Guest guest Posted June 2, 2008 Report Share Posted June 2, 2008 Hi Alyssa- I saw that you posted once, but I'm not sure if anyone responded to your post. If you are in Texas...Dr. Melmed is your best bet for explant. I think the MAJORITY of us have MCS. For many of us, it began after we recevied our implants, and slowly crept up on us over time. I believe the majority of women who had MCS and then had explant, feel A LOT better! Many women here can relate...so ask lots of questions! ~Krista --- In , " amajaawa " <ecoalyssa@...> wrote: > > Hi all, > I'm a new member who is here learning about explant of saline implants > (among other things!). Been reading some of the emails here, and feel > so emotional over what I'm reading! Feeling such compassion and > respect for the women here, anxiety about the explant process, and > relief that I'm headed in the right direction. > > I've had my Mentor H/S implants for 12 years, and been sick for the > last 10. My long list of symptoms pretty much mirrors the ones I've > been seeing online - but big picture -- fibromyalgia, chronic fatigue > and MCS. Been too sick and MCS reactive to work regularly for the > last 5 years. (Just started doing consulting with some clients over > the phone, trying to get back in the swing of things.) > > We're in TX, so I called Dr. Rea's office in Dallas today - and they > referred me to Dr. Mellmed. I also left a message for the other Texas > dr, Dr. Montero. If anyone has any thoughts about these options, > these particular doctors, or anything else for that matter - I'm open > to suggestions and advice! > > Because of the MCS, we live " clean and green " , eat organic, and detox > gently but often. Are there any of you who have MCS and have gone > through the explant process? > > Thank you for being here on this site, and thanks in advance for any > information. > > Warmly, > Alyssa > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2008 Report Share Posted June 2, 2008 Hi Krista,Thank you so much for the email - I've been so anxious about this! I have an appt with Dr. Melmed this week, so I guess I'll get the scoop then about how he deals with MCS, re: drugs, etc. during and after surgery. My MCS crept up on me too - and then Wham! knocked me down completely. It's been an amazing process getting back on my feet - and now, to think that I could get better - boosted up another level in my health - it's pretty exciting. I'm picturing myself with energy again, feeling well, and able to go anywhere, travel, go out, play... I really appreciate this forum, I learn a lot from reading the posts. I'm sure I'll have more questions after meeting with the dr. this week.Thanks again,Alyssa On Mon, Jun 2, 2008 at 10:56 AM, Krista <seekingthetruthaboutimplants@...> wrote: Hi Alyssa- I saw that you posted once, but I'm not sure if anyone responded to your post. If you are in Texas...Dr. Melmed is your best bet for explant. I think the MAJORITY of us have MCS. For many of us, it began after we recevied our implants, and slowly crept up on us over time. I believe the majority of women who had MCS and then had explant, feel A LOT better! Many women here can relate...so ask lots of questions! ~Krista --- In , " amajaawa " <ecoalyssa@...> wrote: > > Hi all, > I'm a new member who is here learning about explant of saline implants > (among other things!). Been reading some of the emails here, and feel > so emotional over what I'm reading! Feeling such compassion and > respect for the women here, anxiety about the explant process, and > relief that I'm headed in the right direction. > > I've had my Mentor H/S implants for 12 years, and been sick for the > last 10. My long list of symptoms pretty much mirrors the ones I've > been seeing online - but big picture -- fibromyalgia, chronic fatigue > and MCS. Been too sick and MCS reactive to work regularly for the > last 5 years. (Just started doing consulting with some clients over > the phone, trying to get back in the swing of things.) > > We're in TX, so I called Dr. Rea's office in Dallas today - and they > referred me to Dr. Mellmed. I also left a message for the other Texas > dr, Dr. Montero. If anyone has any thoughts about these options, > these particular doctors, or anything else for that matter - I'm open > to suggestions and advice! > > Because of the MCS, we live " clean and green " , eat organic, and detox > gently but often. Are there any of you who have MCS and have gone > through the explant process? > > Thank you for being here on this site, and thanks in advance for any > information. > > Warmly, > Alyssa > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2008 Report Share Posted June 2, 2008 Hi Alyssa ( and all),I'm just back home after a vacation . . . Heartsick about all the young implanted women I saw. I wanted to tell everyone of them about us!Alyssa, I had MCS too. I didn't connect it to my implants until a couple years after my explant when I realized my life wasn't controlled by MCS any longer. . . . I have no doubt you will gradually get better too.Right now, you need proper explant (that mean ALL the capsule must come out), then lots of detoxing. We'll help you as much as possible!Hugs and prayers,Rogene Quote Link to comment Share on other sites More sharing options...
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