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Intramuscular Depo Injection resulting in Flare From Hell 3 days later…..
…..anyone else? Excruciating pain from actual injection site after 3 days accompanied by worse flare I’ve ever had. Maybe tomorrow will be better? PS…first couple of days my awful spinal pain lessened, also inflammation in hands. This is just completely debilitating…..and after so many many months
…..anyone else? Excruciating pain from actual injection site after 3 days accompanied by worse flare I’ve ever had. Maybe tomorrow will be better? PS…first couple of days my awful spinal pain lessened, also inflammation in hands. This is just completely debilitating…..and after so many many months
CallMeSunny
in
NRAS
1 year ago
Posterior vitreous detachment
Yesterday feeling great for the first time in ages. Did yoga with no impact on shoulders and then a bit of weeding. Then in the evening I noticed quite a prominent floater. It was still here this morning and joined by a cloud of tiny floaters that were hardly visible. It felt wrong so I got an emergency
Yesterday feeling great for the first time in ages. Did yoga with no impact on shoulders and then a bit of weeding. Then in the evening I noticed quite a prominent floater. It was still here this morning and joined by a cloud of tiny floaters that were hardly visible. It felt wrong so I got an emergency
Viveka
in
PMRGCAuk
1 year ago
itchy eyes
Hi, I have itchy eyes on and off and wondered if it was to do with my thyroid or maybe an allergy. Any help would be much appreciated.
Hi, I have itchy eyes on and off and wondered if it was to do with my thyroid or maybe an allergy. Any help would be much appreciated.
suetatt68
in
Thyroid UK
1 year ago
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GCA Flareup
I hope someone can help me, as I feel like I've been thrown to the wolves and I don't know what to do. I am having a major flare up of PMR and GCA, I have blurred vision and head pains every day for the past 2 weeks but have been feeling awful since February. My body is so sore, plus Iam so tired all
I hope someone can help me, as I feel like I've been thrown to the wolves and I don't know what to do. I am having a major flare up of PMR and GCA, I have blurred vision and head pains every day for the past 2 weeks but have been feeling awful since February. My body is so sore, plus Iam so tired all
Sally001
in
PMRGCAuk
1 year ago
Glaucoma, prednisolone and anxiety supplements
Good morning all I am being treated for GCA and at the moment I’m on 20mg of of prednisilone, I am coping ok and trying to stay as healthy as possible, I already have glaucoma and sadly the steroids have pushed my eye pressure up, I saw my eye consultant yesterday, he is quite concerned, the operation
Good morning all I am being treated for GCA and at the moment I’m on 20mg of of prednisilone, I am coping ok and trying to stay as healthy as possible, I already have glaucoma and sadly the steroids have pushed my eye pressure up, I saw my eye consultant yesterday, he is quite concerned, the operation
Mumdadlove
in
PMRGCAuk
1 year ago
Has anyone had orbital decompression for graves eye disease?
Hi I have Graves eye disease and I am considering orbital decompression. I also have Graves. Will it leave scars? Will it cause numbness due to nerve damage on my face? I am told this is likely. I would like to hear from anyone who has had this surgery. Do you recommend? Thanks
Hi I have Graves eye disease and I am considering orbital decompression. I also have Graves. Will it leave scars? Will it cause numbness due to nerve damage on my face? I am told this is likely. I would like to hear from anyone who has had this surgery. Do you recommend? Thanks
Naples21
in
Thyroid UK
1 year ago
This looks interesting :) I know people with PTSD who have benefited from EMDR ...
... so hope it will be beneficial to p/w FND too :) https://doi.org/10.1136/bmjopen-2023-073727
... so hope it will be beneficial to p/w FND too :) https://doi.org/10.1136/bmjopen-2023-073727
210272
in
Functional Neurological Disorder - FND Hope
1 year ago
Short synathecen test
Hi i have m.e cfs used to be severe was in wheelchair and bedridden now able to walk doctor wants to synathecyn test because i have symptoms of congenital adrenal hyperplasia im scared of a relapse in the m.e and was wondering if there alternative blood test anyone with cfs have this test and what was
Hi i have m.e cfs used to be severe was in wheelchair and bedridden now able to walk doctor wants to synathecyn test because i have symptoms of congenital adrenal hyperplasia im scared of a relapse in the m.e and was wondering if there alternative blood test anyone with cfs have this test and what was
Ester467
in
Thyroid UK
1 year ago
Collagen
Hello all. I've been puzzled by one question for a while already... When looking to buy face cream for example I keep stumbling across wrinkle-reducing skin care products which promise great results through the use of added collagen. Having scleroderma, which is essentially an overproduction of collagen
Hello all. I've been puzzled by one question for a while already... When looking to buy face cream for example I keep stumbling across wrinkle-reducing skin care products which promise great results through the use of added collagen. Having scleroderma, which is essentially an overproduction of collagen
hunkyd0ry
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Dissociative seizures from PTSD
Hi this is my first post to this group. Ive recently been diagnosed with PTSD after seeing a specialist neuropsychiatrist for Non epileptic attack disorder. I was just wondering if there is anyone on here that also has this diagnosis? im really struggling to accept the PTSD diagnosis and the seizures
Hi this is my first post to this group. Ive recently been diagnosed with PTSD after seeing a specialist neuropsychiatrist for Non epileptic attack disorder. I was just wondering if there is anyone on here that also has this diagnosis? im really struggling to accept the PTSD diagnosis and the seizures
ChelseaBlue01
in
Heal My PTSD
1 year ago
WARNING: If you have FND and live in UK
Hi, If you live in UK and have FND you may wish to check your online medical record has not been incorrectly updated. I have had FND for over 12 years following a virus. When I was diagnosed 10 years ago, my consultant neurologist wrote a clear diagnosis letter, stating that I have a physical illness
Hi, If you live in UK and have FND you may wish to check your online medical record has not been incorrectly updated. I have had FND for over 12 years following a virus. When I was diagnosed 10 years ago, my consultant neurologist wrote a clear diagnosis letter, stating that I have a physical illness
sykgirl
in
Functional Neurological Disorder - FND Hope
1 year ago
Kindly suggest me what it is!!
Hi everyone, i have a question which is more like a concern. This is my recent OCT scan on 06/03/2023, as I'm diagnosed macular edema. And taken avastin injection in my eye. The central thickness was 219 (green part) and it remain same 219 after the inj, but the other swelling was reduced. Now my concern
Hi everyone, i have a question which is more like a concern. This is my recent OCT scan on 06/03/2023, as I'm diagnosed macular edema. And taken avastin injection in my eye. The central thickness was 219 (green part) and it remain same 219 after the inj, but the other swelling was reduced. Now my concern
iAdnanShah
in
Macular Society
1 year ago
help me please my ptsd
for years I’ve suffered from ptsd, I haven’t worked on it yet have been to therapy just never invested in it. Now it’s effecting my family and I’m tired of it I just want to learn the tools to use to cope with it because my family deserves better
for years I’ve suffered from ptsd, I haven’t worked on it yet have been to therapy just never invested in it. Now it’s effecting my family and I’m tired of it I just want to learn the tools to use to cope with it because my family deserves better
Zyalishawn
in
Heal My PTSD
1 year ago
filled with sadness and frustration
Taking a medication called roaccutane 20years ago has ruined my life. It has damaged my brain and i’ve been living with these awful side effects all through my 20s and 30s. I’m utterly fed up with chronic head pains, scorched sensations, cognitive problems, brain numbness/deadness, ringing in my head
Taking a medication called roaccutane 20years ago has ruined my life. It has damaged my brain and i’ve been living with these awful side effects all through my 20s and 30s. I’m utterly fed up with chronic head pains, scorched sensations, cognitive problems, brain numbness/deadness, ringing in my head
Dann2
in
Headway
1 year ago
I’m scared of treatment
Venetoclax and Obinutuzumab My Haematologist has suggested that I may need to start treatment with these drugs and Calquence. I’ve been on Watch & Wait since diagnosed in 2014 when WBC count was just above normal range. Now it’s about six times higher than normal range and my red cell count has gone
Venetoclax and Obinutuzumab My Haematologist has suggested that I may need to start treatment with these drugs and Calquence. I’ve been on Watch & Wait since diagnosed in 2014 when WBC count was just above normal range. Now it’s about six times higher than normal range and my red cell count has gone
tigerbeauty
in
CLL Support
1 year ago
Some advice in choosing the best blood tests to go for, please, as am becoming a bit bogged-down with choices!
1)
Starting results and start of treatment from my Bio March ’91-March ’93 – Under Care of [Dr] A, GP At HC1 From Mid ’84-End of March ‘94: a really good, all-round GP who was fully conversant with both my medical and personal history and treated patients in a truly collaborative, advocating on
1)
Starting results and start of treatment from my Bio March ’91-March ’93 – Under Care of [Dr] A, GP At HC1 From Mid ’84-End of March ‘94: a really good, all-round GP who was fully conversant with both my medical and personal history and treated patients in a truly collaborative, advocating on
PRJ20
in
Thyroid UK
1 year ago
cataract op for glaucoma
hi. Has anyone had a cataract operation to reduce eye pressure and did it work? I have not been able to use any eye drops for over a year as developed allergy to all. Laser only reduced pressure slightly. Was told optic nerve had deteriorated slightly over 5 years. As I am 75 I thought it would be ok
hi. Has anyone had a cataract operation to reduce eye pressure and did it work? I have not been able to use any eye drops for over a year as developed allergy to all. Laser only reduced pressure slightly. Was told optic nerve had deteriorated slightly over 5 years. As I am 75 I thought it would be ok
Islandhome
in
Glaucoma UK
1 year ago
Week 6 the down and the ups!!
Did Run 1 last Tuesday morning - went really well mainly because I was a bit wary after reading it catches people out after the glory of finishing Wk 5 Run 3. So I didn't get cocky and went bit slower and it was all lovely so was relieved that went well. Run 2 on Thursday morning was totally different
Did Run 1 last Tuesday morning - went really well mainly because I was a bit wary after reading it catches people out after the glory of finishing Wk 5 Run 3. So I didn't get cocky and went bit slower and it was all lovely so was relieved that went well. Run 2 on Thursday morning was totally different
Dancerunner
in
Couch to 5K
1 year ago
I will eat my diploma
4 years studying psychology through pandemics, wars, terrorism, earthquakes, family abuse, zombie apocalypse and an alien invasion to recieve full A on my final exam and a handshake from the head of the psychology department of the second best university in Bulgaria just for my grandmother to tell me
4 years studying psychology through pandemics, wars, terrorism, earthquakes, family abuse, zombie apocalypse and an alien invasion to recieve full A on my final exam and a handshake from the head of the psychology department of the second best university in Bulgaria just for my grandmother to tell me
Against_the_current
in
Anxiety and Depression Support
1 year ago
Hashimotos double vision
Hello everyone. Just wondering if anyone else here has experienced double vision with Hashimoto's ? I have been feeling tired, heavy, low mood, brain fog, memory problems etc. I went to my optician for a routine check up 3 weeks ago and the letters on the chart were swimming around in a way I'd never
Hello everyone. Just wondering if anyone else here has experienced double vision with Hashimoto's ? I have been feeling tired, heavy, low mood, brain fog, memory problems etc. I went to my optician for a routine check up 3 weeks ago and the letters on the chart were swimming around in a way I'd never
Girtonian
in
Thyroid UK
1 year ago
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