Experiences with

Sodium cromoglicate

I have MCAS and POTS (as well as autoimmune, ME/CFS, histamine intolerance and a raft of other conditions) and recently started on sodium cromoglicate. The outcome has been almost miraculous - the first medication of my many that seems to have had any real effect.

I use sodium cromoglicate drops but again they don’t help much. Sorry for rant but know you understand the struggles On the plus side chest has been good am on spiriva & relvar. Thanks in advance 😊

Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand

Can anyone share their experience getting Intal inhaler since it has been delisted in the UK? Or, do you now take it via a nebulizer instead? If yes, can you share the name of the nebulizer device and the manufacturer of the cromolyn/chromoglycate solution? Pubmed indicates it's less effective than

i have just posted this on pa site, but would also be grateful for any input from those on here who have already got their heads round how to deal with B12 deficiency / low folate / ferritin hi all , i normally hang around on thyroiduk forum as i have autoimmune hypo. My daughter has asked if you

hi all , i normally hang around on thyroiduk forum as i have autoimmune hypo. My daughter has asked if you guys would cast an eye over these results , as you know much more than me about b12 issues . She's 26 , has just been prescribed eod b12 injections due to the following bloods/ symptoms .

I’m a 59 year old woman suffering with Hashimoto Thyroiditis, Fibromyalgia, osteoarthritis and osteoporosis. At my wits end regarding pain and exhaustion. Taking ‘Super B complex with calcium’ and vit DK2 spray daily. Meds prescribed incl: 100g ‘Accord’ levothyroxine ,50mg diclofenac sodium, 15mg lansoprazole

I have low sodium levels but also have water retention which is driving nuts . I can put on 4lb in a day and then it's gone a day or to later. My legs swell I can put up with the pain been in pain my whole life with a rare hereditary neurological condition . It's how tight the skin gets on my legs that

Hello, So after my last blood tests which showed a suppressed TSH and far from optimal T3 and T4 with ongoing symptoms for years, I finally decided to go to a private doctor. After much to’ing and fro’ing with my NHS GP, they finally gave it to me straight, ‘we do not prescribe T3 medication and if

Here I am again asking about availability of liquid thyroxine. I have a wonderful traditional pharmacy now who try really hard for me, however, this time they can only get Zentiva - and I am always noticeably less well on that. I dread having to take it. In fact, I have previously done a Yellow Card

just wondering if any cirrhosis patients suffered from low sodium and high iron levels. Are these levels really bad news for mortality.

Just before Christmas I was in hospital twice. I had a shortage of sodium and had two falls. My doctor was not happy about the sodium though. When I came home I found I had been given this but not a word said about it. I found out it was intended to replace my Omeprazole which I had taken on and off

hey guys. just signed up to this form so i don't really know anything. don't even know where i'm writing to or if i'm making a new post, but that's ok for now. i'll probably get there:) apparently decided to have stage 4 liver cancer about 5-6 months ago. seems like a pretty good hospital, pretty

Hi, My dad is currently in hospital (went in with HE and has been in for pretty much 23 weeks now). He is declining and has End Stage Liver Disease. He is 79. On Friday he had 6litres of fluid drained from his stomach. He was mentally ok before this, no signs of HE but low sodium (127). I was shocked

As I put in my last communication, I now have the results of my blood tests, and need a bit of help with interpretation. My CRP is up to 35, which is way too high for me, as my normal is about 10-12. So I guess 2.5mg will need to be increased. My ESR wasn't done this time, but was 10 on the 20th November

I have had this condition since 1993, ablation in 2019 a good partial success as I still have MAT which could not be ablated and is now kept in check by lifestyle and low (1.5) dose of Bisoopropolol. In this time I have tried with very limited success to establish if it can be cured or at least managed

My husband is now down to 9 eGFR. In the UK they start dialysis as late as possible. I’m not sure why. I assumed at first that it was about money, as it sometimes in with our medical service, which is free to everyone. Then I thought it was because his test results were still good, so it’s wise to delay

I just had nephrectomy and now have an egfr between 49 and 54. I was just told preop that remaining kidney would compensate but not told it frequently didn’t happen in older group, I am 68 and preop egfr was 80. I read about farxiga to prolong kidney function. When do doctors recommend? Is there any

Hi Not sure if anyone else is aware of this. I have high blood pressure - well controlled with exercise, diet and amlodipine 5mg. Regular readings are circa 110/70 I also have SVT and try (normally successfully) to drink a minimum of 2 litres a day. I do this with sugar free lime cordial diluted

As today result my egfr is 44 Creatinine is 137 Uric acid 420 But I have taking some supplement with farmacyst helping like for pre dialysis milk Last few month my egfr was 50 after drink this milk have shoot up to 78 and then suddenly now drop to 44 I have no idea about it my potassium hemoglobin sodium