not resist just apply a bit of light pressure but do not scratch or rub.That only makes it worse.Oh yes, use only a very mild bath soap.I used plain Ivory until it stopped.
Ask your radiation therapyst for cortizone creme. Or get it at the pharmacy or Walmart. 2% is fine but very importantly FOLLOW DIRECTIONS and do not use for a prolonged period of time. You absorb cort creme and to much can make you ill.Thru my process I used about 2 tubes.
Aloe jel helps also. Place the Aloe jel in the freezer until extremely cold then apply to skin. You can also use the jel from an Aloe Vera plant.
My entire process many times a day was as follows..........Cort creme......then cold corn starch.......then ice packs.........and repeated corn starch and ice packs as needed day and night.
Cool bathes anytime. Even cold wet towels on the itching area brings some relief.
I also took Xanax so I could sleep.
Carry the cort. creme, cornstarch and ice packs everywhere you go.
Avoid sunlight or any kind of heat on affected areas.
This is all that gave me any relief at all. And belive it or not, when it was at it's worst I kept telling myself it would stop sooner or later and it does. I itched for a month or two afterwards off and on.
Hope this helps. I feel for you but remember.....it WILL get better!
Blessings!
~SadblossomView Thread

Blessings.....
Pat~sadblossomView Thread
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