Skin

I would love to hear if anyone has experienced similar symptoms or may know what could be causing these.

Key symptoms: faint, subtle outline marks (ie more like a hollow ring, than a filled in disc), pigment coloured, flat not raised, hard to see, which tend to appear after I get an itchy, prickly, burning, sensitisation in a specific spot, followed by a spreading heat sensation, like something blooming on the skin, in that spot. My face and neck are most affected, but I get these point specific sensations head to toe. I also get more generalised persistent itching, burning and pain, as well as pins and needles in hands and feet. Altogether the symptoms, the pain and the lack of effective treatment have been really distressing and have impacted on my quality of life.

It started over 3 months ago. My son developed this first, and was visually diagnosed by GP with tinea, a fungal skin infection. I got it next, and was diagnosed by GP, visually and based an my son, with tinea, however topical and oral antifungals did not help, and the symptoms /progression were not typical of a tinea infection - spread head to toe in a few days, not red or raised or flakey skin, just flat pigment coloured marks, of assorted oval or roundish shapes. My partner got it next. We all had the marks and itchiness, but I am the only one to experience persistent burning, heat and ongoing pain, and many itchy marks still popping up. Two dermatologists found no sign of fungal infection (2 and 4 weeks in) and a third dermatologist described the set of symptoms as unusual, they don’t fit with any common conditions, and the marks are barely visible (and don’t photograph well), while the sensations are significant.

My son and partner get the occasional mark still pop up, but thank goodness, it is only mildly itchy for them. When symptoms started no testing was done, a subsequent skin swab 2 months in and blood tests have not shown anything. Oral antihistamines, and topical and oral corticosteroids also made not impact.

If you have any ideas of what might be causing this, I would love to hear from you!

#Undiagnosed #Skin #itchy #Burning #faint

#Skin picking has a hold on me

#Autism #ADD #PDA #HEDS #Anxiety #Skin Picking disorder #Isolation #parental shame
#chronic Illness

I am so worried about my 5 year old daughter. She will be 6 in November, and is on the autism pathway waiting for assessment. Potentially she has PDA, ADD and a genetic disorder I have called hEDS. She has only recently gone full time at school but they still won’t let her finish at the same time as her peers and I have to pick her up early from the office. Her school friends often overtake her home though, as she walks slow. Often her friends go to the park together or have arranged play dates. They are almost always in pairs. Other parents barely talk to me, let alone arrange play dates. I know my daughter has been feeling increasingly isolated.
Yesterday I picked up my daughter from school and she was already feeling very sensitive, she was crying and fed up. She was passed by several friends talking about their play dates they had arranged. She wanted to go to the park, I also had my 3.5 year old son in a pushchair (he potentially has ADHD and also wanted to go to the park) but it was 30 degrees and I worried it was too hot, and she had already started crying and getting upset. (Of course other parents didn’t care about this). All of this resulted in a full on breakdown of epic proportions. She was so upset and so overwhelmed she struggled with her breath, she couldn’t stop panic crying. Other parents overtook us on the way home and said nothing, didn’t ask if she was ok. My daughter is well-loved at school even though she is very quirky and I find this behaviour from other parents so isolating. I honestly feel so alone sometimes.

We got home and the continuous crying continued for about an hour. She wouldn’t let me touch her. She then proceeded to bite her fingers until they bled. She has been biting her fingers for about 10 months now, since she started reception year. She now has lumps on her fingers caused by scar tissue and infections. I am taking her to the nurse today, thinking she will get diagnosed with skin picking disorder (we are UK). Not sure how much they will do to help her as they continue trying to blame my parenting. I have done 6 parenting courses. Parenting SEND children is honestly so difficult, so thankless and no one helps you.

I am wondering what is going on at school and why she leaves so sensitive. I wonder if it is a build up of trying to fit in over the day and masking. I worry she is being bullied by a couple of kids also (she tells me she was pushed at one point and called a baby by one boy). Also I think the isolation she feels from leaving at different times and being unable to make those connections is finally getting to her. It upsets me so much to see her like this. I have chronic illness (hEDS, fibromyalgia and a blood clotting disorder). Last week I was in hospital with a ruptured ovarian cyst, today I have the migraine from hell (I get bad pain, nausea, aura, blurred vision and unusual smells) and I feel like I can barely walk. Hubby is at work, I have no family near to help. I have to get my daughter into school with my 3 year old in tow. She doesn’t really want to go. Her attendance is already very poor (less than 60%). We are awaiting an EHCP assessment.

I just feel so alone with it all. I am struggling with my own health, my children’s extra needs. How do I calm my daughter’s anxiety? How do I make my GP give us extra help? I have considered taking her out of school and homeschooling her but I feel I am not well enough or capable of that. I am worried about her biting her fingers and causing herself serious infection as her fingers look so scarred and awful and her hygiene is not good (she impulsively touches herself down below and always plays in dirt) and I am forever trying to get her to wash her hands and nails.
My anxiety is through the roof. Just looking for support really also as in very short supply from other parent/carers from her school.

My thumbs and forefingers are severely dry. Nothing works to heal.
#dry skin, #Sarcoidosis , #chronic pain,# fibromyalgia #Skin issues

First diagnosed with Pulmonary Sarcoidosis im 1982 then it went into a remission of sorts, skin Sarcoidosis with ulcers and eye involvement with Sarcoidosis within past 10 yrs.
#chronic pain,#Arthritis ,
#Skin Sarcoidosis,#eye Sarcoidosis,
# Rare Disease,#Sarcoidosis

So I “went” to the doctors about a suspicious mole. He consulted another doc after I sent a photo and then wanted yet another photo . He said they agreed it was best to send photos on to the dermatology dept. At the hospital. But said he didn’t know what the timeline would be as the Coronavirus is affecting hospitals etc so much. Anyone have any idea of the normal timeline for dermatology to get back to you about a mole? Or even wait times generally for dermatology? Thank you! #Moles #Skin #SkinCancer #Doctor #Hospital #NHS #Referrals #Anxiety #Insomnia #Advice #help