Hello I was diagnosed with Dermatomyositis in 2018 and still believe I’m not receiving the right care. I am in hopes to connect with others who can maybe give me some type of hope that there’s Doctors who actually know how to treat my condition.
Dermatomyositis : Hello I was diagnosed with... - Myositis UK
Dermatomyositis
Hi Lucy 4, Dermatomyositis is quite a difficult condition for Medical Staff to diagnose. It took several visits to see a GP, it was eventually after 6 months, my symptoms where getting far worse. They originally put it down to an allergy of some sort. However, I reached the stage where I could not dress myself. Going to work full time left me just about ready to collapse. Eventually, the GP put me on a Waiting List to see a Dermatologist. I was sooooo happy to see a Dermatologist that could actually tell me what was wrong with me. He brought in another Consultant Dermatologist to confirm his findings as this condition is quite rare. You must see a Dermatologist, they can take Skin and Muscles Biopsies to back up their findings. I am still struggling with this disease as it is very active. I also see a Rheumatologist & Neurologist on a regular basis to control my condition.
I am currently on Presnisolene (Steroids) Mycophenolate Mofetil (Auto Immune Suppressant), Adcal-D3 ( Bone Med), Fexofenadone, Atarax, Atentolol, Omeprazole and steroid creams and steroid Scalp Lotion (these meds mayy have a different drug name is the USA)!
Have undergone various types of Scans.
I hope you get the right treatment and are soon on the path to recovery back to having a normal life.
Wishing you all the luck in the world.
Hopegalore20 x
Hello can I ask what the scalp lotion is for? I don't have a rash (I think) but the top of my head is sore on one side. It's different to a headache in that it is surface soreness - if that makes sense.
Hi Periwinkle62, re your question raised on the use of Steroid Scalp Lotion. The name of the lotion that I am currently using is:Elocon.
I use this particular med due to the severe itch and heat suffered all over my Scalp. The lotion does give me relief. But as like most drugs, there are side affects, the lotion will thin the skin. However, I could not live without it. There is also pain with the itch/heat, but the itch is the main issue, you just feel like screaming.
I hope you have a good Doctor who is well versed in Dermatomyositis as each patient with this condition is affected in many different ways.
Take Care All.
Hi Lucy,
I recently opened a Facebook account not in my real name. There’s a page on there which is quite active. X
Hi Lucy
Like you, I took a while to be diagnosed and I would say my then GP was rather more hinderous than helpful and I was eventually diagnosed by a dermatologist. I’ve had DM for nearly thirty years now and enjoy taking similar meds to Hopegalore. I feel it’s trying to find and keep the balance to stay well. I do remember my early days of diagnosis as a nightmare so would be happy to meet you, if easy enough, to have a proper chat to help you through it. I live in north London. Failing that, maybe a phone call. Let me know.
Take care.
Diane
Hello , I would absolutely love to chat more. I don’t think I can make it to London so a phone call is nice.
Hello Lucy. Sorry, I’ve not rechecked this site for your reply as I don’t use it that often. I sort of expected an alert via the site. Anyway, here’s my phone number 07946 332908, so let’s have a chat soon. I’m fairly free this weekend
Take care
Diane