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Chronic Fatigue in Pelvic Pain Disease - Endometriosis/IBD/Bladder Pain
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hidden
in
Endometriosis UK
2 years ago
Chronic Fatigue in Pelvic Pain Diseases - Endometriosis/IBD/Bladder Pain
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hidden
in
Pelvic Pain Support Network
2 years ago
Newbie here. My experience
Had Radioactive
iodine
therapy (RAI) after many years of ups and downs with Graves disease (hyperthyroidism). It's been almost four years since I've had RAI and I feel better being on this side of the battle (hypothyroidism).
Had Radioactive
iodine
therapy (RAI) after many years of ups and downs with Graves disease (hyperthyroidism). It's been almost four years since I've had RAI and I feel better being on this side of the battle (hypothyroidism).
Ellelove_postRAIgirl
in
Thyroid UK
2 years ago
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Deeply upset by A&E visit that was very unhelpful
Where are women supposed to go when they’re in agony with endo flare ups!? I went to my A&E at 4am last night and took 7 hours to see a doctor. I was having horrific pelvic pains, feeling very faint and nauseous and after having taken codeine at home I felt I was that desperate for help I had to go to
Where are women supposed to go when they’re in agony with endo flare ups!? I went to my A&E at 4am last night and took 7 hours to see a doctor. I was having horrific pelvic pains, feeling very faint and nauseous and after having taken codeine at home I felt I was that desperate for help I had to go to
Surfingblue
in
Endometriosis UK
2 years ago
Infection after Laparoscopy - really struggling
Hi everyone, this is my first time posting on here, and I hope that this is ok to share. Buckle up, it’s quite a long post. I had a laparoscopy that I paid for privately back in 2016. That diagnosed Endometriosis and Interstitial Cystitis, and recovery from the surgery actually felt very manageable
Hi everyone, this is my first time posting on here, and I hope that this is ok to share. Buckle up, it’s quite a long post. I had a laparoscopy that I paid for privately back in 2016. That diagnosed Endometriosis and Interstitial Cystitis, and recovery from the surgery actually felt very manageable
AlexB7
in
Endometriosis UK
2 years ago
Hyperthyroidism first appointment
First appointment with consultant and as my liver enzymes were raised, they are taking me off carb, done blood tests and said other options radio active
iodine
or surgery if liver still raised. Wouldn’t entertain the idea of the other medication when I mentioned it as it effects liver.
First appointment with consultant and as my liver enzymes were raised, they are taking me off carb, done blood tests and said other options radio active
iodine
or surgery if liver still raised. Wouldn’t entertain the idea of the other medication when I mentioned it as it effects liver.
SamB22
in
Thyroid UK
2 years ago
Could someone help advise what these skin growths/bumps would be? This might be quite long but any help would be great! :)
Hi all, I really hope somebody can advise me! Sorry if this is long. I've decided to finally post online and ask about this problem because I am getting nowhere with it with the GPs or the hospital (more on those later) So anyway, in August 2021, I noticed a red raised bump, looked similar to a spot
Hi all, I really hope somebody can advise me! Sorry if this is long. I've decided to finally post online and ask about this problem because I am getting nowhere with it with the GPs or the hospital (more on those later) So anyway, in August 2021, I noticed a red raised bump, looked similar to a spot
canaryfan86
in
MY SKIN
2 years ago
Cryo ablation report + 3weeks on (all OK!)
I felt some warmth on the left side of my chest (When I think
iodine
(for contrast) was administered (same as a CT. scan).
I felt some warmth on the left side of my chest (When I think
iodine
(for contrast) was administered (same as a CT. scan).
Towne
in
AF Association
2 years ago
Why is my TSH increasing?
I had my thyroid removed in Jan 2020 due to thyroid cancer and had RAI in June 2020. Since June 2020 my levothyroxine dose has stayed the same. My TSH has always been below range my levels are been suppressed due to cancer. My last blood test at GP surgery showed my TSH has increased to 0.43 from 0.22
I had my thyroid removed in Jan 2020 due to thyroid cancer and had RAI in June 2020. Since June 2020 my levothyroxine dose has stayed the same. My TSH has always been below range my levels are been suppressed due to cancer. My last blood test at GP surgery showed my TSH has increased to 0.43 from 0.22
marmitelover81
in
Thyroid UK
2 years ago
Advice is needed please on Latest labs
I'm talking kelp for low
Iodine
and have lowered my dose of Vitamin D My TSH was tested again yesterday and is now at 6. But I think there is still an error here as I feel ok. However, My FT4 & FT3 are still not converting. My TPO is down to 17 from 600 which is wonderful.
I'm talking kelp for low
Iodine
and have lowered my dose of Vitamin D My TSH was tested again yesterday and is now at 6. But I think there is still an error here as I feel ok. However, My FT4 & FT3 are still not converting. My TPO is down to 17 from 600 which is wonderful.
JannSimpson
in
Thyroid UK
2 years ago
Thyroid
I had to tale RAI twice . what happened
I had to tale RAI twice . what happened
indike
in
Thyroid UK
2 years ago
A and E Aaaaaaaaaaaaaaaaaaaagh.
Woke up at 5 am Sunday morning with severe pain under right shoulder blade which remained all day despite maxing out on paracetamol. In the evening I dug out some codeine tablets I had for sciatica last year and added those with similarly little improvement. Monday was more of the same except by now
Woke up at 5 am Sunday morning with severe pain under right shoulder blade which remained all day despite maxing out on paracetamol. In the evening I dug out some codeine tablets I had for sciatica last year and added those with similarly little improvement. Monday was more of the same except by now
BobD
Volunteer
in
AF Association
2 years ago
Blood test results,advice welcomed.
Hi, I have Graves disease and after having RAI in Feb have been on Levo(currently 100mcg).The only other medication I take is Proplanolol (2 x 40 mg) daily. I took the blood test at 9am,24 hours after any medication. I've been advised to contact my gp in the morning which I will do but am hoping for
Hi, I have Graves disease and after having RAI in Feb have been on Levo(currently 100mcg).The only other medication I take is Proplanolol (2 x 40 mg) daily. I took the blood test at 9am,24 hours after any medication. I've been advised to contact my gp in the morning which I will do but am hoping for
Robbo1972
in
Thyroid UK
2 years ago
My fight and my encouragement
I was diagnosed last year March with graves and I had the radiation
iodine
treatment. Now on the hermone replacement therapy and it's a up hill battle
I was diagnosed last year March with graves and I had the radiation
iodine
treatment. Now on the hermone replacement therapy and it's a up hill battle
Niraf21
in
Graves Disease Support
2 years ago
Pain - where my pain comes from! (2)
I used to visit, my GP for annual bloods, the results = nothing unusual all normal every single year on year. My visits to the GP were mainly due to the constant pain, nightmares and fatigue, we talked in the 15 minute allocated slot to determine my future! I have Pain surely I need pain killers? I
I used to visit, my GP for annual bloods, the results = nothing unusual all normal every single year on year. My visits to the GP were mainly due to the constant pain, nightmares and fatigue, we talked in the 15 minute allocated slot to determine my future! I have Pain surely I need pain killers? I
does-the-NHS-work
in
Fibromyalgia Action UK
2 years ago
Vitamin D causing tinnitus
This has only started since I had radio active
iodine
to ablat my thyroid and now on levothyroxine. My magnesium and potassium levels are high which I'm guessing is because of the meds.
This has only started since I had radio active
iodine
to ablat my thyroid and now on levothyroxine. My magnesium and potassium levels are high which I'm guessing is because of the meds.
Hookie01
in
Tinnitus UK
2 years ago
Iodine
I’m just about to order
iodine
from Amazon. Can anyone help with type, amounts needed etc. I can’t eat fish so struggle to get much
iodine
naturally.
I’m just about to order
iodine
from Amazon. Can anyone help with type, amounts needed etc. I can’t eat fish so struggle to get much
iodine
naturally.
Micharu
in
Thyroid UK
2 years ago
Pain support
good morning I am new to this forum. I am undergoing bloods, x-rays etc to see why I am in constant pain, but my Dr has said Osteoarthritis in my knees and possibly fibromyalgia. I have pain in my knees for approx 8 years and the rest of the pain around 2. There are days/nights where I cry in pain.
good morning I am new to this forum. I am undergoing bloods, x-rays etc to see why I am in constant pain, but my Dr has said Osteoarthritis in my knees and possibly fibromyalgia. I have pain in my knees for approx 8 years and the rest of the pain around 2. There are days/nights where I cry in pain.
French-bear
in
Fibromyalgia Action UK
2 years ago
Salivary Glands Swollen 6 Months Post RAI
Hi everyone and thanks for reading! I had RAI treatment in October of 2021. My dose was 100 mci. I immediately had swollen and painful salivary glands which subsided in a day or two. I have had no issues with them until the beginning of June. Now, they constantly swell when eating. Some days are worse
Hi everyone and thanks for reading! I had RAI treatment in October of 2021. My dose was 100 mci. I immediately had swollen and painful salivary glands which subsided in a day or two. I have had no issues with them until the beginning of June. Now, they constantly swell when eating. Some days are worse
PurpleButterfly7
in
Thyroid Cancer Support
2 years ago
Wife ready to give up on Thyroid Medication, bad reactions like allergic to something in it.
They ran a bunch of tests Scanned her brain but with no
iodine
because of reactions with
iodine
. EKG x-ray chest blood work. Nothing found. Just Thyroid numbers off slightly and it was only because we suggested testing for T-3 and T-4.
They ran a bunch of tests Scanned her brain but with no
iodine
because of reactions with
iodine
. EKG x-ray chest blood work. Nothing found. Just Thyroid numbers off slightly and it was only because we suggested testing for T-3 and T-4.
FredDemeter
in
Thyroid UK
2 years ago
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