I have recently been experiencing symptoms of raynaud's so I'm wondering if there's any link.
Last check all my thyroid numbers were good and been feeling good with that.
My thyroid antibodies were in the normal range when diagnosed, so not sure if that means mine is not autoimmune or if Raynaud's is auto immune?
i had 2 cold nodules in my thyroid and had a total Thyroid lobectomy on 16 sep (8 days ago) and still waiting for the results if the they were benign or malignant so that i start take the hormone replacement in case if benign or start to go into 6 weeks hypo in preparation for the RAI treatment in case if malignant problem is, i fear the result will take more days to finish, and my body is completely without thyroxine now if benign than this wait & deprivation was pointless, and i fear i will need many weeks to fix the damage the hyop state will impose on me so my question is, when will the hypo symptoms start to show in my case (no thyroid at all) ? considering my TSH levels were normal at 2 before the surgery i'm feeling really anxious about this whole thing, and i need your knowledge, i can't even get in touch with my doctor before tomorrow.
View 1 RepliesI have had intense pain in my right kidney area, but kidneys show as clear on ct scan. But I have a 6.5cm ovarian cyst on the other side. Has anyone had anything similar as going out of my mind with the frustration of getting it treated. Should see a gynaecologist within a fortnight
View 1 RepliesI was told by the eye doctor this week that I have a rare fast growing cataract in both eyes. He told me that it can be caused by taking steroids, but I haven't taken them or breast cancer. Just interested in knowing if I should schedule an appointment for a mammogram right away. I did have a mammogram in 12-07 and they felt I should have a ultrasound to look closer at a spot. They thought it was probably just breast tissue after that and I haven't gone back. How important would it be to have the mammogram soon. Thank you, Jacqueline
View 1 RepliesUsually people with hypo are cold but I'm always hot & sweaty even when the temp is chilly. I'm 37, have PCOS and hypothyroid. Since having kids I've gained a lot of weight and can't lose a pound no matter what I do. I'm on Synthroid but I feel like nothing helps.
View 1 RepliesHello All- I have so many symptoms of hypothyroidism and my mother and grandma are as well so I asked my Dr. to test me. She said everything came out perfect, but I still have so many true Hypo symtoms after doing some research on here. Can anybody tell me how normal these ranges are:
TSH- 2.16 (0.3-5.0)
FT3- 3.2 (2.3-4.2)
FT4- 1.02 (0.8-1.8)
Vitamin D- 18
I've been told I have post surgical hypothyroidism (left side, 2010) but TSH is consistently low (0.1) or low normal (.396), I don't understand the hypothyroid diagnosis with a low TSH. Can someone explain? I also had left temporal lobe brain tumors (cancerous) and gamma knife radiation. Could this be affecting the TSH level. I have many hypothyroid symptoms, basal body temp is on avg. 96.5, weight gain, tiredness/fatigue....blah, blah, blah. My endo doesn't do too much. Currently taking 50ug of levothyroxine 6 days/week and feel horrible. There are also 3 nodules in the right side now that continue to enlarge. Any answers? Thanks.
View 2 RepliesHas anyone heard of a special hypothyroid diet?
I would be grateful for any information please as to what foodstuffs to avoid and which ones would help.
Gas anyone heard of any medications that can cause or worsen hypothyroidism?
Many thanks
Jean x
I have hypothyroid and am taking 175 mcg of thyroxine everyday. I eat low fat diet and exercise regularly. But still my cholesterol levels are rising especially triglycerides.
Is there a connection between them? My blood reports show that my thyroid levels are normal with the current medication. Then why is my Cholesterol increasing?
What measures should I take to stop this?
hi, my gf is under treatment for PCOS and hypoThyroid and take Harmoni - F (Cyproterone Acetate, Ethinylestradiol & Folic Acid) and Femella tablets from a week. We had sex last night with protection (condom) i ejaculated outside but i found that the condom was punctured with 4-5 holes . will she get pregnant? Should she take any contraceptive pills to avoid pregnancy?
View 1 RepliesI've been hypothyroid for a long time. I've been taking Synthroid also a long time. I'm confused by my recent blood test. My TSH was 1.180 within normal range and my Thyroxine free 1.81 . The range should be 0.93-1.70. What does this mean. I'm I hypothyroid or hyperthyroid?
View 8 RepliesWondering if anyone has Hashimoto's disease? I saw a specialist a couple of weeks ago who told me I most likely have this. I went from extreme hyperthyroid to hypothyroid. Skinny and energetic to sluggish and heavy. I'm pretty miserable with it. I've just been sent a letter with my levels:
8 May - TSH .03, free T4 29.3, WBC count 5.1
15 June - TSH 15.95, free T4 9.9
6 July - TSH 12.38, free T4 8.3
I was diagnosed with Hashimoto's postpartum about a year ago. I was complaining of excessive fatigue/inability to return to running, and pretty bad carpal tunnel. At the time my TSH was 6.893 and Free T3 282.1 pg/dL [230-420] and of course high antibodies. My primary care put me on NatureThroid 32.5mg (25 mcg T4/T3). I felt better within the week and my carpal tunnel completely resolved in about 2 weeks. I felt great on this for a year. I had my TSH tested once during this time and it came to 2.785. I trained for a 50 mile race, including hard training with back to back long runs on the weekend. I then started training for a marathon in January with a goal time of 3:15-3:20. I was training hard but felt great. I did a half marathon March 20th at a 7:04min/mile pace. I felt on top of the world and was on track to run what I had termed my "comeback marathon". The next week I still felt good, but then the following week I came down with a minor respiratory tract infection. I was completely better in 3 days and just thought it was a small blip. I went out for a long run that weekend and felt good for the first 6 miles, and then got progressively worse and felt like I had no energy, completely flat, defeated. It was not normal but I just chalked it up to a bad run. The following week, I had a strange inexplicable flair of wrist pain/carpal tunnel for about 3 days, but then that resolved, so again I kind of dismissed it. I was able to do my weekly workouts and hit my paces although they did feel a little bit harder than normal. But every time I tried to do a long run, I crashed after just a few miles and finished feeling like complete crap. I started to get worried about my race but again just figured I needed a good taper and I would feel better. Well, my race came it was one of the worst experiences of my life. I ran the first half at my goal pace but after 8-10 miles I started feeling sort of ill, dizzy, and had no energy. Again, I have run several marathons and have had bad marathons, and this was above and beyond anything I'd ever felt. I am not prone to cramping, and by the end I could barely walk and my muscles were just spasming uncontrollably.
Ok, fast forward to the following week. The next day I called my doctor and moved my 6 month follow-up to the next week, and got blood work done (unfortunately he only tested my TSH). That week, I developed progressively worse carpal tunnel. I decided to double up on my thyroid dose, and after a few days of that, I then tripled it (so now I was taking 97.5mg (75 mcg T4/T3). I felt fine energy-wise (although was not running), but still had carpal tunnel. Then I went in to see my doctor. My TSH came to 2.94. He saw that and said my symptoms were probably not thyroid-related but that we could increase my dose by 16.25mg to see if that would help (I knew it wouldn't because I was already taking more than that but I didn't want to say that, and I started second-guessing myself that I was hypo). So I dropped my dose down to 65 mg, then back to 32.5mg. Well a few days later my carpal tunnel got so bad I was waking up in excruciating pain even wearing my braces. I was having shoulder impingement pain as well. I couldn't use my right arm in the morning for 30 mins after waking. I called my doctor asking for further testing and for him to test my free Ts. I did that bloodwork and it came out to TSH 2.58, free T4 0.71 ng/dL [0.6-1.6], free T3 3.59 pg/mL [2.39-6.79]. Seeing that my T4 was on the low end and T3 not super high, I figured that confirmed I was having hypo symptoms, even though they were technically within normal. So I started taking the 97.5mg dose of thyroid again. That weekend I upped my dose, I still felt terrible. I had a horrible run, couldn't move after, my whole body ached, and by Saturday evening I couldn't lift my right arm due to the shoulder impingement. I felt the same Sunday. But Monday (day of three of higher dose), I was SO much better.
Well my doctor looked at my results on Wednesday and said, "Your T3 is excellent." When I protested, he said rather condescendingly, "I've been doing this 30 years." Mind you, he's not an endo, he's a naturopath MD. I argued with him until he agreed to up my dose to 81.25mg. I knew this would not eliminate my musculoskeletal issues, but figured it was at least a move in the right direction. (note: he also tested for RA antibodies and sed rate and that was normal, and I don't have any joint tenderness)
I've still been taking 97.5mg dose this week, but won't be able to continue this once I run out of the extra Rxs from dosage changes. Still have carpal tunnel and morning stiffness, but my arm got better throughout the week, and then Thursday, I had a great run. However, today (Friday), I suddenly developed this shoulder impingement really bad again where I can't lift my arm. I'm thinking somehow running is triggering it, but I've never had a shoulder problem before.
Ok, so now for my question. I cannot think of any possible thing this could be other than hypothyroidism. I've scoured the internet and scientific papers for anything at all. But I'm just confused by how suddenly my symptoms worsened, and how my levels are not super low, but even tripling my dose hasn't completely alleviated my symptoms when I was great on a low dose for a year. I'm seeing a new primary care soon and am going to make an appt with an endo instead of continuing to see my current doctor who I'm really p*ssed with. But this will all take time (the endo I'm planning on takes months to get into), and I'm just curious if anyone has any insight into this or has experienced something similar. I'm nervous that I'm going to have to drop down to 81.25mg again and that I'm just going to be miserable, and that when we test my levels again they will be higher, but that I will still be having symptoms, and so my doctor will not listen to me. I know people say that it takes time to have symptom relief with dosage changes, but in my experience it seems like it happens very quickly. Like when I first started on the NatureThroid, I was almost completely better in a week. Is it normal to feel changes so quickly? And does anyone have experience with exercise worsening symptoms - like maybe free Ts are lowish and then exercise is an added stress that sort of depletes the body if it's not able to compensate with normal thyroid function? I'm not completely sure of the biochemistry (I don't know that anyone is actually), so I'm just kind of postulating.
I am 14 nearly 15 years old and for as long as I can remember i have had this problem and my father also has the same problem but I seem to have it on a much larger scale.
My feet do not warm up naturally, even in bed at night they are freezing cold and if it is cold outside my feet are purple and I have very blotchy looking skin on them and my hands, when they are like this they look like the feet of a dead person.
Also, when it is cold, my hands go white, purple, and then bright red. They are numb during this and when they become bright red, my fingers swell slightly and it looks like they are about to burst. Also at this point, if I touch my hands or fingers together, they will sting and the pain is unbearable, it feels like stepping into a hot bath after being in the snow all day, but 10x worse.
I haven't yet been to see a doctor although I know I probably should. The problem with my hands doesn't affect me unless it is unusually cold, mostly during the winter and the problem with my feet is constant, during all weather and all seasons. I have had multiple friends and family members say it could be circulatory problems but I am yet to know for certain
I have the SLE-Raynaud's-Sjogren's package of auto-immune illness (listed in the order of diagnosis). The Sjogren's is the latest and most burdensome flavor of the decade for me. I was diagnosed with it about 3 years ago but was probably suffering from it for several years prior before the symptoms persisted enough to result in a diagnosis. I guess that's typical. It was with the SLE and the Raynaud's.
I can't imagine it could get any worse, but I get the impression that I might be "early" in the cycle and that scares me. No tears, corneal erosions, no spit, heroic (expensive and painful) dental treatments to save teeth that may already be doomed, pain, fatigue. Little annoyances that by themselves are "nothing" all together its a spirit crusher. Can it possibly get worse?
I was diagnosed with raynaud's back in 2010, but have suffered for about 7 yrs - I'm currently 36. I suffer with typical raynaud's in my hands & feet, they get cold whether it's been outdoors to walking in the fridge isle of a supermarket to holding cold cutlery and now even when I get out of the bath/shower. Back in 2010 my bloods tested positive for the antinuclear factor, so it suggested I had a connective tissue disorder, but with no other symptoms other than raynaud's was left as that. However, I've recently started getting pain in my finger joints - the pain is unrelated to when I have a raynaud's attack. I've been referred for further bloods & X-rays. Anyone else suffer with secondary or similar to my symptoms?
View 2 RepliesI have trouble writing, cooking, even sleeping and living a normal life generally due to my cold hands.
Has anyone found and eventually bought any gloves that helped hands get warmer and be able to work with them on as well?
I am a student and I have great trouble to do my work.
Let me introduce myself as a 57 year old male living in Minnesota. We are currently experiencing one of the longest sub-zero cold spells in my memory. 55 days below zero degrees F already this winter. Yes it is very COLD.
Twenty five years ago, in my early 30's, my fingers began blanching white while carrying items during summertime. I was frightened when several visits to the doc hadn't helped. Carpal tunnel syndrome was ruled out. At that point a neurologist asked if I was a smoker. Yes I was, two pack-a-day. He looked at me very pointedly and told me I'd better quit smoking ASAP. I was crushed, I had tried many times to quit cigs to no avail. I looked down at my white fingertips and bluish toes and decided to quit then and there. That was my last cigarette. Sept 1989. Miraculously, I never saw a white finger tip or blue toe again.
Twenty five years later my left hand has been suddenly reminding me that there is still an issue. Two or three fingers remain cooler than the others and will empty of blood when carrying parcels, or squeezed. Slowly the pink returns. I do not smoke. Hopefully that will keep the symptoms limited.
Someone had posted that what affected you in youth is probably gonna come back to haunt you later in life.
Young people with raynaud's; Quit smoking! Don't move to arctic climates, either.
I had an ultrasound today and it says that there is "a homogeneous appearance to the echotexture of the thyroid gland. Bilateral thyroid nodules are observed. There is evidence of a complex cystic and solid lower pole right thyroid nodule measuring 1.8 x 1.0 x 0.9 cm. Within the left thyroid lobe there is evidence of a hypoechoic midpole left thyroid nodule measuring 0.6 x 0.4 x 0.7 cm. Bilateral thyroid nodules. Dominant nodule is a complex cystic and solid lower pole right thyroid nodule measuring up to 1.8 cm. what does this mean?
View 1 RepliesIs there anyone who has both these conditions? And if yes, do they flare at the same time?
I have had raynaud's since a child (am now 57). I think erythromelalgia has been gradually getting worse since perimenopause began in the early '90s.
But only over recent years has this gradually gotten so bad that I'm relatively lame and housebound
My feet, hands and face are affected. The feet are worst. The NHS rheumy tried my on low dose vasodilator which had to stop cause it made all my symptoms much worse, apparently permanently.
When both conditions flare together my feet are sort of the colour of raw meat. This has been happening daily for nearly 1 year.
The erythromelalgia association website is v helpful, but even on the raynaud's & scleroderma org website it's hard to find anyone with EM, let alone both EM & RP.
If you are out there and have any tips for how to manage these 2 conditions.
I read on the RSA website that Magnesium supplements may be useful in Raynaud's. Anyone got experience of using it, and how much to take?
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