Forum Replies Created
-
AuthorPosts
-
Thank you Jake, appreciate the direction.
Have a wonderful day!
Brenda
in reply to: Armour/Thyrolar?? Any advisement? #1070552I was wondering, I have been taking Armour and I find that I feel alot better, however, my doctor called me on Sunday to say that my brain was not secreating TSH as it is suppose to. He first wanted to drop me from 120mg of the Armour to 60Mg of the Armour, then said that Armour can not be regulated because it is not synthetic, so then he shared to start on 125mg of synthroid.
This confused me, how can Armour be on the market if it can not be standardized? Does anyone know where I can get more information about the Armour?
Thanks for your help
Brenda
Thank you each for your responses. My email address is nshimba@comcast.net
I was hoping to schedule a first meeting at a public place, maybe Dino’s in Castro Valley. They do have a room in the back that we could use. Does evenings work best or is a Saturday around noon better for peoples schedule?Brenda
Thank you Nancy…
I would love to get the materials. I will email you at your email address. I spoke with Sara from Berkely, very wonderful person….she has been so supportive and so informational…..I truly have appreciated all her help. I did speak to her about a support group and she shared that she would love to attend and help as much as possible.
Thank you again Nancy
HUGS
Brenda
Nancy Patterson wrote:Wow! It sounds like you are highly qualified to run a support group! The NGDF Support Groups have training, workbooks, etc. These are provided to you at no charge. IF you will e-mail me at "nancyngdf@bellsouth.net", I will send you the information. You sound as if you have done much of the work already. I can put you in touch with the former support group leader in Berkeley (one of our earliest support groups).Target has just recently changed to Walmart….it actually has not opened yet, but they have completed the construction on the building….we also have a IN and OUT Burger in the parking lot….Bakers Square closed…..
Lots of changes…………..
I’m really glad you like Texas…I was stationed at Ft. Sam Houston in 1978, I went to medical school there………….
HUGS
Brenda
Mickey65 wrote:Hey Brenda –So is the Target gone now across from Kragen?
The Rasputin’s Record store over there was my favorite haunt!
I used to go on a 4 mile walk every day around that area. That’s one of the things I miss the most about living out there.
Texas is okay – a big change from the Bay Area, but at least I finally was able to buy a house – something I would have never been able to do out there! I was living in those little apartments back there behind Kragen for 13 years!
Thanks Bobbi,
I will check the home page and see what information I can get to help. I truly appreciate the concern as the overall stress that comes along with facilitating can be overwhelming when your hormones are off. I am in contact with professionals on a regular basis…and have been looking for a support group in this area…but can not find one. As I find folks that are wanting to participate, I will also pay a professional counselor to facilitate the group.
Please feel confortable to provide me with any additional direction…..
Have a wonderful evening Bobbi…
Brenda
Bobbi wrote:The NGDF provides help for individuals who would like to start a support group, so you may find some information on the home page. NGDF also provides training before conferences. But I think they want folks who have gone through the disease, and are now healthy: it is not necessarily good for someone who is still in the throes of hormone imbalance and illness to take on the running of a support group.Thanks Cathycnm,
I do appreciate the information. I have put together some flyers and am posting them around the area….I will contact the newspapers and see if I can get an ad in the classified….thanks so much….I truly welcome all feedback.
I have been pushed into retirement due to the Graves….my background is Human Development/Counseling and Resource Development. I have worked in the field for over 30 years, 10 in the military and 24 in public education…..it has been difficult for me not to work…I think it has been one of the hardest part of the disease.
Thank you again for taking the time to share…….
Have a wonderful evening….
Brenda
cathycnm wrote:Brenda – Have you thought of writing the area endos a letter announcing your group. Then follow up with a flyer or cards that they could give to patients who had Graves.A couple years ago, I was ready to start a support group through the Osteoporosis Foundation. They send a manual on the process that those were the first steps. Then finding someone to donate space and identifying others who wanted to share the leadership responsibilities.
To be honest – I had a couple women who had started similar support groups say discouraging things. Not meaning to stop my efforts – just a good reality check into the amount of work it takes to start something like that here in this rural, western community. At that same time, my job was turning into more hours than I wanted and since I work in healthcare, it seemed maybe it was not going to create balance in my life to start that group. If there were 2 or 3 people willing to help – I would definately still like to do something like that. I say that not to discourage you – just to encourage you to get some others involved on the ground floor of getting it started. The endos may know of others who have had interest in starting groups, too. Good luck – what a gift that would be for your community.
Hi Mickey,
Yes it is a small world. Grand Auto on Hesperian is now Kragen and Wheel Works….alot of changes here….
How do you like Texas?
Mickey65 wrote:Wow, what a small world!I used to live in San Lorenzo, CA. I moved to Texas 3 years ago from there. I used to live on Albion, right behind the Grand Auto on Lewelling & Hesperian. I miss it!
in reply to: just need to talk #1074638Hi Punkin,
I can really relate to your situation. The emotional rollercoaster is really frustrating and it has totally affected my life. I am a professional working in education for the past 24 years. Specifically, I worked with state and federal funded programs, developing resources, facilitating support groups, developing reporting systems and the list goes on. I was also a Union leader for 13 of these years….even though it took 3 years for the doctors to diagnois the disease, it seems like overnight my life changed and I was pushed into retirement because of the emotional rollercoaster…..
Relationships are difficult because at times I would just break out in tears and could not control them, it made people very unconfortable because they weren’t sure what to say to me or how to say it.
I did have the radiation treatment done in November 2007, I agreed because the doctors could not get my heart rate to slow down and was fearful that I was a heart attack waiting to happen…..
I am on thyroid meds today, but I also meditate once a day at least 1/2 hour, I walk on a treadmill at least 1/2 hour, I take a oil/ebzene salt bath once a day, I write and I meet with a counselor once a week to discuss my emotional ups and downs. These things seem to help me.
My doctors have told me that this disease is a 3 year bell. I am hoping I am on the down side….but it is only the first year for me since the diagnosis and treatment..
Please be patient with yourself…
Brenda
-
AuthorPosts