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#1 Sept. 8, 2012 08:58:54

snelsen
From: Seattle, Wa.
Registered: 2010-01-01
Posts: 1430
Profile  

Well, here goes!

To Angie,
I sent a PM to you, suggesting you post your own thread about your upcoming surgery. There is a lot of good advice and support on the forum. Several people have had a thyroidectomy in the recent past. Kimberly's suggestion is very helpful too, to use the search engine.
You'll read a lot about what to expect both before and after the surgery. So glad you are moving forward on this, so you can begin to get your life back. It is a long process, but it will work.
Your teenagers might appreciate reading about Graves' too. There are good references to explain what it is like, not only for the person who has it, but for the family members.
Shirley


TED 2008-present. OD for pressure on optic nerve 02/02/10
Eye muscle surgery 09/23/10 Upper eyelid surgery 02/01/11
Lower eyelids with grafts from palate, 10/5, 10/25/11
Graves dx/thyroidectomy 1959-Synthroid from 1980

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#2 Sept. 8, 2012 10:41:09

AzGravesGuy
From: Peoria, AZ
Registered: 2012-08-07
Posts: 95
Profile  

Well, here goes!

Glad to see you back Shirley!

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#3 Sept. 8, 2012 10:46:49

metalsrfr
Registered: 2012-09-04
Posts: 13
Profile  

Well, here goes!

Well I was MIA yesterday distracted by video games. My throat pain has seem to subsided, had problems sleeping last night tossed and turned to the wee hours of the morning. Feeling pretty good now still hot but it is around high 70's to low 80's out which is very welcome here in central texas. all windows open and enjoying the fresh air.

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#4 Sept. 9, 2012 18:35:40

AzGravesGuy
From: Peoria, AZ
Registered: 2012-08-07
Posts: 95
Profile  

Well, here goes!

Day 5.

I have to be honest, today was horrible. Something has changed hormone wise. I am no longer having severe hot flashes!

Instead today has been nothing but headaches, physical tremor, tinnitus, and a boat load of anxiety. I feel like I did 6 years ago untreated. Pulse is fast but not over 100. I feel like I want to crawl out of my skin.

Uncomfortable but not worried. Irritated for sure.


I cannot wait to see what tomorrow brings! Hopefully it will b something completely different.

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#5 Sept. 9, 2012 19:06:30

adenure
Registered: 2012-03-22
Posts: 442
Profile  

Well, here goes!

Hang in there! You're doing great- love your positive attitude!


Alexis

Homeschooling mom to 4 wonderful boys!
Diagnosed with Graves Disease after my 4th baby- March 2012
Started on 5 mg. of methimazole daily for 7 weeks
Euthyroid at the end of those 7 weeks, but had to stop methimazole as liver enzymes were 8 times normal range.
Total Thyroidectomy- 6/15/12
Started Synthroid (brand name) 100 mcg. 2nd day after surgery for 6 weeks (TSH: 6.35 & free T4 in upper range and T3 just under mid- range).
Upped Synthroid to 112 mcg. 7/27/12
Euthyroid as of 8/10/12 on 112 mcg. Synthroid (TSH .79 and free T4 in upper range).

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#6 Sept. 10, 2012 10:50:38

Kimberly
Online Facilitator
From: Phoenix, AZ
Registered: 2008-10-14
Posts: 2697
Profile  

Well, here goes!

Yes, hang in there! Hope that you are feeling some relief today, but if not, I would suggest calling the doc's office to see if they can give you some further direction. Take care!


Kimberly
GDATF Forum Facilitator

…through nature's inflexible grace, I'm learning to live…
– Dream Theater

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#7 Sept. 10, 2012 13:35:28

Carito71
Registered: 2012-06-25
Posts: 319
Profile  

Well, here goes!

Great post. I'm so glad you have had your treatment and even though you are not all well yet, I'm glad you are on the road to getting better.

Hope you feel better soon.
Caro


~ Fellow GD patient diagnosed June 2012 with a non-existent TSH, elevated fT3 and fT4, and a TSI of 4.5. On Methimazole 30mg/day for the first 8 weeks. On Methimazole 10mg/day for the next 6 weeks. On Methimazole 5mg/day for a week and a half. On Methimazole 5mg every 4 days for a month. On Methimazole 2.5mg/day starting Nov 15. Current labs show a normal fT4, a normal TSH, and a TSI of 3.2. Diet: Gluten and yeast free. Love to read and learn. Very interested in the immune part of GD ~

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#8 Sept. 10, 2012 14:59:17

AmyG
Registered: 2012-06-28
Posts: 16
Profile  

Well, here goes!

AzGravesGuy - I've been following your story mainly because I'm having RAI on Thursday 9/13 and wanted first second-hand experience and because your no BS approach and positivity are refreshing!

I'm 30 yrs old but feel like my body is at least that of a 50 year old with Graves (no offense to the older posters, I just picked an age). I was allergic to the 2 medications out there so RAI is my last stop to HopeVille.

Keep on posting! If I'm not feeling too out of sorts, I'll start my own thread so others can get as many perspectives of what to expect as possible.


Amy
Diagnosed June 27, 2012
Tried methimazole…allergic
Tried PTU…allergic
RAI treament September 13, 2012

“There is a crack in everything, that's how the light gets in.”

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#9 Sept. 10, 2012 16:00:27

spenanelson
Registered: 2008-11-06
Posts: 33
Profile  

Well, here goes!

Wishing you the best of luck with your journey! We have all been there and are here for you now.

Take care and keep posting.

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#10 Sept. 10, 2012 16:34:40

AzGravesGuy
From: Peoria, AZ
Registered: 2012-08-07
Posts: 95
Profile  

Well, here goes!

Day 6!

Today was a mixed bag. It started with eye pain and anxiety. By noon I was 100% normal. Now it is a lingering heat on my shoulders and ears….but that's it!

I feel good! The best I have felt in over a week.

Wednesday is day 8. I am going to the local cash lab to get my levels checked. I am just curious. My endo said 8 weeks. I have gone every 4 weeks so far this year for a free t3, free t4 and tsh. My reasoning has been that if I feel my hormones shift, waiting 2 months to get in to find out whats happening is foolish. With the monthly levels I have been able to chart the bell curve of my tsh & t3/t4 levels. It's a smile and a grimace on paper.

Thank you everyone for your encouragement and support. This forum greeted me with open arms and a wealth of information. Without everyone here and their collective experience, I would not have been able to come to terms with the RAI, but also the demons of Grave's.

My Grandmother had Grave's and was treated with radioactive seeds in the 80's . I was a kid then and remember seeing her suffer with the effects. This experience made the thought of RAI so scary I put it off for 6 years. It was recommended to me the day I was diagnosed in the ER. I laughed and swore it would never happen.

Today I am 6 days in and kicking myself for not doing it 6 years ago. The statistics that told me I am safe meant nothing. Coming to grips with the disease, reading the experiences of everyone before me…..that is where the fear ended.

Would I prefer not ingesting radioactive iodine? Of course! Who would willingly want to? But I have Grave's and it is destroying my body and mind. I see RAI as an empowerment against Grave's. I have made my stand. Grave's has fought back these last few days, and it gave a good fight.


Pretty sure I won.

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