http://www.breastimplantsupport.org/ Thu, 23 Feb 2012 02:06:29 +0000 MyBB http://www.breastimplantsupport.org/showthread.php?tid=9432 Wed, 22 Feb 2012 20:48:48 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9432 A week from surgery the muscles in my arms ache and hands a bit tingley.
Is this normal?]]> A week from surgery the muscles in my arms ache and hands a bit tingley.
Is this normal?]]> http://www.breastimplantsupport.org/showthread.php?tid=9431 Wed, 22 Feb 2012 13:44:27 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9431
What a great website this is, wished i had found it sooner. My story began 26 years ago when i got silcone implants as a young girl who had no breast tissue which was making me quite depressed so i had the implants put in through my doctor by the NHS. As time went by the left one developed a lot of hard lumps around it and I decided it was time to get them out. When they opened me up they found that the capsule had burst as well as the implant and there was silicone all over my left breast and ribcage, i endured 5 hours of surgery and a blood transfusion as i had lost lots of blood and was put into high dependency for a couple of days as my left lung had deflated a bit as well.When i woke up i was on oxygen, heart moniter and had drains in both breast, i had a couple of funny turns with sugar levels and blood pressure going up and down for the next fews days after the operation, i consider my self lucky to be alive and wished i hadn't waited so long to get them out.

I am now 15 days since explant and i am getting better slowly every day, Im still bruised and sore but i am so glad they are gone! My ps has told me he has removed everything so i don't need to have any more surgery on them. Im looking forward to them healing properly and buying my first A cup bra, size doesn't matter anymore only my health Thanks for listening and its great to know so many people are deciding to have them removed for good]]>
What a great website this is, wished i had found it sooner. My story began 26 years ago when i got silcone implants as a young girl who had no breast tissue which was making me quite depressed so i had the implants put in through my doctor by the NHS. As time went by the left one developed a lot of hard lumps around it and I decided it was time to get them out. When they opened me up they found that the capsule had burst as well as the implant and there was silicone all over my left breast and ribcage, i endured 5 hours of surgery and a blood transfusion as i had lost lots of blood and was put into high dependency for a couple of days as my left lung had deflated a bit as well.When i woke up i was on oxygen, heart moniter and had drains in both breast, i had a couple of funny turns with sugar levels and blood pressure going up and down for the next fews days after the operation, i consider my self lucky to be alive and wished i hadn't waited so long to get them out.

I am now 15 days since explant and i am getting better slowly every day, Im still bruised and sore but i am so glad they are gone! My ps has told me he has removed everything so i don't need to have any more surgery on them. Im looking forward to them healing properly and buying my first A cup bra, size doesn't matter anymore only my health Thanks for listening and its great to know so many people are deciding to have them removed for good]]> http://www.breastimplantsupport.org/showthread.php?tid=9425 Wed, 22 Feb 2012 02:24:33 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9425 http://www.breastimplantsupport.org/showthread.php?tid=9424 Tue, 21 Feb 2012 20:35:35 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9424
I am trying to decide still if I should have the glands with silicone removed. I know Dr. Kolb removes them so they don't become lymphoma and Dr. Feng says leave them in and cleanse. I've been cleansing for 3 yrs since explant and still they are huge. Since I've been doing the detox baths my spleen pain has gotten worse and my glands are throbbing. I've been hoping this is a good sign from detoxing but it's also got me wondering how long I should wait to remove them. As soon as I think I should get them removed, I think, well what about my spleen and liver and all the other glands the ultrasound said had silicone in them. I can't remove everything in me that has silicone so then I just keep detoxing because I don't know what else to do. Is there anyone out there like me?

Cath]]>
I am trying to decide still if I should have the glands with silicone removed. I know Dr. Kolb removes them so they don't become lymphoma and Dr. Feng says leave them in and cleanse. I've been cleansing for 3 yrs since explant and still they are huge. Since I've been doing the detox baths my spleen pain has gotten worse and my glands are throbbing. I've been hoping this is a good sign from detoxing but it's also got me wondering how long I should wait to remove them. As soon as I think I should get them removed, I think, well what about my spleen and liver and all the other glands the ultrasound said had silicone in them. I can't remove everything in me that has silicone so then I just keep detoxing because I don't know what else to do. Is there anyone out there like me?

Cath]]> http://www.breastimplantsupport.org/showthread.php?tid=9423 Tue, 21 Feb 2012 05:00:03 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9423
I will keep this short and sweet, but basically I got implants at the age of 19, fast fwd 4.5 yrs I have food allergies, hypothyroid, very bad RA etc. I got them removed Jan 9th 2012 and feel so much better!!!

I have written a blog and changed direction in my life goals. I was once a model on the cover of magazines and now I am focusing and dedicating my life to helping women and get the word out about what could potentially happen. The response is incredible and the similar stories are so scary.

I hope to make a full recovery and document my bloodwork etc and write articles and stories for magazines etc...

hope you enjoy.

http://www.samanthawhitfield.com
http://www.samanthawhitfield.blogspot.com]]>
I will keep this short and sweet, but basically I got implants at the age of 19, fast fwd 4.5 yrs I have food allergies, hypothyroid, very bad RA etc. I got them removed Jan 9th 2012 and feel so much better!!!

I have written a blog and changed direction in my life goals. I was once a model on the cover of magazines and now I am focusing and dedicating my life to helping women and get the word out about what could potentially happen. The response is incredible and the similar stories are so scary.

I hope to make a full recovery and document my bloodwork etc and write articles and stories for magazines etc...

hope you enjoy.

http://www.samanthawhitfield.com
http://www.samanthawhitfield.blogspot.com]]> http://www.breastimplantsupport.org/showthread.php?tid=9422 Tue, 21 Feb 2012 01:28:01 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9422
Thank you

D]]>
Thank you

D]]> http://www.breastimplantsupport.org/showthread.php?tid=9421 Mon, 20 Feb 2012 20:01:23 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9421 & sobbing & catatonic states down, I was then able to think rationally about what to do next. Here was my concern at this point: I have never in the 13 years of my implants had a mammogram. Why my PCP would not have sent me for breast imaging of some sort after noting 3 years in a row that I had a benign breast lump really had me confused. I most certainly wasn't going under the knife with out Ultrasounds, MRI & Mammogram & blood work done first. I took these steps &
scheduled a 2nd opinion with another Surgeon. By this point a week later I had red streaks & swelling running from my left breast under my arm pit, around to my shoulder blade. I had raised veins on top of my breast that were swollen & fire hot red. The 2nd surgeon said the same thing. Who did this to you? Unknown to me at this point, was my original surgeon in 1998 was not a board certified surgeon nor were my implants FDA approved & the shell of my implant was made out of Silicone & various other toxins. I found out that day at the 2nd surgeons
office. Surgeon advised me yes, we need to get these implants & contracture out & I'm not taking any of your skin until biopsy & pathology reports come back. I had surgery 3 days ago. I have a drain in my left breast & Surgeon called me yesterday at home to let me know I had straw colored fluid where it shouldn't be in my capsular contracture & between my implant, he stated I have clinical presentation of Anaplastic Large Cell Lymphoma, its enough to diagnoses ALCL. Guess we will see what pathology has to say. My 1st Question is this. How can a
woman give informed consent when they are not advised via literature, documents or verbally that the shell of saline implants are indeed silicone & other toxins? Its not possible to give informed consent when you are not informed in any way. I WOULD HAVE NEVER had these implants if I had known. I have basically stayed sick for 12 years. I lost my dignity, my faith, my passion, my husband, my family & friends. Until it reared its ugly head through my breasts I never once considered it was my implants nor did any doctor until now. I can say I am a definite mental & emotional basket case & I have earned the right to be. So, how does a women pick up the pieces & what does she do from here? My heart goes out deeply to every women enduring this hellish nightmare. I too, feel your pain & fears.]]> & sobbing & catatonic states down, I was then able to think rationally about what to do next. Here was my concern at this point: I have never in the 13 years of my implants had a mammogram. Why my PCP would not have sent me for breast imaging of some sort after noting 3 years in a row that I had a benign breast lump really had me confused. I most certainly wasn't going under the knife with out Ultrasounds, MRI & Mammogram & blood work done first. I took these steps &
scheduled a 2nd opinion with another Surgeon. By this point a week later I had red streaks & swelling running from my left breast under my arm pit, around to my shoulder blade. I had raised veins on top of my breast that were swollen & fire hot red. The 2nd surgeon said the same thing. Who did this to you? Unknown to me at this point, was my original surgeon in 1998 was not a board certified surgeon nor were my implants FDA approved & the shell of my implant was made out of Silicone & various other toxins. I found out that day at the 2nd surgeons
office. Surgeon advised me yes, we need to get these implants & contracture out & I'm not taking any of your skin until biopsy & pathology reports come back. I had surgery 3 days ago. I have a drain in my left breast & Surgeon called me yesterday at home to let me know I had straw colored fluid where it shouldn't be in my capsular contracture & between my implant, he stated I have clinical presentation of Anaplastic Large Cell Lymphoma, its enough to diagnoses ALCL. Guess we will see what pathology has to say. My 1st Question is this. How can a
woman give informed consent when they are not advised via literature, documents or verbally that the shell of saline implants are indeed silicone & other toxins? Its not possible to give informed consent when you are not informed in any way. I WOULD HAVE NEVER had these implants if I had known. I have basically stayed sick for 12 years. I lost my dignity, my faith, my passion, my husband, my family & friends. Until it reared its ugly head through my breasts I never once considered it was my implants nor did any doctor until now. I can say I am a definite mental & emotional basket case & I have earned the right to be. So, how does a women pick up the pieces & what does she do from here? My heart goes out deeply to every women enduring this hellish nightmare. I too, feel your pain & fears.]]> http://www.breastimplantsupport.org/showthread.php?tid=9420 Mon, 20 Feb 2012 18:46:03 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9420 i cant find the right bra, what kind of pain am i going to be in, i have low tolerance ..yikes]]> i cant find the right bra, what kind of pain am i going to be in, i have low tolerance ..yikes]]> http://www.breastimplantsupport.org/showthread.php?tid=9419 Mon, 20 Feb 2012 09:47:44 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9419
Many thanks! Xxx]]>
Many thanks! Xxx]]> http://www.breastimplantsupport.org/showthread.php?tid=9418 Sun, 19 Feb 2012 01:47:50 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9418 My name is Louise from the UK and I am a new member to the forum.
I'm 31 years old and was implanted in 2005. For the first 3 years I was really pleased with the results of my surgery and had no health issues, very fit and active, hardly ever went to the doctors or took medications.
In 2009 I started to feel very fatigued, achey and everything began to feel difficult to do. One of the first physical symptom to appear was a patch of skin over the bridge and sides of my nose which started to scab up, ache, and shed skin(very similar to a lupus looking butterfly rash)since it first began it has never stopped, the cycle is continuous, although it has spread more outwardly across my face. Other symptoms not listed include an itchy, burning, crawling sensation all over my body from my scalp to my toes, the skin is now shedding of the bottom of my feet, my scalp and my lower back, all of this is with extreme tiredness and pain throughout my body, which makes even simple tasks so hard to do. I have such pain in my face and throat and my feet and hands feel as though they are sprained all of the time. I have seen so many doctors and specialists, had so many blood tests! I have had all my wisdom teeth out in the hope that they were causing problems, possibly an infection, to no avail, so I have probably had my teeth out when I did not need to. Because of the itchy and crawling nature throughout my body, I autamatically thought it might be some sort of parasite or infection and was given steroid creams by my doctor, which I slathered on not realising the damage it would cause, my facial skin has been thinned and damaged. Doctors suspected lupus, although the tests came back negative twice, Dermatologist said the problem is not coming from my skin and does not know what it is, Rheumatologist could not explain it either. My thyroid results came back as abnormal but then corrected itself, my ana's to begin with were sky high, then returned to normal. I am now in the process of having mri scans and have had to cease going to work as it's gotten so bad. I feel a shadow of the energetic woman I used to be, everything in my life has been put on hold. All the doctors have been so rude and cold, as they can't explain it and I feel that they are starting to believe that it is all in my head. I now feel that there is a good chance that my implants are causing all of this, it was always there in my mind, I guess I hoped it was something else. Can I just mention that I had a bike accident and fractured my back a few months before all of this started..which makes me wonder if I ruptured an implant, although at the time I didn't feel as though I did. My question is has anyone had similar experiences with their skin? symptoms starting from a possible accident? can anyone recommend a breast surgeon in the uk who removes the implants enbloc with good results? do people explanted feel that they are getting better?
I am so sorry for the epic writing. Just i feel it's important to tell people of symptoms possibly not listed or spoke about. I appreciate any information. Many thanks and I hope you all start feeling better very soon
Louise x]]> My name is Louise from the UK and I am a new member to the forum.
I'm 31 years old and was implanted in 2005. For the first 3 years I was really pleased with the results of my surgery and had no health issues, very fit and active, hardly ever went to the doctors or took medications.
In 2009 I started to feel very fatigued, achey and everything began to feel difficult to do. One of the first physical symptom to appear was a patch of skin over the bridge and sides of my nose which started to scab up, ache, and shed skin(very similar to a lupus looking butterfly rash)since it first began it has never stopped, the cycle is continuous, although it has spread more outwardly across my face. Other symptoms not listed include an itchy, burning, crawling sensation all over my body from my scalp to my toes, the skin is now shedding of the bottom of my feet, my scalp and my lower back, all of this is with extreme tiredness and pain throughout my body, which makes even simple tasks so hard to do. I have such pain in my face and throat and my feet and hands feel as though they are sprained all of the time. I have seen so many doctors and specialists, had so many blood tests! I have had all my wisdom teeth out in the hope that they were causing problems, possibly an infection, to no avail, so I have probably had my teeth out when I did not need to. Because of the itchy and crawling nature throughout my body, I autamatically thought it might be some sort of parasite or infection and was given steroid creams by my doctor, which I slathered on not realising the damage it would cause, my facial skin has been thinned and damaged. Doctors suspected lupus, although the tests came back negative twice, Dermatologist said the problem is not coming from my skin and does not know what it is, Rheumatologist could not explain it either. My thyroid results came back as abnormal but then corrected itself, my ana's to begin with were sky high, then returned to normal. I am now in the process of having mri scans and have had to cease going to work as it's gotten so bad. I feel a shadow of the energetic woman I used to be, everything in my life has been put on hold. All the doctors have been so rude and cold, as they can't explain it and I feel that they are starting to believe that it is all in my head. I now feel that there is a good chance that my implants are causing all of this, it was always there in my mind, I guess I hoped it was something else. Can I just mention that I had a bike accident and fractured my back a few months before all of this started..which makes me wonder if I ruptured an implant, although at the time I didn't feel as though I did. My question is has anyone had similar experiences with their skin? symptoms starting from a possible accident? can anyone recommend a breast surgeon in the uk who removes the implants enbloc with good results? do people explanted feel that they are getting better?
I am so sorry for the epic writing. Just i feel it's important to tell people of symptoms possibly not listed or spoke about. I appreciate any information. Many thanks and I hope you all start feeling better very soon
Louise x]]> http://www.breastimplantsupport.org/showthread.php?tid=9417 Sat, 18 Feb 2012 00:38:54 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9417 I have been dx with lupus / mixed connective tissue disease, feeling terrible for about 6 years. Had saline implants put in may 2000. I have had my left breast deflated for about 9 months but dr kept telling me it was not an issue and safe . Since my financial situation is not good presently and I was tired of plastic surgeon wanting t replace rather than remove I have put off dealing with this but now my health is worse!!
I need to take care of it once and for all and at least see if my lupus issues improve after explant. I have an appt with Dr. Ahn on Wednesday in NYC. Im worried bc its very expensive and just the consultation is $200. The only other doctor I see in my area (CT) is Dr. Lyons. Since we have been in financial distress after my husband being laid off I want to do it right the first time since I can't afford multiple surgeries.
Does anyone know if Dr. Ahn will help with getting insurance to cover some? Is she sensitive to saline impacts and autoimmune disease or is she going to react like all other doctors and tell me implants are not the cause at all?
Dr. Lyons is much closer but I have not heard anything about him , can anyone give me feedback on any of these doctors? I would love to talk to any of you who have used either Dr, please.
Thank you
mel]]> I have been dx with lupus / mixed connective tissue disease, feeling terrible for about 6 years. Had saline implants put in may 2000. I have had my left breast deflated for about 9 months but dr kept telling me it was not an issue and safe . Since my financial situation is not good presently and I was tired of plastic surgeon wanting t replace rather than remove I have put off dealing with this but now my health is worse!!
I need to take care of it once and for all and at least see if my lupus issues improve after explant. I have an appt with Dr. Ahn on Wednesday in NYC. Im worried bc its very expensive and just the consultation is $200. The only other doctor I see in my area (CT) is Dr. Lyons. Since we have been in financial distress after my husband being laid off I want to do it right the first time since I can't afford multiple surgeries.
Does anyone know if Dr. Ahn will help with getting insurance to cover some? Is she sensitive to saline impacts and autoimmune disease or is she going to react like all other doctors and tell me implants are not the cause at all?
Dr. Lyons is much closer but I have not heard anything about him , can anyone give me feedback on any of these doctors? I would love to talk to any of you who have used either Dr, please.
Thank you
mel]]> http://www.breastimplantsupport.org/showthread.php?tid=9416 Fri, 17 Feb 2012 13:37:52 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9416
I had bilateral breast augmentation in 1998, In 2000 I noticed that my right implant was not right, it took me four years to get them to believe that something was wrong, in 2005 my right breast was opened up and it was discovered that the implant had ruptured.In 2006 I had to have my left one replaced as that went hard causing a Capsular Contracture. I have developed a range of illnesses since. I am again waiting to have further surgery to remove a capsular contracture to my right breast and the possibility of a ruptured left. Again I am developing the terrible night sweats and joint problems that I experienced in 2000 - 2005, 2006 - 2008. I believe that the silicone from the implant has be a major cause.

Many women who have had implants PIP or NON-PIP have experienced a range of health problems, It is important that the Government and the MHRA recognise that this could impact on the Public monies in long term health care. Thorough testing is needed NOW to acertain the long term effects on health related issues associated with ALL TYPES OF IMPLANTS.

WE NEED TO BE MONITORED AND TESTED ON A REGULAR BASIS

This will provide accurate data on the effects, and will hopefuly increase the guidelines for Implants as a whole.

http://www.change.org/petitions/mhra-and...iends_wall]]>
I had bilateral breast augmentation in 1998, In 2000 I noticed that my right implant was not right, it took me four years to get them to believe that something was wrong, in 2005 my right breast was opened up and it was discovered that the implant had ruptured.In 2006 I had to have my left one replaced as that went hard causing a Capsular Contracture. I have developed a range of illnesses since. I am again waiting to have further surgery to remove a capsular contracture to my right breast and the possibility of a ruptured left. Again I am developing the terrible night sweats and joint problems that I experienced in 2000 - 2005, 2006 - 2008. I believe that the silicone from the implant has be a major cause.

Many women who have had implants PIP or NON-PIP have experienced a range of health problems, It is important that the Government and the MHRA recognise that this could impact on the Public monies in long term health care. Thorough testing is needed NOW to acertain the long term effects on health related issues associated with ALL TYPES OF IMPLANTS.

WE NEED TO BE MONITORED AND TESTED ON A REGULAR BASIS

This will provide accurate data on the effects, and will hopefuly increase the guidelines for Implants as a whole.

http://www.change.org/petitions/mhra-and...iends_wall]]> http://www.breastimplantsupport.org/showthread.php?tid=9415 Fri, 17 Feb 2012 00:45:23 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9415

Now that is over.....

To be honest, I feel like I'm on an emotional roller coaster ride. Up one minute and down the next. This process has drained me emotionally. I wanted to say thank you to everyone. I don't know what I'd do without your support.

I spent this entire week reading threads on this forum, my eyes are blood shot, dry and tired, LOL. I can't believe how much I've learned, even so, I still have questions.

As some of you know, my implants are sub muscular, this concerns me.
Can the muscle re-attach itself to the chest wall if I use a compression wrap? Will wrapping prevent my breast tissue from fluffing?

I won't be getting a lift, stem cell or fat graphing. Would I or could I still benefit from massaging l-arginine powder with Progesterone cream over my breast? Do I have to use the cream indefinitely?

Thats all the questions I have for now. Thanks again ladies.]]>

Now that is over.....

To be honest, I feel like I'm on an emotional roller coaster ride. Up one minute and down the next. This process has drained me emotionally. I wanted to say thank you to everyone. I don't know what I'd do without your support.

I spent this entire week reading threads on this forum, my eyes are blood shot, dry and tired, LOL. I can't believe how much I've learned, even so, I still have questions.

As some of you know, my implants are sub muscular, this concerns me.
Can the muscle re-attach itself to the chest wall if I use a compression wrap? Will wrapping prevent my breast tissue from fluffing?

I won't be getting a lift, stem cell or fat graphing. Would I or could I still benefit from massaging l-arginine powder with Progesterone cream over my breast? Do I have to use the cream indefinitely?

Thats all the questions I have for now. Thanks again ladies.]]> http://www.breastimplantsupport.org/showthread.php?tid=9414 Thu, 16 Feb 2012 20:33:35 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9414 Hello im new to the site, i have p.i.p inplants, i have pain to my right breast i have them behind the muscle and the right one looks a different shape, hurts and uncomfortable the left is ripple.
]]> Hello im new to the site, i have p.i.p inplants, i have pain to my right breast i have them behind the muscle and the right one looks a different shape, hurts and uncomfortable the left is ripple.
]]> http://www.breastimplantsupport.org/showthread.php?tid=9413 Thu, 16 Feb 2012 17:15:54 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9413 http://www.breastimplantsupport.org/showthread.php?tid=9412 Thu, 16 Feb 2012 15:15:24 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9412 I go back to the Dr. that took out the gall bladder tomorrow.
I have been eating a very low fat diet, trying to help liver out. My liver enzymes where elevated 6 days after surgery which I found out when I went back up to hospital on the 8th. I had to have them checked again yesterday.
I'll let you know what Dr. tells me tomorrow, thanks for listening.]]> I go back to the Dr. that took out the gall bladder tomorrow.
I have been eating a very low fat diet, trying to help liver out. My liver enzymes where elevated 6 days after surgery which I found out when I went back up to hospital on the 8th. I had to have them checked again yesterday.
I'll let you know what Dr. tells me tomorrow, thanks for listening.]]> http://www.breastimplantsupport.org/showthread.php?tid=9409 Wed, 15 Feb 2012 23:13:45 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9409 Just wondering is there's any advice on detoxing... And where I can find a detox plan?
Thanks x]]> Just wondering is there's any advice on detoxing... And where I can find a detox plan?
Thanks x]]> http://www.breastimplantsupport.org/showthread.php?tid=9408 Wed, 15 Feb 2012 23:02:20 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9408 Just thought I'd update.
I have booked my explant!!!! March 28th.
I decided not to go with original surgeon/clinic as they basically are struggling to find a specialist breast surgeon who is 'willing' to take me on!?! Hate them, and would not even trust them to operate on my cat!!!
That's another story...
So I have decided to find the money and have booked Wales' top breast reconstruction surgeon 10 mins from my home (so wont have to miss my little girl too much)
Whoopee!!!!
I actually cannot wait to get these out!!
I'm really starting to hate the way I look WITH boobs!!!
Started shopping for padded bras and chicken fillets already! :)

Ladies who have explanted- what size bras should you get? And do you need a sports bra?

Thanks :)
X]]> Just thought I'd update.
I have booked my explant!!!! March 28th.
I decided not to go with original surgeon/clinic as they basically are struggling to find a specialist breast surgeon who is 'willing' to take me on!?! Hate them, and would not even trust them to operate on my cat!!!
That's another story...
So I have decided to find the money and have booked Wales' top breast reconstruction surgeon 10 mins from my home (so wont have to miss my little girl too much)
Whoopee!!!!
I actually cannot wait to get these out!!
I'm really starting to hate the way I look WITH boobs!!!
Started shopping for padded bras and chicken fillets already! :)

Ladies who have explanted- what size bras should you get? And do you need a sports bra?

Thanks :)
X]]> http://www.breastimplantsupport.org/showthread.php?tid=9407 Wed, 15 Feb 2012 19:05:42 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9407 http://www.breastimplantsupport.org/showthread.php?tid=9406 Wed, 15 Feb 2012 18:49:39 +0000 http://www.breastimplantsupport.org/showthread.php?tid=9406
I have Kolbs book but need help as far what I should be taking before and after. It does not reaslly specify. Someone said candida before. I know we are not doctors but if you have been through explant and know of a good before and after protocol please share. I am strapped financially so I don't know if I can afford Kolb. Share your thoughts. Good Bless.

I have saline implants.


Barb]]>
I have Kolbs book but need help as far what I should be taking before and after. It does not reaslly specify. Someone said candida before. I know we are not doctors but if you have been through explant and know of a good before and after protocol please share. I am strapped financially so I don't know if I can afford Kolb. Share your thoughts. Good Bless.

I have saline implants.


Barb]]>