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Leesa
Member in Phase 3
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Posted: Tue Jul 18th, 2006 07:50 |
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This is a letter that I wrote to my friends and family. I hope that It helps some of you in phase one!
My 6-month anniversary and Sarcoidosis Update
James 1:2-4 -- Whenever trouble comes your way, let it be an opportunity for joy. For when your faith is tested your endurance has a chance to grow. So let it grow, for when your endurance is fully developed, you will be strong in character and ready for anything. (NLT)
I received the above by email this morning…what perfect timing, just as I was about to sit down and reflect and write about my progress on my medical treatment. I cannot believe that it has been 6 months since I have started the Marshall Protocol! What a journey…I am grateful that I was brave enough to take it!
My health update:
I am COMPLETELY weaned off of all eye drops since the treatment started I have NOT had uvitus (inflammation of the eye-very painful and dangerous to your eyes). Last year I had it approximately 6 times or more. My eyes are not 100% yet, but they are doing great and I may get to wear my contacts again in the near future J!! By the way, I was at the doctors about 50 times last year total, at lease once a week and this year I can count the times on my hand, what a difference! None of my swelling has returned and over all I feel very good. I still have a bad day here and there and may have a few more as I just started phase 3 (the final phase before maintenance) this past week and have added one more antibiotic to the mix. I may have some reactions to the new combination, but if you remember, it is good, to feel bad at times, it means that you are killing the bugs (the bacteria) and getting better! All in all, I already feel better than I have in almost 2 years…and I am only a third of the way there (or so)J.
I was able to attend a conference in LA a month ago. The Auto Immunity Research Foundation sponsored it; the foundation leads my medical treatment, the Marshall Protocol http://www.marshallprotocol.com (http://www.autoimmunityresearch.org for more info or to make a donation).I took so much away from the conference, but what I wish to share with you all is that before the conference I was pretty sure that I had chose the right path to heal from my chronic illness, but after attending the conference I now am 100% positive that I have chosen the right treatment! If my own healing journey is not enough, I got to see and hear the stories of healing of many others that were way more symptomatic than me. They have now been on the treatment a year or more and are nearly cured or the few who have completed the treatment and are now cured, WOW, what affirmation. We also had the opportunity to listen to doctors speak about the protocol and they told of how and why it works, the science behind it is fascinating. If you know of anyone who suffers an autoimmune disease (Sarcoidosis, chronic fatigue, rheumatoid arthritis, lymes disease, etc…. please send them this info.)
I was honored to be asked to speak at the conference. I spoke about to how I decided to do the protocol and how I let others know about it, and how I have made adjustments to my life to accommodate my treatment and how I am mentally in such a good place now. A positive attitude makes all the difference in the world when healing. Here I am below in the photo at the speaker table and then speaking…do you just love the glasses??
We just got back from a week family vacation. We rented a beach house in Galveston. We had to cover the windows for me…but was so wonderful to spend time together as a family. I wanted to try to thank the ones who have done the most for me, my family. We had a wonderful time; I got to do many activities…some even out in the sun. I made it all day at Moody Gardens, even went out on a big paddleboat! It was sooooooooo wonderful. I am so thankful for that time together. Patrick and the kids loved the beach and I loved sitting out on the balcony overlooking the Gulf at dusk.
Hope this helps to update you. Let me know if you have any questions. Things are really going well for me, maybe a bit better than I had expected (and my doctor thinks so too). I am even planning to go to Guatemala again…my goal is next summer. I plan for me and the kids to go for an extended vacation with Patrick joining us for a week. I am confident that I will be up to much more sun by then and that I will physically being doing so much better!
I truly understand James 1:2-3 (NIV) “Consider it pure joy, whenever you face trials of many kinds, because you know the testing of your faith develops perseverance”. What a blessing to have grown through this trail instead of the alternative.
God Bless,
Leesa
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Sarcoidosis(12-04 biopsy):Uvitus-eyes, Swollen- Parotid Glands, Granulomas-arms, some joint pain & fatigue; Started MP 1-06;Phase 2 03-06 Phase 3 07/06 NO MORE Eye Drops! D test 11-04:1,25D-70 & 25D-46;(9-06)25D-17 (1-07)& 16(2-2008)
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Leesa
Member in Phase 3
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Posted: Sat Aug 12th, 2006 11:07 |
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I am going to cut and paste my last post on the phase 2 and 3 board for those of you who can not access it there. I HOPE IT HELPS...
MP Since Jan 2006, Week 32 of the MP in Phase 3-ramping my 3 abx
Weaned OFF Nevonac eye drops!!
I cannot believe how long it has been since I have posted. I have been soooooo busy with life. That is strange to say since I just came off of 6 months of the slowest pace that life has ever given me in Phase 1 and 2 of the MP! Mentally and physically I started to do better right about conference time (June). Then I think in LA meeting others on the protocol gave me a confidence that I did not have before. A confidence that this treatment/protocol will and is ABSOLUTELY working. After the conference, I began to ease back into life with modifications of course. It has been wonderful to come out of the cave.
All my kids celebrated birthdays in July and we had wonderful indoor parties roller-skating and ice-skating! Then I signed my 5 year olds up for ballet and gymnastics and I now take them to class (I used to have others take them to school for me). I signed my two year old up for gymnastics, music and indoor swimming lessons-mommy and me classes and I take him MYSELF, AND PARTICIPATE and all is well. I started doing some errands and grocery shopping again (yuck to all that J). I also started taking a Spanish class 2X a week (it is my goal in life to be fluent in Spanish and I had to put it on hold while I was sick) and I started working more-about 10 hours a week (out of my home office) and we started going back to church as a family! ALL THAT after staying home and missing out on everything out of the house except doctors appointment and a few school functions. And-most importantly-I am doing and feeling really GREAT. I make a ton of modifications to make what I do MP friendly, but I am living life again and I LOVE IT!
I make sure that the places I go are not full of windows. I still have all of my windows in my home covered, but I took the ready shades out from under the wooden blinds or curtains in the kids rooms and dining room, rooms that I am not in much. I hope to take the blackout curtains out from under my honeycomb blinds in my main kitchen and living areas sometime in the next year and let a bit more light in, but I am not ready yet. I obtained a handicap-parking placard from my doctor and that helps a ton, remember I live in Houston and it is 95-100 degrees everyday, so I try to make my parking lot trips short. I wear all my clothes (a jacket/ or button up shirt over whatever shirt I have on, a hat, gloves (now fingerless, I LOVE THEM), and of course my NoIRS always (but I do not need sunglasses under them any more.) And then sometimes if I am in the first row, I take all that off (never my glasses) and run inside and I shop or whatever and do really well without having so many clothes on and getting so hot. Then I run out and put it all on in the car. And other times, I just wear my layers in and take them off inside, but inside almost any building I can walk around and shop or take my kids to a class and if there are not too many windows I do really well. I can even eat at a restaurant if I am in the middle of the restaurant or not near any windows without being all covered from head to toe. It is great. I even started wearing contacts again sometimes and I ordered the NoIR wrap around (#35) and I now look like I am just wearing sport sunglasses, it is so cool! Not to mention, if I am in my “MP clothes” my confidence is much higher…. funny sunglasses or not J I know I am getting better, so what I look like is not really so important, I do not even notice if people are looking at me anymore and if they are I am sure it because they think I am a movie star and they are trying to figure out just who I am!!
Ok, now how do I feel? I am doing well on Phase 3. I have eye herxes more now than any other type of herx. Every time I up the clindy, I get an eye herx. They feel yucky are a bit red and I have a ton of eye mucus and sometimes a ton of tearing all day long. Every once in a while I feel the need to add a drop of Nevonac Then at the end of a week or so, better. So that is good news, I am excited for when my eyes are “normal” again. I mentioned above that I am in contacts again. I wear soft lenses (always have) but my doctor is trying to get me to go over to gas permeable because he says that overall I will have better results and it may help my dry eyes (they are still a bit dry). I am not sure that I will be able to make the switch cuz of the way my eyes feel with the hard ones in, I am supposed to give it a week or so and if they do not work I can get my money back. I have not had to cancel out on family events cuz of herxes or sun flairs at all in Phase 3, my herxing seems more predictable so far and tolerable, but I do notice body aches when I am tired. I do not have as many mental herx days either.
I now have a nanny to help me out with things at home, she is here part time daily M-F and it really helps. She helps with the kids, takes them out to play and swim while I work and then she helps with household stuff too. Having a nanny and the fact that I consistently feel good have helped me to enter life again. I can actually concentrate in my Spanish class and learn and retain info…I could not do that before the MP. I also started Yoga again and I can do that and it makes me feel real good physically and mentally. I am planning on joining the YMCA in September, when my little boy goes to a preschool program 2 days a week. They have blinds on their windows and I have permission to shut them in the weight room. I will lift weights on the machines at lightest levels and I will not push it. I will also attend Yoga there in a dark room with the lights off. I am excited for this. AND after daylight savings is over I will get out again at night for walks with the dog and family. I bought an Australian swimsuit (after getting that as an idea from another MP’er thanks! And I now can go to indoor water play areas or indoor pools with my kids EVEN if they have windows. I have a long sleeve top and pants that is a swimsuit and it also has a matching hat, my feet and hands and face show…. but I do real well, no sun flares after! IT IS GREAT!! I am hoping to have a family vacation at a large indoor water park in the spring (they are all over up north). I also go outside once in a while when it is not 100 degrees (Houston). We bought a canopy/gazebo for the back patio. It is from Wal-Mart, you can take it up and down real easily and it is has great cover and even sides if the sun is low and shining in. So I now can go out a bit earlier than I could before in the evening and join the family. I even attended a block party, we moved the tent out into the street, and I have to admit after that I did feel a bit yucky; I was out a bit too early and too long. I was real covered up and I think the heat sometimes affects me as much or more than the sun.
The reason this post is so long and detailed is two fold. I want to shout from a mountaintop at how far I have come because I am sooo happy. I feel that if this is a good as it gets, I am lucky. But because I saw and spoke to the other members that are ahead of me on the MP and they are experiencing even more healing, I know for certain that I will too. So that adds even more to my joy to my life. And secondly, I wish to encourage anyone that is on the fence. THIS IS THE ANSWER; THE MP IS THE WAY TO GET BETTER. I AM RECOVERING FROM SARCOIDOSIS. I am doing so well after just 8 months that I know longer think of myself as Leesa: I have an autoimmune disease, Sarcoidosis, and I am a mom and wife…etc. I think I am Leesa, mom, wife, friend…and I am recovering from sarc is on the list somewhere, but not first anymore. I modify my life, but my disease is not my life. I make the life; the disease just makes me modify it slightly. I AM BACK AND I LOVE IT, not to mention the growth that I have gone through in my head and in my heart, it has made me a better person, mom, wife than before. What a blessing.
I know that I have been busy lately, but if can help encourage anyone, please pm me or email me (leesa.shanahan@sbcglobal.net), I am willing to talk to you on the phone or by email and tell you my story or encourage you. Both my doctors are amazed at my recovery and I am too. I encourage you to follow the MP just like we all are. Do the protocol in the beginning just like you are told and then you will know your own personal limitations, but follow those of us who have proven that this works! I have my life and my family back thanks to Dr Marshall and those of you who encouraged me after my first post when I was unsure…THANKS to all of you!
~Unless you change how you are, you will always have what you’ve got~
The MP is the answer
Thanks to all!
Leesa
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Sarcoidosis(12-04 biopsy):Uvitus-eyes, Swollen- Parotid Glands, Granulomas-arms, some joint pain & fatigue; Started MP 1-06;Phase 2 03-06 Phase 3 07/06 NO MORE Eye Drops! D test 11-04:1,25D-70 & 25D-46;(9-06)25D-17 (1-07)& 16(2-2008)
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Leesa
Member in Phase 3
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Posted: Sun Oct 29th, 2006 23:24 |
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I am a mom of three small kids also (5,5 and 2) and I led a very active outdoor life, I was a marathon running in training for a half marathon last year. I SAID all of the same things that you are saying now, over and over. I could not believe I became in as I am an independent distributor for health and nutrition products and was sooo healthy until my quick onset and diagnosis with sarc. (I had uvitus in my eyes and swollen parotids in my face). I started the mp almost 11 months ago and am now feeling better than ever. I have a ways to go but am getting back to real life again. Here is a post that I put out for my 6 MONTH update and I am way better now!!!!!! Read this and then if wish to call me, send me a private message or email and we will talk over the phone. I am happy to help. By the way...the MP was one of the best things that I have ever decided to do in my life!!! I am getting my health back for me and my family and I just know that in about a year or so I will be back to normal! 
James 1:2-4 -- Whenever trouble comes your way, let it be an opportunity for joy. For when your faith is tested your endurance has a chance to grow. So let it grow, for when your endurance is fully developed, you will be strong in character and ready for anything. (NLT)
I received the above by email this morning…what perfect timing, just as I was about to sit down and reflect and write about my progress on my medical treatment. I cannot believe that it has been 6 months since I have started the Marshall Protocol! What a journey…I am grateful that I was brave enough to take it!
My health update:
I am COMPLETELY weaned off of all eye drops since the treatment started I have NOT had uvitus (inflammation of the eye-very painful and dangerous to your eyes). Last year I had it approximately 6 times or more. My eyes are not 100% yet, but they are doing great and I may get to wear my contacts again in the near future J!! By the way, I was at the doctors about 50 times last year total, at lease once a week and this year I can count the times on my hand, what a difference! None of my swelling has returned and over all I feel very good. I still have a bad day here and there and may have a few more as I just started phase 3 (the final phase before maintenance) this past week and have added one more antibiotic to the mix. I may have some reactions to the new combination, but if you remember, it is good, to feel bad at times, it means that you are killing the bugs (the bacteria) and getting better! All in all, I already feel better than I have in almost 2 years…and I am only a third of the way there (or so)
I was able to attend a conference in LA a month ago. The Auto Immunity Research Foundation sponsored it; the foundation leads my medical treatment, the Marshall Protocol http://www.marshallprotocol.com (http://www.autoimmunityresearch.org for more info or to make a donation).I took so much away from the conference, but what I wish to share with you all is that before the conference I was pretty sure that I had chose the right path to heal from my chronic illness, but after attending the conference I now am 100% positive that I have chosen the right treatment! If my own healing journey is not enough, I got to see and hear the stories of healing of many others that were way more symptomatic than me. They have now been on the treatment a year or more and are nearly cured or the few who have completed the treatment and are now cured, WOW, what affirmation. We also had the opportunity to listen to doctors speak about the protocol and they told of how and why it works, the science behind it is fascinating. If you know of anyone who suffers an autoimmune disease (Sarcoidosis, chronic fatigue, rheumatoid arthritis, lymes disease, etc…. please send them this info.)
I was honored to be asked to speak at the conference. I spoke about to how I decided to do the protocol and how I let others know about it, and how I have made adjustments to my life to accommodate my treatment and how I am mentally in such a good place now. A positive attitude makes all the difference in the world when healing. Here I am below in the photo at the speaker table and then speaking…do you just love the glasses??
We just got back from a week family vacation. We rented a beach house in Galveston. We had to cover the windows for me…but was so wonderful to spend time together as a family. I wanted to try to thank the ones who have done the most for me, my family. We had a wonderful time; I got to do many activities…some even out in the sun. I made it all day at Moody Gardens, even went out on a big paddleboat! It was sooooooooo wonderful. I am so thankful for that time together. Patrick and the kids loved the beach and I loved sitting out on the balcony overlooking the Gulf at dusk.
Hope this helps to update you. Let me know if you have any questions. Things are really going well for me, maybe a bit better than I had expected (and my doctor thinks so too). I am even planning to go to Guatemala again…my goal is next summer. I plan for me and the kids to go for an extended vacation with Patrick joining us for a week. I am confident that I will be up to much more sun by then and that I will physically being doing so much better!
I truly understand James 1:2-3 (NIV) “Consider it pure joy, whenever you face trials of many kinds, because you know the testing of your faith develops perseverance”. What a blessing to have grown through this trail instead of the alternative.
____________________
Sarcoidosis(12-04 biopsy):Uvitus-eyes, Swollen- Parotid Glands, Granulomas-arms, some joint pain & fatigue; Started MP 1-06;Phase 2 03-06 Phase 3 07/06 NO MORE Eye Drops! D test 11-04:1,25D-70 & 25D-46;(9-06)25D-17 (1-07)& 16(2-2008)
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heenie
Member
| Joined: | Wed Feb 7th, 2007 |
| Location: | Pennsylvania USA |
| Posts: | 35 |
| Status: |
Offline
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Posted: Fri Feb 16th, 2007 13:22 |
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Hi Leesa,
I love the fact you are a believer. I am almost ready to start the MP but honestly am a little scared. I somehow came across a post you wrote (this site is H-U-G-E!! I feel like this after a couple hours- !!).
Anyway, you said "I spoke about to how I decided to do the protocol and how I let others know about it, and how I have made adjustments to my life to accommodate my treatment ". Can you share with me these things?
I believe I have been led to this protocol, but as an over-thinker, we can talk ourselves in or out of most things. This is my, and especially my husband's, problem right now.
Look forward to hearing from you l,
Heenie
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MP2/27/07;Chr.lyme(17yrs),CF,FM,systemic OA,DGD,comp.hyster@36,hypothryd.,Insomnia,Renauds,Migraines,MVP,Armour thyr.BID,T3BID,BioHRT estr/prog/test,25D-36, 1,25D pending
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Belinda
Research Team
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Posted: Fri Feb 16th, 2007 14:02 |
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Heenie,
Leesa shared her compelling story and her tips at our 2006 Conference in Los Angeles, "Recovery from Chronic Disease," and it is all on DVD. The DVD is great, because you get to see and hear what Leesa says in her own words in the session on "Reaching Out - Letting Family and Friends Know About the MP."
I suspect you will want to obtain a copy of our DVD, which is available by clicking on the DVD images in the upper right-hand corner of the page. We have a webpage with a form that allows you to make a donation to the Autoimmunity Research Foundation and receive that DVD "Recovery from Chronic Disease."
All the best,
Belinda
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areeser
Member
| Joined: | Mon Mar 26th, 2007 |
| Location: | |
| Posts: | 26 |
| Status: |
Offline
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Posted: Wed May 9th, 2007 09:09 |
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Dear Leesa,
I read read your posts. Thanks. I am a single mom with five daughters.
Four of these precious gals have lyme. They are very ill. We are in the
process of implementing the MP. We are excited but are aware a lot
of work and discipline is ahead.
We are part of the family of God. OUr goal is two fold: to find healing through
the MP, and to honor our Father during this time. His plans and purposes are
always good.
Thanks for your very encouraging words and courage.
In Him,
Susie(areeser)
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Res MP: 5 daughters w Lyme: meds:
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Mary21
Member in Phase 3
| Joined: | Sun Aug 26th, 2007 |
| Location: | USA |
| Posts: | 121 |
| Status: |
Offline
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Posted: Fri Aug 31st, 2007 14:13 |
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Leesa-
First of all thank you for sharing your story. I am originally from Houston and now live in Oklahoma City. My life sounds very similiar to yours. I am very active, have always been athletic, very independent and love to have several aggressive projects going at all times.
I have been diagnosed with Sjogrens and RA but think that I have more extensive problems than that. My mother died from autoimmune and I see myself following in her footsteps at this point.
I am planning to start the MP in early October. I have to get some things done before I begin.
VickiLast edited on Fri Aug 31st, 2007 15:54 by Aussie Barb
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RA, Sjogrens/Ph 1 1/7/07/Ph 2 12/4/07/,calcium & mag, Noirs 2%, 25-D-28.4. I-25-47.5
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Deb Grabetz
Member in Phase 2
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Posted: Fri Aug 31st, 2007 15:41 |
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Leesa...Thank you ever so much for your report it is so encouraging to read success stories over and over...I've been on Phase I now for about six weeks and although I am pushing through the herx, I know I'm in the right place. Oddly enough with this Sarc that I've carried around with me for 16 years now, I didn't suffer much pain (not the kind I'm experiencing now with IP!)...but struggled with so many symptoms through the years I WAS beginning to think I was a little nuts. I never imagined what it could be like to live in a body that is "well"...
With debilitating Neuro symptoms in 1991, I raised my three children...I tried to be a good mom along the way...and my kids learned to do laundry for themselves and take care of a lot for each other, which has made them very responsible adults! I went unDx'd...there was not enough energy to keep going to docs who would tell me it was this, it was that, only to know I had something very serious going on, much deeper than what they were seeing...
So greatful today I am, that this year, in a very severe second flare I was finally Dx'd through my lymph. I spend most of my time reading MP...and dreaming of a time when I will be back on my feet and traveling...I'm on a medical right now and my energy span is only about two hours a day on my feet TOTAL! So, it is a very challenging time...but I find my strength right here on this site...and your scripture reading was the ultimate...as I totally believe we are always tested for a greater purpose! Thank you for sharing! Deb
Last edited on Fri Aug 31st, 2007 15:42 by Deb Grabetz
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Sarcoidosis/lungs, lymph,liver, GI, neuro, D125,42, Ph1,7/07, Ph2,3/08,cover up, NoIRs, low lux home, not working, 4/07D25/11 1/08D25-0 Weaned Pred with MP/ CranialSacral weekly
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Leesa
Member in Phase 3
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Posted: Sat Sep 1st, 2007 01:55 |
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Wow, I just logged into my own thread from last OCTOBER, I have been so busy that almost a year has gone by and I did not read any of the comments that were beneath my own post. I am so SORRY, I guess I thought that I got notified if I received a reply. OOPS!
Where do I start? To you all above post that I did not answer, I am so sorry that I did not reply to you, the purpose of writing that post was partially for me, but mostly for others. I would have replied if I had known.
Since last Oct… we decided that I was well enough to take the black out curtains off the windows and attempt to put our house on the market. We wanted to move to a place in Houston that had more trees; it is called Kingwood, The Livable Forest! There are trees everywhere and hiking and biking trails and really SHADED parks for the kids. We decided that this would improve the quality of life for all of us with me on the MP and wanting to live life at the same time as getting better! I took the blinds down and did okay, we put our house on the market and it sold in 2 weeks and we had to be out 1½ weeks after that if we wanted to sell. We had 2 back-to-back family vacations, nowhere to live and I was on the MP! Wow what now??? J We did it all and I am okay, we went on a vacation to the beach with my family for a week, I stayed inside most all of the time, but did great! Then we moved into my brother in laws house (he had no blinds on his living room windows, I was scared), then we went to our ski house in Tamarack Idaho and I even want skiing for 2 of the days! (How much more covered up can you get than skiing? J) Then we moved into our new house as I was celebrating 1 year on the MP: no more Uvitus, no more facial swelling, no more grandulomas on my skin, my vitamin D going down and the fact that I NEW I was getting better.
I checked my kids into school and began life again. Let me tell you, I modify everything I do, but not too much any more. I look pretty normal, but I wear longer pants and a light shirt over my t-shirts outside in the sun and a cute little hat most of the time and sun glasses all the time outside when it is sunny. But I go for walks in the woods, I watch my kids sports, I take them everywhere, I go where ever I want indoors and sometimes even outdoor if it is really covered, we had the kids b’day party at an outside cowboy ranch under a totally covered barn area, I did fine and loved every minute of it. I even went boating recently under a cover all day wearing a long sleeve and long pants swim suit, a matching hat and sunglasses! I have to be honest…I even went on the tube behind the boat with each of the kids-one time each. That may have been over doing it, but it was GREAT, in other words it was worth it, I felt so good and so alive, I almost cried! What a great time I had. I do almost everything that I wish, with modifications. I go everywhere and feel pretty normal. I have to cut my outside time short, I still herx so I know that I am getting better still and I have mini set backs sometimes, but it all comes with getting better. I just take each day as it comes. However, what I do know for certain is: I am WAY better than I would have been, I am on the road to recovery, and I will be healed from this Sarc. Someday and all of its related issues. I am a better person; a better wife, a better mother and I have a way better life because I did this. I trusted the MP, God and my family. Because of my faith, I am getting there little by little, inch by inch, and mile by mile. I know that I will even run again (maybe not another marathon, but a 5K or 10 K), play again and some of the time maybe even outside and live a full life again, in the not so distant future…
If you wish to know more and I do not reply to you, it just means that 3 little kids need me almost all of the time, and thank goodness, the computer can wait! So send me an email or a pm.
With all of you in mind- my best for you all,
Leesa
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Sarcoidosis(12-04 biopsy):Uvitus-eyes, Swollen- Parotid Glands, Granulomas-arms, some joint pain & fatigue; Started MP 1-06;Phase 2 03-06 Phase 3 07/06 NO MORE Eye Drops! D test 11-04:1,25D-70 & 25D-46;(9-06)25D-17 (1-07)& 16(2-2008)
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Mary21
Member in Phase 3
| Joined: | Sun Aug 26th, 2007 |
| Location: | USA |
| Posts: | 121 |
| Status: |
Offline
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Posted: Sat Sep 15th, 2007 02:18 |
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Leesa-
I am starting the Benicar last night. I really appreciated our conversation on the phone. Say a prayer for me and wish me luck!
Vicki
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RA, Sjogrens/Ph 1 1/7/07/Ph 2 12/4/07/,calcium & mag, Noirs 2%, 25-D-28.4. I-25-47.5
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Leesa
Member in Phase 3
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Posted: Sat Sep 15th, 2007 02:23 |
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I will pray for you and keep up with your posts...
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Sarcoidosis(12-04 biopsy):Uvitus-eyes, Swollen- Parotid Glands, Granulomas-arms, some joint pain & fatigue; Started MP 1-06;Phase 2 03-06 Phase 3 07/06 NO MORE Eye Drops! D test 11-04:1,25D-70 & 25D-46;(9-06)25D-17 (1-07)& 16(2-2008)
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